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Clinical Trials in the EU / 2026-525836-41-00
Authorised Phase I

Bioequivalence of Tramadol retard 200 mg Prolonged-Release Tablets in Healthy Participants Under Fasting Conditions

2026-525836-41-00 · tracked via the Priya Life Science EU tracker
Sponsor
Laboratorios Cinfa S.A.
Sponsor type
Pharmaceutical company
Therapeutic area
Nervous System Diseases
Decision date
30/07/2026
Enrollment target
36
Sites
Czechia

Condition studied

Not applicable (submitted trial is a bioavailability trial in healthy participants).

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 2026-525836-41-00 on CTIS ↗ ← All trials in the EU