CLINICAL_TRIALS ClinicalTrials.gov record update

A Single-center, Open-label, Parallel Study With Single Subcutaneous Injection for Pharmacokinetics and Pharmacodynamics Comparison of Two Pegfilgrastim Formulations in Both Male and Female Healthy Volunteers, Test Formulation is an Injectable Solution Containing 6 mg of Pegfilgrastim, Manufactured by Eurofarma Laboratórios S/A, and Reference Formulation (Neulastim® Injectable Solution Containing 6 mg) Marketed by Produtos Roche Químicos e Farmacêuticos S/A

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT02589301
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:36:18.186854+00:00
Published At: 2017-02-07T00:00:00+00:00
Record Updated At: 2017-02-07
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: ["Neutropenia", "Healthy"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2017-02-07"
protocolSection.identificationModule.nctId: "NCT02589301"
protocolSection.identificationModule.officialTitle: "A Single-center, Open-label, Parallel Study With Single Subcutaneous Injection for Pharmacokinetics and Pharmacodynamics Comparison of Two Pegfilgrastim Formulations in Both Male and Female Healthy Volunteers, Test Formulation is an Injectable Solution Containing 6 mg of Pegfilgrastim, Manufactured by Eurofarma Laborat\u00f3rios S/A, and Reference Formulation (Neulastim\u00ae Injectable Solution Containing 6 mg) Marketed by Produtos Roche Qu\u00edmicos e Farmac\u00eauticos S/A"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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