AZD0305 as Monotherapy or in Combination With Anticancer Agents in Participants With Multiple Myeloma
NCT06106945 · Status: RECRUITING · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 226
Last updated 2026-05-06
Summary
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 efficacy of AZD0305 as monotherapy and in combination with other anticancer agents in participants with MM.
Conditions
Interventions
- DRUG
-
AZD0305
AZD0305 Investigational product
- DRUG
-
Module 2 Investigational product
- DRUG
-
Module 3 Standard of Care (background treatment)
- DRUG
-
Module 3 Standard of Care (background treatment)
Sponsors & Collaborators
- lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-12-05
- Primary Completion
- 2027-08-16
- Completion
- 2027-08-16
- FDA Drug
- Yes
Countries
- United States
- Australia
- Canada
- China
- France
- Germany
- Japan
- Spain
Study Locations
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