Study to Evaluate the Safety and Analgesic Activity of ATx08-001 in Subjects With Postherpetic Neuralgia

PHASE2CompletedINTERVENTIONAL
Enrollment

61

Participants

Timeline

Start Date

March 31, 2011

Primary Completion Date

July 31, 2011

Study Completion Date

July 31, 2011

Conditions
Postherpetic Neuralgia
Interventions
DRUG

ATx08-001

ATx08-001 will be administered as a 6mm white film coated tablet of 2.5 mg strength, to be taken orally at a dose of 2.5 mg or 7.5 mg, twice a day approximately every 12 hours over an 8 day period.

DRUG

Placebo

Placebo will be administered as a 6mm white film coated tablet, twice a day approximately every 12 hours over an 8 day period. Placebo is identical in appearance to the ATx 08-001 tablet.

Trial Locations (9)

33015

San Marcus Research Clinic, Miami

33189

Homestead Clinical Research, Cutler Bay (Miami)

48025

Quest Research Institute, Bingham Farms

75231

Radiant Research, Dallas

85225

Radiant Research, Chandler

85381

Premier Research Center, Peoria

89106

Affiliated Clinical Research, Las Vegas

89146

Radiant Research, Las Vegas

02135

Boston Clinical Trials, Boston

Sponsors
All Listed Sponsors
collaborator

National Institute of Neurological Disorders and Stroke (NINDS)

NIH

collaborator

Symbiance, Inc

UNKNOWN

collaborator

Parallax Clinical Research, LLC

OTHER

lead

Aestus Therapeutics

INDUSTRY