Condition: Advanced HR - Positive, HER2 - Negative Breast Cancer · Resistant to (Neo)Adjuvant Endocrine Therapy · Sponsor: Fudan University
This study adopts a single-center, open-label, non-randomized trial design. It plans to enroll patients with HR- positive, HER2- negative advanced breast cancer who are resistant to (neo)adjuvant endocrine therapy. Dose-escalation and dose-expansion studies will be carried out to evaluate the safety, tolerability, and preliminary efficacy of sirolimus (albumin-bound) in combination with palbociclib and fulvestrant in this patient population, and to confirm the recommended phase 2 dose (RP2D)
This description comes directly from the study's public registry record.
Zhimin Shao, PhD,MD · +086 64175590 · zhimingshao@yahoo.com
Always discuss trial participation with your own doctor first.
| Cancer Hospital Affiliated to Fudan University | Shanghai, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06856200