A Safety, PK and Efficacy Study of CC-92480 Monotherapy and in Combination With Dexamethasone in Subjects With Relapsed and Refractory Multiple Myeloma (RRMM)
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- STATUS
- Recruiting
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- End date
- Feb 8, 2027
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- participants needed
- 201
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- sponsor
- Celgene
Summary
This is an open-label, multi-center, international, Phase 1/2 study to assess the safety, PK and efficacy of CC-92480 monotherapy and in combination with dexamethasone in subjects with relapsed and refractory multiple myeloma (RRMM).
RRMM patient previously treated with at least 3 prior regimens including lenalidomide or pomalidomide, a proteasome inhibitor and a CD38 antibody will be eligible.
Details
| Condition | Multiple Myeloma |
|---|---|
| Treatment | Dexamethasone, CC-92480 |
| Clinical Study Identifier | NCT03374085 |
| Sponsor | Celgene |
| Last Modified on | 4 October 2022 |
Eligibility
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
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