Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
AZD5069 + durvalumab is a combination therapy comprising AZD5069, an oral small molecule inhibitor of CXC chemokine receptor 2 (CXCR2), and durvalumab, a monoclonal antibody targeting programmed death-ligand 1 (PD-L1). AZD5069 acts by blocking CXCR2-mediated neutrophil recruitment and reprogramming neutrophil phenotypes in the tumor microenvironment. Durvalumab inhibits the interaction between PD-L1 and its receptors, enhancing T cell-mediated antitumor immunity. This combination is under investigation for use in advanced malignancies, primarily hepatocellular carcinoma and head and neck squamous cell carcinoma, aiming to synergize immunomodulation and targeted therapeutic effects[1][3][5]. It is being evaluated in phase I/II clinical trials for antitumor efficacy, safety, and recommended dosing[1][3][5].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on AZD5069 + durvalumab.