Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
NMT.004 is an antisense oligonucleotide (ASO) drug candidate developed by Neumirna Therapeutics ApS, currently in preclinical development for the treatment of epilepsy and other nervous system diseases. The specific molecular target and mechanism of action have not been publicly disclosed, but as an ASO, it is designed to modulate gene expression at the RNA level, likely by binding to a specific mRNA sequence involved in disease pathology[1]. No clinical trial data or additional indications are available at this time.
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 NMT.004.