Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Terminated Phase 2 Interventional Results available

A Phase 2 Study to Evaluate the Safety, Efficacy and PK of Tildacerfont in Children Aged 2-17 Years With CAH

ClinicalTrials.gov ID: NCT05128942

Public ClinicalTrials.gov record NCT05128942. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 4, 2026, 3:41 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

An investigation of the safety and efficacy of tildacerfont in participants with CAH.

Study identification

NCT ID
NCT05128942
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Spruce Biosciences
Industry
Enrollment
67 participants

Conditions and interventions

Eligibility (public fields only)

Age range
2 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 10, 2021 (Actual)
Primary completion
Jan 31, 2025 (Actual)
Completion
Jan 31, 2025 (Actual)
Last update posted
Dec 24, 2025

2021 – 2025

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
Spruce Study Site Sacramento California 95821 —
Spruce Study Site San Diego California 92123 —
Spruce Study Site Chicago Illinois 60611 —
Spruce Study Site Minneapolis Minnesota 55454 —
Spruce Study Site Buffalo New York 14203 —
Spruce Study Site Providence Rhode Island 02903 —
Spruce Study Site Columbia South Carolina 29203 —
Spruce Study Site Dallas Texas 75231 —
Spruce Study Site Edinburg Texas 78539 —
Spruce Study Site Fort Worth Texas 76104 —
Spruce Study Site Salt Lake City Utah 84113 —
Spruce Study Site Charlottesville Virginia 22903 —
Spruce Study Site Richmond Virginia 23284 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05128942, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 24, 2025 · Synced Nov 4, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05128942 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →