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NCT04932005

A Study of DZD2269 in Healthy Adult Participants

Completed Phase 1 Last updated 1 July 2022
What this trial tests

Phase 1 trial testing DZD2269 in Healthy Volunteers in 72 participants. Completed in 12 April 2022.

Timeline
29 June 2021
Primary endpoint
1 April 2022
12 April 2022

Quick facts

Lead sponsorDizal Pharmaceuticals
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment72
Start date29 June 2021
Primary completion1 April 2022
Estimated completion12 April 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Dizal Pharmaceuticals — full company profile →

Who can join

Adults 18 to 55, any sex, with Healthy Volunteers. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a research study in healthy participants. The purpose of this study is to see how safe the study drug is and how well it is tolerated after dosing. This study will also investigate pharmacokinetics of DZD2269; renal excretion of DZD2269 will also be evaluated. The study will also measure biomarkers such as pCREB in the blood.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Overcoming high level adenosine-mediated immunosuppression by DZD2269, a potent and selective A2aR antagonist.
    Bai Y, Zhang X, Zheng J, Liu Z, et al · · 2022 · cited 21× · PMID 36229853 · DOI 10.1186/s13046-022-02511-1

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Other trials of DZD2269

Trials testing the same drug.

Other recruiting trials for Healthy Volunteers

Currently open trials in the same condition.

Other Dizal Pharmaceuticals trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04932005.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing