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TERMINATED
NCT04916002
PHASE2

A Trial To Find Out If Vidutolimod Together With Cemiplimab Is Safe And If It Works In Adult Participants With Advanced Cancer Or Metastatic Cancer

Sponsor: Regeneron Pharmaceuticals

View on ClinicalTrials.gov

Summary

The goal of this study is to learn if giving cemiplimab and vidutolimod together could be effective in treating advanced cancer. The main questions it aims to answer are: * How many participants' cancers respond to vidutolimod together with cemiplimab? * Is vidutolimod together with cemiplimab safe and well-tolerated? * How well does vidutolimod together with cemiplimab treat participants' cancer? Participants will receive trial treatment for up to 2 years. 30 days after stopping treatment, participants will have a follow-up visit. After that visit, the trial staff will continue to follow up with participants about every 3 months, until the trial ends.

Official title: A Multicenter, Open-label, Phase 2 Study of Intratumoral Vidutolimod (CMP-001) in Combination With Intravenous Cemiplimab in Subjects With Selected Types of Advanced or Metastatic Cancer

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

77

Start Date

2021-11-30

Completion Date

2024-10-31

Last Updated

2026-06-09

Healthy Volunteers

No

Interventions

DRUG

vidutolimod

Participants will receive vidutolimod for up to 2 years as follows: 10 mg IT weekly for 7 doses after which vidutolimod will be administered every 3 weeks (Q3W). The first dose of vidutolimod may be administered subcutaneously (SC) or IT at the discretion of Investigator. All subsequent doses will be IT. The initial 7 doses of vidutolimod, delivered on a weekly dosing schedule, must be completed before starting the Q3W vidutolimod dosing schedule.

DRUG

cemiplimab

Participants will receive cemiplimab for up to 2 years as follows: 350 mg IV infusion over 30 minutes at week 1 dose 1 (W1D1) and Q3W thereafter.

Locations (24)

University of Alabama

Birmingham, Alabama, United States

City of Hope

Duarte, California, United States

UC San Diego Moores Cancer Center

La Jolla, California, United States

University of California

Los Angeles, California, United States

GenesisCare USA

Jacksonville, Florida, United States

Orlando Health Cancer Institute

Orlando, Florida, United States

University of Iowa

Iowa City, Iowa, United States

Norton Cancer Institute

Louisville, Kentucky, United States

VA Maryland Health Care System

Baltimore, Maryland, United States

Dana-Farber Cancer Institute

Boston, Massachusetts, United States

Karmanos Cancer Institute

Detroit, Michigan, United States

Dartmouth Clinical Trial Office

Lebanon, New Hampshire, United States

Memorial Sloan Kettering Cancer Center

New York, New York, United States

East Carolina University

Greenville, North Carolina, United States

Ohio State University

Columbus, Ohio, United States

OU Health Stephenson Cancer Center

Oklahoma City, Oklahoma, United States

University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania, United States

Oncology Consultants

Houston, Texas, United States

University of Utah Huntsman Cancer Center

Salt Lake City, Utah, United States

University of Washington

Seattle, Washington, United States

St. Vincent's Hospital

Darlinghurst, New South Wales, Australia

Princess Alexandra Hospital

Woolloongabba, Queensland, Australia

Peter MacCallum Cancer Centre (PMCC) and The Royal Melbourne Hospital

Melbourne, Victoria, Australia

Fiona Stanley Hospital

Murdoch, Western Australia, Australia