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Spruce Biosciences
Industry · 6 registered clinical trials.
Status
Trial
Phase
Started
Terminated
A Study of Safety and Efficacy of Tildacerfont in Females With Polycystic Ovary Syndrome and Elevated Adrenal
Polycystic Ovary Syndrome
Phase 2
2022-05-15
Terminated
A Phase 2 Study to Evaluate the Safety, Efficacy and PK of Tildacerfont in Children Aged 2-17 Years With CAH
Congenital Adrenal Hyperplasia, 21-OHD
Phase 2
2021-12-10
Terminated
A Ph2b to Evaluate Tildacerfont in the Reduction of Glucocorticoid Steroid Doses in Adult CAH
Congenital Adrenal Hyperplasia
Phase 2
2021-02-22
Terminated
A Ph2b to Evaluate Clinical Efficacy and Safety of Tildacerfont in Adult CAH
Congenital Adrenal Hyperplasia
Phase 2
2020-08-26
Completed
Study to Evaluate the Safety and Efficacy of SPR001 in Subjects With Classic Congenital Adrenal Hyperplasia
Congenital Adrenal Hyperplasia, CAH - Congenital Adrenal Hyperplasia, CAH - 21-Hydroxylase Deficiency
Phase 2
2018-09-06
Completed
Study of SPR001 in Adults With Classic Congenital Adrenal Hyperplasia
Congenital Adrenal Hyperplasia, CAH - Congenital Adrenal Hyperplasia
Phase 2
2017-07-12