Study on the Safety, Drug Levels, and Effectiveness of CC-92480 with Other Treatments for Relapsed or Refractory Multiple Myeloma
Sponsor: Bristol-Myers Squibb
ClinicalTrials ID:NCT05372354
This clinical trial is testing the safety and effectiveness of a new drug, CC-92480, when used with other treatments for patients with multiple myeloma that has returned or not responded to previous treatments.
Patient Parameters
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Program Overview
The aim of this study is to evaluate how safe and effective the drug CC-92480 (also known as BMS-986348) is when combined with other treatments for patients with multiple myeloma that has either come back after treatment or has not responded to previous therapies. Researchers will assess how well patients tolerate the drug and its preliminary effectiveness in managing the disease.
Eligibility Criteria
Inclusion Criteria
- Have multiple myeloma that has returned or not responded to previous treatments.
- Show signs of disease progression during or after the last treatment.
- Be unable to benefit from existing treatments due to resistance, intolerance, or ineligibility.
- Have measurable disease that can be tracked.
- Be in good general health, with a performance status score of 0 or 1, indicating full activity or some restriction in strenuous activities.
- Agree to follow a specific plan to prevent pregnancy during the study.
Exclusion Criteria
- Have active or past involvement of multiple myeloma in the central nervous system.
- Have certain other blood disorders, such as plasma cell leukemia or Waldenstrom's macroglobulinemia.
- Have significant heart problems or diseases affecting the heart.
- Have had a COVID-19 infection recently, with specific timeframes for mild or severe cases.
- Have received certain treatments before, such as CC-92480 or other specified drugs, depending on the study part.
- Have had a stem-cell transplant recently or at any time for certain types.
- Have undergone certain procedures or treatments within 14 days before starting the study, such as major surgery or radiation therapy.
- Have used any investigational drugs recently, within 28 days or a specific time based on the drug's half-life.
- Have received a COVID-19 vaccine within 14 days before starting the study.
- Other specific criteria as defined by the study protocol.
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