Safety Study of Gene Therapy in Treating Critical Leg Ischemia

PHASE1CompletedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

April 3, 2007

Primary Completion Date

October 19, 2009

Study Completion Date

December 11, 2023

Conditions
Critical Limb Ischemia
Interventions
BIOLOGICAL

VM202 2 mg

2 mg intramuscular injection with the first half of the total dose given on Day 1 and the second half on Day 15

BIOLOGICAL

VM202 4 mg

4 mg intramuscular injection, with half of the total dose given on Day 1 and the second half given on Day 15

BIOLOGICAL

VM202 8 mg

8 mg intramuscular injection. The first half of the total dose given on Day 1 and the second half on Day 15.

BIOLOGICAL

VM202 16 mg

16 mg dose intramuscular injection. The first half of the total dose given on Day 1 and the second half on Day 15.

Trial Locations (1)

55407

Minneapolis Heart Institute Foundation/ Abbott Northwestern Hospital, Minneapolis

All Listed Sponsors
lead

Helixmith Co., Ltd.

INDUSTRY

NCT00696124 - Safety Study of Gene Therapy in Treating Critical Leg Ischemia | Biotech Hunter | Biotech Hunter