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CLINICAL_TRIALS ClinicalTrials.gov record update

Post-marketing Phase 4 Study to Evaluate Safety, Tolerability, and Efficacy of Kyprolis® (Carfilzomib) in Indian Patients With Relapsed or Refractory Multiple Myeloma: A Prospective, Open-label, Non-comparative, Multicenter Study

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT03934684
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:27:29.816176+00:00
Published At
2024-01-02T00:00:00+00:00
Record Updated At
2025-08-06
Results Posted At
2024-01-02
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
["Relapsed Refractory Multiple Myeloma"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2025-08-06"
protocolSection.identificationModule.nctId
"NCT03934684"
protocolSection.identificationModule.officialTitle
"Post-marketing Phase 4 Study to Evaluate Safety, Tolerability, and Efficacy of Kyprolis\u00ae (Carfilzomib) in Indian Patients With Relapsed or Refractory Multiple Myeloma: A Prospective, Open-label, Non-comparative, Multicenter Study"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE4"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2024-01-02"

Study condition terms

  • Relapsed Refractory Multiple Myeloma (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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