Oral Budesonide vs. Oral Mesalazine in Active Crohn's Disease (CD)
Information source: Dr. Falk Pharma GmbH
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Crohn's Disease
Intervention: budesonide (Drug); mesalazine (Drug)
Phase: Phase 3
Status: Completed
Sponsored by: Dr. Falk Pharma GmbH Official(s) and/or principal investigator(s): Andreas Tromm, Professor, Principal Investigator, Affiliation: Ev. Krankenhaus Hattingen GmbH
Summary
The purpose of this study is to determine whether mesalazine or budesonide is more active in
the treatment of active Crohn's disease.
Clinical Details
Official title: Double-Blind, Double-Dummy, Randomized, Multicentre Study to Compare the Efficacy and Safety of Oral Budesonide (9 mg) and Oral Mesalazine (4.5 g) in Moderately Active Crohn's Disease Patients
Study design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Active Control, Parallel Assignment, Safety/Efficacy Study
Primary outcome: Rate of remission
Secondary outcome: Response to treatmentTime to response Time to remission PGA QoL
Detailed description:
Crohn's disease is often treated with glucocorticoids or mesalazine. Both drugs are indicated
for active Crohn's disease. Treatment with mesalazine is indicated for the treatment of
mildly to moderately active Crohn's disease. Budesonide 9 mg/day or mesalazine 4. 5 g/day are
better than lower doses.
So far only one trial compares the efficacy and safety of budesonide and 5-ASA. The result of
this trial is that budesonide is more effective in inducing remission than mesalazine. The
primary objective of this trial is to confirm this result for other presentations of
budesonide and mesalazine; i. e. Budenofalk® capsules (9 mg/day) and Salofalk® tablets
(Eudragit-L-coated oral mesalazine; 4. 5 g/day) in moderately active Crohn's disease.
Mesalazine is used in this trial as a comparator.
Eligibility
Minimum age: 18 Years.
Maximum age: 70 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria (main):
- 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 localization, pain intensity, blood
in stool) and behaviour (according to Vienna classification) should be unchanged
compared to former episodes]
- Localisation of CD either in terminal ileum, ascending colon or ileocolitis
- Active phase of disease (200 < CDAI < 400)
Exclusion Criteria (main):
- Known Crohn's lesion in the upper GI-tract (up to and including the jejunum) with
present symptoms
- CD in the rectum currently present
- Short bowel syndrome
- Septic complications
- Baseline stool positive for germs causing bowel disease
- 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
- Clinical signs of stricturing disease
- Subileus within the last 6 months
- Suspicion of ileus, subileus or corresponding symptomatology
- Contra-indications, special warnings and precautions mentioned in SmPC
- Treatment with immunosuppressants, cytostatics, 6-TG, methotrexate, 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, ciprofloxacin or other CYP3A inhibitors within the last
month before baseline visit
- Treatment with anti-TNF-a therapy within 6 months before baseline visit
- Conventional steroids (iv, po, rectal) within 2 weeks before the study
- > 6 mg/d budesonide po or > 3 g/d mesalazine po within 2 weeks before the study
- Patients known to be steroid-refractory or steroid-dependent from former CD episodes
- Treatment of study disease with oral antibiotics (e. g., metronidazole) within the last
2 weeks
Locations and Contacts
Ev. Krankenhaus Hattingen GmbH, Hattingen 45525, Germany
Additional Information
Starting date: September 2004
Ending date: May 2008
Last updated: May 29, 2008
|