ID
32515
Description
Study ID: 105229 Clinical Study ID: GLP105229 Study Title: A double-blinded, randomized, placebo-controlled, staggered-parallel, escalating dose study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of subcutaneous injections of GSK 716155 in healthy volunteers. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: albiglutide Trade Name: Tanzeum,Eperzan Study Indication: Diabetes Mellitus, Type 2
Keywords
Versions (3)
- 10/5/18 10/5/18 -
- 11/6/18 11/6/18 -
- 11/6/18 11/6/18 -
Copyright Holder
GlaxoSmithKline
Uploaded on
November 6, 2018
DOI
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License
Creative Commons BY-NC 3.0
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Subcutaneous injections of GSK 716155 in healthy volunteers; Study ID: 105229
Day 7
- StudyEvent: ODM
Description
Capillary Blood Glucose
Alias
- UMLS CUI-1
- C0457578
Description
Capillary Blood Glucose measurement; Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0457578
- UMLS CUI [1,2]
- C0011008
Description
Capillary Blood Glucose measurement; relative time
Data type
text
Alias
- UMLS CUI [1,1]
- C0457578
- UMLS CUI [1,2]
- C0439564
Description
Capillary Blood Glucose measurement; Time
Data type
time
Alias
- UMLS CUI [1,1]
- C0457578
- UMLS CUI [1,2]
- C0040223
Description
Capillary Blood Glucose measurement; Result
Data type
float
Alias
- UMLS CUI [1,1]
- C0457578
- UMLS CUI [1,2]
- C1274040
Description
Capillary Blood Glucose measurement; Unit of measure
Data type
text
Alias
- UMLS CUI [1,1]
- C0457578
- UMLS CUI [1,2]
- C1519795
Description
Anti-Diabetic Agent Tolerability Scale (ADATS)
Alias
- UMLS CUI-1
- C0935929
- UMLS CUI-2
- C3274448
Description
Antidiabetics; Tolerability Study;Date in Time
Data type
date
Alias
- UMLS CUI [1,1]
- C0935929
- UMLS CUI [1,2]
- C3274448
- UMLS CUI [1,3]
- C0011008
Description
Adverse event; Serious Adverse Event; Hypoglycaemic episode
Data type
boolean
Alias
- UMLS CUI [1]
- C0877248
- UMLS CUI [2]
- C1519255
- UMLS CUI [3]
- C0745153
Description
Adverse event; Quantity
Data type
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C1265611
Description
Adverse events
Alias
- UMLS CUI-1
- C0877248
Description
Adverse Event
Data type
text
Alias
- UMLS CUI [1]
- C0877248
Description
Adverse event; Page, Number
Data type
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C1704732
- UMLS CUI [1,3]
- C0237753
Description
Adverse event; row (table), number
Data type
integer
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C1552840
- UMLS CUI [1,3]
- C0237753
Description
Anti-Diabetic Agent Tolerability Scale (ADATS) - Worksheet
Alias
- UMLS CUI-1
- C0935929
- UMLS CUI-2
- C3274448
- UMLS CUI-3
- C2349155
Description
Adverse event, Not at all bothersome; Adverse event, Slightly bothersome; Adverse event, Moderately bothersome; Adverse event, Quite a bit bothersome; Adverse event, Extremely bothersome
Data type
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C4489383
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C4489382
- UMLS CUI [3,1]
- C0877248
- UMLS CUI [3,2]
- C4489381
- UMLS CUI [4,1]
- C0877248
- UMLS CUI [4,2]
- C4489380
- UMLS CUI [5,1]
- C0877248
- UMLS CUI [5,2]
- C4489379
Description
Adverse event, Not at all bothersome; Adverse event, Slightly bothersome; Adverse event, Moderately bothersome; Adverse event, Quite a bit bothersome; Adverse event, Extremely bothersome
Data type
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C4489383
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C4489382
- UMLS CUI [3,1]
- C0877248
- UMLS CUI [3,2]
- C4489381
- UMLS CUI [4,1]
- C0877248
- UMLS CUI [4,2]
- C4489380
- UMLS CUI [5,1]
- C0877248
- UMLS CUI [5,2]
- C4489379
Description
Adverse event, Not at all bothersome; Adverse event, Slightly bothersome; Adverse event, Moderately bothersome; Adverse event, Quite a bit bothersome; Adverse event, Extremely bothersome
Data type
text
Alias
- UMLS CUI [1,1]
- C0877248
- UMLS CUI [1,2]
- C4489383
- UMLS CUI [2,1]
- C0877248
- UMLS CUI [2,2]
- C4489382
- UMLS CUI [3,1]
- C0877248
- UMLS CUI [3,2]
- C4489381
- UMLS CUI [4,1]
- C0877248
- UMLS CUI [4,2]
- C4489380
- UMLS CUI [5,1]
- C0877248
- UMLS CUI [5,2]
- C4489379
Description
Experimental drug; Adverse reaction to drug; Impaired
Data type
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0041755
- UMLS CUI [1,3]
- C0221099
Similar models
Day 7
- StudyEvent: ODM
C0011008 (UMLS CUI [1,2])
C0439564 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,2])
C3274448 (UMLS CUI-2)
C3274448 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C1519255 (UMLS CUI [2])
C0745153 (UMLS CUI [3])
C1265611 (UMLS CUI [1,2])
C1704732 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])
C1552840 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])
C3274448 (UMLS CUI-2)
C2349155 (UMLS CUI-3)
C4489383 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C4489382 (UMLS CUI [2,2])
C0877248 (UMLS CUI [3,1])
C4489381 (UMLS CUI [3,2])
C0877248 (UMLS CUI [4,1])
C4489380 (UMLS CUI [4,2])
C0877248 (UMLS CUI [5,1])
C4489379 (UMLS CUI [5,2])
C4489383 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C4489382 (UMLS CUI [2,2])
C0877248 (UMLS CUI [3,1])
C4489381 (UMLS CUI [3,2])
C0877248 (UMLS CUI [4,1])
C4489380 (UMLS CUI [4,2])
C0877248 (UMLS CUI [5,1])
C4489379 (UMLS CUI [5,2])
C4489383 (UMLS CUI [1,2])
C0877248 (UMLS CUI [2,1])
C4489382 (UMLS CUI [2,2])
C0877248 (UMLS CUI [3,1])
C4489381 (UMLS CUI [3,2])
C0877248 (UMLS CUI [4,1])
C4489380 (UMLS CUI [4,2])
C0877248 (UMLS CUI [5,1])
C4489379 (UMLS CUI [5,2])
C0041755 (UMLS CUI [1,2])
C0221099 (UMLS CUI [1,3])