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A Trial to Learn How Safe AZD9750 is and How Well it Works in People With Metastatic Prostate Cancer When Given With or Without Other Anticancer Drugs

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NCT07336446 · readout in 891 d

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

Phase
Phase 1/2
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
300estimated
Sites
18
Countries
Australia, Canada, China +5

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
Start2026-01-27actualWhen the study began enrolling
Primary completion2029-01-26estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2029-01-26estimatedThe whole study's end, after follow-up
First posted2026-01-13actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-10actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Prostate Cancer

Interventions

  • Drug: AZD9750
  • Drug: AZD5305 — also filed as Saruparib

Primary outcomes

what the primary-completion date above is the date OF
Number of participants with dose-limiting toxicity (DLT), as defined in the protocol (Part A only)
measured From first dose of study intervention to 28 days post first dose
Number of participants with Adverse Events and Serious Adverse Events
measured From first dose of study intervention up to 37 days after the last dose of study treatment
Number of participants with Adverse Events leading to discontinuation of study intervention
measured From first dose of study intervention up to 37 days after the last dose of study treatment
Clinically significant changes from baseline in vital signs.
measured From first study dose up to 37 days after the last dose of study treatment
Clinically significant changes from baseline in physical examination.
measured From first dose of study intervention up to 37 days after the last dose of study treatment
Clinically significant changes from baseline in ECOG PS.
measured From first dose of study intervention up to 37 days after the last dose of study treatment
Clinically significant changes from baseline in ECGs.
measured From first dose of study intervention up to 37 days after the last dose of study treatment
Clinically significant changes from baseline in laboratory parameters.
measured From first dose of study intervention up to 37 days after the last dose of study treatment
Proportion of participants achieving a ≥50% decrease in PSA from baseline (PSA50) (Part B only)
measured From first dose of study intervention up to 14 days after the last dose of study treatment

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