Study of Nitazoxanide Tablets in the Treatment of Mild to Moderate Active Crohn's Disease

Romark Laboratories

Status and phase

Terminated

Phase 2

Conditions

Crohn's Disease

Treatments

Drug: Nitazoxanide

Other: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT00130390

RM01-2018

Details and patient eligibility

About

The primary objective of this study is to evaluate the efficacy and safety of nitazoxanide compared to a placebo in reducing the signs and symptoms of mild to moderate active Crohn's disease in adults.

Full description

There is a significant need for a safe and effective treatment of Crohn's disease. It is recognized that bacteria in the gut lumen may have a role in the etiology and/or symptoms of this disease. Antimicrobials have often been used in treating Crohn's disease although their effectiveness has not been well established. Pro-inflammatory cytokines are also believed to play an important role in this disease. Nitazoxanide, a thiazolide anti-infective, is active in vitro against a broad spectrum of anaerobic bacteria, and it inhibits secretion of pro-inflammatory cytokines including IL-2, -4, -5, -6, -8, -10 and TNF alpha. The drug is also highly concentrated in the gastrointestinal tract. With these characteristics, nitazoxanide offers a unique approach to treatment of Crohn's disease.

Enrollment

98 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≥18 years.
Diagnosis of Crohn's disease with colonic or perianal involvement confirmed by endoscopic, histologic and/or radiologic data.
CDAI score ≥200 and ≤400.

Exclusion criteria

Subjects known to have stool positive for Clostridium difficile toxin A or B, bacterial enteric pathogens, rotavirus, Cryptosporidium species (spp.), and/or ova/parasites.
Evidence of bowel obstruction.
Females that are pregnant, breast-feeding or not using birth control and are sexually active.
Serious systemic disorders incompatible with the study.
History of hypersensitivity to nitazoxanide or any inactive ingredient in the formulation.
Uncontrolled gastro-intestinal bleeding.
Evidence of intestinal abscess, non-perianal fistula or stricture.
Patients who have received antibiotics in the past 7 days.
Patients receiving >20 mg of prednisone, or its equivalent.
Patients receiving Anucort-HC or rectal steroids.
Patients receiving immunosuppressive therapy that has not been stabilized.
Patients who have received TNF-alpha inhibitor treatments such as infliximab or other biological agents within three months prior to start of treatment.
Patients with Crohn's disease confined to the esophagus, stomach and small bowel.