Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Opicinumab is a fully human monoclonal antibody developed as an experimental therapy for demyelinating diseases such as multiple sclerosis (MS) and acute optic neuritis. Its mechanism of action is antagonism of the LINGO-1 protein, a negative regulator of oligodendrocyte differentiation and axonal regeneration in the central nervous system. By blocking LINGO-1, opicinumab aims to promote the maturation of oligodendrocytes—the cells responsible for producing and maintaining myelin sheaths around nerve fibers—thereby facilitating remyelination and potentially reversing or preventing disability progression in MS. Despite promising preclinical data and early clinical trials, phase II studies did not demonstrate significant efficacy on primary endpoints in relapsing or progressive MS populations. As a result, further development has been discontinued by its developer[2][3][4][5].
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 opicinumab.