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 May 17, 2026, 7:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. 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)

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

Interventions

  • Tildacerfont Drug

Drug

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 9, 2021
Primary completion
Jan 30, 2025
Completion
Jan 30, 2025
Last update posted
Dec 23, 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 23, 2025 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05128942 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →