Clinical Trials Directory

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

TypeNameDescription
DRUGIpilimumabMonoclonal antibody administered through intravenous infusion
DRUGNivolumabMonoclonal antibody administered through intravenous infusion
PROCEDURECryoablationProcedure 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

Source: ClinicalTrials.gov record NCT05779423. Inclusion in this directory is not an endorsement.