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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: EUCTR
Last refreshed on: 17 March 2014
Main ID:  EUCTR2008-002783-33-NL
Date of registration: 05/11/2008
Prospective Registration: Yes
Primary sponsor: Millennium Pharmaceuticals, Inc.
Public title: A Phase 3, Randomized, Placebo-Controlled, Blinded, Multicenter Study of the Induction and Maintenance of Clinical Response and Remission by Vedolizumab (MLN0002) in Patients with Moderate to Severe Crohn’s Disease
Scientific title: A Phase 3, Randomized, Placebo-Controlled, Blinded, Multicenter Study of the Induction and Maintenance of Clinical Response and Remission by Vedolizumab (MLN0002) in Patients with Moderate to Severe Crohn’s Disease
Date of first enrolment: 18/02/2009
Target sample size: 1060
Recruitment status: Not Recruiting
URL:  https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2008-002783-33
Study type:  Interventional clinical trial of medicinal product
Study design:  Controlled: yes Randomised: yes Open: yes Single blind: no Double blind: yes Parallel group: yes Cross over: yes Other: no If controlled, specify comparator, Other Medicinial Product: no Placebo: yes Other: no  
Phase: 
Countries of recruitment
Austria Belgium Bulgaria Czech Republic Denmark Estonia France Germany
Greece Hungary Iceland Ireland Italy Latvia Malta Netherlands
Portugal Slovakia Spain Sweden United Kingdom
Contacts
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Key inclusion & exclusion criteria
Inclusion criteria:
1.Age 18-80. 2.Male/female patient voluntarily able to give consent 3.Female patients must:be post-menopausal for =1year before screening visit,OR be surgically sterile,OR(of childbearing potential)agree to practice 2 effective methods of contraception,at the same time,from time of signing informed consent form through to 6months after last dose of study drug,OR agree to completely abstain from heterosexual contact.Male patients,even if surgically sterilized, must agree to practice effective barrier contraception during entire study treatment period and through 6months after last dose of study drug,OR agree to completely abstain from heterosexual contact. 4.Diagnosis of Crohn’s disease established at least 3 months prior to enrollment by clinical & endoscopic evidence & corroborated by histopathology report.Cases of Crohn’s disease established =6 months prior to enrollment for which a histopathology report is not available will be considered.5. Moderate to severe CD determined by CDAI score of 220-450 within 7days of first administration of study drug and 1 of the following:a)CRP level>2.87mg/L during the screening period OR b)Ileocolonoscopy with photographic documentation of a minimum of 3 nonanastomotic ulcerations (each>0.5cm in diameter)or 10 aphthous ulcerations(involving a minimum 10 contiguous cm of intestine) consistent with CD =4 months prior to randomization OR c)Fecal calprotectin>250mcg/g stool during the screening period in conjunction with CT enterography,MR enterography, contrast-enhanced small bowel radiography,or wireless capsule endoscopy revealing Crohn’s ulcerations (aphthae not sufficient),4months prior to screening.(Patients with evidence of fixed stenosis or small bowel stenosis with prestenotic dilation should not be included.).6.CD involvement of ileum and/or colon,atat minimum 7.Patients with extensive colitis or pancolitis of>8years duration or left-sided colitis of>12years duration must have evidence of a surveillance colonoscopy within 12months of initial screening visit. 8.Patients with family history of colorectal cancer, personal history of increased colorectal cancer risk,age>50 years,or other known risk factor must be up-to-date on colorectal cancer surveillance. 9.Over the previous 5year period, an inadequate response to,loss of reponse to,or intolerance of at least one of the following agents as defined below:•Corticosteroids,Symptoms of persistently active disease despite a history of at least one 4-week induction regimen that included a dose equivalent to prednisone 30mg daily orally for 2weeks or intravenously for 1 week OR Two failed attempts to taper corticosteroids to below a dose equivalent to prednisone 10mg daily orally on two separate occasions OR History of intolerance of corticosteroids (including Cushing’s syndrome,osteopenia/osteoporosis, hyperglycemia, insomnia,infection) •Immunomodulators. Symptoms of persistently active disease despite history of =8week regimen of oral azathioprine (=1.5mg/kg)or 6-mercaptopurine mg/kg (=0.75mg/kg)OR Symptoms of persistently active disease despite a history of at least one 8week regimen of methotrexate (=12.5 mg/week)OR History of intolerance of at least one immunomodulator(including nausea/vomiting,abdominal pain,pancreatitis,LFT abnormalities,lymphopenia,TPMT genetic mutation,infection)•TNF antagonists. Symptoms of persistently active disease despite history of at least one 4week induction regimen of one of the following agents:Infliximab 5mg/kg IV

