Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Niraparib + tebotelimab is an investigational combination therapy consisting of niraparib, an oral poly(ADP-ribose) polymerase (PARP) inhibitor, and tebotelimab (MGD013), a first-in-class bispecific monoclonal antibody targeting PD-1 and LAG-3. Developed by Zai Lab in collaboration with MacroGenics, this combination aims to leverage the synergistic effects of PARP inhibition and dual immune checkpoint blockade. Niraparib induces DNA damage and promotes an inflammatory tumor microenvironment, while tebotelimab reactivates exhausted T cells by simultaneously blocking the PD-1 and LAG-3 pathways. The combination was evaluated in Phase 1b trials for advanced solid tumors, including gastric cancer, triple-negative breast cancer, biliary tract carcinoma, and endometrial carcinoma. However, due to limited antitumor activity, further clinical development for this specific combination has been discontinued.
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 niraparib + tebotelimab.