ID
33376
Descrizione
Study ID: 107806 Clinical Study ID: RA3107806 Study Title: An open label study to determine the safety, tolerability, excretion balance and pharmacokinetics of Losmapimod, administered as a single dose of an oral solution to healthy adult male subjects Patient Level Data: Clinicaltrials.gov Identifier: NCT00599612 https://clinicaltrials.gov/ct2/show/NCT00599612 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: losmapimod Trade Name: losmapimod Study Indication: Pulmonary Disease, Chronic Obstructive The study consists of a screening, study visit and follow-up. The protocol identifier for all: RA3107806 This document contains the liver events form. It has to be filled in if a liver event occurs during study (including screening and study visit).
collegamento
https://clinicaltrials.gov/ct2/show/NCT00599612
Keywords
versioni (2)
- 04/12/18 04/12/18 -
- 07/12/18 07/12/18 -
Titolare del copyright
GlaxoSmithKline
Caricato su
7 dicembre 2018
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY-NC 3.0
Commenti del modello :
Puoi commentare il modello dati qui. Tramite i fumetti nei gruppi di articoli e articoli è possibile aggiungere commenti a quelli in modo specifico.
Commenti del gruppo di articoli per :
Commenti dell'articolo per :
Per scaricare i modelli di dati devi essere registrato. Per favore accesso o registrati GRATIS.
Safety, tolerability, excretion balance and pharmacokinetics of Losmapimod in healthy males, NCT00599612
Liver events
- StudyEvent: ODM
Descrizione
Liver events
Alias
- UMLS CUI-1
- C0023884
- UMLS CUI-2
- C0877248
- UMLS CUI-3
- C0220825
Descrizione
day month year
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C2985720
Descrizione
Time period to the onset of ALT ≥ 2xUpper Limit Normal (ULN). Note: Although stopping criteria is ALT 3x ULN, GSK are interested in capturing ALT≥2x ULNto assess the probability of drug relatedness of liver event
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C0201836
Descrizione
AST
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C0201899
Descrizione
Total bilirubin
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C0201913
Descrizione
Alkaline phosphatase
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C0201850
Descrizione
Other
Tipo di dati
boolean
Alias
- UMLS CUI [1]
- C0205394
Descrizione
Liver events assessment
Alias
- UMLS CUI-1
- C0023884
- UMLS CUI-2
- C0877248
- UMLS CUI-3
- C0220825
Descrizione
If Yes, stop investigational product, complete date stopped on lnvestigational Product form, contact GSK within 24 hours of occurrence, complete Liver Events Form and obtain the following tests: PK blood sample within 24 hours of last dose (or 3x the investigational product half-life or t1/2). Hepatitis A: Hepatitis A lgM antibody. Hepatitis B: Hepatitis B surface antigen and Hepatitis B Core Antibody (/gM). Hepatitis C: Hepatitis C RNA. Hepatitis E /gM antibody (if subject resides or hastravelled in past 3 months outside the USA or Canada). Cytomegalovirus lgM antibody (CMV) EBV (Epstein Barr viral capsid antigen /gM antibody) or if unavailable, obtain heterophile antibody or monospot testing. CPK (serum creatine phosphokinase) LDH (factate dehydrogenase) Bilirubin fractionation, if bilirubin ≥ 1,5xULN The following are only needed when ALT ≥ 3xULN and bilirubin ≥ 1,5xULN (>35% direct): Anti-nuclear antibody Anti-smooth muscle antibody Type 1 anti-liver kidney microsomal antibodies (if available) Liver Imaging (ultrasound, magnetic resonance, or computerised tomography
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C0023884
- UMLS CUI [1,2]
- C0008000
- UMLS CUI [1,3]
- C1254595
- UMLS CUI [1,4]
- C2746065
- UMLS CUI [1,5]
- C0243161
Descrizione
Treatment periods applicable to the onset of ALT≥2x ULN
Alias
- UMLS CUI-1
- C0087111
- UMLS CUI-2
- C1948053
- UMLS CUI-3
- C0201836
Descrizione
If the liver event occurred during treatment period record start and stop date of investigational product for that treatment period. If the liver event occurred after treatment period record start and stop date of investigational product for the most recent period prior to the liver event. Tick for each period/event
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0439564
- UMLS CUI [1,2]
- C0023884
- UMLS CUI [1,3]
- C0877248
Descrizione
Start Date lnvestigational Date
Tipo di dati
date
Alias
- UMLS CUI [1,1]
- C0808070
- UMLS CUI [1,2]
- C0304229
Descrizione
End Date lnvestigational Product
Tipo di dati
date
Alias
- UMLS CUI [1,1]
- C0806020
- UMLS CUI [1,2]
- C0304229
Descrizione
Liver events, Diagnositics
Alias
- UMLS CUI-1
- C0023884
- UMLS CUI-2
- C0877248
- UMLS CUI-3
- C0430022
Descrizione
Age of subject
Tipo di dati
text
Alias
- UMLS CUI [1]
- C0001779
Descrizione
If Yes, ensure Pregnancy Notification Form has been completed.
