Methotrexate in Induction and Maintenance of Steroid Free Remission in Ulcerative Colitis

Completed · Phase 2 · Has a placebo group

Conditions studied: Ulcerative Colitis

In brief

There are fewer therapeutic options for patients with active ulcerative colitis (UC) compared to patients with active Crohn's disease (CD) and the investigators are facing a persistent unmet need for additional effective and affordable therapies for patients with UC. Methotrexate (MTX) 25 mg once weekly administered subcutaneously (sq) or intramuscularly (im) is an efficient therapy to induce and maintain steroid free remission in patients with CD. To evaluate the efficacy of a similar approach in patients with active ulcerative colitis the investigators conduct a double-blind, placebo controlled, randomized, multicenter, parallel group trial to investigate the safety and efficacy of 25 mg MTX applied subcutaneously once weekly in patients with active UC, who either failed 5-ASA therapy, or are steroid dependent or are intolerant or not responding to azathioprine/6-mercaptopurine therapy or have no response/ lost response to infliximab prior to the study inclusion. The study is designed as a drug withdrawal trial and includes two periods, the Induction Period (week 0-16) and the Maintenance Period (week 17-48). In the open label Induction Period every patient will receive a steroid taper, MTX 25 mg sq once weekly + daily folic acid 1 mg tablets for the induction of clinical response or remission. Patients responding to the open label MTX therapy and being off steroids between week 12-16 will be randomized at week 16 1:1 to Placebo sq once weekly + daily folic acid 1 mg tablets + 2.4 g mesalamine or to MTX 25 mg sq once weekly + daily folic acid 1 mg tablets+ 2.4 g mesalamine. The Specific Aims of the trial are: i) To evaluate the safety and tolerability of 25 mg MTX applied sq once weekly over a time period of 48 weeks; ii) To evaluate the relapse-free survival of MTX maintenance therapy compared to placebo over a time period of 32 weeks; iii) To evaluate the efficacy of MTX over a time period of 16 weeks to induce steroid free remission; iiii) To establish a DNA, plasma and serum library to enable the evaluation of clinical and pharmacogenomic models to predict the response to MTX therapy in patients with UC. With 25-30 participating centers actively enrolling, the investigators anticipate to complete enrollment for this study in a time period of 3 years. Completion of this trial will define the therapeutic value of MTX in UC, potentially changing the current therapeutic strategy in UC.

Key facts

Study ID

NCT01393405

Run by

University of North Carolina, Chapel Hill

People needed

179

Starts

2012-02-01

Expected to finish

2017-04-01

Last updated by the study team

2018-04-17

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Signed informed consent.
• Man or woman between 18 and 70 years of age.
• UC diagnosed by routine clinical, radiographic, endoscopic, and pathological criteria.
• Active UC with a Mayo score of 6 to 12 points and moderate-to severe active disease on sigmoidoscopy (Mayo endoscopic subscore of at least 2)
• and at least ONE of the following criteria:
• Steroid dependent UC *
• Primary failure or loss of response to an anti-TNF (infliximab, adalimumab, golimumab) in the past
• Primary failure or loss of response to vedolizumab in the past
• Intolerance/failure of azathioprine/6-MP therapy in the past
• Failure of 5-ASA therapy
• Steroid dependence is defined as a clinical response to treatment with prednisone 40 to 60 mg/day and relapse within 30 days after prednisone treatment was completed or as a requirement for a daily dosage of not less than 10 mg of prednisone and impossibility of weaning the patient off steroid without clinical relapses (two attempts to discontinue the medication within the preceding six months of the start of the study).

You may not qualify if…

• Failure to respond to 40 mg of prednisone or higher/day in the last 2 weeks before inclusion
• Concomitant use of azathioprine (AZA) or 6-mercaptopurine (6-MP) must be discontinued at least 2 weeks before inclusion into the study (Week 0 visit)
• Anti-TNF therapy in the 2 weeks before the Week 0 visit
• Failure of cyclosporine therapy in the previous 6 months prior to Screening visit
• Patients with serum albumin < 2.5 g/dl at baseline
• Low serum folate defined as decrease of >10% below normal range
• Patients with WBC< 3.0 x109th/L at baseline
• Patients with platelet count < 100 x109th/L
• Patients with an underlying infection with C. difficile at Screening visit
• Patients with pre-existing hepatic disease
• Patients with known non-alcoholic fatty liver disease (NAFLD)
• Patients with known Hepatitis B or Hepatitis C
• Patients with pre-existing renal dysfunction (creatinine >1.5 mg/dl).
• Patients with a pre-existing chronic lung disease other than well controlled asthma
• Patients with interstitial lung disease of unknown cause
• Patients with a BMI >35
• Known previous or concurrent malignancy (other than that considered surgically cured, with no evidence for recurrence for 5 years - basal cell does not exclude)
• Existing pregnancy, lactation, or planned pregnancy* (men and women) within the next 12 months. (*Methotrexate should not be used for at least 3 months before planned pregnancy for men and women and should not be used during pregnancy or breast feeding)
• High alcohol consumption (more than seven drinks per week)
• Non - steroidal inflammatory medications (NSAIDs) as long-term treatment, defined as use for at least 4 days a week each month
• Continuous treatment with one of the following drugs:
• Probenecid,
• Trimethoprim/sulfamethoxazole
• Sulfasalazine
• Acitretin

Where it is running

• University of Southern California — Los Angeles, California, United States
• University of Colorado — Denver, Colorado, United States
• Shafran Gastroenterology — Winter Park, Florida, United States
• Atlanta Gastroenterology — Atlanta, Georgia, United States
• Northwestern University — Chicago, Illinois, United States
• The University of Chicago — Chicago, Illinois, United States
• Indiana University IU Health — Indianapolis, Indiana, United States
• University of Iowa — Iowa City, Iowa, United States
• University of Kentucky — Lexington, Kentucky, United States
• University of Louisville — Louisville, Kentucky, United States
• University of Maryland — Baltimore, Maryland, United States
• Metropolitan Gastroenterology Group, PC, Chevy Chase Clinical Research — Chevy Chase, Maryland, United States
• Massachusetts General Hospital — Boston, Massachusetts, United States
• Henry Ford Health System — Novi, Michigan, United States
• Minnesota Gastroenterology — Plymouth, Minnesota, United States
• Mayo Clinic — Rochester, Minnesota, United States
• Dartmouth College — Lebanon, New Hampshire, United States
• Mt Sinai School of Medicine — New York, New York, United States
• Asheville Gastroenterology Associates — Asheville, North Carolina, United States
• University of North Carolina — Chapel Hill, North Carolina, United States
• Charlotte Gastroenterology & Hepatology — Charlotte, North Carolina, United States
• Case Western Reserve University — Cleveland, Ohio, United States
• Great Lakes Gastroenterology — Mentor, Ohio, United States
• University of Pennsylvania — Philadelphia, Pennsylvania, United States
• Penn State University — State College, Pennsylvania, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.