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Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting

Pembrolizumab With or Without Vismodegib in Treating Metastatic or Unresectable Basal Cell Skin Cancer

This phase 1/2 trial studies how well pembrolizumab with or without vismodegib works in treating patients with skin basal cell cancer that has spread to other places in the body or cannot be removed by surgery. Monoclonal antibodies, such as pembrolizumab, are checkpoint inhibitors that stimulate immune response. Vismodegib may stop the growth of tumor cells by blocking signals needed for cell growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Anne Chang

Collaborator: National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Biological: Pembrolizumab
  • Drug: Vismodegib

Phase:

Phase 1/Phase 2

Eligibility


INCLUSION CRITERIA

   - Histologically-proven basal cell carcinoma (BCC) in which curative resection is
   unlikely without significant morbidity, or have nodal or distantly metastatic disease
   which has progressed on vismodegib (ARM 1) or has achieved partial response or stable
   disease on smoothened inhibitor (ARM 2). Individuals who are intolerant or have a
   medical contra-indication to smoothened inhibitor will be enrolled into ARM 1.

   - Have measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST)
   version 1.1.

   - ≥ 18 years of age on day of consent.

   - Willing to provide tissue from a core or excisional biopsy of a tumor lesion up to 6
   weeks (42 days) prior to initiation of treatment on Day 1, or availability of adequate
   archival specimens.

   - Eastern Cooperative Oncology Group (ECOG) Performance Status = 0 or 1

   - Absolute neutrophil count (ANC) ≥ 1,500/mcL

   - Platelets ≥ 100,000/mcL

   - Hemoglobin ≥ 9 g/dL, or ≥ 5.6 mmol/L, without transfusion or EPO dependency (within 7
   days of assessment)

   - Serum creatinine ≤ 1.5 x upper limit of normal (ULN) OR measured or calculated
   creatinine clearance ≥ 60 mL/min for subject(s) with creatinine levels > 1.5 x ULN

   - Serum total bilirubin ≤ 1.5 x ULN OR direct bilirubin ≤ ULN for subjects with total
   bilirubin levels > 1.5 x ULN

   - Aspartate aminotransferase (AST) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - alanine aminotransferase (ALT) ≤ 2.5 x ULN, OR ≤ 5 x ULN for subjects with liver
   metastases

   - Albumin ≥ 2.5 mg/dL

   - International normalized ratio (INR) or prothrombin time (PT) ≤ 1.5 x ULN unless
   subject is receiving anticoagulant therapy, in which case PT/INR must be within
   therapeutic range of intended use of anticoagulants

   - Activated partial thromboplastin time (aPTT) ≤ 1.5 x ULN unless subject is receiving
   anticoagulant therapy, in which case PTT must be within therapeutic range of intended
   use of anticoagulants

   - Female subject of childbearing potential should have a negative urine or serum
   pregnancy within 72 hours prior to receiving the first dose of study medication. If
   the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
   will be required.

   - Female subjects of childbearing potential should be willing to use 2 methods of birth
   control or be surgically sterile, or be willing to abstain from heterosexual activity
   for the course of the study through 120 days after the last dose of study medication.
   Subjects of childbearing potential are those who have not been surgically sterilized
   or have not been free from menses for > 1 year.

   - If female, is postmenopausal; is surgically sterile; or agrees to use 2 acceptable
   methods of birth control throughout the trial, until 120 days after the last dose of
   treatment

   - If female, agree to use an adequate method of contraception starting with the first
   dose of study therapy through 120 days after the last dose of study therapy

   - Male with female partner of childbearing potential agrees to use adequate method of
   contraception throughout study, until 120 days after last dose of treatment or last
   blood draw.

   - Willing and able to provide written informed consent/assent for the trial. Consent may
   be obtained by legally authorized representative (LAR).

EXCLUSION CRITERIA

   - Currently receiving investigational study therapy, or has received investigational
   study therapy, or used an investigational device, within 4 weeks of the first dose of
   treatment.

   - Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other
   form of immunosuppressive therapy within 7 days prior to the first dose of trial
   treatment (EXCEPTIONS: topical, intraarticular, intralesional, and inhaled steroids)

   - Known history of active Bacillus Tuberculosis (TB) infection

   - Hypersensitivity to pembrolizumab or any of its excipients.

   - Has received an anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
   Day 1, or who has not recovered (ie, ≤ Grade 1 or at baseline) from adverse events due
   to agents administered more than 4 weeks earlier.

   - Has received chemotherapy, targeted small molecule therapy, or radiation therapy
   within 2 weeks prior to study Day 1, or who has not recovered (ie, ≤ Grade 1 or at
   baseline) from adverse events due to a previously administered agent. (EXCEPTION:
   Subjects with ≤ Grade 2 neuropathy may qualify for the study).

   - If subject received major surgery, they must have recovered adequately from the
   toxicity and/or complications from the intervention prior to starting therapy.

   - Known additional malignancy that is progressing or requires active treatment.
   (EXCEPTIONS: basal cell carcinoma of the skin or squamous cell carcinoma of the skin
   that has undergone potentially curative therapy, or in situ cervical cancer)

   - Carcinomatous meningitis without consideration of clinical stability

   - Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
   Subjects with previously treated brain metastases may participate provided they are
   stable (without evidence of progression by imaging for at least four weeks prior to
   the first dose of trial treatment and any neurologic symptoms have returned to
   baseline), have no evidence of new or enlarging brain metastases, and are not using
   steroids for at least 7 days prior to trial treatment.

   - Active autoimmune disease that has required systemic treatment in the past 2 years
   (ie, with use of disease modifying agents, corticosteroids or immunosuppressive
   drugs). Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid
   replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
   form of systemic treatment. Intraarticular, inhaled, and intralesional doses of
   steroids are allowed at screening and during the study.

   - Known history of, or any evidence of active, non-infectious pneumonitis that required
   steroids or current pneumonitis.

   - Active infection requiring systemic therapy.

   - History or current evidence of any condition, therapy, or laboratory abnormality that
   might confound the results of the trial, interfere with the subject's participation
   for the full duration of the trial, or is not in the best interest of the subject to
   participate, in the opinion of the treating investigator.

   - Has known psychiatric or substance abuse disorders that would interfere with
   cooperation with the requirements of the trial.

   - Is pregnant or breastfeeding

   - Expecting to conceive or father children within the projected duration of the trial,
   starting with the pre-screening or screening visit through 120 days after the last
   dose of trial treatment.

   - Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.

   - Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1-2 antibodies).

   - Has known active Hepatitis B (eg, HBsAg reactive) or Hepatitis C (eg, HCV RNA
   [qualitative] is detected).

   - Has received a live vaccine within 30 days of planned start of study therapy. Note:
   Seasonal influenza vaccines for injection are generally inactivated flu vaccines and
   are allowed; however intranasal influenza vaccines (eg, Flu-Mist) are live attenuated
   vaccines, and are not allowed.

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
CCTO
650-498-7061
Not Recruiting