drugset / Trial / NCT06428396

Study of Belzutifan (MK-6482) Plus Fulvestrant for ER+/HER2- Metastatic Breast Cancer (MK-6482-029/LITESPARK-029)

NCT06428396

Phase 2 Active not recruiting 120 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the efficacy and safety of belzutifan (MK-6482) plus fulvestrant compared to everolimus plus endocrine therapy (ET) (investigator's choice of fulvestrant or exemestane) in adults with estrogen receptor-positive, human epidermal growth factor receptor 2-negative (ER+/HER2-) unresectable metastatic breast cancer. There is no formal hypothesis testing in this study.

Timeline

Start
2024-11-27
Primary completion
2027-05-05
Completion
2028-12-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Belzutifan Small molecule 120 mg Oral
Comparator Everolimus Small molecule 10 mg Oral
Comparator Exemestane Small molecule 25 mg Oral
Subject Fulvestrant Small molecule 500 mg Intramuscular

Indications