Conditions
Metastatic Castration-resistant Prostate Cancer, Prostatic Neoplasms
The purpose of this study is to assess the efficacy and safety of opevesostat plus hormone replacement therapy (HRT) compared to alternative abiraterone acetate or enzalutamide in participants with Metastatic Castration-resistant Prostate Cancer (mCRPC) previously treated with one next-generation hormonal agent (NHA). The primary study hypotheses are that opevesostat is superior to alternative abiraterone acetate or enzalutamide with respect to radiographic progression free survival (rPFS) per Prostate Cancer Working Group (PCWG) Modified Response Evaluation Criteria in Solid Tumours (RECIST 1.1) as assessed by Blinded Independent Central Review (BICR) and overall survival (OS), in androgen receptor ligand binding domain (AR LBD) mutation positive and negative participants.
NATIONAL TRIAL REFERENCE NUMBER
NCT06136650
EU CT
2023-504957-11
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Conditions
Metastatic Castration-resistant Prostate Cancer, Prostatic Neoplasms
Age Range
18+
Sex
All
Tests the medicine or vaccine in large groups of trial participants (from several hundred to several thousand). For medicines, volunteers have the disease or condition the medicine is designed to treat. In vaccine studies, the volunteers may be healthy or have diseases or conditions. Phase 3 trials take place in hospitals, clinics or doctors’ offices.
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I understand that the information on this page relates to clinical trials and is intended for Australian residents only. Clinical trials may be conducted using unapproved therapeutic goods in Australia. That is, therapeutic goods that have not been evaluated by the Therapeutics Goods Administration in Australia – for quality, safety and efficacy, and have not been entered into the Australian Register of Therapeutic Goods (ARTG). This website is not intended to suggest that any unapproved therapeutic good is appropriate for use outside the specific circumstances of a clinical trial.
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