Study on Cemsidomide and Dexamethasone for Treating Relapsed or Refractory Multiple Myeloma

Sponsor: C4 Therapeutics, Inc.

Sponsor score: 0

ClinicalTrials ID:NCT07284758

This clinical trial is testing the effectiveness and safety of a new treatment combination using cemsidomide and dexamethasone for patients with multiple myeloma that has returned or not responded to previous treatments.

Patient Parameters

Program Overview

This Phase 2 study is designed to evaluate how well the combination of cemsidomide and dexamethasone works in treating patients with multiple myeloma that has either come back or not responded to other treatments. The study will also look at the safety and how the body processes these medications.

Eligibility Criteria

Inclusion Criteria

  • Be 18 years or older and able to provide consent to participate.
  • Have a confirmed diagnosis of multiple myeloma with measurable disease.
  • Have received at least three previous treatments for multiple myeloma, including specific types of drugs and therapies, unless unavailable locally.
  • Have good organ function as determined by medical tests.
  • Any side effects from previous cancer treatments must have improved to a mild level or returned to baseline.
  • Women must not be pregnant, planning to become pregnant, breastfeeding, or planning to breastfeed during the study and for 30 days after the last treatment.
  • Men must agree to use condoms during intercourse with women who can become pregnant and avoid donating sperm during the study and for 30 days after the last treatment.
  • Participants must not donate blood during the study and for 30 days after the last treatment.

Exclusion Criteria

  • Have multiple myeloma affecting the brain or spinal cord.
  • Have certain other medical conditions, such as systemic light chain amyloidosis, POEMS syndrome, or myelodysplastic syndrome.
  • Have been previously treated with cemsidomide.
  • Have significant heart problems or diseases.
  • Have had a blood clot within three months before joining the study.
  • Have another cancer that has progressed or needed treatment in the past three years.
  • Have an uncontrolled active infection.
  • Have difficulty swallowing tablets.

Locations

FACILITYZIPCITYSTATE
Berenson Cancer Center90069West HollywoodCalifornia
START Midwest49546Grand RapidsMichigan
START San Antonio78229San AntonioTexas

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