Clinical Trials Directory

Trials / Completed

CompletedNCT04701918

Cryoablation With Pembrolizumab Or Avelumab In Urothelial Carcinoma

A Multicenter, Single-Arm Open Label Phase II Trial of Cryoablation in Combination With Pembrolizumab or Avelumab in Patients With Metastatic Urothelial Carcinoma

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
9 (actual)
Sponsor
Massachusetts General Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This research study is examining the effectiveness of pembrolizumab plus cryoablation or aveluma plus cryoablation on people with urothelial carcinoma, including bladder cancer, that has spread.

Detailed description

This is an open label Phase 2, single-arm, multi-institutional clinical trial designed to study the combination of pembrolizumab and cryoablation or avelumab and cryoablation on people with urothelial carcinoma, including bladder cancer, that has spread. The U.S. Food and Drug Administration (FDA) has approved both cryoablation, pembrolizumab, and avelumab as treatment options for urothelial carcinoma, including bladder cancer, that has spread. However, the FDA has not yet approved the combination of the drugs, pembrolizumab or avelumab, and intervention, cryoablation, for urothelial carcinoma, including bladder cancer, that has spread. Pembrolizumab is believed to work by binding to a chemical called PD-1 that is found on a special type of white blood cell in your body. Avelumab is believed to work by binding a similar molecule called PD-L1. This may help your body to be better at finding and destroying tumor cells. Cryoablation is an intervention which may kill cancer cells using extreme cold. It may help the immune system better recognize tumors and act against it. The research study procedures include screening for eligibility and study treatment, including evaluations and follow up visits. Participants will receive study treatment as long as their disease does not get worse or they do not have any unacceptable side effects for up to two years. Participants will be followed for up to 2 years after ending the study treatment. It is expected that about 30 people will take part in this research study. Biocompatibles UK Ltd, a device company under Boston Scientific, is supporting this research study by providing funding for the needles used in the study intervention.

Conditions

Interventions

TypeNameDescription
DRUGPembrolizumabIntravenous injection through a vein (IV) every 3 weeks
PROCEDURECryoablationNeedle inserted through the skin and into the tumor using CT guidance
DRUGAvelumabIntravenous injection through a vein (IV) every 2 weeks

Timeline

Start date
2021-06-04
Primary completion
2025-12-01
Completion
2025-12-01
First posted
2021-01-08
Last updated
2026-01-22

Locations

2 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04701918. Inclusion in this directory is not an endorsement.