tildacerfont
tildacerfont: developed by 1 company · 4 clinical trials tracked.
tildacerfont evidence translation
What we can confirm
4 tracked trials
What it means
What to watch
Prepared research question
How could tildacerfont → SPRB affect its developer, and what evidence supports the link?
Traceable citations · Unknowns marked
See linked entities and source evidence2 indications · 0 study sponsors
Related indications
Study sponsors
No additional listed-company sponsor is linked.
Development Pipeline (1)
| Company | Phase |
|---|---|
| SPRUCE BIOSCIENCES, INC. (SPRB) Polycystic Ovary Syndrome; Congenital Adrenal Hyperplasia | Phase 2 |
Clinical Trials (4)
A Randomized, Placebo-Controlled, Dose Escalation Study to Evaluate the Safety and Efficacy of Tildacerfont in Adult Subjects With Polycystic Ovary Syndrome (PCOS) and Elevated Adrenal Androgens
Primary endpoint: Change in DHEAS
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 (CAH)
Primary endpoint: Number of Participants With Treatment-emergent Adverse Event (TEAE) as Assessed by Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0
A 3-Month Phase 2 Study to Evaluate the Safety and Efficacy of SPR001 in Subjects With Classic Congenital Adrenal Hyperplasia
Primary endpoint: The Incidence of Treatment-emergent Adverse Events (Safety and Tolerability) in Subjects With CAH
A Phase 2, Multiple-Dose, Dose-Escalation Study to Evaluate the Safety and Efficacy of SPR001 in Adults With Classic Congenital Adrenal Hyperplasia (CAH)
Primary endpoint: Safety of SPR001 in Patients With CAH
Frequently asked questions
Who is developing tildacerfont?
tildacerfont is being developed by SPRUCE BIOSCIENCES, INC..
How many clinical trials involve tildacerfont?
BioSniper tracks 4 clinical trials involving tildacerfont.