Exclusion criteria:
Gastrointestinal Exclusion Criteria
1. Evidence of abdominal abscess at the initial screening visit
2. Extensive colonic resection, subtotal or total colectomy
3. History of >3 small bowel resections or diagnosis of short bowel syndrome
4. Have received tube feeding, defined formula diets, or parenteral alimentation within 21 days prior to the administration of the first dose of study drug
5. Ileostomy, colostomy, or known fixed symptomatic stenosis of the intestine
6. Within 30 days prior to enrollment, have received any of the following for the treatment of underlying disease:
a) Non-biologic therapies (eg, cyclosporine, thalidomide) other than those permitted
b) A non-biologic investigational therapy
c)An approved non-biologic therapy in an investigational protocol
7. Within 60 days prior to enrollment, have received any of the following:
a) Infliximab, adalimumab, or certolizumab pegol
b)Other investigational or approved biological agent
8. Any prior exposure to natalizumab, efalizumab or rituximab
9. Use of topical (rectal) treatment with 5-ASA or corticosteroid enemas/suppositories within 2 weeks of the administration of the first dose of study drug
Evidence of or treatment for C. difficile infection or other intestinal pathogen
within 28 days prior to enrollment
11. Currently require or are anticipated to require surgical intervention for CD during the study
12. History or evidence of adenomatous colonic polyps that have not been removed
13. History or evidence of colonic mucosal dysplasia
14. Diagnosis of ulcerative colitis or indeterminate colitis
Infectious Disease Exclusion Criteria
1. Any chronic hepatitis B or C infection
2. Active or latent tuberculosis, regardless of treatment history, as evidenced by any of the following:
a) History of tuberculosis
b) A positive diagnostic tuberculosis (TB) test within one month of enrollment defined as:
i) a positive QuantiFERON test or 2 successive indeterminate QuantiFERON tests OR
ii)a tuberculin skin test reaction = 10 mm (= 5 mm in patients receiving the equivalent of > 15 mg/day prednisone).
c) Chest x-ray within 3 months of enrollment in which active or latent pulmonary tuberculosis cannot be excluded
3. Any identified congenital or acquired immunodeficiency (eg, common variable immunodeficiency, human immunodeficiency virus [HIV] infection, organ transplantation)
4. Any live vaccinations within 30 days prior to study drug administration except for the influenza vaccine
5. Clinically significant extra-intestinal infection (eg, pneumonia, pyelonephritis) within 30 days of the initial screening visit
General Exclusion Criteria
1. Previous exposure to MLN0002
2. Female patients who are lactating or have a positive serum pregnancy test during the screening period or a positive urine pregnancy test on Day 1 prior to study drug administration.
3. Any unstable or uncontrolled cardiovascular, pulmonary, hepatic, renal, gastrointestinal, genitourinary, hematological, coagulation, immunological, endocrine/metabolic, or other medical disorder that, in the opinion of the investigator, would confound the study results or compromise patient safety
4. Had any surgical procedure requiring general anesthesia within 30 days prior to enrollment or is planning to undergo surgery during the study period
5. Any history of malignancy, except for the following:
• adequately-treated non-metastatic basal cell skin cancer;
• Squamous cell skin cancer that has been adequately treated and has not r


Age minimum:
Age maximum:
Gender:
Female: yes
Male: yes
Health Condition(s) or Problem(s) studied
Moderate to Severe Crohn's Disease
MedDRA version: 9.1 Level: LLT Classification code 10013099 Term: Disease Crohns
Intervention(s)

Product Name: VEDOLIZUMAB
Product Code: MLN0002
Pharmaceutical Form: Powder for solution for infusion
INN or Proposed INN: VEDOLIZUMAB
CAS Number: 943609-66-3
Current Sponsor code: MLN0002
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 300mg-
Pharmaceutical form of the placebo: Solution for infusion
Route of administration of the placebo: Intravenous use

Primary Outcome(s)
Main Objective: Co-Primary Objectives for the Induction Phase

• To determine the effect of MLN0002 induction treatment on clinical remission at 6 weeks (primary)

• To determine the effect of MLN0002 induction treatment on enhanced clinical
response at 6 weeks (co-primary)

Primary Objective for the Maintenance Phase

• To determine the effect of MLN0002 maintenance treatment on clinical remission at 52 weeks





Primary end point(s): Co-Primary Endpoints for the Induction Phase

• Proportion of patients in clinical remission at Week 6 (primary)

• Proportion of patients with enhanced clinical response at Week 6 (co-primary)

Primary Endpoint for the Maintenance Phase

• Proportion of patients in clinical remission at Week 52
Secondary Objective: Secondary Objectives for the Induction Phase

• To determine the effect of MLN0002 induction treatment on serum C-reactive protein (CRP) levels at 6 weeks in patients with elevated CRP levels at baseline

Secondary Objectives for the Maintenance Phase

• To determine the effect of MLN0002 maintenance treatment on enhanced clinical response at 52 weeks

• To determine the effect of MLN0002 maintenance treatment on corticosteroid-free remission at 52 weeks

• To determine the effect of MLN0002 maintenance treatment on durability of clinical remission over 52 weeks
Secondary Outcome(s)
Secondary ID(s)
2008-002783-33-ES
C13007
Source(s) of Monetary Support
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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