A Ph2b to Evaluate Clinical Efficacy and Safety of Tildacerfont in Adult CAH
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- STATUS
- Recruiting
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- End date
- Nov 22, 2024
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- participants needed
- 72
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- sponsor
- Spruce Biosciences
Summary
An investigation of the efficacy and safety of up to 70 weeks of treatment with Tildacerfont in subjects with classic CAH who have elevated biomarkers at baseline on their current GC regimen. Optional open label treatment extension period up to 240 weeks with 200mg tildacerfont QD.
Description
This is a study that will test the efficacy and safety of Tildacerfont. The first 12-weeks will be a double-blind, placebo controlled, dose ranging study. The following 58-weeks will assess the long term safety of Tildacerfont. Optional open label treatment extension period up to 240 weeks with 200mg tildacerfont QD.
Details
| Condition | Congenital Adrenal Hyperplasia |
|---|---|
| Treatment | Tildacerfont/Placebo |
| Clinical Study Identifier | NCT04457336 |
| Sponsor | Spruce Biosciences |
| Last Modified on | 7 October 2022 |
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