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Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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

Evaluation of Pharmacodynamic Effects of IT-pIL12-EP in Patients With TNBC

The purpose of this study is to investigate plasmid electroporation. The patient will be injected with pIL-12 (plasmid interleukin-12). pIL-12 is created using human genetic material (DNA). We hope to learn more about pIL-12 as a whether this is an effective treatment for this type of cancer.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

OncoSec Medical Incorporated

Stanford Investigator(s):

Intervention(s):

  • Biological: IT-pIL12-EP

Phase:

Phase 1

Eligibility


Inclusion Criteria:

   - Patients with histologically confirmed diagnosis of locally-advanced, inoperable,
   metastatic and/or treatment-refractory triple negative breast cancer (TNBC).
   *Treatment refractory disease is defined as the persistence of tumor lesions following
   at least one intervention that may include chemotherapy, radiation and/or surgery, or
   any combination thereof. *Patients must have both ER and PR staining < 5% and be
   HER2-negative. Patients with ER or PR staining of 5-10%, but who have historically
   been treated as TNBC may also be enrolled. *Patients must not have disease that, in
   the opinion of the investigator, is considered amenable to potentially curative
   treatment.

   - Age ≥ 18 years.

   - ECOG Performance Status of 0-1.

   - Life expectancy ≥ 6 months.

   - Patients may have had radiation therapy, but must have progressive disease after
   radiation therapy if the lesions to be treated are within the radiation field.
   Radiation treatment must be completed ≥ 4 weeks prior to Cycle 1 Day 1.

   - Adequate hepatic function with total bilirubin and ALT < 1.5X the upper limit of
   normal (ULN), except in patients with Gilbert's Syndrome must have a total bilirubin <
   3X ULN and ALT < 3X ULN. In cases of known liver metastases, ALT ≤ 5X ULN is
   acceptable (total bilirubin must be < 1.5X ULN).

   - Adequate renal function, estimated or calculated creatinine clearance of > 50 mL/min
   (calculated using the formula of Cockcroft and Gault) -or- serum creatinine ≤ 2.0
   mg/dL.

   - Adequate hematological function, defined as ANC ≥ 1,500/mm3, Hb ≥ 9.0 g/dL, and
   platelet count ≥ 100,000/mm3.

   - Lesions that are accessible for injection and electroporation, defined as cutaneous or
   subcutaneous disease.

   - At least 2 anatomically distinct lesions accessible for biopsy.

   - Must consent to study-specific biopsies at two separate timepoints: pre-treatment
   (Screening) and post-treatment (Day 28 or EOS).

   - Tumor lesions in the CNS are permitted but lesions must have been stable for at least
   3 months prior to Cycle 1 Day 1 (C1D1). Stable CNS lesions are defined as not
   requiring steroid prophylaxis or other medications to prevent seizures or other
   complications associated with CNS lesions and no evidence of worsening of CNS disease.

   - Female patients of childbearing potential must have a negative serum or urine
   pregnancy test within 3 days prior to C1D1 and agree to use dual methods of
   contraception during the study and for a minimum of 30 days following the last
   treatment. Post menopausal females (>45 years old and without menses for > 1 year) and
   surgically sterilized females are exempt from these requirements.

Male patients must use an effective barrier method of contraception during the study and
for a minimum of 30 days following the last treatment if sexually active with a female of
childbearing potential.

   - Resolution of all treatment-related toxicities, except alopecia, anemia and
   neuropathy, from any previous cancer therapy to ≤ Grade 1 prior to the first dose of
   study treatment.

   - Ability to provide written informed consent.

Exclusion Criteria:

   - Any other current or previous malignancy within the past three years that, in the
   opinion of the Principal Investigator, will interfere with study-specific objectives.

   - Patients with electronic pacemakers or defibrillators.

   - Chemotherapy or hormonal therapy for anti-cancer treatment within 28 days prior to
   Cycle 1 Day 1.

   - Immunotherapy or biological therapy (e.g., monoclonal antibodies) within 28 days prior
   to Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Treatment with unapproved investigational therapeutic agent within 28 days prior to
   Cycle 1 Day 1, unless pre-approval is obtained from the Sponsor Medical Monitor.

   - Patients receiving systemic steroid therapy for a chronic inflammatory condition
   (e.g., rheumatoid arthritis, Crohn's Disease, etc.). Topical steroids are also
   excluded. Nasal and inhaled steroids are permitted.

   - Unstable/inadequate cardiac function:

      - symptomatic ischemia

      - uncontrolled or clinically significant conduction abnormalities; first degree AV
      block or asymptomatic LAFB/RBBB are eligible

      - myocardial infarction in the previous six months

      - congestive heart failure (New York Heart Association class III to IV)

   - Major surgery within 28 days prior to C1D1.

   - Infection requiring parenteral antibiotics, antivirals, or antifungals within 2 weeks
   prior to C1D1.

   - Patients who are known to have HIV infection/seropositivity.

   - Active Hepatitis A, B, or C infection or known to be positive for HCV RNA or HBV
   surface antigen. Patients who have been vaccinated against Hepatitis B and who are
   positive for ONLY the Hepatitis B surface antibody are permitted to participate in the
   study.

   - Serious psychiatric or medical conditions that could interfere with treatment or
   protocol-related procedures.

   - Patients who are pregnant or lactating.

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