Efficacy and Safety Study of Ataciguat Versus Placebo in Patients With Neuropathic Pain

PHASE2CompletedINTERVENTIONAL
Enrollment

62

Participants

Timeline

Start Date

November 30, 2008

Primary Completion Date

June 30, 2009

Study Completion Date

September 30, 2009

Conditions
Pain
Interventions
DRUG

ataciguat (HMR1766)

oral administration 200mg once daily for 28 days

DRUG

placebo

oral administration once daily for 28 days

Trial Locations (3)

Unknown

Sanofi-Aventis Administrative Office, Vienna

Sanofi-Aventis Administrative Office, Prague

Sanofi-Aventis Administrative Office, Bucharest

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Sanofi

INDUSTRY

NCT00799656 - Efficacy and Safety Study of Ataciguat Versus Placebo in Patients With Neuropathic Pain | Biotech Hunter | Biotech Hunter