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CLINICAL_TRIALS ClinicalTrials.gov record update

A First-in-Human Phase I Study of Intravesical sEphB4-HSA in Patients With "BCG-Unresponsive" Bladder Carcinoma In Situ (CIS), Completely Resected High Grade Ta/T1, to Establish the Maximum Tolerated Dose (MTD) or Recommended Phase II Dose (RP2D)

This page presents selected fields from the linked source record. It does not add a medical interpretation.

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT03552796
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:39:05.855067+00:00
Published At
2023-06-26T00:00:00+00:00
Record Updated At
2023-06-26
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
["Recurrent Bladder Carcinoma", "Bladder Cancer Stage 0", "Bladder Cancer Stage I"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2023-06-26"
protocolSection.identificationModule.nctId
"NCT03552796"
protocolSection.identificationModule.officialTitle
"A First-in-Human Phase I Study of Intravesical sEphB4-HSA in Patients With \"BCG-Unresponsive\" Bladder Carcinoma In Situ (CIS), Completely Resected High Grade Ta/T1, to Establish the Maximum Tolerated Dose (MTD) or Recommended Phase II Dose (RP2D)"
protocolSection.statusModule.overallStatus
"WITHDRAWN"
protocolSection.designModule.phases
["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Recurrent Bladder Carcinoma (protocolSection.conditionsModule.conditions)
  • Bladder Cancer Stage 0 (protocolSection.conditionsModule.conditions)
  • Bladder Cancer Stage I (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.