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Clinical Trial Summary

This is a Phase 1/2, open-label, randomized, dose finding and dose expansion study to evaluate the safety, preliminary efficacy, and PK of gedatolisib in combination with darolutamide in subjects with mCRPC.


Clinical Trial Description

This is a Phase 1/2, open-label, randomized, dose finding and dose expansion study to evaluate the safety, preliminary efficacy, and pharmacokinetics of gedatolisib, a pan-PI3K/mTOR inhibitor, in combination with darolutamide, a next-generation androgen receptor inhibitor, in patients with metastatic castration-resistant prostate cancer following progression on a next-generation androgen receptor inhibitor. The aim of the Phase 1 portion of the study is to evaluate dose limiting toxicities and to determine the recommended Phase 2 dose. The aim of the Phase 2 portion of the study is to further assess the safety and preliminary efficacy of the drug combination. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06190899
Study type Interventional
Source Celcuity Inc
Contact Genelle Brower, RN
Phone 844-310-3900
Email gbrower@celcuity.com
Status Recruiting
Phase Phase 1/Phase 2
Start date January 1, 2024
Completion date November 2027

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