Stopped: Homology Medicines has discontinued the development of this program.
This is a Phase 1/2, open-label, randomized, concurrently-controlled, dose escalation study to evaluate the safety and efficacy of HMI-102 in adult PKU subjects with PAH deficiency. Participants will receive a single administration of HMI-102 and will be followed for safety and efficacy for 1 year.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Incidence and severity of treatment-emergent adverse events (TEAEs) (Dose Escalation Phase)
Timeframe: Baseline to Week 52
Change from baseline in clinical laboratory values (Dose Escalation Phase)
Timeframe: Baseline to Week 52
Change from baseline in 12-lead electrocardiograms (ECGs), vital signs, physical examinations (Dose Escalation Phase)
Timeframe: Baseline to Week 52
Incidence of sustained plasma Phe concentration of ≤360 μmol/L at 28 weeks post dose (Dose Escalation Phase)
Timeframe: Week 28
Change from baseline in Plasma Phe Concentration (Dose Escalation Phase)
Timeframe: Weeks 24-28
Change from baseline in mean Plasma Phe Concentration (Dose Expansion Phase)
Timeframe: Weeks 24-28