A 52-Week, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Evaluate the Efficacy and Safety of a 200-mcg Dose of IPP-201101 Plus Standard of Care in Patients With Systemic Lupus Erythematosus

PHASE3CompletedINTERVENTIONAL
Enrollment

202

Participants

Timeline

Start Date

March 31, 2015

Primary Completion Date

January 31, 2018

Study Completion Date

January 31, 2018

Conditions
Lupus Erythematosus, Systemic
Interventions
DRUG

IPP-201101

DRUG

Placebo

OTHER

Standard of Care

Trial Locations (30)

1097

Egyesitett Szt.István és Szt. László Kórház, Budapest

5700

Synexus Gyula AS, Gyula

8000

Mentaház Magánorvosi Központ Kft., Székesfehérvár

33614

McILwain Medical Group, Tampa

Unknown

WALLACE, Los Angeles

East Bay Rheumatology Medical, San Leandro

Denver Arthritis Clinic, Denver

Arthritis and Rheumatic Disease Specialties, Aventura

Arthritis Research & Treatment Center, Stockbridge

Innovative Health Research, Las Vegas

Thurston Arthritis Research Center, Chapel Hill

DJL Clinical Research, PLLC, Charlotte

Revmatologie s.r.o., Brno

CHU Felix Guyon, Saint-Denis

Hopital Haut Lévêque, Bordeaux

Hôpital européen, Marseille

GHR Mulhouse Sud-Alsace, Mulhouse

Hôpital Cochin, Paris

CHU Strasbourg Hôpital de Hautepierre, Strasbourg

CHU Strasbourg Nouvel Hôpital Civil, Strasbourg

Schlosspark-Klinik Berlin, Berlin

Clinic for Rheumatology and Internal Medicine, Freiburg im Breisgau

University of Debrecen Medical Center Department of Clinical Immunology, Debrecen

Cap Research, Phoenix

Centrum Medyczne Plejady, Krakow

Krakowskie Centrum Medyczne, Krakow

Centrum Medyczne Hetmańska, Poznan

Centrum Medyczne Oporow, Wroclaw

128 50

Revmatologický ústav v Praze, Prague

00909

Latin Clinical Trial Center, San Juan

Sponsors

Lead Sponsor

All Listed Sponsors
lead

ImmuPharma

INDUSTRY