Tipo di dati
text
Alias
- UMLS CUI [1]
- C0032961
Descrizione
Performance of diagnostic imaging tests of the liver or hepatobiliary system (liver ultrasound, computerized tomography or CAT scan, magnetic resonance imaging or MRI, or endoscopic retrograde cholangiopancreatography)
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C0011923
- UMLS CUI [1,2]
- C0023884
- UMLS CUI [2,1]
- C0011923
- UMLS CUI [2,2]
- C1711359
- UMLS CUI [3,1]
- C0023884
- UMLS CUI [3,2]
- C0041618
- UMLS CUI [4]
- C0040405
- UMLS CUI [5]
- C0024485
- UMLS CUI [6]
- C0008310
- UMLS CUI [7]
- C0205394
Descrizione
If No, record the details on the Non-Serious Adverse Events form or Serious Adverse Event form.
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C0086143
- UMLS CUI [1,2]
- C0456984
- UMLS CUI [1,3]
- C0205307
Descrizione
If Yes, complete Liver Biopsy form.
Tipo di dati
text
Alias
- UMLS CUI [1]
- C0193388
Descrizione
If Yes, record on the appropriate Concomitant Medication form.
Tipo di dati
text
Alias
- UMLS CUI [1]
- C2240391
- UMLS CUI [2]
- C0002346
- UMLS CUI [3]
- C0242295
- UMLS CUI [4]
- C0086190
Descrizione
Dietary Change, Fasting
Tipo di dati
text
Alias
- UMLS CUI [1]
- C3671772
- UMLS CUI [2]
- C0015663
Descrizione
An unscheduled PK blood sample must be obtained within 24 hours of last dose (or 3x the investigational product half-life or t1!2).
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C0031328
- UMLS CUI [1,2]
- C0005834
Descrizione
day month year
Tipo di dati
date
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0011008
Descrizione
00:00-23:59
Tipo di dati
time
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0040223
Descrizione
day month year
Tipo di dati
date
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [2,1]
- C1517741
- UMLS CUI [2,2]
- C0304229
- UMLS CUI [2,3]
- C0678766
- UMLS CUI [2,4]
- C0332152
- UMLS CUI [2,5]
- C0031327
Descrizione
00:00-23:59
Tipo di dati
time
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0040223
- UMLS CUI [2,1]
- C1517741
- UMLS CUI [2,2]
- C0304229
- UMLS CUI [2,3]
- C0678766
- UMLS CUI [2,4]
- C0332152
- UMLS CUI [2,5]
- C0031327
Descrizione
Sample Identifier Label
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0600091
Descrizione
Sample Number
Tipo di dati
text
Alias
- UMLS CUI [1]
- C1299222
Descrizione
Alcohol intake
Alias
- UMLS CUI-1
- C0001948
Descrizione
LIVER DISEASE MEDICAL CONDITIONS
Alias
- UMLS CUI-1
- C0023895
Descrizione
Tick only one response for each condition
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C0012634
- UMLS CUI [1,2]
- C2348235
Descrizione
Definitions: CURRENT MEDICAL CONDITIONS Conditionsfrom which the subject is currentlysuffering, regardlessof how long they have been present. If the subject has had a recurring condition that is not present at the time of the assessment, it can be classed as current if, in the Investigator's opinion it is likely to recur during the study. PAST MEDICAL CONDITIONS Conditions from which the subject has sufferedin the past, but are no longer present. A past condition may have stoppedas recently as the day prior to being assessed. NO MEDICAL CONDITION No current or past condition.
