ID

38073

Description

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

Keywords

  1. 9/15/19 9/15/19 -
Copyright Holder

GlaxoSmithKline

Uploaded on

September 15, 2019

DOI

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License

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
Description

PK Rpt

Alias
UMLS CUI-1
C0031328
Actual date/time
Description

Pharmacokinetic aspects, Date in time, Time

Data type

datetime

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

Pharmacokinetic aspects, Sampling, Identifier

Data type

text

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

Similar models

PK Rpt

  1. StudyEvent: ODM
    1. PK Rpt
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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