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Clinical Trial · NCT06139575
Overview
The study is being conducted to evaluate the safety, tolerability, pharmacokinetics, radiation dosimetry, and preliminary efficacy of Lutetium Lu 177 JH020002 Injection in adult patients with advanced prostate cancer.
Sponsor
Bivision Pharmaceuticals, Inc.
Phase
Phase 1/2
Contacts
Bivision Pharmaceuticals, Inc.
bivision.public1@bivisionpharma.com
86-21-50886996
ClinicalTrials.gov
NCT06139575Drug / Compound
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