Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NBI-74788 (Crinecerfont) in Pediatric Participants With Congenital Adrenal Hyperplasia

Completed · Phase 2

Conditions studied: CAH - Congenital Adrenal Hyperplasia

In brief

This is a Phase 2, open-label, multiple-dose, study to assess the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of NBI-74788 (crinecerfont) in pediatric participants (14 to 17 years of age) with a documented medical diagnosis of classic 21-hydroxylase deficiency congenital adrenal hyperplasia (CAH).

Key facts

Study ID

NCT04045145

Run by

Neurocrine Biosciences

People needed

8

Starts

2019-12-12

Expected to finish

2021-07-02

Last updated by the study team

2024-07-18

Who can join

Age: 14 and older, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Be in good general health.
• Have a medically confirmed diagnosis of classic 21-hydroxylase deficiency CAH.
• Be on a stable regimen of steroidal treatment for CAH that is expected to remain stable throughout the study.
• Participants of childbearing potential must be instructed on the proper use of barrier methods of contraception and agree to use hormonal or two forms of nonhormonal contraception (dual contraception) consistently from screening until the final study visit or a prespecified window after the last dose of study drug, whichever is longer.
• Participants of childbearing potential must have a negative pregnancy test at screening and negative urine pregnancy test at baseline.
• Have a negative urine drug (for illegal drugs) and alcohol breath test at screening and baseline.
• Be willing and able to adhere to the study regimen and study procedures described in the protocol and informed consent/assent form, including all requirements at the study center and return for the follow-up visit.

You may not qualify if…

• Have a clinically significant unstable medical condition or chronic disease, or malignancy.
• Had a medically significant illness within 30 days of screening.
• Have a known or suspected differential diagnosis of any of the other known forms of classic CAH.
• Have a history that includes bilateral adrenalectomy, hypopituitarism, or other condition requiring daily therapy with orally administered glucocorticoids.
• Are pregnant or lactating females.
• Have a history of epilepsy or serious head injury.
• Have a known history of long QT syndrome or cardiac tachy-arrhythmia.
• Have hypersensitivity to any corticotropin releasing hormone antagonists.
• Test positive at screening for hepatitis B, hepatitis C, or human immunodeficiency virus (HIV), or have a history of a positive result.
• Have a recent history of alcohol or drug abuse, or current evidence of substance dependence or abuse criteria.
• Used any anticoagulants or antiplatelet therapies within 30 days before screening.
• Have an active bleeding disorder.
• Used any other investigational drug within 30 days before initial screening, or plans to use an investigational drug (other than the study drug) during the study.
• Have a blood loss ≥250 mL or donated blood within 56 days or donated plasma within 7 days before baseline.

Where it is running

• Neurocrine Clinical Site — San Diego, California, United States
• Neurocrine Clinical Site — Aurora, Colorado, United States
• Neurocrine Clinical Site — Ann Arbor, Michigan, United States
• Neurocrine Clinical Site — Minneapolis, Minnesota, United States
• Neurocrine Clinical Site — Philadelphia, Pennsylvania, United States
• Neurocrine Clinical Site — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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