Drug intelligence / Profile preview

DZD2269

Development stage
Phase 1
Lead developer
Dizal Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

DZD2269 is a potent and selective small molecule antagonist of the adenosine A2A receptor (A2AR; also known as ADORA2A), developed as an immune checkpoint inhibitor with immunomodulating and antineoplastic activities. By selectively binding to and inhibiting A2AR expressed on T lymphocytes, DZD2269 reverses adenosine-induced immunosuppression in the tumor microenvironment, thereby restoring immune cell function. Preclinical studies have shown that DZD2269 can enhance antitumor activity when combined with anti-PD1 antibodies or radiotherapy. Clinical trials are ongoing to evaluate its safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy in patients with metastatic castration-resistant prostate cancer[1][2][5][7].

02

Targets

ADORA2A (Adenosine A₂A Receptor)

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