Project Details
Description
A Phase 1/2a Open-label Study to Investigate the Safety and Tolerability, Efficacy, Pharmacokinetics, and Immunogenicity of TAK-573 (formerly TEV-48573) Administered Intravenously as a Single Agent in Patients With Refractory Multiple Myeloma
Status | Finished |
---|---|
Effective start/end date | 8/14/19 → 8/30/24 |
Funding
- TAKEDA CAMBRIDGE LTD
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