A Phase 2 Study to Evaluate the Safety, Efficacy and Pharmacokinetics of SPR001 (Tildacerfont) in Children Aged 2 to 17 Years with Congenital Adrenal Hyperplasia
Latest Information Update: 16 Dec 2024
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At a glance
- Drugs Tildacerfont (Primary)
- Indications Congenital adrenal hyperplasia
- Focus Adverse reactions
- Acronyms CAHptain-205
- Sponsors Spruce Biosciences
- 10 Dec 2024 According to a Spruce Biosciences media release, In the interim, the CAHmelia-204 and CAHptain-205 clinical trials will be discontinued.
- 10 Dec 2024 Results presented in the Spruce Biosciences Media Release.
- 03 Dec 2024 Planned number of patients changed from 55 to 70.