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Clinical Trials in the EU / 2026-525478-21-00
Authorised, recruiting Phase I

A randomized, multiple ascending doses, clinical trial to evaluate safety, tolerability, pharmacokinetics, and pharmacodynamics of CV-01 after double-blind, placebo-controlled multiple oral administrations for 2 weeks in healthy volunteers, and multiple oral administrations open-label for 2 weeks in a cohort of participants with drug resistant epilepsy

2026-525478-21-00 · tracked via the Priya Life Science EU tracker
Sponsor
Angelini Pharma Italia Aziende Chimiche Riunite Angelini Francesco A.C.R.A.F. S.p.A. Enunciabile Anche Angelini Pharma Italia S.p.A. Angelini Pharma S.p.A. A.C.R.A.F. S.p.A. Acraf S.p.A. Angelini S.p.A. aziende Chimiche Riunite Angelini Francesco A.C.R.A.F. S.p.A
Sponsor type
Pharmaceutical company
Therapeutic area
Nervous System Diseases
Decision date
08/06/2026
Enrollment target
36
Sites
Sweden

Condition studied

Drug resistant epilepsy

Eligibility

Age group
18-64 years, 65+ 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 2026-525478-21-00 on CTIS ↗ ← All trials in the EU