A Study to Learn About the Effects of Cemsidomide in Combination With Elranatamab in Relapsed/Refractory Multiple Myeloma Subjects
Part of paid clinical trials in Gilbert, Arizona.
- Sponsor
- C4 Therapeutics, Inc.
- Study ID
- NCT07280013
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Multiple Myeloma (MM)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Cemsidomide — DRUGIKZF1/3 degrader
- Elranatamab — BIOLOGICAL• BCMA-CD3 bispecific antibody
Study Details
The main purpose of the study is to understand the safety and tolerability of cemsidomide when given along with elranatamab in subjects with relapsed or refractory multiple myeloma. The first part of the study will evaluate different dose levels of cemsidomide in combination with elranatamab in a limited number of subjects. Approximately 3 different dose levels of cemsidomide in combination with elranatamab may be explored. Once a dose level is determined safe, additional subjects may be enrolled through expansion of the dose level. This expansion will provide further exploration of the safety and evaluation of preliminary antimyeloma activity. Cemsidomide will be taken orally each cycle for 14 days on/14 days off (1 cycle=28 days). Elranatamab will be administered by subcutaneous injection twice a month. Dexamethasone will be administered weekly until a confirmed response but no longer than 4 cycles.
Key Dates
- Start date
- Feb 6, 2026
- Status verified
- Apr 2026
- Primary completion
- Dec 31, 2028
- Completion
- Jun 30, 2029
Study Design
- Enrollment
- 60 participants (estimated)
- Allocation
- NA
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Non-randomized cemsidomide (tablet) plus elranatamab (subcutaneous injection)
Primary Outcome Measure
Safety and tolerability of cemsidomide in combination with elranatamab [ Time Frame: Cycle 1 approximately 28 days ]
Central Contacts
- Study Medical Officer(617) 231-0700
Locations (16)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Banner MD Anderson Cancer Center | Gilbert | Arizona | 85234 | - |
| UCLA Health, Jonsson Comprehensive Cancer Center | Santa Monica | California | 90404 | - |
| Tampa General Hospital | Tampa | Florida | 33606 | - |
| Winship Cancer Institute, Emory University | Atlanta | Georgia | 30322 | - |
| Loyola University Medical Center | Maywood | Illinois | 60153 | - |
| Indiana University | Indianapolis | Indiana | 46202 | - |
| Norton Cancer Institute St. Matthews | Louisville | Kentucky | 40207 | - |
| University of Maryland Greenbaum Comprehensive Cancer Center | Baltimore | Maryland | 21201 | - |
| START Midwest | Grand Rapids | Michigan | 49546 | - |
| University of Nebraska | Omaha | Nebraska | 68105 | - |
| Dartmouth-Hitchcock Medical Center | Lebanon | New Hampshire | 03756 | - |
| Perlmutter Cancer Center at NYU Langone Hospital | Brooklyn | New York | 11203 | - |
| Memorial Sloan Kettering Cancer Center | New York | New York | 10021 | - |
| Duke Cancer Center | Durham | North Carolina | 27710 | - |
| MD Anderson Cancer Center | Houston | Texas | 77030 | - |
| Huntsman Cancer Institute, University of Utah | Salt Lake City | Utah | 84112 | - |
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