Phase II Intratumoral IL12 Plasmid Electroporation in Cutaneous Lymphoma

NCT ID: NCT01579318

Last Updated: 2023-05-15

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 2 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-06-08
• Study Completion Date: 2014-06-03

Brief Summary

A single arm, open label, multi-center, phase 2 study to assess the safety and anti-tumor activity of ImmunoPulse IL-12® in participants with stage IB to IIIB mycosis fungoides. ImmunPulseIL12® is the combination of intrtumoral interleukin-12 gene (also known as tavokinogene telseplasmid [tavo]) and in vivo electroporation-mediated plasmid deoxyribonucleic acid [DNA] vaccine therapy (tavo-EP) administered using the OncoSec Medical System (OMS).

All participants may receive up to four cycles of treatment consisting of three treatment days, Days 1, 5 and 8, in a 12-week cycle as per Protocol version 6 (see Limitations and Caveats section of this record for protocol version information). Patients will receive intra-tumoral injection of tavo at a concentration of 1.0 mg/mL (maximum volume of 1 mL/day distributed over 2-4 lesions), followed immediately by electrical discharge around the tumor site resulting in electroporation of plasmid deoxyribonucleic acid (DNA) into tumor cells.

Detailed Description

This is a single arm, open label, multi-center phase 2 study to assess the safety and anti-tumor activity of intratumoral tavo electroporation in participants with stage IB to IIIB mycosis fungoides. All participants received up to four cycles of treatment consisting of three treatment days, Days 1, 5 and 8, in a 12-week cycle. Patients will receive intra-tumoral injection of tavo at a concentration of 1.0 mg/mL (maximum volume of 1 mL/day distributed over 2-4 lesions), followed immediately by electrical discharge around the tumor site resulting in electroporation of plasmid deoxyribonucleic acid (DNA) into tumor cells. Prior to the first cycle of treatment, the investigator will select at least one lesion, or affected area in erythrodermic patients, to be left untreated for the duration of the study to allow for clinical observation of an untreated site. Participants will be followed for safety and clinical evaluation every 4 weeks. Quality of Life will be assessed using the Skindex29, Functional Assessment of Cancer Therapy - General (FACT-G) and Visual Analog Scale for Pruritus (VAS-P) instruments. Survival follow up will occur at 3-month intervals over 2 years following end of study.

Conditions

Cutaneous T Cell Lymphomas (CTCL); Mycosis Fungoides (MF)

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment

Participants received up to 4 cycles of treatment (3 daily treatments on Days 1, 5 and 8, in a 12-week cycle) of intratumoral injection(s) of tavo at a concentration of 1.0 mg/mL (maximum volume of 1 mL/day distributed over 2-4 lesions), followed immediately by electrical discharge around the tumor site resulting in electroporation of plasmid deoxyribonucleic acid (DNA) into tumor cells.

Group Type: EXPERIMENTAL

Tavokinogene Telseplasmid (tavo)

Intervention Type: BIOLOGICAL

Patients received intratumoral injection(s) of tavo.

OncoSec Medical System (OMS)

Intervention Type: DEVICE

Electroporation via OMS was performed immediately following intratumoral injection of tavo. A sterile applicator containing 6 stainless steel electrodes arranged in a circle were placed around the tumor. The applicator was connected to the OMS power supply and six pulseswere administered to each tumor lesion at the approximate point of tavo injection.

Interventions

Tavokinogene Telseplasmid (tavo)

Patients received intratumoral injection(s) of tavo.

Intervention Type: BIOLOGICAL

OncoSec Medical System (OMS)

Electroporation via OMS was performed immediately following intratumoral injection of tavo. A sterile applicator containing 6 stainless steel electrodes arranged in a circle were placed around the tumor. The applicator was connected to the OMS power supply and six pulseswere administered to each tumor lesion at the approximate point of tavo injection.

