CLINICAL_TRIALS ClinicalTrials.gov record with results posted

A Phase I, Randomised, Open Label, Single Center, Single Oral Dose, Three Treatment, Three Period, Three Sequence, Change-over Bioequivalence Study of Paracetamol Orodispersible Tablet 500 mg (Haleon) to Assess Bioequivalence With Alvedon 500 mg Film-Coated Tablet (Haleon, Sweden) and Panadol 500 mg Film-Coated Tablet (Haleon, Australia) in Healthy Adult Subjects Under Fasting Conditions

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT06855576
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-07-02T00:08:23.778422+00:00
Published At: 2026-07-01T00:00:00+00:00
Record Updated At: 2026-07-01
Results Posted At: 2026-07-01
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: ["Fever", "Pain"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2026-07-01"
protocolSection.identificationModule.nctId: "NCT06855576"
protocolSection.identificationModule.officialTitle: "A Phase I, Randomised, Open Label, Single Center, Single Oral Dose, Three Treatment, Three Period, Three Sequence, Change-over Bioequivalence Study of Paracetamol Orodispersible Tablet 500 mg (Haleon) to Assess Bioequivalence With Alvedon 500 mg Film-Coated Tablet (Haleon, Sweden) and Panadol 500 mg Film-Coated Tablet (Haleon, Australia) in Healthy Adult Subjects Under Fasting Conditions"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: "2026-07-01"

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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