Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
miR-92a inhibitors are a class of RNA-based therapeutics, typically antisense oligonucleotides or antagomirs, designed to silence the activity of microRNA-92a. Research from the Brigham and Women’s Hospital and Harvard Medical School has identified miR-92a as a critical regulator of the immune balance in central nervous system (CNS) autoimmune diseases like multiple sclerosis (MS). miR-92a is often elevated in MS patients and promotes neuroinflammation by inhibiting the transcription factor Foxo1, which in turn suppresses the development of regulatory T cells (Tregs) and enhances the differentiation of inflammatory Th17 cells. Preclinical studies in experimental autoimmune encephalomyelitis (EAE) models have demonstrated that miR-92a inhibition can attenuate disease severity by recalibrating the Treg/Th17 ratio, suggesting its potential as a therapeutic strategy for autoimmune disorders.
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 miR-92a inhibitor.