Intervention Type: DEVICE

Other Intervention Names

interleukin-12 gene; IL-12 gene; pIL-12; plasmid DNA encoding human interleukin-12; plasmid IL-12; MedPulser

Eligibility Criteria

Inclusion Criteria

1. Biopsy confirmed mycosis fungoides of stage IB - IIIB;

2. Participants must have failed or have been intolerant to at least one standard of care therapy;

3. Participants must have a minimum of one lesion, or affected area in erythrodermic patients (T4/stage III), that meets all following criteria:

• Accessible for pIL-12 electroporation;
• Adequate size such that 6-mm biopsy can be collected prior to treatment;

4. Participants must have one additional lesion, or affected area in erythrodermic patients, that remains untreated for the duration of the study;

5. Age ≥ 18 years old;

6. Participants must have Eastern Cooperative Oncology Group (ECOG) performance status 0-2;

7. Required wash out period of 4 weeks from last dose for the following prior therapies:

• Topical therapy;
• Radiotherapy (including photo therapy);
• Multi-agent chemotherapy;
• Systemic biological therapy;
• Histone deacetylase inhibitors (HDAC) inhibitors;
• Interferon alpha and other investigational therapies;

8. For women of childbearing potential, negative pregnancy serum test within 14 days to the first study drug administration, and use of birth control from 30 days prior to the first day study drug administration and 30 days following last day study drug administration;

9. Male participants must be surgically sterile, or must agree to use contraception during the study and at least 30 days following the last day of study drug administration.

10. Life expectancy of at least 6 months;

11. The patient must have adequate renal and hepatic function as assessed by standard laboratory criteria within 4 weeks prior to enrollment:

• Creatinine < 2 x upper limit of normal (ULN);
• Serum bilirubin within institutional normal limits;
• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 1.5 x ULN;
• Absolute neutrophil count (ANC) > 1000/mm;
• Platelet count > 100,000 /mm;

12. Able to give informed consent and able to follow guidelines given in the study.

Exclusion Criteria

1. Prior therapy with IL-12 or prior gene therapy;

2. Prior treatment with Campath (alemtuzumab) within 1 year of enrollment;

3. Concurrent immunotherapy, chemotherapy, or radiation therapy for duration of patient participation on study;

4. Concurrent steroid therapy;

5. Concurrent anticoagulant therapy (acetylsalicylic acid [ASA]≤ 325mg/day allowed);

6. Evidence of significant active infection (e.g., pneumonia, cellulitis, wound abscess, etc.) at time of study enrollment;

7. Patients with current evidence of large cell transformation (LCT) with aggressive disease at study entry (patients with a history of LCT are eligible if pathologic evidence at study entry indicates there is no presence of LCT);

8. Known history of human immunodeficiency virus (HIV), Human T-cell leukemia virus (HTLV) -1/2 infection, hepatitis B or hepatitis C (active, prior treatment, or both);

9. No other prior malignancy is allowed except for the following: adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, adequately treated Stage I or II cancer from which the patient is currently in complete remission, or any other cancer from which the patient has been disease-free for 2 years;

10. Significant cardiovascular disease (i.e. New York Heart Association [NYHA] class 3 congestive heart failure; myocardial infarction within the past 6 months; unstable angina; coronary angioplasty with the past 6 months; uncontrolled atrial or ventricular cardiac arrhythmias);

11. Any other medical history, including laboratory results, deemed by the investigator to be likely to interfere with patient's participation in the study, or to interfere with the interpretation of the results;

12. Participants with electronic pacemakers or defibrillators are excluded from this study as the effect of electroporation on these devices is unknown;

13. Pregnant and breast-feeding women are excluded from the study as effects on the fetus are unknown and there may be a risk of increased fetal wastage.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

OncoSec Medical Incorporated

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

UCSF Helen Diller Comprehensive Cancer Center

San Francisco, California, United States

Countries

United States

Other Identifiers

OMS-I120

Identifier Type: -

Identifier Source: org_study_id