drugset / Trial / NCT03687242
Study to Evaluate the Safety and Efficacy of SPR001 in Subjects With Classic Congenital Adrenal Hyperplasia
NaSingle-groupOpen-labelTreatment
Summary
This is a Phase 2 study of SPR001 for the treatment of classic CAH that will provide 12 weeks of open-label treatment to eligible subjects.
Timeline
- Start
- 2018-09-06
- Primary completion
- 2019-07-08
- Completion
- 2019-08-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tildacerfont | Small molecule | 400 mg | Oral |