CLINICAL_TRIALS ClinicalTrials.gov record update

An Open-Label, 2-Part, Randomized, Crossover Study to Compare the Bioavailability of Intranasal Administration of 200 and 400 µg of OPTINOSE™ FLUTICASONE With 400 µg of Flonase® (Fluticasone Propionate) Nasal Spray (Part 1), and Intranasal Administration of 200 and 400 µg or 400 µg Alone of OPTINOSE™ FLUTICASONE With 440 µg of Flovent® HFA (Fluticasone Propionate) Inhalation Aerosol (Part 2) (Current Investigation is Part 2 Only)

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT02266927
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:36:00.546613+00:00
Published At: 2016-02-03T00:00:00+00:00
Record Updated At: 2016-02-03
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: ["Mild to Moderate Asthma"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2016-02-03"
protocolSection.identificationModule.nctId: "NCT02266927"
protocolSection.identificationModule.officialTitle: "An Open-Label, 2-Part, Randomized, Crossover Study to Compare the Bioavailability of Intranasal Administration of 200 and 400 \u00b5g of OPTINOSE\u2122 FLUTICASONE With 400 \u00b5g of Flonase\u00ae (Fluticasone Propionate) Nasal Spray (Part 1), and Intranasal Administration of 200 and 400 \u00b5g or 400 \u00b5g Alone of OPTINOSE\u2122 FLUTICASONE With 440 \u00b5g of Flovent\u00ae HFA (Fluticasone Propionate) Inhalation Aerosol (Part 2) (Current Investigation is Part 2 Only)"
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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