Acute Safety, Tolerability, Feasibility and Pharmacokinetics of Intrath. Administered ATI355 in Patients With Acute SCI

PHASE1CompletedINTERVENTIONAL
Enrollment

52

Participants

Timeline

Start Date

May 31, 2006

Primary Completion Date

September 30, 2011

Study Completion Date

September 30, 2011

Conditions
Acute Spinal Cord Injury
Interventions
DRUG

ATI355

Trial Locations (14)

8008

Novartis Investigative site, Zurich

21033

Novartis Investigative site, Hamburg

34537

Novartis Investigative site, Bad Wildungen

44789

Novartis Investigative site, Bochum

69118

Novartis Investigative site, Heidelberg

72076

Novartis Investigative site, Tübingen

76307

Novartis Investigative site, Karlsbad-Lagensteinbach

82418

Novartis Investigative site, Murnau am Staffelsee

89081

Novartis Investigative site, Ulm

Unknown

Novartis Investigative site, Calgary

Novartis Investigative site, Montreal

Novartis Investigative site, Toronto

Novartis Investigative site, Vancouver

09445

Novartis Investigative site, Bayreuth

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Novartis

INDUSTRY

NCT00406016 - Acute Safety, Tolerability, Feasibility and Pharmacokinetics of Intrath. Administered ATI355 in Patients With Acute SCI | Biotech Hunter | Biotech Hunter