Clinical Trials Detalhe
Efficacy and Safety Study of Mongersen (GED-0301) for the Treatment of Subjects With Active Crohn's Disease
General Information
Gender
ALL
Age
N/A
Phase
PHASE3
Study Type
INTERVENTIONAL
Location
Hospital de Braga (Braga, Portugal)
Centro Hospitalar E Universitario de Coimbra EPE (Coimbra, Portugal)
Hospital da Senhora da Oliveira Guimaraes (Guimarães, Portugal)
Hospital Da Luz (Lisbon, Portugal)
Centro Hospitalar de Sao Joao, EPE (Porto, Portugal)
Centro Hospitalar do Alto Minho - Unidade Local de Saúde do Alto Minho, EPE (Viana do Castelo, Portugal)
Clinicaltrial.gov
https://classic.clinicaltrials.gov/ct2/show/NCT02596893Summary
The purpose of study is to test the effects of an experimental medication GED-0301 (mongersen) in patients who have active Crohn's disease. The study will test GED-0301 compared to placebo for 52 weeks. The study treatment is blinded which means that patients and the study doctor will not know which treatment has been assigned. Patients in this study will be allowed treatment with stable doses of oral aminosalicylates, oral corticosteroids, immunosupressants and antibiotics for the treatment of Crohn's disease. After 12 weeks in the study until the end of the study, patients who do not have an improvement in their Crohns disease symptoms will have the option to enter a long term active treatment study. Participants who discontinued the study anytime or completed the study at Week 52 were then observed for an additional 4 weeks.
Conditions
Crohn Disease
Eligibility
Inclusion Criteria: Subjects must satisfy the following criteria to be enrolled in the study: * Male or female ≥ 18 years * Active Crohn's disease (CD) disease as determined by the Crohn's Disease Activity Index (CDAI) score and the Simple Endoscopic Score for Crohn's Disease (SES-CD) * Must meet a determined average minimum number of daily stools or rating of abdominal pain over a 7 day period * Subject must have failed or experienced intolerance to at least one of the following: budesonide; systemic corticosteroids; immunosuppressants (eg, azathiopurine, 6-mercaptopurine, or methotrexate); or biologics for the treatment of CD. Exclusion Criteria: The presence of any of the following will exclude a subject from enrollment: * Diagnosis of ulcerative colitis (UC), indeterminate colitis, ischemic colitis, microscopic colitis, radiation colitis or diverticular disease-associated colitis * Local manifestations of Crohn's Disease (CD) such as symptomatic/severe strictures, abscesses, short bowel syndrome; or other disease complications for which surgery might be indicated or could confound the evaluation of efficacy * Intestinal resection within 6 months or any intra-abdominal surgery within 3 months prior to the Screening Visit * Ileostomy or a colostomy * Subject has a history of any clinically significant medical condition that, in the investigator's opinion, would prevent the subject from participating in the study.