Comparison of Methotrexate vs Placebo in Corticosteroid-dependent Ulcerative Colitis (METEOR)
Primary Purpose
Ulcerative Colitis
Status
Completed
Phase
Phase 2
Locations
International
Study Type
Interventional
Intervention
methotrexate
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Ulcerative Colitis
Eligibility Criteria
Inclusion Criteria:
- UC diagnosed according to the Lennard-Jones criteria (Appendix 1) with endoscopic colorectal lesions, whatever their extension may be
- A Mayo Disease Activity Index £ 4, with no item >1 for the clinical part of the score and from 0 to 2 for the endoscopic part at the time of inclusion
- Steroid-dependence defined by at least 1 unsuccessful attempt to stop systemic steroid therapy during the last 12 weeks. Steroid therapy might have been completely stopped if it has been restarted within the last 30 days
- To be receiving a treatment of prednisone at a dose between 10 and 40mg, stable for at least 2 weeks at the time of inclusion
- Under an adequate contraception for male or female subjects of childbearing potential
Exclusion Criteria:
- Indication to a colectomy.
- Alcoholism (more than 21 glasses per week for male subjects and 14 glasses per week for female subjects). 1 glass corresponds to 3 cl of strong alcohol, 10 cl glass of wine or a half pint of beer.
- Pregnant or breast-feeding female subjects.
- No efficacious contraception.
- NSAIDS or cotrimoxazole intake upon inclusion, or probenecid intake within 1 month prior to inclusion.
- Anti-TNFa treatment within 2 months prior to inclusion.
- Azathioprine, mercaptopurine, cyclosporin or thalidomide within 1 month prior to inclusion.
- Modification of mesalazine or olsalazine dosage within 1 month prior to inclusion.
- Chronic (broncho) pneumopathy.
- Renal failure (creatinaemia > upper limit of normal laboratory values limit).
- Liver disease apart from primary sclerosing cholangitis.
- Unexplained rise higher than twice the normal level for transaminases, alkaline phosphatases and/or bilirubin.
- Folate level < normal level.
- Past history of malignant condition (including leukaemia, lymphoma and myelodysplasia) except for baso-cellular cutaneous cancers.
Sites / Locations
- University Hospital of Vienna
- ULB - Cliniques Saint Luc
- CHU Amiens - Hôpital Nord
- CH Avignon
- Centre Hospitalier Universitaire de Besançon
- CHU Clermont-Ferrand - Hôpital Hotel Dieu
- APHP - Hôpital Beaujon
- APHP - Hôpital Bicêtre
- CHRU Lille - Hôpital Huriez
- CHU Nantes - Hôpital Hôtel Dieu
- CHU Nice - Hôpital de l'Archet 2
- APHP - Hôpital Saint Louis
- APHP - Hôpital Saint Antoine
- APHP - Hôpital Cochin
- CHU Bordeaux - Hôpital Haut L'Eveque
- CHU Rouen - Hôpital Charles Nicolle
- CHU St Etienne - Hôpital NOrd
- CHU Toulouse - Hôpital Rangueil
- Sheba Medical Center
- Istituto Clinico Humanitas
- Ospedale Casa Sollievo Della Sofferenza
- LUMC
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Placebo Comparator
Arm Label
1
2
Arm Description
Methotrexate IM or SC 25 mg/week vs placebo IM or SC for 24 weeks
1 IM or SC of placebo per week during 24 weeks
Outcomes
Primary Outcome Measures
Remission without steroids, immunosuppressives and without colectomy
Secondary Outcome Measures
Full Information
NCT ID
NCT00498589
First Posted
July 9, 2007
Last Updated
February 4, 2015
Sponsor
Centre Hospitalier Universitaire de Besancon
1. Study Identification
Unique Protocol Identification Number
NCT00498589
Brief Title
Comparison of Methotrexate vs Placebo in Corticosteroid-dependent Ulcerative Colitis
Acronym
METEOR
Official Title
A Controlled, Randomized, Double-blind, Multicenter Study, Comparing Methotrexate vs Placebo in Corticosteroid-dependent Ulcerative Colitis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2015
Overall Recruitment Status
Completed
Study Start Date
September 2007 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
June 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centre Hospitalier Universitaire de Besancon
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
PHASE: II
TYPE OF STUDY : With direct benefit
DESCRIPTIVE: Multicenter, randomized, double-blind study
INCLUSION CRITERIA: Steroid-dependent ulcerative colitis
OBJECTIVES: To show superiority of methotrexate vs placebo in inducing steroid-free remission in steroid-dependent ulcerative colitis
STUDY TREATMENTS: Methotrexate 1 intramuscular injection (25 mg) per week Placebo 1 intramuscular injection per week
NUMBERS OF PATIENTS: 55 patients in each group, i.e. a total of 110 patients
INCLUSION PERIOD: 24 months
STUDY DURATION: 36 months
EVALUATION CRITERIA: Remission without steroids, immunosuppressives and without colectomy at 16 weeks of treatment.
