Drug intelligence / Profile preview

adavosertib + durvalumab

Development stage
Unknown
Lead developer
AstraZeneca
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Oral, Intravenous
01

Overview

Adavosertib + durvalumab is a combination of two investigational drugs for cancer therapy. **Adavosertib** (AZD1775) is an orally administered, first-in-class, selective small molecule inhibitor of Wee1 kinase, which disrupts the G2/M checkpoint in tumor cells, leading to cell cycle arrest and apoptosis, particularly in p53-deficient tumors. **Durvalumab** (MEDI4736) is a monoclonal antibody that inhibits the programmed death ligand 1 (**PD-L1**), blocking its interaction with PD-1 and CD80 receptors, and thereby promoting an immune-mediated anti-tumor response. The combination aims to increase anti-tumor efficacy by simultaneously targeting tumor cell division and enhancing immune activity. This drug combination has been evaluated in phase 1 clinical trials for advanced solid tumors, focusing on safety, tolerability, and dose determination[1][2].

Brand names
Durvalumab
Other names
adavosertib + durvalumabAZD1775 + MEDI4736
02

Targets

CD274 (Programmed cell death protein 1 ligand 1)WEE1 (WEE1 G2 checkpoint kinase)

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