ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional Results available

Global Safety and Efficacy Registration Study of Crinecerfont for Congenital Adrenal Hyperplasia

ClinicalTrials.gov ID: NCT04490915

Public ClinicalTrials.gov record NCT04490915. 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 18, 2026, 6:06 AM 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 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Crinecerfont (NBI-74788) in Adult Subjects With Classic Congenital Adrenal Hyperplasia, Followed by Open-Label Treatment

Study identification

NCT ID
NCT04490915
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Neurocrine Biosciences
Industry
Enrollment
182 participants

Conditions and interventions

Interventions

  • Crinecerfont Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 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 15, 2020
Primary completion
Jul 18, 2023
Completion
Jul 31, 2027
Last update posted
May 10, 2026

2020 – 2027

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
Neurocrine Clinical Site Los Angeles California 90027
Neurocrine Clinical Site San Diego California 92123
Neurocrine Clinical Site San Francisco California 94143
Neurocrine Clinical Site Aurora Colorado 80045
Neurocrine Clinical Site Atlanta Georgia 30329
Neurocrine Clinical Site Indianapolis Indiana 46202
Neurocrine Clinical Site Bethesda Maryland 20982
Neurocrine Clinical Site Boston Massachusetts 02115
Neurocrine Clinical Site Ann Arbor Michigan 48109
Neurocrine Clinical Site Minneapolis Minnesota 55454
Neurocrine Clinical Site Rochester Minnesota 55905
Neurocrine Clinical Site St Louis Missouri 63110
Neurocrine Clinical Site Great Neck New York 11021
Neurocrine Clinical Site New York New York 10029
Neurocrine Clinical Site Winston-Salem North Carolina 27157
Neurocrine Clinical Site Tulsa Oklahoma 74135
Neurocrine Clinical Site Philadelphia Pennsylvania 19104
Neurocrine Clinical Site Pittsburgh Pennsylvania 15224
Neurocrine Clinical Site Dallas Texas 75390
Neurocrine Clinical Site Seattle Washington 98105

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 50 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04490915, 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 May 10, 2026 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04490915 live on ClinicalTrials.gov.

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