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NCT04045145 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Neurocrine Biosciences.

Completed
Registry status
Phase 2
Development phase
8
Enrollment target

NCT04045145 is a Phase 2 study that has completed, run by Neurocrine Biosciences. The registered enrollment target is 8 participants.

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The verdict

NCT04045145, a Phase 2 study, has completed, sponsored by Neurocrine Biosciences.

COMPLETED
Registry status
Phase 2
Development phase
8 participants
Enrollment target

Study Summary

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).

Interventions

  • DRUG Crinecerfont

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2019-12-12
Est. Completion 2021-07-02
Phase Phase 2

Sponsor

Neurocrine Biosciences

65 total trials

What the Registry Record Tells You About NCT04045145

The ClinicalTrials.gov registry entry for NCT04045145 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Neurocrine Biosciences, which has 65 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Crinecerfont is the first listed.

NCT04045145 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04045145 about?

NCT04045145 is a clinical study titled "Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NBI-74788 (Crinecerfont) in Pediatric Participants With Congenital Adrenal Hyperplasia". 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 a...

What is the current status of trial NCT04045145?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 8 participants. The study started on 2019-12-12. Estimated completion is 2021-07-02.

What interventions are being tested in trial NCT04045145?

The interventions under investigation include: Crinecerfont (DRUG).

Who is sponsoring clinical trial NCT04045145?

This trial is sponsored by Neurocrine Biosciences, which has 65 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.