Study of Daclatasvir (BMS-790052) and Simeprevir (TMC435) in Patients With Genotype 1 Chronic Hepatitis C Virus

PHASE2CompletedINTERVENTIONAL
Enrollment

230

Participants

Timeline

Start Date

July 31, 2012

Primary Completion Date

August 31, 2013

Study Completion Date

November 30, 2013

Conditions
Hepatitis C Virus
Interventions
DRUG

Daclatasvir

Tablets, oral, 30 mg, once daily

DRUG

Simeprevir

Capsule, oral, 150 mg, once daily

DRUG

Ribavirin

Tablets, oral, 500-600 mg, twice daily

Trial Locations (26)

1097

Local Institution, Budapest

1119

Local Institution, Buenos Aires

1126

Local Institution, Budapest

5700

Local Institution, Gyula

10969

Local Institution, Berlin

13285

Local Institution, Marseille

20099

Local Institution, Hamburg

21093

Johns Hopkins University, Lutherville

22031

Metropolitan Research, Fairfax

28046

Local Institution, Madrid

33600

Local Institution, Pessac

37205

Nashville Medical Research Institute, Nashville

46010

Local Institution, Valencia

46202

Indiana University, Indianapolis

50937

Local Institution, Cologne

54511

Local Institution, Vandœuvre-lès-Nancy

60590

Local Institution, Frankfurt

75651

Local Institution, Paris

75679

Local Institution, Paris

76012

Texas Clinical Research Institute, Llc, Arlington

87042

Local Institution, Limoges

94010

Local Institution, Créteil

94110

San Francisco General Hospital, San Francisco

94118

Kaiser Permanente Med Ctr, San Francisco

C1181ACH

Local Institution, Buenos Aires

08035

Local Institution, Barcelona

Sponsors
All Listed Sponsors
collaborator

Janssen Research & Development, LLC

INDUSTRY

lead

Bristol-Myers Squibb

INDUSTRY

NCT01628692 - Study of Daclatasvir (BMS-790052) and Simeprevir (TMC435) in Patients With Genotype 1 Chronic Hepatitis C Virus | Biotech Hunter | Biotech Hunter