drugset / Trial / NCT05304169

Study to Evaluate the Safety and Efficacy of Switching From Zoladex® Monthly or Quarterly, to Eligard® Semiannual.

NCT05304169

Phase 4 Completed 48 enrolled Zodiac Produtos Farmaceuticos S.A.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy, quality of life and safety of switching from monthly (3.6 mg) or quarterly (10.8 mg) goserelin acetate (Zoladex®) to semiannual leuprorelin acetate 45 mg (Eligard® 45 mg) in prostate cancer patients with adequate hormonal castration level (plasma testosterone levels ≤50 ng/dL).

Timeline

Start
2017-11-14
Primary completion
2018-06-15
Completion
2020-06-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Leuprolide Other / unclassified 45 mg Subcutaneous

Indications