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fluzoparib + apatinib + paclitaxel
- Development stage
- Phase 1
- Lead developer
- Hengrui Therapeutics
- Modality
- Small Molecules
- Administration
- Oral, Intravenous
01
Overview
This combination consists of **fluzoparib** (a small molecule poly (ADP-ribose) polymerase [PARP] inhibitor), **apatinib** (a small molecule vascular endothelial growth factor receptor 2 [VEGFR2] inhibitor/anti-angiogenic agent), and **paclitaxel** (a taxane-based small molecule chemotherapeutic that stabilizes microtubules to inhibit mitosis). The combination is being explored for synergistic anti-tumor effects, particularly in recurrent ovarian cancer and triple-negative breast cancer, based on mechanisms that include DNA damage, inhibition of homologous recombination repair, anti-angiogenesis, and disruption of cell division. Preclinical and early clinical studies suggest enhanced antitumor efficacy compared to monotherapy regimens[1][3][5].
- Other names
- SHR-1209SHR1209SHR 1209rivoceranibYN-968D1YN968D1YN 968D1
02
Targets
VEGFR2 (Vascular endothelial growth factor receptor 2)PARP1 (Poly (adp-ribose) polymerase 1)TUBB (Tubulin (alpha and beta subunits))
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