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Study identifier: NCT07570979 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study to Investigate the Safety and Tolerability of Oral INR731 Single Agent or in Combination With Androgen Receptor Pathway Inhibitor (ARPI) in Patients With Metastatic Prostate Cancer

Condition: Metastatic Castration-resistant Prostate Cancer (mCRPC)  ·  Sponsor: Novartis Pharmaceuticals

PhasePhase 1
Planned participants208
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to assess the safety, tolerability, pharmacokinetics/pharmacodynamics, preliminary anti-tumor activity, and recommended dose of INR731 as a single agent and in combination with standard-of-care androgen receptor pathway inhibitors (ARPIs) in adult patients with metastatic prostate cancer.

This description comes directly from the study's public registry record.

Talk to the study team

Novartis Pharmaceuticals  ·  1-888-669-6682  ·  novartis.email@novartis.com

Novartis Pharmaceuticals  ·  +41613241111

Always discuss trial participation with your own doctor first.

Locations (3)

Mary Crowley Cancer ResearchDallas, Texas, United StatesRecruiting
Novartis Investigative SiteMelbourne, Victoria, AustraliaRecruiting
Novartis Investigative SiteHirakata, Osaka, JapanRecruiting

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Source record: clinicaltrials.gov/study/NCT07570979