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Clinical Trials in the EU / 2025-524218-27-00
Authorised Phase I

An open label, randomized, single-dose, two-treatment, two-period, cross-over bioequivalence study comparing Pyridostigmine Bromide, P.R.Tab, 180 mg/tab, VIANEX S.A., Greece versus Mestinon® retard 180 mg/prolonged-release tablet, Viatris Healthcare GmbH, Germany, in healthy male and female volunteers under fed conditions.

2025-524218-27-00 · tracked via the Priya Life Science EU tracker
Sponsor
Vianex S.A.
Sponsor type
Pharmaceutical company
Therapeutic area
Musculoskeletal Diseases
Decision date
19/12/2025
Enrollment target
44
Sites
Czechia

Condition studied

treatment of myasthenia gravis

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 2025-524218-27-00 on CTIS ↗ ← All trials in the EU