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tildacerfont

Generic: Tildacerfont

tildacerfont: 4 clinical trials tracked.

tildacerfont evidence translation

What we can confirm

4 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about tildacerfont, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 1 study sponsors
Clinical Trial Registry Records (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

NCT05370521Registry updated 2025-10-09·Phase 2·SPRB
Terminated

Primary endpoint: Change in DHEAS

InterventionalRandomizedtriple27 targetStarted 2022-05Completion 2023-0821 sites · United StatesSpruce Biosciences

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)

NCT05128942Registry updated 2025-12-24·Phase 2·SPRB
Terminated

Primary endpoint: Number of Participants With Treatment-emergent Adverse Event (TEAE) as Assessed by Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0

Interventionalopen67 targetStarted 2021-12Completion 2025-0113 sites · United StatesSpruce Biosciences

A 3-Month Phase 2 Study to Evaluate the Safety and Efficacy of SPR001 in Subjects With Classic Congenital Adrenal Hyperplasia

NCT03687242Registry updated 2025-04-01·Phase 2·SPRB
Completed

Primary endpoint: The Incidence of Treatment-emergent Adverse Events (Safety and Tolerability) in Subjects With CAH

Interventionalopen11 enrolledStarted 2018-09Completion 2019-088 sites · United StatesSpruce Biosciences

A Phase 2, Multiple-Dose, Dose-Escalation Study to Evaluate the Safety and Efficacy of SPR001 in Adults With Classic Congenital Adrenal Hyperplasia (CAH)

NCT03257462Registry updated 2025-10-22·Phase 2·SPRB
Completed

Primary endpoint: Safety of SPR001 in Patients With CAH

Interventionalopen24 enrolledStarted 2017-07Completion 2019-039 sites · United StatesSpruce Biosciences