drugset / Trial / NCT03687242

Study to Evaluate the Safety and Efficacy of SPR001 in Subjects With Classic Congenital Adrenal Hyperplasia

NCT03687242 ↗

Phase 2 Completed 11 enrolled Spruce Biosciences
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

EvaluationDrugModalityDoseRoute
Subject Tildacerfont Small molecule 400 mg Oral