Status:

UNKNOWN

Changing the coUrse of cRohn's Disease With an Early Use of Adalimumab

Lead Sponsor:

Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives

Conditions:

CD

Eligibility:

All Genders

18-75 years

Phase:

PHASE4

Brief Summary

This is a prospective, longitudinal, multicenter study conducted in a cohort of patients with early CD. This study will not change the patient/physician relationship.

Detailed Description

The main objective will be to evaluate the sustained deep remission rate one year after discontinuation of a 12 month course of adalimumab in adult patients with early CD who have achieved deep remiss...

Eligibility Criteria

Inclusion

  • Male or female patient aged 18 years old to 75 years old 2. Patient with early luminal Crohn's disease (less than 24 months since diagnosis), 3. Patient who is
  • intolerant to immunosuppressants or steroids, or
  • primarily not responders to immunosuppressants for at least 3 months \[azathioprine: at least 2.5 mg/kg/d; 6-mercaptopurine: at least 1.5 mg/kg/d; methotrexate: 25 mg/week (subcutaneous or intramuscular route)\], and/or
  • not responder to steroids \[prednisolone equivalent at least 40 mg/d\], and/or
  • steroid-dependent \[unable to reduce corticosteroids below the equivalent of prednisolone 10 mg/d or budesonide \< 6 mg/d within 3 months of starting corticosteroids without recurrent active disease, or who have a relapse within 3 months of stopping corticosteroids\], 4. Patient with CDAI \> 150, 5. Patient with at least one ulcer in at least one affected segment (Magnetic Resonance Imaging (MRI) of gastrointestinal tract or colonoscopy or by video capsule conducted after failure of conventional therapy and within 12 weeks before inclusion in the study), 6. Patient naïve for anti-TNF, 7. Patient whose physician decides to start adalimumab as monotherapy independently from the study protocol, 8. Patient followed in a centre belonging to the GETAID network. 9. Written consent.

Exclusion

  • Patient with active complex perianal fistula according to the definition of the American Gastroenterological Association (AGA) \[high anal fistula, abscess, proctitis, multiple external openings\],
  • Patient with stoma,
  • previous surgery in IBD
  • Pregnant or breastfeeding women, absence of contraception
  • Patient with any contra-indication to adalimumab.
  • Patient with any contra-indication to MRI
  • Minors and people unable to give their consent (because of their physical or mental state).
  • Subject who has not given his/her consent to participate.
  • Subject participating in another study.

Key Trial Info

Start Date :

March 17 2015

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 1 2025

Estimated Enrollment :

203 Patients enrolled

Trial Details

Trial ID

NCT03306446

Start Date

March 17 2015

End Date

March 1 2025

Last Update

May 31 2023

Active Locations (23)

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Page 1 of 6 (23 locations)

1

Chu Liege

Liège, Belgium

2

Chu Amiens

Amiens, France

3

Chu Besancon

Besançon, France

4

CHU de Caen- Hopital de la Cote de Nacre

Caen, France, 14033