Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
ASHA-091 is a novel mitochondrial dynamics targeting drug developed by Asha Therapeutics designed to inhibit mitochondrial fragmentation by specifically inhibiting DRP1 activation, a regulatory protein involved in mitochondrial fragmentation. This inhibition restores normal mitochondrial function and has demonstrated disease-modifying efficacy as a functional cure in preclinical models of neurodegenerative diseases such as Parkinson’s Disease and Alzheimer’s Disease. It also shows promise for treating other conditions linked to mitochondrial dysfunction including ME/CFS (Myalgic Encephalomyelitis/Chronic Fatigue Syndrome), Long COVID, Amyotrophic Lateral Sclerosis (ALS), stroke, and post-viral fatigue syndromes. The drug acts as a degradable molecular glue with mechanisms involving DENR inhibitors (density regulated re-initiation and release factor inhibitors) and UTRN modulators (Utrophin modulators). Preclinical studies have shown robust efficacy in reversing motor impairment in Parkinson’s disease mouse models and improving activity levels in ME/CFS models. Clinical trials are planned to begin by late 2024[1][2][3][4][5][7].
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 ASHA-091.