ID

32736

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

Versies (1)
  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

Engels

Pharmacokinetics

1 Formulieren  
  1. StudyEvent: ODM
    1. Pharmacokinetics
Pharmacokinetics
Beschrijving

Pharmacokinetics

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

Pharmacokinetic aspects, Blood, Sampling

Datatype

boolean

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

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

Datatype

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
Beschrijving

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

Datatype

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
Beschrijving

Pharmacokinetic aspects, Blood, Sample Identification Number

Datatype

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 Formulieren
  1. StudyEvent: ODM
    1. Pharmacokinetics
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

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