drugset / Trial / NCT04693507

Teverelix Evaluated in Advanced Prostate Cancer

NCT04693507 ↗

Phase 2 Completed 50 enrolled Antev Ltd.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety and efficacy of teverelix TFA in the treatment of advanced prostate cancer

Timeline

Start
2021-03-04
Primary completion
2022-12-05
Completion
2023-02-06

Drugs

EvaluationDrugModalityDoseRoute
Subject teverelix TFA Unknown 120 mg Subcutaneous
Subject teverelix TFA Unknown 180 mg Subcutaneous

Indications