A Study of CC-95251, a Monoclonal Antibody Directed Against SIRPα, in Participants With Advanced Solid and Hematologic Cancers
Stopped early · Phase 1
Conditions studied: Neoplasms
In brief
The purpose of this study is to evaluate the safety, tolerability, and preliminary clinical activity of CC-95251 as a single agent and in combination with cetuximab and rituximab in participants with advanced solid and hematologic cancers.
Key facts
- Study ID
- NCT03783403
- Run by
- Celgene
- People needed
- 206
- Starts
- 2019-03-01
- Expected to finish
- 2024-08-05
- Last updated by the study team
- 2024-09-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Progressed on standard anticancer therapy or for whom no other approved conventional therapy exists and have histological or cytological confirmation of advanced unresectable solid tumors, advanced unresectable colorectal cancer, or squamous cell carcinoma of the head and neck, or CD20-positive non-Hodgkin's lymphoma, or diffuse large B cell lymphoma, or follicular lymphoma
- Solid tumors must have at least one site of measurable disease as determined by RECIST v1.1
- Eastern cooperative oncology group performance status of 0 or 1
You may not qualify if…
- High-grade lymphomas (Burkitt's or lymphoblastic)
- Has cancer with symptomatic central nervous system (CNS) involvement
- History of class III or IV congestive heart failure (CHF) or severe non-ischemic cardiomyopathy, unstable angina, myocardial infarction, or ventricular arrhythmia within the previous 6 months
- Other protocol-defined inclusion/exclusion criteria apply
Where it is running
- Local Institution - 105 — Birmingham, Alabama, United States
- Local Institution - 101 — Scottsdale, Arizona, United States
- Local Institution - 112 — Sacramento, California, United States
- Rocky Mountain Cancer Centers, LLP [Aurora-COAU] — Aurora, Colorado, United States
- Local Institution - 115 — St Louis, Missouri, United States
- Local Institution - 110 — New York, New York, United States
- Local Institution - 109 — Charlotte, North Carolina, United States
- Local Institution - 106 — Oklahoma City, Oklahoma, United States
- Local Institution - 113 — Portland, Oregon, United States
- Local Institution - 107 — Pittsburgh, Pennsylvania, United States
- Local Institution - 102 — Nashville, Tennessee, United States
- Local Institution - 108 — Houston, Texas, United States
- Local Institution - 103 — San Antonio, Texas, United States
- Local Institution - 301 — Heidelberg, Victoria, Australia
- Local Institution - 303 — Melbourne, Victoria, Australia
- Local Institution - 201 — Edmonton, Alberta, Canada
- Local Institution - 202 — Toronto, Ontario, Canada
- Local Institution - 402 — Borddeaux Cedex, France
- Local Institution - 406 — Créteil, France
- Local Institution - 405 — Marseille, France
- Local Institution - 404 — Nantes, France
- Local Institution - 403 — Rouen, France
- Local Institution - 401 — Villejuif, France
- Local Institution - 604 — Seoul, South Korea
- Local Institution - 603 — Seoul, South Korea
Full record on ClinicalTrials.gov
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