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Active, not recruiting No phase listed Observational

Non-interventional Study on Osilodrostat in Patients With Endogenous Cushing's Syndrome

ClinicalTrials.gov ID: NCT05382156

Public ClinicalTrials.gov record NCT05382156. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 2:45 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Non-interventional Study to Assess the Long-term Safety and Efficacy of Osilodrostat in Patients With Endogenous Cushing's Syndrome

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a non-interventional, multinational, multi-centre study with primary data collection, to further document the safety and efficacy of osilodrostat administered in routine clinical practice in patients treated with osilodrostat for endogenous Cushing's Syndrome

Study identification

NCT ID
NCT05382156
Recruitment status
Active, not recruiting
Study type
Observational
Phase
Not listed
Lead sponsor
RECORDATI GROUP
Industry
Enrollment
206 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 13, 2022 (Actual)
Primary completion
Jun 2027 (Estimated)
Completion
Aug 2027 (Estimated)
Last update posted
Nov 20, 2025

2022 – 2027

United States locations

U.S. sites
15
U.S. states
14
U.S. cities
14
Facility City State ZIP Site status
Barrow Neurological Institute Phoenix Arizona 85013 —
Emory University School Atlanta Georgia 30322 —
Northwestern University Chicago Illinois 60611 —
Indiana University Schl-med Indianapolis Indiana 46202 —
St Elizabeth Physicians Covington Kentucky 41011 —
Massachusetts General Hospital Boston Massachusetts 02114-2696 —
University of Michigan Ann Arbor Michigan 48109 —
Mayo Clinic - Rochester Rochester Minnesota 55905 —
Washington University School of Medicine St Louis Missouri 63110 —
NYU Grossman School of Medicine New York New York 10017 —
Memorial Sloan-Kettering Cancer Center (MSKCC) - New York New York New York 10021 —
Endocrinology Research Associates, Inc. Columbus Ohio 43201 —
Oregon Health And Science University Portland Oregon 97239 —
University of Pennsylvania Medical Center Philadelphia Pennsylvania 19104 —
Froedtert Hospital Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 28 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05382156, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 20, 2025 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05382156 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →