CLINICAL_TRIALS
ClinicalTrials.gov record update
A Phase II, Open-label, Dose Titration, Multi-center Study to Assess the Safety/Tolerability and Efficacy of Osilodrostat in Patients With All Types of Endogenous Cushing's Syndrome Except Cushing's Disease
This page presents selected fields from the linked source record. It does not add a medical interpretation.
Record identity and dates
- Source
- ClinicalTrials.gov
- Source record ID
- NCT02468193
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-28T10:37:43.474339+00:00
- Published At
- 2020-03-11T00:00:00+00:00
- Record Updated At
- 2020-05-06
- Results Posted At
- 2020-03-11
- Timestamp Basis
- source retrieval time was not retained by the feed adapter
- Date limitation
- source retrieval time was not retained by the feed adapter
Fields recorded by this source
- protocolSection.conditionsModule.conditions
["Cushing\u0027s Syndrome", "Ectopic Corticotropin Syndrome", "Adrenal Adenoma", "Adrenal Carcinoma", "AIMAH", "PPNAD"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2020-05-06"- protocolSection.identificationModule.nctId
"NCT02468193"- protocolSection.identificationModule.officialTitle
"A Phase II, Open-label, Dose Titration, Multi-center Study to Assess the Safety/Tolerability and Efficacy of Osilodrostat in Patients With All Types of Endogenous Cushing\u0027s Syndrome Except Cushing\u0027s Disease"- protocolSection.statusModule.overallStatus
"COMPLETED"- protocolSection.designModule.phases
["PHASE2"]- protocolSection.statusModule.resultsFirstPostDateStruct.date
"2020-03-11"
Study condition terms
Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.
This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.