Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Fulvestrant + vinorelbine is a combination regimen of two pharmaceutical agents used in the treatment of hormone receptor-positive (HR+), human epidermal growth factor receptor 2-negative (HER2−) recurrent or metastatic breast cancer. Fulvestrant is a selective estrogen receptor degrader (SERD) that binds, blocks, and accelerates degradation of the estrogen receptor, thereby inhibiting estrogen signaling in breast cancer cells. Vinorelbine is a semi-synthetic vinca alkaloid chemotherapeutic agent that inhibits microtubule assembly, disrupting mitosis and leading to cell death. The combination has shown synergistic antitumor effects both in vitro and in clinical studies for ER-positive breast cancer, with fulvestrant downregulating chemoresistance factors such as Bcl2 and microtubule-associated protein tau. This dual approach targets both endocrine pathways and proliferative mechanisms to improve outcomes for patients with advanced HR+/HER2− breast cancer[1][2][5].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on fulvestrant + vinorelbine.