CLINICAL_TRIALS ClinicalTrials.gov record update

A Single-Dose, Open-Label, Three-Period Crossover Study to Assess the Bioequivalence of Famotidine 20 mg Film-Coated Tablets (FCT) Compared to Famotidine 20 mg Chewable Tablets (CT) Without Water and Famotidine 20 mg Chewable Tablets (CTw) With Water (Protocol 144)

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT00945750
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:36:38.999297+00:00
Published At: 2015-12-09T00:00:00+00:00
Record Updated At: 2017-03-10
Results Posted At: 2015-12-09
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: ["Heartburn"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2017-03-10"
protocolSection.identificationModule.nctId: "NCT00945750"
protocolSection.identificationModule.officialTitle: "A Single-Dose, Open-Label, Three-Period Crossover Study to Assess the Bioequivalence of Famotidine 20 mg Film-Coated Tablets (FCT) Compared to Famotidine 20 mg Chewable Tablets (CT) Without Water and Famotidine 20 mg Chewable Tablets (CTw) With Water (Protocol 144)"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: "2015-12-09"

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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