Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
MEDI9197 + durvalumab is a combination regimen investigated for advanced solid tumors, comprising intratumoral MEDI9197, a toll-like receptor 7 and 8 (TLR7/8) agonist, with intravenous durvalumab, a monoclonal antibody checkpoint inhibitor targeting programmed cell death ligand-1 (PD-L1)[1][2][3][4]. MEDI9197 stimulates local and systemic antitumor immune responses via TLR7/8 activation, resulting in increased CD8+ T cells, PD-L1+ cells, induction of type 1 and 2 interferons, and a T helper 1 response. Durvalumab blocks PD-L1, preventing T cell inhibition and facilitating immune-mediated tumor cell killing. Developed to be administered by intratumoral injection for MEDI9197 and intravenous infusion for durvalumab, the combination was tested in a phase 1 trial for safety, pharmacodynamics, and anti-tumor activity. No objective responses were observed, but immune activation was demonstrated, and disease stabilization occurred in some participants[1][2][3][4].
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 MEDI9197 + durvalumab.