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A Study to Evaluate the Safety and PK of CRN04894 for the Treatment of Cushing's Syndrome

← catalyst calendar

NCT05804669 · readout ≤ 73 d

Sponsored by Crinetics Pharmaceuticals Inc. (industry) · CRNX — their whole pipeline →.

Phase
Phase 1/2
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
19actual
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2023-10-12actualWhen the study began enrolling
Primary completionOct 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionOct 2026estimatedThe whole study's end, after follow-up
First posted2023-04-07actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-19actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Cushing Syndrome
  • Cushing Disease
  • Ectopic ACTH Syndrome

Intervention

  • Drug: atumelnant

Primary outcomes

what the primary-completion date above is the date OF
Proportion of participants with treatment emergent adverse events (TEAEs)
measured Up to Day 15
Proportion of participants with adrenal insufficiency
measured Up to Day 15
Proportion of participants with safety findings determined by laboratory testing
measured Up to Day 15
Assessment of the maximum observed plasma concentration of CRN04894
measured Up to Day 15
Assessment of the time to achieve maximum observed plasma concentration of CRN04894
measured Up to Day 15
Assessment of the plasma area under the curve of CRN04894
measured Up to Day 15

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