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Clinical Trials in the EU / 2025-525078-12-00
Authorised, not yet recruiting Phase I

A randomized, balanced, two-treatment, two-sequence, single oral dose, two stage crossover adaptative bioequivalence study of Rifaximin 200 mg film-coated tablets (Antibiotice SA) vs. Normix® 200 mg, film- coated tablets (Alfasigma S.P.A) in healthy subjects under fed conditions

2025-525078-12-00 · tracked via the Priya Life Science EU tracker
Sponsor
Antibiotice S.A
Sponsor type
Pharmaceutical company
Therapeutic area
Bacterial Infections and Mycoses
Decision date
22/05/2026
Enrollment target
64
Sites
Romania

Condition studied

healthy subjects

Eligibility

Age group
18-64 years
Sex
Female, Male
Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-525078-12-00 on CTIS ↗ ← All trials in the EU