Project Details
Description
A Phase 2 Open-label, Dose Escalation Study of HST5040 in Subjects with Propionic or Methylmalonic Acidemia Followed by a 6-Month, Randomized, Double-blind, Placebo-controlled, 2-period Crossover and an Open-label, Long-term Extension
Status | Active |
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Effective start/end date | 6/1/20 → 7/31/25 |
Funding
- HEMOSHEAR THERAPEUTICS, LLC
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