ID
40951
Beschrijving
The primary focus of this first time in human (FTIH) study was to evaluate the safety and tolerability of GSK1292263 and to estimate GSK1292263 pharmacokinetic (PK) parameters and pharmacodynamic (PD) effects in healthy volunteers. Subject: FTIH, oral, safety, tolerability, pharmacokinetics, glucose, pharmacodynamics, male, female, gastric emptying Indication Studied: Type 2 Diabetes Mellitus Study ID: 111596 Clinical Study ID: 111596 Study Title: A study in healthy volunteers of single doses of orally administered GSK1292263 to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of the compound alone and when co-administered with sitagliptin Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00783549 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: GSK1292263, Sitagliptin Trade Name: N/A Study Indication: Dyslipidaemias
Trefwoorden
Versies (2)
- 24-04-20 24-04-20 -
- 07-06-20 07-06-20 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
7 juni 2020
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY-NC 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
A study in healthy volunteers of single doses of orally administered GSK1292263 to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of the compound alone and when co-administered with sitagliptin
Liver Events, Liver Event 2-DF
- StudyEvent: ODM
Beschrijving
Liver events
Alias
- UMLS CUI-1
- C0023884
- UMLS CUI-2
- C0877248
Beschrijving
subject age
Datatype
boolean
Alias
- UMLS CUI [1]
- C0205847
- UMLS CUI [2]
- C0596728
- UMLS CUI [3]
- C0178694
Beschrijving
If yes, ensure Pregnancy Notification Form has been completed.
Datatype
text
Alias
- UMLS CUI [1]
- C0032961
Beschrijving
diagnostic imaging of liver or hepatobiliary system
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1711359
- UMLS CUI [1,2]
- C0011923
- UMLS CUI [2,1]
- C0011923
- UMLS CUI [2,2]
- C0023884
Beschrijving
If No, record the details on the Non-Serious Adverse Events form or Serious Adverse Event form.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1711359
- UMLS CUI [1,2]
- C0011923
- UMLS CUI [1,3]
- C1319347
- UMLS CUI [2,1]
- C0011923
- UMLS CUI [2,2]
- C0023884
- UMLS CUI [2,3]
- C1319347
Beschrijving
If yes, complete Liver Biopsy form.
Datatype
boolean
Alias
- UMLS CUI [1]
- C0193388
Beschrijving
If yes, record on the appropriate Concomitant Medication form.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0681850
- UMLS CUI [1,2]
- C1524063
- UMLS CUI [1,3]
- C1360419
- UMLS CUI [2,1]
- C0681850
- UMLS CUI [2,2]
- C1524063
- UMLS CUI [2,3]
- C0936077
- UMLS CUI [3,1]
- C0681850
- UMLS CUI [3,2]
- C1524063
- UMLS CUI [3,3]
- C0242295
- UMLS CUI [4,1]
- C0681850
- UMLS CUI [4,2]
- C0281875
Beschrijving
dietary change
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0681850
- UMLS CUI [1,2]
- C3671772
- UMLS CUI [2,1]
- C0681850
- UMLS CUI [2,2]
- C0015663
Similar models
Liver Events, Liver Event 2-DF
- StudyEvent: ODM
C1254595 (UMLS CUI-2)
C2746065 (UMLS CUI-3)
C0243161 (UMLS CUI-4)
C4688482 (UMLS CUI-5)
C2599718 (UMLS CUI-6)
C1550543 (UMLS CUI-7)
C0587081 (UMLS CUI [1,2])
C0023901 (UMLS CUI [1,3])
C0205394 (UMLS CUI [1,4])
C0596728 (UMLS CUI [2])
C0178694 (UMLS CUI [3])
C0011923 (UMLS CUI [1,2])
C0011923 (UMLS CUI [2,1])
C0023884 (UMLS CUI [2,2])
C0011923 (UMLS CUI [1,2])
C1319347 (UMLS CUI [1,3])
C0011923 (UMLS CUI [2,1])
C0023884 (UMLS CUI [2,2])
C1319347 (UMLS CUI [2,3])
C1524063 (UMLS CUI [1,2])
C1360419 (UMLS CUI [1,3])
C0681850 (UMLS CUI [2,1])
C1524063 (UMLS CUI [2,2])
C0936077 (UMLS CUI [2,3])
C0681850 (UMLS CUI [3,1])
C1524063 (UMLS CUI [3,2])
C0242295 (UMLS CUI [3,3])
C0681850 (UMLS CUI [4,1])
C0281875 (UMLS CUI [4,2])
C3671772 (UMLS CUI [1,2])
C0681850 (UMLS CUI [2,1])
C0015663 (UMLS CUI [2,2])