Study of GC1008 in Patients With Idiopathic Pulmonary Fibrosis (IPF)

PHASE1CompletedINTERVENTIONAL
Enrollment

25

Participants

Timeline

Start Date

July 31, 2005

Primary Completion Date

September 30, 2008

Study Completion Date

September 30, 2008

Conditions
Idiopathic Pulmonary Fibrosis
Interventions
BIOLOGICAL

GC1008

0.3 mg/kg, IV on Day 0 and return to the clinic on 3,7, 10, 14, 21, 28, 42, 56, 84, 112, 140 post infusion for safety follow-up.

BIOLOGICAL

GC1008

1.0 mg/kg, IV on Day 0 and return to the clinic on 3,7, 10, 14, 21, 28, 42, 56, 84, 112, 140 post infusion for safety follow-up.

BIOLOGICAL

GC1008

2.0 mg/kg, IV on Day 0 and return to the clinic on 3,7, 10, 14, 21, 28, 42, 56, 84, 112, 140 post infusion for safety follow-up.

BIOLOGICAL

GC1008

4.0 mg/kg, IV on Day 0 and return to the clinic on 3,7, 10, 14, 21, 28, 42, 56, 84, 112, 140 post infusion for safety follow-up.

BIOLOGICAL

GC1008

8.0 mg/kg, IV on Day 0 and return to the clinic on 3,7, 10, 14, 21, 28, 42, 56, 84, 112, 140 post infusion for safety follow-up.

Trial Locations (8)

37232

Nashville

48109

Ann Arbor

55905

Rochester

60637

Chicago

80206

Denver

98195

Seattle

Unknown

Minneapolis

Belgium

All Listed Sponsors
lead

Genzyme, a Sanofi Company

INDUSTRY

NCT00125385 - Study of GC1008 in Patients With Idiopathic Pulmonary Fibrosis (IPF) | Biotech Hunter | Biotech Hunter