Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Mavrostobart + docetaxel is a combination therapy consisting of **mavrostobart** (PT199), an anti-CD73 monoclonal antibody, and **docetaxel**, a small molecule chemotherapy agent. **Mavrostobart** inhibits both soluble and membrane-bound CD73 enzyme, countering the adenosine-mediated immunosuppressive tumor microenvironment and increasing antitumor immune activation. It offers full inhibition without “hook effect” at higher concentrations, overcoming limitations of other CD73 antibodies.[1][2][5][6] **Docetaxel** is a cytotoxic taxane that stabilizes microtubules and induces cell cycle arrest and apoptosis in dividing cells.[3][7] In combination, mavrostobart enhances immune activation while docetaxel exerts direct cytotoxic effects on tumor cells. The combination as investigated in the MORNINGSTAR (NCT05431270) clinical study is being used to evaluate safety, efficacy, and immune activation in advanced malignancies, with particular focus on solid tumors expressing high levels of CD73.[1][2][4][5][6]
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 mavrostobart + docetaxel.