Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
**MIW815 + PDR001** is a combination investigational immunotherapy regimen designed for patients with advanced or metastatic solid tumors or lymphomas. MIW815, also known as ADU-S100, is a synthetic cyclic dinucleotide and a stimulator of interferon genes (STING) pathway agonist, administered via intratumoral injection to activate innate immune responses within the tumor microenvironment. PDR001, also known as spartalizumab, is a fully human monoclonal antibody directed against programmed cell death protein 1 (PD-1), functioning as a checkpoint inhibitor and administered by intravenous infusion. The combination was evaluated primarily for safety, tolerability, pharmacokinetics, preliminary antitumor efficacy, and immune activation. Novartis sponsored and developed the clinical study. The program was terminated before dose expansion due to lack of meaningful antitumor activity in the dose-escalation phase, not for safety reasons[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 MIW815 + PDR001.