drugset / Trial / NCT03370120

Study to Test the Safety and Efficacy of Padsevonil as Adjunctive Treatment of Focal-onset Seizures in Adult Subjects With Drug-resistant Epilepsy

NCT03370120 ↗

Phase 2 Terminated 406 enrolled UCB Biopharma SRL
NaSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to evaluate the long-term safety and tolerability of Padsevonil administered at individualized doses as adjunctive treatment for subjects with drug-resistant epilepsy.

Timeline

Start
2018-08-27
Primary completion
2020-12-11
Completion
2020-12-11

Outcome

Outcome not reported

Stopped: “Based on available data, UCB has decided to stop development of padsevonil as adjunctive treatment of focal-onset seizure”

Drugs

EvaluationDrugModalityDoseRoute
Subject Padsevonil Small molecule — Oral

Indications