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CLINICAL_TRIALS ClinicalTrials.gov record update

A Phase 1B Double Blinded Randomized Trial Evaluating Safety, Tolerability, and Immune Response of OSU-2131 a BZLF1 Peptide Vaccine With Stimulon™ QS-21 Solution Adjuvant in Healthy Volunteers and Patients Awaiting Solid Organ Transplantation

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT06741072
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:29:07.213510+00:00
Published At
2026-04-21T00:00:00+00:00
Record Updated At
2026-04-21
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
["Chronic Kidney Disease, Stage 4", "Chronic Kidney Disease, Stage 5", "EBV-Related Lymphoproliferative Disorder", "EBV-Related Malignant Neoplasm", "Post-Transplant Lymphoproliferative Disorder"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2026-04-21"
protocolSection.identificationModule.nctId
"NCT06741072"
protocolSection.identificationModule.officialTitle
"A Phase 1B Double Blinded Randomized Trial Evaluating Safety, Tolerability, and Immune Response of OSU-2131 a BZLF1 Peptide Vaccine With Stimulon\u2122 QS-21 Solution Adjuvant in Healthy Volunteers and Patients Awaiting Solid Organ Transplantation"
protocolSection.statusModule.overallStatus
"SUSPENDED"
protocolSection.designModule.phases
["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Chronic Kidney Disease, Stage 4 (protocolSection.conditionsModule.conditions)
  • Chronic Kidney Disease, Stage 5 (protocolSection.conditionsModule.conditions)
  • EBV-Related Lymphoproliferative Disorder (protocolSection.conditionsModule.conditions)
  • EBV-Related Malignant Neoplasm (protocolSection.conditionsModule.conditions)
  • Post-Transplant Lymphoproliferative Disorder (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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