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NCT07144163 · ClinicalTrials.gov registry record · Phase 3

A Study to Evaluate Atumelnant in Adults With Congenital Adrenal Hyperplasia

A Phase 3 study of Congenital Adrenal Hyperplasia and Classic Congenital Adrenal Hyperplasia, sponsored by Crinetics Pharmaceuticals.

Recruiting
Registry status
Phase 3
Development phase
150
Enrollment target
8
Study locations

NCT07144163 is a Phase 3 study of Congenital Adrenal Hyperplasia and Classic Congenital Adrenal Hyperplasia that is actively recruiting participants, run by Crinetics Pharmaceuticals. The registered enrollment target is 150 participants, above the 84-participant average among 8 other Congenital Adrenal Hyperplasia trials with a reported enrollment target (79% higher). The trial reports 8 study locations across 7 states.

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The verdict

NCT07144163, a Phase 3 study of Congenital Adrenal Hyperplasia and Classic Congenital Adrenal Hyperplasia, is actively recruiting participants, sponsored by Crinetics Pharmaceuticals.

RECRUITING
Registry status
Phase 3
Development phase
150 participants
Enrollment target
8
Study locations

Study Summary

The purpose of this study is to evaluate the efficacy, safety, PK, and PD of atumelnant in adults with classic CAH due to 21-OHD.

Interventions

  • DRUG Placebo
  • DRUG Atumelnant

Study Locations (8)

Queensland

  • Crinetics Study Site - Herston
  • Crinetics Study Site - Woolloongabba

Michigan

  • Crinetics Study Site - Ann Arbor

Buenos Aires F.D.

  • Crinetics Study Site - Buenos Aires

South Australia

  • Crinetics Study Site - Adelaide

Victoria

  • Crinetics Study Site - Parkville

Western Australia

  • Crinetics Study Site - Nedlands

São Paulo

  • Crinetics Study Site - São Paulo

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2025-12-11
Est. Completion 2027-05
Phase Phase 3

Sponsor

Crinetics Pharmaceuticals

16 total trials

What the Registry Record Tells You About NCT07144163

The ClinicalTrials.gov registry entry for NCT07144163 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 84-participant average among 8 other Congenital Adrenal Hyperplasia trials with a reported enrollment target (79% higher). The listed sponsor is Crinetics Pharmaceuticals, which has 16 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Congenital Adrenal Hyperplasia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07144163 reports 8 study locations spanning 7 distinct geographic areas - top geographies include Queensland, Michigan, Buenos Aires F.D..

Frequently Asked Questions

What is clinical trial NCT07144163 about?

NCT07144163 is a clinical study titled "A Study to Evaluate Atumelnant in Adults With Congenital Adrenal Hyperplasia". The purpose of this study is to evaluate the efficacy, safety, PK, and PD of atumelnant in adults with classic CAH due to 21-OHD.

What is the current status of trial NCT07144163?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 150 participants. The study started on 2025-12-11. Estimated completion is 2027-05.

What conditions does trial NCT07144163 study?

This clinical trial studies the following conditions: Congenital Adrenal Hyperplasia, Classic Congenital Adrenal Hyperplasia.

What interventions are being tested in trial NCT07144163?

The interventions under investigation include: Placebo (DRUG), Atumelnant (DRUG).

Who is sponsoring clinical trial NCT07144163?

This trial is sponsored by Crinetics Pharmaceuticals, which has 16 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07144163 being conducted?

This trial has 8 study locations across Michigan, Buenos Aires F.D., Queensland, South Australia, Victoria. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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