0 Evaluaciones
ID

32736

Descripción

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

Palabras clave

Versiones (1)
  1. 13/11/18 13/11/18 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

13 de noviembre de 2018

DOI

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Licencia

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

    Inglés

    Pharmacokinetics

    1 formularios  
    1. StudyEvent: ODM
      1. Pharmacokinetics
    Pharmacokinetics
    Descripción

    Pharmacokinetics

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

    Pharmacokinetic aspects, Blood, Sampling

    Tipo de datos

    boolean

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

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

    Tipo de datos

    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
    Descripción

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

    Tipo de datos

    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
    Descripción

    Pharmacokinetic aspects, Blood, Sample Identification Number

    Tipo de datos

    datetime

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

    Pharmacokinetics

    1 formularios
    1. StudyEvent: ODM
      1. Pharmacokinetics
    Name
    Tipo
    Description | Question | Decode (Coded Value)
    Tipo de datos
    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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