Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Ad.hIFN-β is a recombinant, replication-defective adenoviral gene therapy vector encoding human interferon-β (hIFN-β). After local administration into tumors or serosal cavities, transduced cells express hIFN-β, producing antiproliferative, pro-apoptotic, and immunomodulatory effects, including induction of tumor cell apoptosis and stimulation of innate immune responses such as NK cell activity. Clinical phase 1 studies have evaluated intratumoral administration in malignant glioma and intrapleural administration in pleural malignancies, demonstrating detectable intratumoral hIFN-β, dose-dependent vector DNA distribution, feasibility, and a safety profile with occasional dose-limiting neurotoxicity at higher intratumoral doses.
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 Ad.hIFN-β.