0 Beoordelingen

ID

32735

Beschrijving

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

Trefwoorden

  1. 13-11-18 13-11-18 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

13 november 2018

DOI

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Licentie

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

    Repeat Pharmacokinetics Blood

    Repeat Pharmacokinetics Blood
    Beschrijving

    Repeat Pharmacokinetics Blood

    Alias
    UMLS CUI-1
    C0031328
    UMLS CUI-2
    C0005767
    UMLS CUI-3
    C0205341
    Actual date/time
    Beschrijving

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

    Datatype

    datetime

    Alias
    UMLS CUI [1,1]
    C0031328
    UMLS CUI [1,2]
    C0005767
    UMLS CUI [1,3]
    C0205341
    UMLS CUI [1,4]
    C0011008
    UMLS CUI [1,5]
    C0040223

    Similar models

    Repeat Pharmacokinetics Blood

    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    Repeat Pharmacokinetics Blood
    C0031328 (UMLS CUI-1)
    C0005767 (UMLS CUI-2)
    C0205341 (UMLS CUI-3)
    Pharmacokinetic aspects, Blood, Repeat, Date in time, Time
    Item
    Actual date/time
    datetime
    C0031328 (UMLS CUI [1,1])
    C0005767 (UMLS CUI [1,2])
    C0205341 (UMLS CUI [1,3])
    C0011008 (UMLS CUI [1,4])
    C0040223 (UMLS CUI [1,5])

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