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Clinical Trials · NCT00832091

Study of Thymosin Beta 4 in Patients With Venous Stasis Ulcers

CompletedPhase 2TB-500 (Approved)
Phase
Phase 2
Recruitment status
Completed
Sponsor
RegeneRx Biopharmaceuticals, Inc.
Enrollment
72
Start date
Jul 2006
Locations
8 sites, Italy, Poland
Primary endpoint
Safety and Tolerability of Thymosin Beta 4 (Tβ4) Applied to Patients With Venous Stasis (VS) Ulcers for up to 84 Days
View TB-500 compound reference