CLINICAL_TRIALS
ClinicalTrials.gov record update
Phase 2 Study of Oral Ezatiostat Hydrochloride (Telintra®) in Patients With Lenalidomide (Revlimid®) Refractory or Resistant, Low to Intermediate-1 Risk, Deletion 5q Myelodysplastic Syndrome
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
- NCT01422486
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-04-28T10:35:35.969862+00:00
- Published At
- 2013-11-25T00:00:00+00:00
- Record Updated At
- 2013-11-25
- 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
["Myelodysplastic Syndrome (MDS)"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2013-11-25"- protocolSection.identificationModule.nctId
"NCT01422486"- protocolSection.identificationModule.officialTitle
"Phase 2 Study of Oral Ezatiostat Hydrochloride (Telintra\u00ae) in Patients With Lenalidomide (Revlimid\u00ae) Refractory or Resistant, Low to Intermediate-1 Risk, Deletion 5q Myelodysplastic Syndrome"- protocolSection.statusModule.overallStatus
"TERMINATED"- protocolSection.designModule.phases
["PHASE2"]- protocolSection.statusModule.resultsFirstPostDateStruct.date
""
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.