62
Participants
Start Date
February 27, 2018
Primary Completion Date
February 5, 2019
Study Completion Date
February 5, 2019
IPP-201101
200 mcg of IPP-201101 will be administered subcutaneously every 4 weeks for 24 weeks.
Arthritis and Rheumatic Disease Specialties, Aventura
Innovative Health Research, Las Vegas
WALLACE, Los Angeles
East Bay Rheumatology Medical, San Leandro
Revmatologie s.r.o., Brno
Revmatologický ústav v Praze, Prague
GHR Mulhouse Sud-Alsace, Mulhouse
CHU de la Réunion, Saint-Denis
Schlosspark-Klinik Berlin, Berlin
Clinic for Rheumatology and Internal Medicine, Freiburg im Breisgau
University of Debrecen Medical Center Department of Clinical Immunology, Debrecen
Mentaház Magánorvosi Központ Kft., Székesfehérvár
CAP Research, Phoenix
Latin Clinical Trial Center, San Juan
Lead Sponsor
ImmuPharma
INDUSTRY