PER-001
Phase 2- Indications
- Glaucoma
Company intelligence / Profile preview
Perfuse Therapeutics has completed a Phase 1/2a trial for PER-001 in glaucoma patients. The 24-week data showed that PER-001 was well-tolerated and demonstrated proof of concept with both functional and structural improvements. Patients treated with PER-001 on top of IOP reducing therapies experienced a mean improvement in visual field mean deviation of 1 decibel per year and a mean increase in retinal nerve fiber layer thickness of 3 microns at 24 weeks. The Phase 2a Dose 2 cohort is ongoing with topline data expected in Q2 2025.
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