Induction of Clinical Response Using Rifaximin in Crohn's Disease

Sponsor

Scott Lee (Other)

Overall Status

Completed

CT.gov ID

NCT00603616

Collaborator

Bausch Health Americas, Inc. (Industry)

Enrollment

Location

Arms

144.1

Duration (Months)

0.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Antibiotics have been used to treat Crohn's disease symptoms with the best studied antibiotics being Cipro and Flagyl. Rifaximin is a poorly absorbed oral antibiotic that is FDA approved for travelers' diarrhea. It works by inhibiting bacterial reproduction. It is very poorly absorbed and over 97% of the drug taken orally is excreted in the feces.

The purpose of this study is to evaluate the potential benefits and safety of Rifaximin for the treatment of moderate to severe symptoms of Crohn's Disease.

Condition or Disease	Intervention/Treatment	Phase
Crohn's Disease	Drug: Placebo Comparator Drug: Rifaximin	Phase 2

Detailed Description

Inflammatory bowel disease (IBD) is a debilitating chronic inflammatory disease conventionally categorized into Crohn's disease (CD) and Ulcerative Colitis (UC). CD affects nearly 630,000 people in North America with up to 50,000 new people being diagnosed every year. It is a chronic debilitating disease characterized by abdominal pain, malnutrition, bloody diarrhea, fistula formation, intestinal perforations and strictures, and even extra-intestinal manifestations such as joint pains and skin rashes. Nearly 80% of people with CD will need surgical treatment at some point in their disease process. The majority of CD subjects are diagnosed in young adulthood thereby subjecting them to many decades of discomfort and medical intervention.

Antibiotics have been used to treat CD with variable response rates. The basis for antibiotic therapy is that breakdown of the integrity of the mucosal barrier in the gastrointestinal (GI) tract leads to a heightened inflammatory response to commensurate luminal bacteria. By changing the composition or bacterial load in the intestinal lumen, it may be possible to alter the immune response. Ciprofloxacin (Cipro) and metronidazole (Flagyl) are the best studied antibiotics that have shown efficacy, but the effect is temporal and long term use can lead to serious side effects. Rifaximin is a recent FDA approved antibiotic with broad spectrum of activity, excellent safety profile, and minimal absorption from the GI tract. Open label and small studies in IBD subjects show response rates up to 80% in CD subjects. These studies were limited however in that they were not randomized placebo controlled trials.

The investigators propose to conduct a randomized placebo controlled crossover trial of rifaximin in CD subjects to assess initial clinical response compared to placebo.

Study Design

Study Type:

Interventional

Actual Enrollment :

36 participants

Allocation:

Randomized

Intervention Model:

Crossover Assignment

Masking:

Triple (Participant, Care Provider, Investigator)

Primary Purpose:

Treatment

Official Title:

A Randomized, Prospective, Double-blind, Placebo-controlled, Crossover Study to Evaluate the Safety and Efficacy of Rifaximin for the Treatment of Moderate to Severe Crohn's Disease

Study Start Date :

Nov 1, 2008

Actual Primary Completion Date :

Nov 3, 2020

Actual Study Completion Date :

Nov 3, 2020

Arms and Interventions

Arm	Intervention/Treatment
Placebo Comparator: 1 Placebo pills	Drug: Placebo Comparator Matching oral placebo pills to be taken twice daily for a total of 8 weeks
Active Comparator: 2 Rifaximin	Drug: Rifaximin Oral rifaximin 550mg to be taken twice daily for a total of 8 weeks Other Names: Xifaxan

Arm

Intervention/Treatment

Placebo Comparator: 1

Placebo pills

Drug: Placebo Comparator

Matching oral placebo pills to be taken twice daily for a total of 8 weeks

Active Comparator: 2

Rifaximin

Drug: Rifaximin

Oral rifaximin 550mg to be taken twice daily for a total of 8 weeks

Other Names:

Xifaxan

Outcome Measures

Primary Outcome Measures

Evaluate the efficacy of rifaximin 550 mg bid compared to placebo in achieving clinical response in moderate to severe Crohn's Disease (CD) subjects as determined by a > 100 point decrease in the Crohn's Disease Activity Index (CDAI) [8 weeks]

