Comparison of Azathioprine to Methotrexate in Combination Therapy With Adalimumab in Crohn's Disease: an Open-label Randomized Controlled Trial

Who is this study for? Patients with Crohn's disease
Status: Recruiting
Location: See location...
Intervention Type: Biological, Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Combination therapy, the association of an anti-Tumor Necrosis Factor (TNF) to an immunosuppressant, is recognized as the most effective treatment during Crohn's disease (CD). Several mechanisms have been proposed to explain the superiority of combination therapy over monotherapy, the additive effect of two effective drugs or the prevention of anti-TNF immunogenicity. As the best combination therapy is unknown, both azathioprine (AZA) and methotrexate (MTX) are used. Some retrospective studies suggest a higher effectiveness of AZA. MTX may have an advantage in terms of safety. The investigators hypothesize that AZA is more effective than MTX as combination therapy with adalimumab to improve short-term endoscopic, clinical and pharmacological outcomes in CD patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Male or female patients with age \> 18 years

• Crohn's disease for at least 6 weeks,

• Clinically active with CDAI \> 150

• Active inflammation by endoscopy (CDEIS \> 4) at baseline

• Not responder to conventional therapy or are intolerant to or have medical contraindications for such therapies and initiating treatment with adalimumab

• Patient followed in a center belonging to the GETAID network

• Fertile men and women of childbearing potential included in the protocol should use adequate methods of contraception according to study drug SMPCs.

• Written consent

Locations
Other Locations
France
CHU Amiens
RECRUITING
Amiens
Contact Information
Primary
Mathurin Fumery, Pr
Fumery.mathurin@chu-amiens.fr
03 22 08 88 51
Time Frame
Start Date: 2021-08-26
Estimated Completion Date: 2027-05
Participants
Target number of participants: 166
Treatments
Experimental: AZA group
Combination of sub-cutaneous administration of adalimumab at a dose of 160mg(W0)-80mg(W2)-40mg(W6) and then 40mg EOW and oral AZA capsules at a daily dose of 2.5 mg/kg
Experimental: MTX group
Combination of sub-cutaneous administration of adalimumab at a dose of 160mg (week (W) 0)-80mg(W2)-40mg(W6) and then 40mg EOW and sub-cutaneous MTX 25mg once a week
Sponsors
Collaborators: CMC Ambroise Paré, Pierre Cherest, Hartmann, CHU NICE, CHI TOULON LA SEYNE, University Hospital, Montpellier, CH ROUBAIX, CHRU TOURS, Hospices Civils de Lyon, CHU Rennes,France, Nantes University Hospital, Hopitaux Civils de Colmar, CHU REIMS, University Hospital, Clermont-Ferrand, CHU ROUEN - HOPITAL DE BOIS-GUILLAUME, Henri Mondor University Hospital, Centre Hospitalier Universitaire de Besancon, CH COTE BASQUE, University Hospital, Toulouse, University Hospital, Bordeaux, AP-HP - HU BEAUJON, CH VALENCE, CHU CAEN, CHU SAINT-ETIENNE, CH TOURCOING, CHU NANCY, CHRU LILLE, CHI CRETEIL
Leads: Centre Hospitalier Universitaire, Amiens

This content was sourced from clinicaltrials.gov