Company intelligence / Profile preview
Akashi Therapeutics
- Ownership
- Private
- Employees
- ~5
- Development stage
- Phase 1
Overview
Akashi’s lead candidate HT-100 demonstrated promising anti-fibrotic and muscle-regenerative effects in early-stage trials for Duchenne muscular dystrophy, with favorable safety data at lower doses. However, the program was halted after a serious adverse event at the highest dose cohort; subsequent discussions with the FDA allowed resumption of development at lower doses. Additional candidates include DT‑200 and AT‑300 for DMD.
- Therapeutic areas
- OtherRare Diseases
- Modalities
- Small molecules (HT-100/halofuginone)Selective Androgen Receptor Modulator (SARM; DT-200)Cation channel modulator (AT-300)
- Industry
- Biotech
Drug pipeline
1 assetPartnerships
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