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C3854307
- UMLS CUI [1,2]
- C0012634
Descrizione
DRUG RELATED LIVER DISEASE CONDITIONS (All drugs including lnvestigational Product)
Descrizione
OTHER LIVER DISEASE CONDITIONS
Alias
- UMLS CUI-1
- C0023895
- UMLS CUI-2
- C0205394
Descrizione
Other liver disease
Tipo di dati
text
Alias
- UMLS CUI [1,1]
- C0023895
- UMLS CUI [1,2]
- C0205394
Descrizione
Definitions: CURRENT MEDICAL CONDITIONS Conditionsfrom which the subject is currentlysuffering, regardlessof how long they have been present. If the subject has had a recurring condition that is not present at the time of the assessment, it can be classed as current if, in the Investigator's opinion it is likely to recur during the study. PAST MEDICAL CONDITIONS Conditions from which the subject has sufferedin the past, but are no longer present. A past condition may have stoppedas recently as the day prior to being assessed.
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C3854307
- UMLS CUI [1,2]
- C0012634
Descrizione
OTHER MEDICAL CONDITIONS
Alias
- UMLS CUI-1
- C0012634
- UMLS CUI-2
- C0205394
Descrizione
Disease
Tipo di dati
integer
Alias
- UMLS CUI [1]
- C0012634
Descrizione
Definitions: CURRENT MEDICAL CONDITIONS Conditionsfrom which the subject is currentlysuffering, regardlessof how long they have been present. If the subject has had a recurring condition that is not present at the time of the assessment, it can be classed as current if, in the Investigator's opinion it is likely to recur during the study. PAST MEDICAL CONDITIONS Conditions from which the subject has sufferedin the past, but are no longer present. A past condition may have stoppedas recently as the day prior to being assessed. NO MEDICAL CONDITION No current or past condition.
Tipo di dati
integer
Alias
- UMLS CUI [1,1]
- C3854307
- UMLS CUI [1,2]
- C0012634
Similar models
Liver events
- StudyEvent: ODM
C0877248 (UMLS CUI-2)
C0220825 (UMLS CUI-3)
C0877248 (UMLS CUI-2)
C0220825 (UMLS CUI-3)
C0008000 (UMLS CUI [1,2])
C1254595 (UMLS CUI [1,3])
C2746065 (UMLS CUI [1,4])
C0243161 (UMLS CUI [1,5])
C1948053 (UMLS CUI-2)
C0201836 (UMLS CUI-3)
C0023884 (UMLS CUI [1,2])
C0877248 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
C0877248 (UMLS CUI-2)
C0430022 (UMLS CUI-3)
C0023884 (UMLS CUI [1,2])
C0011923 (UMLS CUI [2,1])
C1711359 (UMLS CUI [2,2])
C0023884 (UMLS CUI [3,1])
C0041618 (UMLS CUI [3,2])
C0040405 (UMLS CUI [4])
C0024485 (UMLS CUI [5])
C0008310 (UMLS CUI [6])
C0205394 (UMLS CUI [7])
C0456984 (UMLS CUI [1,2])
C0205307 (UMLS CUI [1,3])
C0002346 (UMLS CUI [2])
C0242295 (UMLS CUI [3])
C0086190 (UMLS CUI [4])
C0015663 (UMLS CUI [2])
C0005834 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C1517741 (UMLS CUI [2,1])
C0304229 (UMLS CUI [2,2])
C0678766 (UMLS CUI [2,3])
C0332152 (UMLS CUI [2,4])
C0031327 (UMLS CUI [2,5])
C0040223 (UMLS CUI [1,2])
C1517741 (UMLS CUI [2,1])
C0304229 (UMLS CUI [2,2])
C0678766 (UMLS CUI [2,3])
C0332152 (UMLS CUI [2,4])
C0031327 (UMLS CUI [2,5])
C0600091 (UMLS CUI [1,2])
C0560579 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C0277579 (UMLS CUI [1,2])
C0205394 (UMLS CUI-2)
C0205394 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,2])
C0205394 (UMLS CUI-2)
C0012634 (UMLS CUI [1,2])