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Clinical Trials in the EU / 2025-524832-20-00
Authorised Phase I

A PHASE 1, OPEN-LABEL STUDY TO ASSESS THE ABSORPTION, DISTRIBUTION, METABOLISM, AND EXCRETION, INCLUDING THE MASS BALANCE, OF A SINGLE ORAL DOSE OF [14C]-VAFIDEMSTAT IN HEALTHY MALE PARTICIPANTS

2025-524832-20-00 · tracked via the Priya Life Science EU tracker
Sponsor
Oryzon Genomics S.A.
Sponsor type
Pharmaceutical company
Therapeutic area
Not possible to specify
Decision date
30/04/2026
Enrollment target
8
Sites
Netherlands

Condition studied

Healthy volunteers

Eligibility

Age group
18-64 years
Sex
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 2025-524832-20-00 on CTIS ↗ ← All trials in the EU