Phase IIb One Year Efficacy and Safety Study of S-2367 in Obese Subjects With Reduced Calorie Diet

PHASE2CompletedINTERVENTIONAL
Enrollment

724

Participants

Timeline

Start Date

June 30, 2007

Primary Completion Date

November 30, 2008

Study Completion Date

January 31, 2009

Conditions
Obesity
Interventions
DRUG

S-2367 Placebo

four placebo tablets (total dose = 0 mg/day S-2367) administered orally once-a-day with morning meal while on a reduced calorie diet for a total of 54 weeks,

DRUG

S-2367 800 mg

two 400 mg S-2367 tablets (total dose = 800 mg/day S-2367) administered orally once-a-day with morning meal while on a reduced calorie diet for a total of 54 weeks

DRUG

S-2367 1600 mg

four 400 mg S-2367 tablets (total dose = 1600 mg/day S-2367) administered orally once-a-day with morning meal while on a reduced calorie diet for total of 54 weeks,

OTHER

Reduced Calorie Diet

A diet with restricted calorie content

Trial Locations (38)

13104

Manlius

14609

Rochester

23294

Richmond

27612

Raleigh

28025

Concord

28144

Salisbury

29615

Greenville

30328

Atlanta

32216

Jacksonville

33134

Coral Gables

34996

Stuart

36608

Mobile

37029

Burns

37620

Bristol

37920

Knoxville

39501

Gulfport

44122

Cleveland

44260

Mogadore

47714

Evansville

54303

Green Bay

60607

Chicago

62704

Springfield

63141

St Louis

66218

Shawnee Mission

68134

Omaha

71913

Hot Springs

77024

Houston

77566

Jackson

78229

San Antonio

85701

Tucson

95608

Carmichael

95661

Roseville

95816

Sacramento

98057

Renton

06905

Stamford

01757

Milford

08009

Berlin

02920

Cranston

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Shionogi

INDUSTRY

NCT00747929 - Phase IIb One Year Efficacy and Safety Study of S-2367 in Obese Subjects With Reduced Calorie Diet | Biotech Hunter | Biotech Hunter