Drug intelligence / Profile preview

benmelciclib + irinotecan

Development stage
Unknown
Lead developer
Chia Tai-Tianqing Pharmaceutical Group
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

Benmelciclib + irinotecan is a combination therapy consisting of benmelciclib (TQB3616), an orally bioavailable selective inhibitor of cyclin-dependent kinases 4 and 6 (CDK4/6), and irinotecan, a topoisomerase I inhibitor. Benmelciclib works by blocking the transition from the G1 to the S phase of the cell cycle, thereby inhibiting tumor cell proliferation. Irinotecan, a derivative of camptothecin, induces double-strand DNA breaks by stabilizing the topoisomerase I-DNA complex. This combination is primarily being investigated by Chia Tai Tianqing Pharmaceutical Group for the treatment of advanced solid tumors, including colorectal cancer and small cell lung cancer, where CDK4/6 inhibition may enhance the cytotoxic effects of chemotherapy or overcome resistance.

Brand names
Camptosar
Other names
TQB3616 + irinotecanbenmelciclib + irinotecan hydrochloride
02

Targets

TOP1 (DNA Topoisomerase I)CDK6 (Cyclin-dependent kinase 6)CDK4 (Cyclin-dependent kinase 4)

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