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Clinical Trials · NCT02646189

Therapeutic Safety and Efficacy of REP 2139 (REP 9AC') in HBV Infected Patients

CompletedPhase 1/Phase 2Thymosin-Alpha-1 (Approved)
Phase
Phase 1/Phase 2
Recruitment status
Completed
Sponsor
Replicor Inc.
Enrollment
12
Start date
Aug 2011
Locations
1 site, Bangladesh
Primary endpoint
Safety and tolerability of REP 2139-Ca + immunotherapy
View Thymosin-Alpha-1 compound reference