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Study of AZD0516 as Monotherapy and in Combination in Participants With Metastatic Prostate Cancer

← catalyst calendar

NCT07181161 · readout in 883 d

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →. With Parexel.

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
177estimated
Sites
52
Countries
Brazil, China, France +7

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-10-01actualWhen the study began enrolling
Primary completion2029-01-18estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-01-18estimatedThe whole study's end, after follow-up
First posted2025-09-18actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-15actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Metastatic Prostate Cancer

Interventions

  • Drug: AZD0516
  • Drug: AZD9574

Primary outcomes

what the primary-completion date above is the date OF
Module 1 and 2: Parts A and B: Number of participants with Adverse Events (AEs), Serious Adverse Events (SAEs) and Adverse Event of Special Interests (AESIs)
measured From Day 1 up to approximately 3 years
Module 1 and 2: Part A: Number of participants with Dose Limiting Toxicities (DLTs)
measured From Day 1 up to end of DLT period (approximately 21 days)
Module 1: Parts B and C and Module 2: Part B: Percentage of participants with Prostate-Specific Antigen (PSA) 50 response rate
measured Up to approximately 2 years

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