A Study to Assess the Analgesic Efficacy and Safety of ASP8062 in Subjects With Fibromyalgia

PHASE2CompletedINTERVENTIONAL
Enrollment

183

Participants

Timeline

Start Date

May 8, 2017

Primary Completion Date

March 6, 2018

Study Completion Date

March 6, 2018

Conditions
Fibromyalgia
Interventions
DRUG

ASP8062

ASP8062 30 mg was administered orally as a single daily dose, taken preferably in the morning with or without food.

DRUG

Placebo

Placebo was administered orally as a single daily dose, taken preferably in the morning with or without food.

Trial Locations (24)

11235

NY Scientific, Brooklyn

11516

Neurobehavioral Research, Inc, Cedarhurst

18104

Lehigh Center for Clinical Research, Allentown

27103

PMG of Winston-Salem, LLC, Winston-Salem

27609

Private Practice, Raleigh

32720

Avail Clinical Research, LLC, DeLand

32801

Clinical Neuroscience Solutions, Inc, Orlando

33511

PAB Clinical Research, Brandon

37421

ClinSearch, LLC, Chattanooga

39202

Elite Clinical Research, LLC, Jackson

44718

Neuro-Behavioral Clinical Research, Inc, Canton

45219

University of Cincinnati, Cincinnati

47714

Medisphere Medical Research Center, LLC, Evansville

53142

Clinical Investigation Specialists, Inc, Kenosha

57049

Meridian Clinical Research, Dakota Dunes

60634

Chicago Research Center, Inc, Chicago

64114

The Center For Pharmaceutical Research, Kansas City

85032

Noesis Pharma, LLC, Phoenix

89123

Advanced Biomedical Research of America, Las Vegas

90502

Collaborative Neuroscience Network, LLC., Torrance

92056

Excell Research, Inc, Oceanside

97210

Summit Research Network, Portland

02747

Infinity Medical Research, Inc, North Dartmouth

02886

Omega Medical Research, Warwick

All Listed Sponsors
lead

Astellas Pharma Global Development, Inc.

INDUSTRY

NCT03092726 - A Study to Assess the Analgesic Efficacy and Safety of ASP8062 in Subjects With Fibromyalgia | Biotech Hunter | Biotech Hunter