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RECRUITING Phase 2

An Extension Study to Evaluate Safety and Efficacy in Participants Treated With CRN04894

NCT06712823 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the long-term safety, tolerability, and efficacy of atumelnant (CRN04894).

Interventions

  • DRUG atumelnant (CRN04894)

Study Locations (9)

Other

  • Crinetics Study Site — São Paulo
  • Crinetics Study Site — Roma
  • Crinetics Study Site — Birmingham
  • Crinetics Study Site — London

Minnesota

  • Crinetics Study Site, Minneapolis, Minnesota 55454 — Minneapolis

North Carolina

  • Crinetics Study Site — Morehead City

Córdoba Province

  • Crinetics Study Site — Córdoba

São Paulo

  • Crinetics Study Site — Botucatu

Bavaria

  • Crinetics Study Site — Munich

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2025-02-25
Est. Completion 2027-11
Phase Phase 2

Sponsor

Crinetics Pharmaceuticals

9 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06712823

The ClinicalTrials.gov registry entry for NCT06712823 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Crinetics Pharmaceuticals, which has 9 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 2 conditions, with Congenital Adrenal Hyperplasia appearing as the primary indexed condition, and to 1 intervention — of which atumelnant (CRN04894) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06712823 reports 9 study locations spanning 6 distinct geographic areas — top geographies include Other, Minnesota, North Carolina. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06712823 about?

NCT06712823 is a clinical study titled "An Extension Study to Evaluate Safety and Efficacy in Participants Treated With CRN04894". The purpose of this study is to evaluate the long-term safety, tolerability, and efficacy of atumelnant (CRN04894).

What is the current status of trial NCT06712823?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 150 participants. The study started on 2025-02-25. Estimated completion is 2027-11.

What conditions does trial NCT06712823 study?

This clinical trial studies the following conditions: Congenital Adrenal Hyperplasia, Classic Congenital Adrenal Hyperplasia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06712823?

The interventions under investigation include: atumelnant (CRN04894) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06712823?

This trial is sponsored by Crinetics Pharmaceuticals, which has 9 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06712823 being conducted?

This trial has 9 study locations across Minnesota, North Carolina, Córdoba Province, São Paulo, Bavaria. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

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