Condition: Locally Advanced or Metastatic Breast Cancer · Sponsor: MediLink Therapeutics (Suzhou) Co., Ltd.
The study will evaluate the safety and efficacy of YL202, when compared with treatment of physician's choice (eribulin, capecitabine, vinorelbine, gemcitabine or sacituzumab govitecan) in participants with unresectable locally advanced, recurrent or metastatic hormone receptor-positive and human epidermal growth factor receptor 2-negative (HR+/HER2-) breast cancer who had failed at least one line of chemotherapy.
This description comes directly from the study's public registry record.
Medilink Study Team · +86 0512-62858368 · clinicaltrials@medilinkthera.com
Always discuss trial participation with your own doctor first.
| Fudan University Shanghai Cancer Center | Shanghai, Shanghai Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07461454