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Clinical Trial Summary

ACCEL is a multicenter, open label phase I/II study of [Ac-225]-PSMA-62 in participants with prostate-specific membrane antigen (PSMA)-positive prostate cancer.


Clinical Trial Description

The primary aim of the phase I study is to evaluate the safety and tolerability of [Ac-225]-PSMA-62 to determine recommended phase II doses for patients with mCRPC and BCR prostate cancer. The aim of the phase II study for patients with mCRPC is to evaluate the efficacy of [Ac-225]-PSMA-62. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06229366
Study type Interventional
Source POINT Biopharma, a wholly owned subsidiary of Eli Lilly and Company
Contact Richard Cioci
Phone (647) 812-2417
Email rcioci@pointbiopharma.com
Status Recruiting
Phase Phase 1
Start date March 26, 2024
Completion date March 2032

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