CLINICAL_TRIALS ClinicalTrials.gov record update

Comparative, Randomized, Single-Dose, 2-Way Crossover Bioavailability Study of Par and Bristol-Myers Squibb (Buspar) 15 mg Buspirone HCl Tablets in Healthy Adult Males Under Fasting Conditions Following Administration of a 30 mg Dose

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT00653419
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:34:52.028825+00:00
Published At: 2008-04-04T00:00:00+00:00
Record Updated At: 2008-04-04
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["To Determine Bioequivalence Under Fasting Conditions"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2008-04-04"
protocolSection.identificationModule.nctId: "NCT00653419"
protocolSection.identificationModule.officialTitle: "Comparative, Randomized, Single-Dose, 2-Way Crossover Bioavailability Study of Par and Bristol-Myers Squibb (Buspar) 15 mg Buspirone HCl Tablets in Healthy Adult Males Under Fasting Conditions Following Administration of a 30 mg Dose"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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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