Adoptive Cell Therapy Following a Non-myeloablative, Lymphodepleting Induction Regimen in Metastatic Melanoma Patients
- Sponsor
- Sheba Medical Center
- Study ID
- NCT03166397
- Phase
- PHASE2
- Status
- Unknown
Conditions
- Malignant Melanoma Stage IV
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Fludarabine — DRUGCyclophosphamide 30mg/kg/day with Fludarabine (25 mg/m2/d) followed by 3 consecutive days of Fludarabine 25mg/m2/d.
- Cyclophosphamide — DRUGCyclophosphamide 30mg/kg/day with Fludarabine (25 mg/m2/d) followed by 3 consecutive days of Fludarabine 25mg/m2/d.
- TIL — BIOLOGICALTIL administration
- IL-2 — DRUGBolus high-dose (720,000 IU/kg) IL-2 will be administered to each patient every 8 hours, to tolerance. A maximum of 10 doses will be administered per patient.
- Nivolumab — DRUGNivolumab 480 mg fixed dose
- Ipilimumab — DRUGIpilimumab 1 mg/kg up to 100 mg
- FMT Protocol — DRUGFMT given both directly into the colon via colonoscopy and orally using capsules (12 capsules each time). FMT will be taken from melanoma patients treated with Anti PD-1 who achieved a durable response of more than 12 months.
Study Details
Adoptive cell therapy (ACT) with tumor-infiltrating lymphocytes (TILs) in combination with lymphodepletion and high-dose interleukin 2 (IL-2) has demonstrated reproducible objective response rates of approximately 50 percent in patients with highly advanced, refractory metastatic melanoma. Recent developments in theTIL ACT procedure facilitate the use of a reduced-intensity, non-myeloablative, lympho-depleting preparative regimen which is expected to be both less toxic and equally efficient compared to previous regimens. Recently patients recruited post Anti PD-1 therapy had inferior responses in comparison to the pre immune checkpoint inhibitors era. Therefore 2 new arms were added: 1. TIL-ACT with combination of 2 doses of Nivolumab fixed dose 480mg, pre and post TIL. 2. TIL-ACT with FMT given using colonoscopy once and 2 maintenance doses of 12 orally ingested capsules, concurrently with a single dose of Ipilimumab 1 mg/kg up to 100 mg.
Key Dates
- Start date
- Jun 5, 2017
- Status verified
- Jan 2023
- Primary completion
- Jan 1, 2025
- Completion
- Jun 1, 2026
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: ACT TIL1. Reduced Intensity, non-myeloablative, lymphodepleting induction regimen using Cyclophosphamide 30mg/kg/day with Fludarabine (25 mg/m2/d) followed by 3 consecutive days of Fludarabine 25mg/m2/d.. 2. Preparation and administration of TIL 3. Bolus high-dose (720,000 IU/kg) IL-2 will be administered to each patient every 8 hours, to tolerance. A maximum of 10 doses will be administered per patient.
- Experimental: ACT TIL + Anti PD-11. Single dose of Nivolumab 480 mg fixed dose 2. Reduced Intensity, non-myeloablative, lymphodepleting induction regimen using Cyclophosphamide 30mg/kg/day with Fludarabine (25 mg/m2/d) followed by 3 consecutive days of Fludarabine 25mg/m2/d.. 3. Preparation and administration of TIL 4. Bolus high-dose (720,000 IU/kg) IL-2 will be administered to each patient every 8 hours, to tolerance. A maximum of 10 doses will be administered per patient. 5. Second dose of Nivolumab 480 mg fixed dose (at least 4 weeks from the first dose)
- Experimental: ACT TIL FMT + Anti CTLA41. FMT loading dose given via colonoscopy 2. FMT 12 oral capsules as maintenance - given 2 times 3. Single dose of Ipilimumab 1mg/kg up to 100 mg 4. Reduced Intensity, non-myeloablative, lymphodepleting induction regimen using Cyclophosphamide 30mg/kg/day with Fludarabine (25 mg/m2/d) followed by 3 consecutive days of Fludarabine 25mg/m2/d.. 5. Preparation and administration of TIL 6. Bolus high-dose (720,000 IU/kg) IL-2 will be administered to each patient every 8 hours, to tolerance. A maximum of 10 doses will be administered per patient.
Primary Outcome Measure
Objective tumor responses [ Time Frame: 3 years ]
Central Contacts
- Meital Bar972-3-5305201
Related Studies
- Phase 2b of RAPA-201 Cell Therapy in Post-PD-(L)-1 MelanomaPHASE2 · Not Yet Recruiting · Rapa Therapeutics LLC · Hackensack, New Jersey