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CORTCorcept TherapeuticsFinished

A Study of the Efficacy and Safety of Relacorilant in Patients With Endogenous Cushing Syndrome

Cushing Syndrome

4Calmworry score, out of 100

No strong warning signs right now. The score counts warning signs; it is not a prediction.

Why this score

  • 3 insiders sold shares within a month

    Since Aug 26, 2026 · was worth 10, fading over time

    +4.4
Worry score4

Score over time

Stage
Phase 3
Patients
152 (final count)
Started
Nov 15, 2018
Main results expected
Apr 8, 2024
Fully finished
Apr 15, 2024
Results posted
Apr 24, 2025

What counts as success

The trial's main goal(s), called the “primary outcome.”

  • Number of Patients With Loss of Response With Respect to Hypertension During the RW Phase.

    Measured over: Week 22 (end of OL Phase) and Week 36 (Week 12 of RW Phase)

  • Number of Patients With 1 or More Treatment-emergent Adverse Events (TEAEs) as Graded by CTCAE v5.0.

    Measured over: OL Phase: Up to 22 weeks; RW Phase: up to 18 weeks after completion of the OL Phase

Changes Tremor has spotted

No changes since Tremor started watching this trial.
Show details (technical version)

Score inputs

  • insider_selling_cluster: base 10, now 4.4, since 2026-08-26, fades (half-life)

Raw record changes

  • none yet

Trial ID NCT03697109 · record last updated 2025-07-16 · checked 2026-11-09 15:42 UTC

See the official record on ClinicalTrials.gov (NCT03697109) ↗