Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**Vepdegestrant + ribociclib** is an investigational oral combination therapy composed of vepdegestrant, a potent PROteolysis TArgeting Chimera (PROTAC) estrogen receptor degrader, and ribociclib, a cyclin-dependent kinase 4/6 (CDK4/6) inhibitor. Vepdegestrant induces proteasome-mediated degradation of estrogen receptor, blocking estrogen signaling and potentially leading to inhibition of ER+ breast cancer cell proliferation and survival. Ribociclib inhibits CDK4 and CDK6, preventing cell cycle progression from G1 to S phase in actively dividing tumor cells. The combination is targeted towards estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. Preclinical and early clinical studies suggest synergistic antitumor activity when these agents are used together, particularly in patients whose disease has progressed after prior endocrine or CDK4/6 inhibitor therapies[3][5][7].
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 vepdegestrant + ribociclib.