Condition: Breast Cancer Early Stage Breast Cancer (Stage 1-3) · Sponsor: Yale University
This is a phase II, randomized, double-blinded, placebo-controlled trial designed to evaluate the efficacy of fezolinetant (45 mg a day) vs. placebo in reducing moderate to severe vasomotor symptoms (VMS) in breast cancer survivors on endocrine therapy (tamoxifen, aromatase inhibitors). The trial will proceed in a single stage, and the total of 92 participants will be randomized in 1:1 fashion to fezolinetant or placebo arm respectively.
This description comes directly from the study's public registry record.
Laura Kane · 773-369-6904 · laura.kane@yale.edu
Always discuss trial participation with your own doctor first.
| Yale University | New Haven, Connecticut, United States | Recruiting |
| The Ohio State University Comprehensive Cancer Center | Columbus, Ohio, United States | Not Yet Recruiting |
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Source record: clinicaltrials.gov/study/NCT06917313