drugset / Trial / NCT05149898
Open-Label Study of ZYN002 Administered as a Transdermal Gel to Children and Adolescents With 22q11.2 Deletion Syndrome (INSPIRE)
Phase 2
Completed
20 enrolled
Harmony Biosciences Management, Inc.
Zynerba Pharmaceuticals, Inc. · collab
NaSingle-groupOpen-labelTreatment
Summary
To evaluate the safety and tolerability of ZYN002 administered as a transdermal gel formulation, for up to 38 weeks, in participants ages 4 to \<18 years, in the treatment of 22q.11.2 Deletion syndrome (22qDS).
Timeline
- Start
- 2020-02-19
- Primary completion
- 2022-11-09
- Completion
- 2022-11-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ZYN002 | Unknown | 125 mg | Other |
| Subject | ZYN002 | Unknown | 250 mg | Other |
| Subject | ZYN002 | Unknown | 500 mg | Other |
| Subject | ZYN002 | Unknown | 750 mg | Other |