Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ATG-037 + pembrolizumab is an investigational combination therapy for advanced and metastatic solid tumors, particularly in checkpoint inhibitor (CPI)-resistant cancers such as melanoma and non-small cell lung cancer (NSCLC). ATG-037 is an orally available, small molecule inhibitor of CD73 (ecto-5'-nucleotidase), an immune checkpoint that generates immunosuppressive adenosine in the tumor microenvironment. By blocking CD73, ATG-037 can counteract adenosine-mediated suppression of anti-tumor immune responses. Pembrolizumab is an approved monoclonal antibody that targets programmed cell death protein 1 (PD-1), functioning as an immune checkpoint inhibitor to restore antitumor immunity. The combination is currently being studied in the ongoing STAMINA-01 trial, which has shown promising preliminary efficacy, including overall response rates (ORR) of 36.4% in melanoma and 22% in NSCLC, with manageable safety profiles[2][3][9][10]. ATG-037 was developed by Antengene, and pembrolizumab by Merck & Co. (MSD).
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 ATG-037 + pembrolizumab.