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Post-marketing Observational Study of Remitoro® Intravenous Injection 300 μg - Safety of Remitoro in Patients With Recurrent or Refractory Peripheral T Cell Lymphoma and Cutaneous T Cell Lymphoma (All Case Study)

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT05137847
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:39:25.552505+00:00
Published At
2023-12-12T00:00:00+00:00
Record Updated At
2023-12-12
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
["Lymphoma, T-cell, Peripheral", "Lymphoma, T-cell, Cutaneous"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2023-12-12"
protocolSection.identificationModule.nctId
"NCT05137847"
protocolSection.identificationModule.officialTitle
"Post-marketing Observational Study of Remitoro\u00ae Intravenous Injection 300 \u03bcg - Safety of Remitoro in Patients With Recurrent or Refractory Peripheral T Cell Lymphoma and Cutaneous T Cell Lymphoma (All Case Study)"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
[]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Lymphoma, T-cell, Peripheral (protocolSection.conditionsModule.conditions)
  • Lymphoma, T-cell, Cutaneous (protocolSection.conditionsModule.conditions)

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.