A Study Evaluating the Safety, Pharmacokinetics, and Preliminary Activity of GDC-1261 in Participants With Advanced or Metastatic Prostate Cancer
Condition(s) studied
Investigational drug(s) / intervention(s)
GDC-1261: Participants will receive GDC-1261 as per the schedule described in the protocol.
Study summary
The purpose of this study is to evaluate the safety, pharmacokinetics (PK), and preliminary activity of GDC-1261 in participants with advanced or metastatic prostate cancer. It's also to identify a recommended dose(s) and regimen for GDC-1261 for subsequent studies.
Eligibility
Primary outcome measure(s)
- Percentage of Participants With Adverse Events (AEs) — Up to approximately 24 months
- Incidence and Nature of DLTs Dose-limiting Toxicities (DLTs) — From Day 1-28 of Cycle 1 (1 Cycle = 28 days)
Trial sites (5)
| Facility | City | Region | Status |
|---|---|---|---|
| Honor Health Research Institute | Scottsdale | Arizona | Recruiting |
| Sarah Cannon Research Institute | Nashville | Tennessee | Recruiting |
| St Vincent's Hospital Sydney | Darlinghurst | New South Wales | Recruiting |
| Austin Hospital | Heidelberg | Victoria | Recruiting |
| The Royal Marsden in Sutton, Surrey - Downs Rd | Sutton | Surrey | Recruiting |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07567846 on ClinicalTrials.gov ↗ ← All trials in the USA