Detailed Description
Ulcerative colitis (UC) is a chronic inflammatory bowel disease that slightly reduces life expectancy, strongly reduces its quality and can lead to serious complications such as acute colitis, dysplasia and colon cancer. About 40'000 patients are affected in France Among them, 15% suffer from a chronic active form that often leads to an extended steroid therapy, and its known side effects. Azathioprine has already proven its efficacy in this indication but brings a lasting remission without steroid in only 41% of the patients (1-4). What are the medications available for the patients who failed in maintaining a remission with azathioprine ? Cyclosporin is designed for severe or steroid-resistant forms. (5). The results of two recent studies have showed that infliximab is more efficacious than placebo in active UC (6, 7). Infliximab is expensive, its efficacy in steroid-dependent UC has not been specifically tested yet, and its tolerance on the long term remains uncertain. Methotrexate proved its efficacy in Crohn's disease with an intramuscular dose of 25mg/week (8). In UC a controlled trial has been negative with an oral dose of 12.5mg/week (9). Another study compared mercaptopurine, methotrexate (15mg/week) and 5-aminosalicylate in 72 steroid-dependent patients with CD or UC (10). The remission rates obtained were 58% after 30 weeks with methotrexate (not significantly different from 5-ASA) and 14% after 106 weeks (not significantly different from 5-ASA). Few data are available on the efficacy of methotrexate in UC, at a dose which is active in Crohn's disease (25mg intramuscular/week). Several uncontrolled series have been published, including 91 patients whose remission failed under azathioprine.
Methotrexate is cheap and its patent has fallen in the public domain. Only institutional research will be able to finance a study in this new indication.
This is a prospective, controlled, randomized, double-blind study of methotrexate with an intramuscular dose of 25mg/week vs placebo in patients with steroid-dependent UC.
This multicenter study will take place under the aegis of the Therapeutic Study Group for Inflammatory Digestive Diseases (G.E.T.A.I.D.) and with the help of the gastroenterologists network of the CIC. The issue of this study is important. If the hypothesis is borne out, a cheap, efficacious medication will be available for chronic active UC.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
110 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Placebo Comparator
Arm Description
Methotrexate IM or SC 25 mg/week vs placebo IM or SC for 24 weeks
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
1 IM or SC of placebo per week during 24 weeks
Intervention Type
Drug
Intervention Name(s)
methotrexate
Intervention Description
25 mg per week IM or SC during 24 weeks
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
one intramuscular injection per week
Primary Outcome Measure Information:
Title
Remission without steroids, immunosuppressives and without colectomy
Time Frame
week 16
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
UC diagnosed according to the Lennard-Jones criteria (Appendix 1) with endoscopic colorectal lesions, whatever their extension may be
A Mayo Disease Activity Index £ 4, with no item >1 for the clinical part of the score and from 0 to 2 for the endoscopic part at the time of inclusion
Steroid-dependence defined by at least 1 unsuccessful attempt to stop systemic steroid therapy during the last 12 weeks. Steroid therapy might have been completely stopped if it has been restarted within the last 30 days
To be receiving a treatment of prednisone at a dose between 10 and 40mg, stable for at least 2 weeks at the time of inclusion
Under an adequate contraception for male or female subjects of childbearing potential
Exclusion Criteria:
Indication to a colectomy.
Alcoholism (more than 21 glasses per week for male subjects and 14 glasses per week for female subjects). 1 glass corresponds to 3 cl of strong alcohol, 10 cl glass of wine or a half pint of beer.
Pregnant or breast-feeding female subjects.
No efficacious contraception.
NSAIDS or cotrimoxazole intake upon inclusion, or probenecid intake within 1 month prior to inclusion.
Anti-TNFa treatment within 2 months prior to inclusion.
Azathioprine, mercaptopurine, cyclosporin or thalidomide within 1 month prior to inclusion.
Modification of mesalazine or olsalazine dosage within 1 month prior to inclusion.
