0 Avaliações

ID

32736

Descrição

Study ID: 109059 Clinical Study ID: OTB109059 Study Title: TXA107979:A Phase II Study to Evaluate: Delay in Intravaginal Ejaculatory Latency Time (IELT), Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Two Oral Doses of GSK557296 in a Randomized, Double Blind, Placebo-Controlled, Parallel Group Study in Men with Premature Ejaculation Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01021553 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: epelsiban Trade Name: Study Indication: Premature Ejaculation

Palavras-chave

  1. 13-11-18 13-11-18 -
Titular dos direitos

GlaxoSmithKline

Transferido a

13 november 2018

DOI

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Licença

Creative Commons BY-NC 3.0

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    Delay in IELT, Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GSK557296 in Men with Premature Ejaculation, 109059

    Pharmacokinetics

    1. StudyEvent: ODM
      1. Pharmacokinetics
    Pharmacokinetics
    Descrição

    Pharmacokinetics

    Alias
    UMLS CUI-1
    C0031328
    Was a pharmacokinetic blood sample obtained?
    Descrição

    Pharmacokinetic aspects, Blood, Sampling

    Tipo de dados

    boolean

    Alias
    UMLS CUI [1,1]
    C0031328
    UMLS CUI [1,2]
    C0005767
    UMLS CUI [1,3]
    C0870078
    Date and time sample taken
    Descrição

    Pharmacokinetic aspects, Blood, Sampling, Date in time, Time

    Tipo de dados

    datetime

    Alias
    UMLS CUI [1,1]
    C0031328
    UMLS CUI [1,2]
    C0005767
    UMLS CUI [1,3]
    C0870078
    UMLS CUI [1,4]
    C0011008
    UMLS CUI [1,5]
    C0040223
    Date and time of last investigational product dose prior to PK sample
    Descrição

    Pharmacokinetic aspects, Blood, Experimental drug, Date last dose, Time last dose

    Tipo de dados

    datetime

    Alias
    UMLS CUI [1,1]
    C0031328
    UMLS CUI [1,2]
    C0005767
    UMLS CUI [1,3]
    C0304229
    UMLS CUI [1,4]
    C1762893
    UMLS CUI [1,5]
    C0946444
    Sample Identifier
    Descrição

    Pharmacokinetic aspects, Blood, Sample Identification Number

    Tipo de dados

    datetime

    Alias
    UMLS CUI [1,1]
    C0031328
    UMLS CUI [1,2]
    C0005767
    UMLS CUI [1,3]
    C1299222

    Similar models

    Pharmacokinetics

    1. StudyEvent: ODM
      1. Pharmacokinetics
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de dados
    Alias
    Item Group
    Pharmacokinetics
    C0031328 (UMLS CUI-1)
    Pharmacokinetic aspects, Blood, Sampling
    Item
    Was a pharmacokinetic blood sample obtained?
    boolean
    C0031328 (UMLS CUI [1,1])
    C0005767 (UMLS CUI [1,2])
    C0870078 (UMLS CUI [1,3])
    Pharmacokinetic aspects, Blood, Sampling, Date in time, Time
    Item
    Date and time sample taken
    datetime
    C0031328 (UMLS CUI [1,1])
    C0005767 (UMLS CUI [1,2])
    C0870078 (UMLS CUI [1,3])
    C0011008 (UMLS CUI [1,4])
    C0040223 (UMLS CUI [1,5])
    Pharmacokinetic aspects, Blood, Experimental drug, Date last dose, Time last dose
    Item
    Date and time of last investigational product dose prior to PK sample
    datetime
    C0031328 (UMLS CUI [1,1])
    C0005767 (UMLS CUI [1,2])
    C0304229 (UMLS CUI [1,3])
    C1762893 (UMLS CUI [1,4])
    C0946444 (UMLS CUI [1,5])
    Pharmacokinetic aspects, Blood, Sample Identification Number
    Item
    Sample Identifier
    datetime
    C0031328 (UMLS CUI [1,1])
    C0005767 (UMLS CUI [1,2])
    C1299222 (UMLS CUI [1,3])

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