XmAb®20717 (Vudalimab) Alone or in Combination With Chemotherapy or Targeted Therapy in Patients With Metastatic Castration-Resistant Prostate Cancer
Part of paid clinical trials in Anchorage, Alaska.
- Sponsor
- Xencor, Inc.
- Study ID
- NCT05005728
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- MALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- vudalimab + carboplatin + cabazitaxel — COMBINATION_PRODUCTVudalimab IV, carboplatin IV, cabazitaxel IV
- vudalimab + olaparib — COMBINATION_PRODUCTVudalimab IV, olaparib oral
- vudalimab monotherapy — BIOLOGICALVudalimab IV
- vudalimab + docetaxel — COMBINATION_PRODUCTVudalimab IV, docetaxel IV
- vudalimab + cabazitaxel or docetaxel — COMBINATION_PRODUCTVudalimab IV, cabazitaxel or docetaxel IV
Study Details
This Phase 2 study will investigate the safety and clinical activity of vudalimab (XmAb20717) alone or in combination with standard of care anticancer therapies in patients with metastatic castration-resistant prostate cancer (mCRPC) who have progressed on prior therapy.
Key Dates
- Start date
- Oct 22, 2021
- Status verified
- May 2026
- Primary completion
- Jun 10, 2025
- Completion
- Jun 10, 2025
Study Design
- Enrollment
- 72 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Cohort A - AVPCa
- Experimental: Cohort B - HRD/CDK12 PARP - Progressors
- Experimental: Cohort C - HRD/CDK12 PARP Naïve
- Experimental: Cohort D - MSI-H, MMRD or TMB-H
- Experimental: Cohort E - No Targetable Mutations
Primary Outcome Measure
Incidence of treatment-emergent adverse events (safety and tolerability of vudalimab) [ Time Frame: 8 weeks ]
Locations (26)
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