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NCT05804669 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate the Safety and PK of CRN04894 for the Treatment of Cushing's Syndrome
A Phase 1 study of Cushing Syndrome and Cushing Disease, sponsored by Crinetics Pharmaceuticals.
- Recruiting
- Registry status
- Phase 1
- Development phase
- 18
- Enrollment target
- 1
- Study location
NCT05804669 is a Phase 1 study of Cushing Syndrome and Cushing Disease that is actively recruiting participants, run by Crinetics Pharmaceuticals. The registered enrollment target is 18 participants, below the 178-participant average among 9 other Cushing Syndrome trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05804669, a Phase 1 study of Cushing Syndrome and Cushing Disease, is actively recruiting participants, sponsored by Crinetics Pharmaceuticals.
- RECRUITING
- Registry status
- Phase 1
- Development phase
- 18 participants
- Enrollment target
- 1
- Study location
Study Summary
A Phase 1b/2a, first-in-disease, open-label, multiple-ascending dose exploratory study to evaluate safety, tolerability, pharmacokinetics (PK), and pharmacodynamic biomarker responses associated with CRN04894 (an adrenocorticotropic hormone \[ACTH\] receptor antagonist) in participants with ACTH-dependent Cushing's syndrome (Cushing's disease or Ectopic ACTH Syndrome \[EAS\])
Conditions Studied
Interventions
- DRUG atumelnant
Study Locations (1)
Maryland
- National Institutes of Health (NIH) - National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) - Bethesda
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2023-10-12 |
| Est. Completion | 2026-10 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05804669
The ClinicalTrials.gov registry entry for NCT05804669 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 178-participant average among 9 other Cushing Syndrome trials with a reported enrollment target (90% lower). The listed sponsor is Crinetics Pharmaceuticals, which has 16 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Cushing Syndrome appearing as the primary indexed condition, and to 1 intervention - of which atumelnant is the first listed.
NCT05804669 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.
Frequently Asked Questions
What is clinical trial NCT05804669 about?
NCT05804669 is a clinical study titled "A Study to Evaluate the Safety and PK of CRN04894 for the Treatment of Cushing's Syndrome". A Phase 1b/2a, first-in-disease, open-label, multiple-ascending dose exploratory study to evaluate safety, tolerability, pharmacokinetics (PK), and pharmacodynamic biomarker responses associated with CRN04894 (an adrenocorticotropic hormone \[ACTH\] receptor antagonist) in participants with ACTH-dep...
What is the current status of trial NCT05804669?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 18 participants. The study started on 2023-10-12. Estimated completion is 2026-10.
What conditions does trial NCT05804669 study?
This clinical trial studies the following conditions: Cushing Syndrome, Cushing Disease, Ectopic ACTH Syndrome.
What interventions are being tested in trial NCT05804669?
The interventions under investigation include: atumelnant (DRUG).
Who is sponsoring clinical trial NCT05804669?
This trial is sponsored by Crinetics Pharmaceuticals, which has 16 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05804669 being conducted?
This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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