Cure8

Why This Matters

This trial tests whether adding nitazoxanide—an antiparasitic with reported antimicrobial and anti-inflammatory effects—can improve symptoms in people with mild-to-moderate ulcerative colitis. If effective, it could point to a novel adjunctive therapy targeting microbes and inflammation.

Who Should Pay Attention

Adult patients with mild-to-moderate ulcerative colitis, clinicians who treat UC, and researchers interested in microbiome-targeted or repurposed-drug strategies.

Study Snapshot

Story typeClinical Reference
Trial phasePhase 2, Phase 3
Enrollment44 participants
Study statusNot_yet_recruiting
Source depthTrial registry record

What To Know

This clinicaltrials.gov record describes a randomized, double-blind, placebo-controlled Phase 2/3 trial testing nitazoxanide 500 mg twice daily as an add-on to standard therapy for adults (18–65) with mild-to-moderate ulcerative colitis over 12 weeks. The study plans to enroll 44 participants and lists change in Mayo score at 12 weeks as the primary outcome.

The registry summary notes preclinical rationale (antimicrobial, anti-inflammatory, and barrier-protective effects of nitazoxanide) but emphasizes that clinical evidence to date is limited.

Key eligibility points include stable UC therapy for ≥8 weeks and exclusion of recent antibiotics/probiotics, active intestinal infection, recent biologic initiation or dose change, and pregnancy/lactation. This is a trial record (NOT_YET_RECRUITING) describing planned methods and outcomes; it does not report results or safety findings.

People should not interpret this as evidence that nitazoxanide is effective or safe for UC outside a trial.

Keep In Mind

This is a registered trial record (Phase 2/3) that is not yet recruiting and does not include results. The registry provides planned design, dose, duration, and outcomes but not efficacy or safety data. Nitazoxanide is not an established UC therapy; enrollment criteria exclude recent antibiotic/probiotic use and recent biologic changes, which may limit generalizability.

Source Details

Review the original publication for the complete reporting, methods, and context.

Read Original Source
Clinical trial Evidence type derived from source or registry metadata.
PublicationClinicalTrials.gov
SponsorTanta University
Trial IDNCT07820046
Study typeInterventional
Trial phasePhase 2, Phase 3
Enrollment44 participants
Indexed viaClinicalTrials.gov
Source typeTrial registry record
PublishedSep 15, 2026, 12:00 AM
Content availableTrial registry record

This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.

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