Trials / Recruiting
RecruitingNCT05779423
Cryoablation+Ipilimumab+Nivolumab in Melanoma
A Phase II Study of Core Needle Biopsy and Cryoablation of an Enlarging Tumor in Patients With Advanced Melanoma Receiving Post-progression Dual Immune Checkpoint Inhibitor Therapy
- Status
- Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 37 (estimated)
- Sponsor
- Massachusetts General Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this study is to find out whether the combination of two approved drugs, ipilimumab and nivolumab, in combination with cryoablation are safe and effective for participants who have an unresectable melanoma that is resistant, or is growing, after receiving immunotherapy with a PD-1 inhibitor. The names of the study interventions involved in this study are: * Cryoablation (an interventional radiology procedure that freezes part of a tumor) * Ipilimumab (an immunotherapy) * Nivolumab (an immunotherapy)
Detailed description
This is a single-arm, two-stage, Phase II clinical trial to test the safety and effectiveness of an investigational treatment, the combination of ipilimumab and nivolumab with cryoablation, for the treatment of metastatic melanoma resistant to PD-1 inhibition. Ipilimumab and nivolumab are types of inhibitors. Ipilimumab targets and blocks specific proteins in cancer cells which are responsible for stopping the immune system from working correctly. Nivolumab targets a receptor on cancer cells that causes programmed cell death. The U.S. Food and Drug Administration has approved Ipilimumab and Nivolumab for the treatment of melanoma. Cryoablation is an approved procedure that consists of freezing a tumor and surgically removing it. The use of the study drugs and cryoablation combination is experimental. Study procedures including screening for eligibility, study treatment including in-clinic visits, blood sample collections, Computerized Tomography (CT) scans, and tumor biopsies. Participation in this research study is expected to last up to 3 years. It is expected that about 37 people will take part in this research study. The William M. Wood Foundation is supporting this research by providing funding for the cryoablation and research activities.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ipilimumab | Monoclonal antibody administered through intravenous infusion |
| DRUG | Nivolumab | Monoclonal antibody administered through intravenous infusion |
| PROCEDURE | Cryoablation | Procedure of freezing a tumor performed via CT-guidance by interventional radiologist. |
Timeline
- Start date
- 2023-09-23
- Primary completion
- 2028-01-01
- Completion
- 2028-01-01
- First posted
- 2023-03-22
- Last updated
- 2026-01-06
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05779423. Inclusion in this directory is not an endorsement.