9 mg Budesonide Once Daily (OD) Versus 3 mg Budesonide Three Times Daily (TID) in Active Crohn's Disease

Phase 3

Completed

• Conditions: Crohn´s Disease
• Interventions: Drug: budesonide

• Registration Number: NCT01086553
• Lead Sponsor: Dr. Falk Pharma GmbH

Brief Summary

This study aims to evaluate the efficacy of 9 mg budesonide once daily (OD) versus 3 mg budesonide three-times daily (TID) for the induction of remission in Crohn's disease.

Detailed Description

Not available

Study Timeline

• Study Start: 2009-11
• Study First Submitted: 2010-03-12
• Study First Submitted QC: 2010-03-12
• Study First Posted: 2010-03-15
• Primary Completion: 2012-05
• Study Completion: 2012-12
• Status Verified: 2014-10
• Last Update Submitted: 2014-10-29
• Last Update Posted: 2014-10-30

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 471

Inclusion Criteria

• Signed informed consent,
• Age 18 to 75 years,
• Symptoms of Crohn's disease since at least 3 months; diagnosis confirmed by endoscopic and histological, or endoscopic and radiological criteria [endoscopy not older than 12 months or if older, then clinical signs (e.g., pain localisation, pain intensity, blood in stool) and behaviour (according to Montreal classification) should be unchanged compared to former episodes],
• Localisation of CD either in terminal ileum, coecum, ascending colon, or ileocolitis,
• Active phase of disease (200 < CDAI < 400),
• Negative pregnancy test in females of childbearing potential,
• Women of child-bearing potential have to apply appropriate contraceptive methods, e.g., hormonal contraception, intrauterine device (IUD), double-barrier method of contraception (e.g., use of a condom and spermicide), or partner has undergone vasectomy. The investigator is responsible for determining whether the subject has adequate birth control for study participation.

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Exclusion Criteria

• Known Crohn's lesions in the upper GI-tract (up to and including the jejunum) or rectum with present symptoms,
• Septic complications,
• Evidence of infectious diarrhoea (i.e., pathogenic bacteria in stool culture),
• Abscess, perforation, or active fistulas,
• Ileostomy or colostomy,
• Resection of more than 50 cm of the ileum,
• Bowel surgery within the last 3 months,
• Immediate surgery required (e.g., major stenosis, serious bleeding, peritonitis, ileus),
• Clinical signs of stricturing disease,
• Subileus within the last 6 months (subileus with inflammatory hint allowed),
• Suspicion of ileus, subileus or corresponding symptoms,
• Parenteral or tube feeding,
• Active peptic ulcer disease, local intestinal infection, or known established cataract,
• Diabetes mellitus, infection, osteoporosis, glaucoma, tuberculosis, or hypertension if careful medical monitoring is not ensured,
• Abnormal hepatic function (ALT or ALP > 2.5 x upper limit of normal [ULN]), liver cirrhosis, or portal hypertension,
• Abnormal renal function (Cystatin C > ULN),
• Any severe concomitant cardiovascular, renal, endocrine, or psychiatric disorder,
• History of cancer in the last five years (except for non-metastatic cancers, e.g., basalioma),
• Treatment with immunosuppressants or anti-cancer drugs, e.g., 6 TG, methotrexate, tacrolimus, cyclophosphamide, or cyclosporine within the last 3 months; in case of treatment with azathioprine or 6 MP the drugs have to be used for maintenance of remission only and dosage has to be unchanged within the last 3 months before baseline visit and during the study,
• Treatment with ketoconazole or other CYP3A inhibitors within the last month before baseline visit,
• Treatment with anti-TNF-alpha therapy within 3 months before baseline visit,
• Conventional steroids (iv, po, rectal) within 2 weeks before baseline visit,
• > 6 mg/d budesonide po within 2 weeks before baseline visit,
• Steroids for inhalation within 2 weeks before baseline visit,
• Patients known to be steroid-refractory,
• Treatment of study disease with oral antibiotics (e.g., metronidazole or ciprofloxacin) within the last 2 weeks,
• Application of non-steroidal anti-inflammatory drugs (NSAIDs) within 2 weeks before baseline visit except ≤ 350 mg/d or short-term acetylsalicylic acid (paracetamol is allowed),
• Known intolerance/hypersensitivity to study drug,
• Well-founded doubt about the patient's cooperation, e.g., because of addiction to alcohol or drugs,
• Existing or intended pregnancy or breast-feeding,
• Participation in another clinical trial within the last 30 days, simultaneous participation in another clinical trial, or previous participation in this trial.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
A	budesonide	9mg budesonide OD
B	budesonide	3mg budesonide TID

Primary Outcome Measures

Name	Time	Method
Rate of clinical remission, defined as a CDAI < 150, at week 8 (LOCF)	8 weeks

Secondary Outcome Measures

Name	Time	Method
Response to treatment defined as CDAI < 150 or CDAI reduction of > 100 points	8 weeks
Adverse events	8 weeks

Trial Locations

Locations (1)

Med. Klinik I - Markus-Krankenhaus - Frankfurter Diakonie-Kliniken; 🇩🇪 Frankfurt, Germany