Study Evaluating the Long-Term Safety and Efficacy of ABX464 in Patients With Moderate to Severe Rheumatoid Arthritis

PHASE2CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

October 24, 2019

Primary Completion Date

April 30, 2021

Study Completion Date

January 23, 2023

Conditions
Rheumatoid Arthritis
Interventions
DRUG

ABX464

All subjects will receive ABX464 administered at 50 mg o.d for an overall period of 2 years (104 weeks).

Trial Locations (24)

Unknown

Cliniques Universitaires Saint-Luc, Brussels

UZ Gent, Ghent

UZ Leuven, Leuven

ZNA Jan Palfijn, Merksem

Fakultni Tomayerova nemocnice, Prague

Revmatologicky ustav, Prague

CHU de Brest - Hôpital Cavale Blanche, Brest

CHD Vendée, La Roche-sur-Yon

CHU DE MONTPELLIER - Hôpital Lapeyronie, Montpellier

GHR Mulhouse Sud-Alsace, Mulhouse

CHU de Nice - Hôpital Pasteur, Nice

CHR d'Orléans, Orléans

APHP - Hôpital Salpétrière, Paris

CHU de Tours - Hôpital Trousseau, Tours

Complex Medical Centre - Déli Klinika, Budapest

CRU Hungary Ltd., Miskolc

CMed Rehabilitációs és Diagnosztikai Központ, Székesfehérvár

ClinicMed Daniluk, Nowak Sp. J., Bialystok

Pratia MCM, Krakow

Zespół Poradni Specjalistycznych REUMED, Lublin

NZOZ Lecznica MAK-MED S.C., Nadarzyn

Medyczne Centrum Hetmańska, Poznan

National Institute of Geriatrics, Warsaw

RHEUMA MEDICUS Zakład Opieki Zdrowotnej, Warsaw

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Abivax S.A.

INDUSTRY