drugset / Trial / NCT06065748

A Study to Evaluate Efficacy and Safety of Giredestrant Compared With Fulvestrant (Plus a CDK4/6 Inhibitor), in Participants With ER-Positive, HER2-Negative Advanced Breast Cancer Resistant to Adjuvant Endocrine Therapy (pionERA Breast Cancer)

NCT06065748

Phase 3 Recruiting 1050 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase III, randomized, open-label multicenter study that will evaluate the efficacy and safety of giredestrant compared with fulvestrant, both in combination with the investigator's choice of a CDK4/6 inhibitor (palbociclib, ribociclib or abemaciclib), in participants with estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) advanced breast cancer who have developed resistance to adjuvant endocrine therapy.

Timeline

Start
2023-12-11
Primary completion
2027-02-19
Completion
2029-02-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Fulvestrant Small molecule 500 mg Intramuscular
Subject Giredestrant Small molecule 30 mg Oral
Background Abemaciclib Small molecule 150 mg Oral
Background Palbociclib Small molecule 125 mg Oral
Background Ribociclib Small molecule 600 mg Oral