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CLINICAL_TRIALS ClinicalTrials.gov record update

A Single Dose Oral Bioavailability Study of PanCytoVir™ Oral Suspension (100 mg/ml) 1000 mg Versus Probenecid 500 mg Tablets, 1000 mg (2 X 500 mg) in Healthy, Adult, Human Subjects Under Fasting Conditions

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT06025344
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-25T22:27:07.247931+00:00
Published At
2024-11-21T00:00:00+00:00
Record Updated At
2024-11-21
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
["Relative Bioavailability"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2024-11-21"
protocolSection.identificationModule.nctId
"NCT06025344"
protocolSection.identificationModule.officialTitle
"A Single Dose Oral Bioavailability Study of PanCytoVir\u2122 Oral Suspension (100 mg/ml) 1000 mg Versus Probenecid 500 mg Tablets, 1000 mg (2 X 500 mg) in Healthy, Adult, Human Subjects Under Fasting Conditions"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Relative Bioavailability (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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