Drugs / DZD2269
last change Oct 2022 re-read 3 minutes ago

DZD2269

targets ADORA2A via inhibition

Developed for
castration-resistant prostate carcinoma
Investigated by
Dizal Pharmaceuticals

Trials 2

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT04932005 Jun 2021 → Apr 2022 — Dizal Pharmaceuticals Completed No outcome recorded
Phase 1 NCT04634344 Apr 2021 → May 2022 castration-resistant prostate carcinoma Dizal Pharmaceuticals Terminated No outcome recorded Stop: Business

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2022-10-18 Dizal Pharmaceuticals Results Dizal Announces the Latest Publication of DZD2269 in Journal of Experimental & Clinical Cancer Research dizalpharma.com ↗
DZD2269 alone showed anti-tumor activity in immunocompetent mouse models, and when in combination with radiotherapy, chemotherapy, or immune checkpoint inhibitors, its anti-tumor effect was significantly enhanced.
2022-05-27 Dizal Pharmaceuticals Results Dizal to Demonstrate the Strength and Rapid Acceleration of its Clinical Portfolio at ASCO 2022 dizalpharma.com ↗
Results from the Phase 1 healthy volunteer trial, which is evaluating the safety, PK, and effect on biomarkers, showed DZD2269 was safe and well tolerated from 5 mg to 160 mg, with no ≥ grade 3 TEAE or SAE reported.

Evidence & citations 4 cited values

Every value below carries the sentence it was read from. 3 sources stand behind the page.

FieldValueCited text
Known as DZD2269 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04634344 ↗
1

NCT04932005 ↗

Action Inhibit “DZD2269, a novel A2aR antagonist which can fully block A2aR mediated immunosuppression commonly found in TME.” PMID 36229853 ↗ Oct 2022
Route Oral “Part A: A single oral dose at 5mg, 10mg, 20mg, 40mg, 80mg, 160mg.” NCT04932005 ↗
Target ADORA2A “DZD2269, a novel A2aR antagonist which can fully block A2aR mediated immunosuppression commonly found in TME.” PMID 36229853 ↗ Oct 2022