Study to Assess the Safety of Dupilumab (REGN668/SAR231893) Administered Concomitantly With Topical Corticosteroids (TCS) in Patients With Moderate-to-severe Atopic Dermatitis (AD)

PHASE2CompletedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

July 31, 2012

Primary Completion Date

December 31, 2012

Study Completion Date

December 31, 2012

Conditions
Atopic Dermatitis
Interventions
DRUG

Dupilumab

Dupilumab 300 mg once weekly (QW) for 4 weeks

DRUG

Placebo (for Dupilumab)

Placebo (for Dupilumab) once weekly (QW) for 4 weeks

OTHER

Topical Corticosteroid (TCS)

TCS such as methylprednisolone aceponate 0.1%, mometasone furoate 0.1%, or betamethasone valerate 0.1%

Trial Locations (13)

Unknown

Berlin

Dresden

Dülmen

Frankfurt

Gera

Langenau

Münster

Szeged-Hungary

Szolnok

Gdansk

Lodz

Lublin

Warsaw

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Sanofi

INDUSTRY

lead

Regeneron Pharmaceuticals

INDUSTRY