Phase II Study to Analyze Sarilumab in Non-Infectious Uveitis

PHASE2CompletedINTERVENTIONAL
Enrollment

58

Participants

Timeline

Start Date

October 31, 2013

Primary Completion Date

July 31, 2015

Study Completion Date

April 30, 2016

Conditions
Uveitis
Interventions
DRUG

Sarilumab

Pharmaceutical form: Prefilled syringes; Route of administration: Subcutaneous

DRUG

Prednisone

Pharmaceutical form: Tablet or Capsule; Route of administration: Oral

DRUG

Methotrexate

Pharmaceutical form: Tablet or Capsule or Suspension; Route of administration: Orally or intravenously or intramuscular

DRUG

Folic/folinic acid

Pharmaceutical form: Tablet or Capsule; Route of administration: Oral

OTHER

Placebo (for Sarilumab)

Pharmaceutical form: Prefilled syringes; Route of administration: Subcutaneous

Trial Locations (20)

12159

Investigational Site Number 840005, Slingerlands

12808

Investigational Site Number 203002, Prague

20132

Investigational Site Number 380001, Milan

34093

Investigational Site Number 792002, Istanbul

34098

Investigational Site Number 792003, Istanbul

35100

Investigational Site Number 792004, Izmir

Investigational Site Number 792006, Izmir

35128

Investigational Site Number 380003, Padua

42100

Investigational Site Number 380004, Reggio Emilia

44195

Investigational Site Number 840007, Cleveland

62500

Investigational Site Number 203001, Brno

75013

Investigational Site Number 250001, Paris

75571

Investigational Site Number 250002, Paris

76012

Investigational Site Number 840006, Arlington

01608

Investigational Site Number 840008, Worcester

68198-5540

Investigational Site Number 840009, Omaha

08028

Investigational Site Number 724003, Barcelona

08907

Investigational Site Number 724001, Barcelona

06100

Investigational Site Number 792001, Ankara

Investigational Site Number 792005, Ankara

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Sanofi

INDUSTRY

NCT01900431 - Phase II Study to Analyze Sarilumab in Non-Infectious Uveitis | Biotech Hunter | Biotech Hunter