Dose Finding Study of BIRB 796 BS in Patients With Moderate to Severe Crohn's Disease

Crohn Disease Clinical Trial

Official title:

A Randomised, Double-blind, Placebo-controlled, Five* Parallel Groups, Dose Finding Study of BIRB 796 BS (10, 20, 30, and 60 mg*) Administered Twice a Day Orally Over 8 Weeks in Patients With Moderate to Severe Crohn's Disease Followed by a 18 Weeks Treatment Extension in Patients With Clinical Remission or Clinical Response After 8 Weeks Treatment With the Respective Dose of BIRB 796 BS - Extension Phase. * Subsequent to Amendment 4 (Dated 11 Jun 2002) a 60 mg b.i.d. Group Was Included.

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02209792
• Other study ID #: 1175.12
• Status: Terminated
• Phase: Phase 2
• First received: August 5, 2014
• Last updated: August 5, 2014
• Start date: October 2001

Study information

• Verified date: August 2014
• Source: Boehringer Ingelheim
• Contact: n/a
• Is FDA regulated: No
• Health authority: Belgium: Federal Agency for Medicines and Health Products, FAMHPFrance: Agence Nationale de Sécurité du Médicament et des produits de santéGermany: Federal Institute for Drugs and Medical DevicesItaly: National Monitoring Centre for Clinical Trials - Ministry of HealthNetherlands: Medicines Evaluation Board (MEB)Russia: Ministry of Health of the Russian FederationSouth Africa: Medicines Control CouncilSwitzerland: Swissmedic
• Study type: Interventional

Clinical Trial Summary

The primary objective of this extension study was to obtain long-term safety data for BIRB 796 BS in patients with moderate to severe Crohn's disease after 26 weeks of treatment. Secondary objectives were the evaluation of efficacy of BIRB 796 BS to induce clinical remission and response over 26 weeks of treatment.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 284
• Est. primary completion date: January 2004
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria:

• Male or female patient of 18 to 65 years of age

• Provision of written informed consent in accordance with Good Clinical Practice and local legislation prior to any study procedures

• Diagnosis of Crohn's disease documented for at least 6 months. Preferably, inflammatory activity of the bowel should be confirmed by endoscopy within the last 3 months

• Moderate to severe Crohn's disease, CDAI =220 to =450, at baseline (visit 2)

• Any of the following therapy, provided the respective criteria for dosage, duration and stability were satisfied:

• Prednisone or other systemic corticosteroids for at least 12 weeks with a stable oral dosage =25 mg/d or equivalent for at least two weeks prior to visit 2

• Budesonide with a stable dose of = 9 mg/d for at least 2 weeks prior to visit 2 (changed by amendment 1, dated 16 January 2002)

• 5-Aminosalicylic Acid drugs/derivatives, provided they were given for 3 months or more and the dosage was stable for at least 4 weeks prior to visit 2

• 6-Mercaptopurine or azathioprine, provided they were taken for 6 months or more and the dosage was stable for at least 12 weeks prior to visit 2

• Methotrexate, provided it was taken for 6 months or more and the dosage was stable and =25 mg per week for at least 12 weeks prior to visit 2

The following patients were included in the 18-week treatment extension:

• Patients who received BIRB 796 BS for 8 weeks and reached:

• Clinical remission (defined as CDAI <150) after 8 weeks or

• Clinical response (reduction of CDAI =70) after 8 weeks

• Patients who were willing to continue with their treatment

Exclusion Criteria:

• Pregnancy (to be excluded at visit 2 by urine ß-human chorion-gonadotropin-test in women of childbearing potential) or breast feeding

• Female patients of childbearing potential (not 6 months post-menopausal or surgically sterilised) not using an approved form of birth control (hormonal contraceptives orally or in depot, intrauterine device)

• Patients without signs of inflammation of the bowel in the initial colonoscopy of the substudy

• Patients with colostomy or ileostomy

• Planned or needed surgery during the conduct of the trial due to Crohn's disease or for active gastrointestinal bleeding, peritonitis, intestinal obstruction, or intra-abdominal or pancreatic abscess requiring surgical drainage

• Known or suggested severe fixed symptomatic stenosis of the small or large intestine

• Severe underlying disease in particular of the GI tract (e.g. irritable bowel syndrome, celiac disease, infectious colitis)

• Patients with pathogens or Clostridium difficile toxin detected in the stool culture in the screening period

• Other infectious, ischemic, or immunological diseases with gastrointestinal involvement

• Patients with short bowel syndrome

• Patients who had had a treatment failure with a tumor necrosis factor (TNF)-blocking agent. Treatment failure was defined as not achieving a clinical response (improvement of =70 points in CDAI within 4 weeks) in a clinical trial or - in clinical practice -discontinuation of the TNF-blocking agent due to ineffectiveness (changed according to amendment 1, dated 16 January 2002)

• Treatment with cyclosporine A within 12 weeks prior to visit 2

• Last dose given within the specified time period before visit 2 for the following compounds:

• infliximab (Remicade®): 8 weeks,

• investigational agent: 4 weeks or 5 half-lives, whichever is longer

• Treatment with anti-inflammatory medication deviating from the criteria for dosage, and stability as provided in the inclusion criteria

• Patients treated with any of the following therapy:

• antibiotics provided the dosage had not been stable within 2 weeks prior to visit 2;

• parenteral or elemental diet;

• intrarectal therapy for Crohn's disease 2 weeks prior to visit 2 (added by amendment 1, dated 16 January 2002)

• Treatment with:

• Nonsteroidal anti-inflammatory drugs (NSAIDs) within 2 weeks prior to visit 2;

• Acetylsalicylic acid >100 mg/d;

• Paracetamol (acetaminophen) >3 g/day;

• Drug classified as proton pump inhibitor: 7 days prior to visit 2. This exclusion criterion was deleted after amendment 2 dated 11 June 2002.

