Trial Purpose

Inhloso yalolu cwaningo ukuhlola ukusebenza kahle nokuphepha kwe-opevesostat plus hormone replacement therapy (HRT) uma kuqhathaniswa nenye i-abiraterone acetate noma i- enzalutamide kubahlanganyeli abanomdlavuza wendlala yesinye we-Metastatic Castration-resistant (mCRPC) owake waphathwa ngomenzeli wamahomoni wesizukulwane esilandelayo (NHA). Imibono yocwaningo eyinhloko iwukuthi i-opevesostat iphakeme kunenye i-abiraterone acetate noma i- enzalutamide ngokuphathelene nokusinda kwamahhala kwe-radiographic (rPFS) ngeqembu le-Prostate Cancer Working Group (PCWG) Imibandela Yokuhlola Ukusabela Okuguquliwe Kuma-Solid Tumors (RECIST 1.1) njengoba ihlolwe yi-Blinded androgenval receptor (i-BICRval Independent) Isibuyekezo se-OS Ephakathi (i-BICRval Independent) kanye ne-OS Ephakathi isizinda esibophezelayo se-ligand (AR LBD) ukuguqulwa kwabahlanganyeli abalungile nabangalungile.

View full trial information on Clinicaltrials.gov

NATIONAL TRIAL REFERENCE NUMBER

I-NCT06136650

EU CT Number

2023-504957-11-00

When speaking to your doctor or clinical trial representative, please have the trial reference number available.

Eligibility

Age Range Icon

Age Range

18+

Sex Icon

Sex

KONKE

About The Study

Trial phase Icon Trial Phase
Trial start Icon Trial start and end dates
  • Actual study start date Disemba 18, 2023
  • Estimated primary completion date Disemba 2, 2030
  • Estimated study completion date Disemba 2, 2030

Trial locations

What can you do next?

NATIONAL TRIAL REFERENCE NUMBER

I-NCT06136650

EU CT Number

2023-504957-11-00

When speaking to your doctor or clinical trial representative, please have the trial reference number available.

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