CLINICAL_TRIALS ClinicalTrials.gov record update

An Open Label, Randomised, Single Center, 2 Way Crossover Study to Assess Bioequivalence Between a Commercial HPMC Capsule of D961H 20 mg and a Pellets Based Sachet Formulation of D961H 20 mg by Pharmacodynamics (Intragastric pH) After Once-daily Repeated Oral Administration in Japanese Healthy Male Subjects

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT01964131
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:35:34.466192+00:00
Published At: 2013-12-31T00:00:00+00:00
Record Updated At: 2013-12-31
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: ["Gastric Ulcer", "Duodenal Ulcer", "Anastomotic Ulcer", "Reflux Esophagitis", "Etc."]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2013-12-31"
protocolSection.identificationModule.nctId: "NCT01964131"
protocolSection.identificationModule.officialTitle: "An Open Label, Randomised, Single Center, 2 Way Crossover Study to Assess Bioequivalence Between a Commercial HPMC Capsule of D961H 20 mg and a Pellets Based Sachet Formulation of D961H 20 mg by Pharmacodynamics (Intragastric pH) After Once-daily Repeated Oral Administration in Japanese Healthy Male Subjects"
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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