• Drug classified as H2-receptor-blocker or antacid: 2 days prior to visit 2. This exclusion criterion was deleted after amendment 2 dated 11 June 2002.

• Active infection or serious infectious diseases resulting in hospitalisation or requiring systemic anti-infective therapy within 4 weeks before visit 2

• Serologic evidence of active hepatitis B and/or C

• Known HIV-infection

• History of prior tuberculosis infection or suspicion of active infection at screening based on chest X-ray done within 6 months prior to treatment phase

• History of cardiovascular, renal, neurologic, psychiatric, liver, immunologic, or endocrine dysfunction if they were clinically significant. A clinically significant disease was defined as one which, in the opinion of the investigator, may have either put the patient at risk because of participation in the study or as a disease which may have influenced the results of the study or the patient's ability to participate in the study

• Recent history of heart failure (one year or less) or myocardial infarction or patients with any cardiac arrhythmia requiring drug therapy (changed by amendment 1, dated 16 January 2002)

• ECG results outside of the reference range of clinical relevance including, but not limited to QTcB >480 msec, PR interval >240 msec, QRS interval >110 msec

• History of malignant disease in the last 5 years or suspicion of active malignant disease except successfully treated squamous or basal cell carcinoma of the skin and except patients with cervical carcinoma in situ who have had adequate treatment and follow up

• Clinically significant abnormal baseline haematology, blood chemistry or urinalysis if the abnormality defines a disease listed as an exclusion criterion

• Any of the following specific laboratory abnormalities at visit 1:

• alanine aminotransferase (ALT), aspartate aminotransferase (AST) greater than upper limit of normal range (ULN)

• Total bilirubin greater than ULN except for patients with documented Gilbert's disease

• Gamma-glutamyltransferase, alkaline phosphatase or lactate dehydrogenase greater than 1.5 x ULN

• White blood cell count greater than 1.5 ULN which was not due to Crohn's disease as assessed by the investigator

• Serum creatinine above 1.5 x ULN

• History of drug or alcohol abuse within the past two years or active drug or alcohol abuse

• Participation in another clinical trial within 4 weeks or 5 half-lives of the respective investigational agent, whichever was longer

• Hypersensitivity to trial drug

• Inability to comply with the protocol

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Crohn Disease

Intervention

Drug:
• Placebo

• BIBR 796 BS, 5 mg

• BIBR 796 BS, 20 mg

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Boehringer Ingelheim

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical Remission defined as Crohn's Disease Activity Index (CDAI) < 150		at week 8	No
Secondary	Clinical remission (defined as a CDAI score below 150)		at week 26	No
Secondary	Stabilised clinical remission at the end of the main treatment phase		at week 8 and 10	No
Secondary	Time to clinical remission		up to 26 weeks	No
Secondary	Duration of maintenance of clinical remission		up to 26 weeks	No
Secondary	Clinical response (defined as a reduction of CDAI score =70)		up to 26 weeks	No
Secondary	Time to clinical response		up to 26 weeks	No
Secondary	Duration of maintenance of clinical response		up to 26 weeks	No
Secondary	Changes from baseline in the CDAI score		up to 26 weeks	No
Secondary	Changes from baseline in the Inflammatory Bowel Disease Questionnaire (IBDQ) score		up to 26 weeks	No
Secondary	Number of patients with 50% fistulae reduction	defined as an at least 50% reduction from baseline in the number of draining fistulae	up to 26 weeks	No
Secondary	Changes from baseline in the number of draining fistulae		up to 26 weeks	No
Secondary	Changes from baseline in C-reactive protein (CRP) measurements		up to 26 weeks	No
Secondary	Changes from baseline in the daily corticosteroid dose	measured in mg prednisone equivalent	after week 10	No
Secondary	Number of drop-outs due to treatment failure		up to 26 weeks	No
Secondary	Number of patients with adverse events		up to 40 weeks	No
Secondary	Number of patients with clinically relevant changes in laboratory parameters		up to week 38	No
Secondary	Number of patients with relevant findings in electrocardiogram (ECG)		up to 26 weeks	No
Secondary	Extended clinical response (defined as a reduction of CDAI score = 100)		week 10 to 26	No
Secondary	Time to extended clinical response		week 10 to 26	No
Secondary	Duration of maintenance of extended clinical response		week 10 to 26	No
Secondary	Changes from baseline in the Crohn's Disease Endoscopic Index of Severity (CDEIS) score	for patients in the endoscopic substudy only	at the end of week 8	No
Secondary	Changes from baseline in the histological scoring of biopsy specimens	for patients in the endoscopic substudy only	at the end of week 8	No

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