Drug intelligence / Profile preview

ABSK061 + ABSK043

Development stage
Unknown
Lead developer
Abbisko Therapeutics
Modality
Small Molecules
Administration
Oral
01

Overview

ABSK061 + ABSK043 is a combination of two investigational small molecule drugs developed by Abbisko Therapeutics for the treatment of solid tumors with FGFR2/3 alterations. - **ABSK061** is a novel, orally bioavailable, highly potent and selective inhibitor of fibroblast growth factor receptor 2 (FGFR2) and fibroblast growth factor receptor 3 (FGFR3). It was designed to minimize inhibition of FGFR1 in order to reduce side effects while maintaining efficacy against FGFR2/3-driven cancers. - **ABSK043** is an oral small molecule inhibitor targeting programmed death-ligand 1 (PD-L1), blocking the PD-1/PD-L1 interaction to enhance anti-tumor immune responses. Compared to antibody-based checkpoint inhibitors, it offers lower immunogenic risk and oral administration convenience. The combination is being evaluated in phase II clinical trials for metastatic or unresectable solid tumors harboring FGFR2/3 alterations—including non-small cell lung cancer, gastric/gastroesophageal junction carcinoma (HER2 negative), urothelial carcinoma, esophageal cancer, and other solid tumors—with or without chemotherapy. Both agents are also being explored for potential use in non-oncology indications such as achondroplasia[1][4][5][7].

02

Targets

FGFR2 (Keratinocyte growth factor receptor)FGFR3 (Fibroblast growth factor receptor 3)CD274 (Programmed cell death protein 1 ligand 1)

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