Efficacy and Safety of Ustekinumab, a Human Monoclonal Anti-IL-12/IL-23 Antibody, in Patients With Behçet Disease

PHASE2CompletedINTERVENTIONAL
Enrollment

16

Participants

Timeline

Start Date

June 14, 2017

Primary Completion Date

May 7, 2019

Study Completion Date

November 19, 2019

Conditions
Behçet Disease
Interventions
DRUG

Subcutaneous Ustekinumab

Injections of ustekinumab at 90 mg at week 0, week 4 and week 16. Patients in treatment failure at week 24 will terminate the study. Responder patients at week 24 will receive additional 2 injections of ustekinumab at week 28 and week 40 with a final evaluation at week 52.

Trial Locations (1)

75014

Hôpital Cochin, Department of Internal Medicine, National Reference Center for Autoimmune and Systemic Diseases, Paris

All Listed Sponsors
collaborator

URC-CIC Paris Descartes Necker Cochin

OTHER

lead

Assistance Publique - Hôpitaux de Paris

OTHER

NCT02648581 - Efficacy and Safety of Ustekinumab, a Human Monoclonal Anti-IL-12/IL-23 Antibody, in Patients With Behçet Disease | Biotech Hunter | Biotech Hunter