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Clinical Trials · NCT01786915

Safety and Pharmacokinetic (PK) Study of Oral Bendavia Administered for 7 Days

CompletedPhase 1Elamipretide (Approved)
Phase
Phase 1
Recruitment status
Completed
Sponsor
Stealth BioTherapeutics Inc.
Enrollment
30
Start date
Feb 2013
Locations
1 site, United States
Primary endpoint
Mean peak plasma concentration (Cmax) of Bendavia (ng/ml) on Day 1 in each cohort.
View Elamipretide compound reference