Secondary Outcome Measures

Evaluate the efficacy of rifaximin compared to placebo at inducing clinical remission in CD subjects [8 weeks]
Evaluate the safety profile of rifaximin in subjects with active CD [16 weeks for those subjects who do not cross over, 32 weeks for those who do cross over]
Evaluate the effect rifaximin has on the quality of life in subjects with CD compared to placebo [8 weeks]
Evaluate if there are any clinical parameters which might predict response to rifaximin [8 weeks]
Compare mean changes in CDAI scores between rifaximin and placebo treated subjects [8 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 80 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Male or female subjects, 18 to 80 years of age, inclusive, that can themselves provide written, informed consent and authorization of use of protected health information prior to any study-related procedures and who are, in the opinion of the investigator(s), likely to comply with all the requirements of the study
Subjects must have a prior diagnosis of CD established by endoscopy and clinical parameters as determined by the investigator(s) for at least 3 months prior to randomization
Subjects must be able to participate in all required follow-up visits and fill out all related documentation (e.g. symptom diary)
Subjects currently with moderately active disease defined as a CDAI 250-450
Concomitant medications:
If subjects are taking sulfasalazine or 5-ASA products prior to entry, the dose must be stable for at least 4 weeks prior to the randomization
If subjects are on azathioprine, 6-mercaptopurine, or methotrexate, they will have had to be on a stable dosage for at least 8 weeks
Subjects are allowed to be on corticosteroids at a dose equivalent to 20 mg or less of prednisone, IF the dose has been stable for a minimum of 2 weeks. Steroids must be held stable throughout the induction portion of the study. The maximum dose of budesonide must not exceed 9mg per day and must also have been stable for a minimum of 2 weeks.
No oral or intravenous antibiotics within 4 weeks prior to randomization
No current or past use of biological treatment within 6 weeks of randomization into study (e.g. infliximab)
If subjects have previously been on any of the above products but are no longer taking them, they should not have received any of the relevant therapeutic products within 4 weeks prior to randomization
No other experimental or non-FDA approved medications are allowed. If the subject has previously been on an experimental therapy, they must have not received the therapy within the prior 8 weeks prior to randomization
Subjects on concomitant medications for CD will not be allowed to change dosages during the study
If subjects are at increased risk of colorectal cancer (defined as having an 8-year history of pan-colitis or 12 year history of left sided colitis), they will need to have undergone a colonoscopy with pan-colonic surveillance biopsies within 2 years of the screening visit. The biopsies must be negative for dysplasia
Female or male subjects who are surgically sterilized or who are prepared to and agree to practice a double-barrier form of birth control from the screening visit through 30 days (females) and 30 days (males), respectively, from the last dose of study medication. Females who are more than 12 months post-menopausal are also eligible to participate in the study

Exclusion Criteria:

Evidence of active infection which may include any of the following
Febrile ( > 38.5ºC)
Positive blood culture within 2 weeks prior to randomization
Evidence of toxic megacolon or abscess
Positive stool culture for enteric pathogens, pathogenic ova or parasite, or a positive assay for C. difficile toxin at screening
Subjects with CDAI > 450
Any current use or use within the last 8 weeks of an investigational drug
Current or past use (within past 12 wks) of biological treatment
Current or use within the last 4 weeks of any oral or intravenous antibiotic
Anticipated increased dosage of any medication to treat CD
Anticipated need for surgery within 12 weeks
Known obstructive diseases of the gastrointestinal system
Medical conditions requiring in-patient hospitalization
Proctocolectomy, total colectomy, ileostomy, or stoma
Severe cardiopulmonary disease:
Congestive heart failure (NYHA Class III or IV)
Severe cardiovascular or peripheral vascular disease
Myocardial infarction, percutaneous coronary intervention, or bypass surgery within the past 6 months
Significant liver disease:
Levels of SGOT [AST], SGPT [ALT], or alkaline phosphatase > 2.5x the upper limit of the normal range for the laboratory performing test
History of cirrhosis
Renal insufficiency, defined as serum creatinine > 150% of the upper limit of the normal range for the laboratory performing the test
Abnormal hematology parameters defined as severe anemia with hemoglobin < 8.5 g/dL and/or white blood cell count of < 3,500/ul
Malignancy within the past 2 years other than surgically cured skin carcinoma or cervical dysplasia (CIN I-II)
History of dysplasia or carcinoma of the colon
Pregnant, lactating, or planning to become pregnant during the course of the investigational study
Known history of allergic reaction to rifaximin or allergy to any of the rifamycin antimicrobial agents (which include rifampin, rifabutin, and rifapentine)