0 Beoordelingen

ID

38073

Beschrijving

Study ID: 105036 Clinical Study ID: 105036 Study Title: A single-blind, randomized, placebo-controlled study to investigate the safety, tolerability, and potential effects on betamethasone pharmacokinetics of a co-administered infusion of GSK221149A in healthy female subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: betamethasone Trade Name: Retosiban Study Indication: Women's Health & Pregnancy - Other, pre-term labour

Trefwoorden

  1. 15-09-19 15-09-19 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

15 september 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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    Betamethasone pharmacokinetics of a co-administered infusion of GSK221149A; 105036

    1. StudyEvent: ODM
      1. PK Rpt
    PK Rpt
    Beschrijving

    PK Rpt

    Alias
    UMLS CUI-1
    C0031328
    Actual date/time
    Beschrijving

    Pharmacokinetic aspects, Date in time, Time

    Datatype

    datetime

    Alias
    UMLS CUI [1,1]
    C0031328
    UMLS CUI [1,2]
    C0011008
    UMLS CUI [1,3]
    C0040223
    Sample ID
    Beschrijving

    Pharmacokinetic aspects, Sampling, Identifier

    Datatype

    text

    Alias
    UMLS CUI [1,1]
    C0031328
    UMLS CUI [1,2]
    C0870078
    UMLS CUI [1,3]
    C0600091

    Similar models

    1. StudyEvent: ODM
      1. PK Rpt
    Name
    Type
    Description | Question | Decode (Coded Value)
    Datatype
    Alias
    Item Group
    PK Rpt
    C0031328 (UMLS CUI-1)
    Pharmacokinetic aspects, Date in time, Time
    Item
    Actual date/time
    datetime
    C0031328 (UMLS CUI [1,1])
    C0011008 (UMLS CUI [1,2])
    C0040223 (UMLS CUI [1,3])
    Pharmacokinetic aspects, Sampling, Identifier
    Item
    Sample ID
    text
    C0031328 (UMLS CUI [1,1])
    C0870078 (UMLS CUI [1,2])
    C0600091 (UMLS CUI [1,3])

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