Chronic (broncho) pneumopathy.
Renal failure (creatinaemia > upper limit of normal laboratory values limit).
Liver disease apart from primary sclerosing cholangitis.
Unexplained rise higher than twice the normal level for transaminases, alkaline phosphatases and/or bilirubin.
Folate level < normal level.
Past history of malignant condition (including leukaemia, lymphoma and myelodysplasia) except for baso-cellular cutaneous cancers.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Franck Carbonnel
Organizational Affiliation
CHU Besançon
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria
Facility Name
ULB - Cliniques Saint Luc
City
Bruxelles
ZIP/Postal Code
1200
Country
Belgium
Facility Name
CHU Amiens - Hôpital Nord
City
Amiens
ZIP/Postal Code
84000
Country
France
Facility Name
CH Avignon
City
Avignon
ZIP/Postal Code
84000
Country
France
Facility Name
Centre Hospitalier Universitaire de Besançon
City
Besançon
ZIP/Postal Code
25000
Country
France
Facility Name
CHU Clermont-Ferrand - Hôpital Hotel Dieu
City
Clermont-Ferrand
ZIP/Postal Code
63000
Country
France
Facility Name
APHP - Hôpital Beaujon
City
Clichy
ZIP/Postal Code
92110
Country
France
Facility Name
APHP - Hôpital Bicêtre
City
Le Kremlin Bicetre
ZIP/Postal Code
94270
Country
France
Facility Name
CHRU Lille - Hôpital Huriez
City
Lille
ZIP/Postal Code
59037
Country
France
Facility Name
CHU Nantes - Hôpital Hôtel Dieu
City
Nantes
ZIP/Postal Code
44000
Country
France
Facility Name
CHU Nice - Hôpital de l'Archet 2
City
Nice
ZIP/Postal Code
06202
Country
France
Facility Name
APHP - Hôpital Saint Louis
City
Paris
ZIP/Postal Code
75010
Country
France
Facility Name
APHP - Hôpital Saint Antoine
City
Paris
ZIP/Postal Code
75012
Country
France
Facility Name
APHP - Hôpital Cochin
City
Paris
ZIP/Postal Code
75014
Country
France
Facility Name
CHU Bordeaux - Hôpital Haut L'Eveque
City
Pessac
ZIP/Postal Code
33604
Country
France
Facility Name
CHU Rouen - Hôpital Charles Nicolle
City
Rouen
ZIP/Postal Code
76000
Country
France
Facility Name
CHU St Etienne - Hôpital NOrd
City
Saint Priest
ZIP/Postal Code
42270
Country
France
Facility Name
CHU Toulouse - Hôpital Rangueil
City
Toulouse
ZIP/Postal Code
31403
Country
France
Facility Name
Sheba Medical Center
City
Tel aviv
ZIP/Postal Code
52621
Country
Israel
Facility Name
Istituto Clinico Humanitas
City
Rozzano , Milano
ZIP/Postal Code
20089
Country
Italy
Facility Name
Ospedale Casa Sollievo Della Sofferenza
City
San Giovanni Rotondo
ZIP/Postal Code
71013
Country
Italy
Facility Name
LUMC
City
Leiden
ZIP/Postal Code
2333
Country
Netherlands
12. IPD Sharing Statement
Citations:
PubMed Identifier
26632520
Citation
Carbonnel F, Colombel JF, Filippi J, Katsanos KH, Peyrin-Biroulet L, Allez M, Nachury M, Novacek G, Danese S, Abitbol V, Bossa F, Moreau J, Bommelaer G, Bourreille A, Fumery M, Roblin X, Reinisch W, Bouhnik Y, Brixi H, Seksik P, Malamut G, Farkkila M, Coulibaly B, Dewit O, Louis E, Deplanque D, Michetti P, Sarter H, Laharie D; European Crohn's and Colitis Organisation; Groupe d'Etude Therapeutique des Affections Inflammatoires Digestives. Methotrexate Is Not Superior to Placebo for Inducing Steroid-Free Remission, but Induces Steroid-Free Clinical Remission in a Larger Proportion of Patients With Ulcerative Colitis. Gastroenterology. 2016 Feb;150(2):380-8.e4. doi: 10.1053/j.gastro.2015.10.050. Epub 2015 Nov 26.
Results Reference
derived
Learn more about this trial
Comparison of Methotrexate vs Placebo in Corticosteroid-dependent Ulcerative Colitis
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