Drug intelligence / Profile preview

QR-6401

Development stage
Preclinical
Lead developer
Genentech
Modality
Small Molecules
Administration
Oral
01

Overview

QR-6401 is an orally active, highly potent, and selective macrocyclic small molecule inhibitor of cyclin-dependent kinase 2 (CDK2). Discovered by Regor Therapeutics in collaboration with Tencent AI Lab using generative artificial intelligence models and structure-based drug design, QR-6401 is designed to target CDK2-dependent cancers and overcome resistance to CDK4/6 inhibitors. In preclinical studies, QR-6401 demonstrated robust antitumor efficacy in OVCAR3 ovarian cancer xenograft models. In September 2024, Genentech (a member of the Roche Group) acquired Regor's portfolio of next-generation CDK inhibitors, which includes QR-6401, for global clinical development, manufacturing, and commercialization.

02

Targets

CDK1 (Cyclin-dependent kinase 1)CDK2 (Cyclin-dependent kinase 2)CDK4 (Cyclin-dependent kinase 4)CDK6 (Cyclin-dependent kinase 6)CDK9 (Cyclin-dependent kinase 9)CCNE1 (Cyclin E1)GSK3 (Glycogen synthase kinase 3 beta)

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