AZD0305

AZD0305 as Monotherapy or in Combination With Anticancer Agents in Participants With Relapsed/​Refractory Multiple Myeloma

What will happen during the trial?

This is a Phase I/II, modular, open-label, multicenter, dose escalation, and dose expansion/optimization study to evaluate the safety, tolerability, PK, immunogenicity, pharmacodynamics, and preliminary efficacy of AZD0305 in participants with RRMM. This study will follow a modular protocol design evaluating AZD0305 as monotherapy and in combination with other anticancer agents.

The study includes dose escalation and dose expansion phases. This study will enroll subjects with RRMM who received at least 3 prior lines of treatment including at least one proteasome inhibitor (PI), one immunomodulator (IMiD), and an anti-CD38 antibody. Subjects will be administered AZD0305 intravenously.

More Information

Trial Status
Accepting patients
Trial Phase
Phase 1/2
Enrollment
84 patients (estimated)
Sponsors
AstraZeneca
Tags
PARP Inhibitor
Trial Type
Treatment
Last Update
1 week ago
SparkCures ID
1787
NCT Identifier
NCT06106945

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