drugset / Trial / NCT05816382

A Study of TAK-861 for the Treatment of Selected Central Hypersomnia Conditions

NCT05816382

Phase 2/3 Recruiting 500 enrolled Takeda
NaSingle-groupOpen-labelTreatment

Summary

The main aim is to evaluate the safety and tolerability of TAK-861 in participants with type 1 narcolepsy, who were exposed to previously tested doses of TAK-861.

Timeline

Start
2023-04-05
Primary completion
2028-02-28
Completion
2028-02-28

Drugs

EvaluationDrugModalityDoseRoute
Subject oveporexton Small molecule

Indications