drugset / Trial / NCT07051252
A Study of HBS-201 (Pitolisant Delayed-release)
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to assess the tolerability of HBS-201 when starting at a therapeutic dose in adult participants with narcolepsy.
Timeline
- Start
- 2025-05-21
- Primary completion
- 2025-10-13
- Completion
- 2025-10-13
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HBS-201 | Unknown | 35.6 mg | Oral |