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CLINICAL_TRIALS ClinicalTrials.gov record update

Recombinant SeV-hFGF2 / dF Injection (BF30) Single-dose Therapy in Patients With Peripheral Arterial Occlusive Disease, a Dose Escalation, Safety, Tolerability Phase I Clinical Trial

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
NCT03668353
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:37:06.896022+00:00
Published At
2018-10-25T00:00:00+00:00
Record Updated At
2018-10-25
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
["PAOD - Peripheral Arterial Occlusive Disease", "PAD", "Critical Limb Ischemia"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2018-10-25"
protocolSection.identificationModule.nctId
"NCT03668353"
protocolSection.identificationModule.officialTitle
"Recombinant SeV-hFGF2 / dF Injection (BF30) Single-dose Therapy in Patients With Peripheral Arterial Occlusive Disease, a Dose Escalation, Safety, Tolerability Phase I Clinical Trial"
protocolSection.statusModule.overallStatus
"UNKNOWN"
protocolSection.designModule.phases
["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • PAOD - Peripheral Arterial Occlusive Disease (protocolSection.conditionsModule.conditions)
  • PAD (protocolSection.conditionsModule.conditions)
  • Critical Limb Ischemia (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.