ID
38601
Descripción
Study ID: 110951 Clinical Study ID: 110951 Study Title: A two-part, randomised, placebo-controlled study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of single doses of intravenously infused GSK1995057 in healthy subjects. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01476046 See https://clinicaltrials.gov/ct2/show/NCT01476046 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: N/A, Placebo Trade Name: N/A Study Indication: Respiratory Disorders The single-centre study consists of two parts A and B with seven cohorts/ten subcohorts in total. Part A includes ascending doses of the investigational product given to subjects negative or positive for pre-existing human anti-heavy chain variable domain (HAVH) antibodies (Cohorts 1 to 3 with Subcohorts 1a, 2a and 3a negative for HAVH and 1b, 2b, 3b positive for HAVH). Part B includes only subjects negative for HAVH, with ascending doses given to Cohorts 4 to 6. Cohort 7 receives the same dose as Cohort 6, but whereas the other Cohorts are single-blinded, Cohort 7 is open-label and additionally receives a bronchoalveolar lavage (BAL). The study consists of a Screening Visit (up to 56 days before Day 1, the day of the drug administration), Visits on Day -1, 1, 2, 3, 5, 7, 14, 28 and Follow-Up Visits on Day 57 and 85. This form contains general information on any Liver Event happening during the study, including whether and when a pharmacokinetic sample has been obtained as well as information on the subject's general and liver-related medical conditions and alcohol intake. There are seperate forms for Imaging and Biopsy in case of a Liver Event.
Link
https://clinicaltrials.gov/ct2/show/NCT01476046
Palabras clave
Versiones (1)
- 26/10/19 26/10/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
26 de octubre de 2019
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 3.0
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Phase I Trial of Intravenous TNFR1 Antagonist GSK1995057 in Healthy Subjects - NCT01476046
Liver Events incl. Pharmacokinetics, Medical Conditions, Alcohol
- StudyEvent: ODM
Descripción
Liver Event Seriousness
Alias
- UMLS CUI-1
- C1710056
- UMLS CUI-2
- C0023884
Descripción
Notification Sent
Alias
- UMLS CUI-1
- C0422202
- UMLS CUI-2
- C0023884
Descripción
[read-only]
Tipo de datos
partialDatetime
Alias
- UMLS CUI [1,1]
- C1264639
- UMLS CUI [1,2]
- C0013849
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C1708968
Descripción
[read-only]
Tipo de datos
partialDatetime
Alias
- UMLS CUI [1,1]
- C1264639
- UMLS CUI [1,2]
- C0205435
- UMLS CUI [1,3]
- C0013849
- UMLS CUI [1,4]
- C1708968
Descripción
[read-only]
Tipo de datos
partialDatetime
Alias
- UMLS CUI [1,1]
- C1264639
- UMLS CUI [1,2]
- C0013849
- UMLS CUI [1,3]
- C1517741
- UMLS CUI [1,4]
- C3899555
Descripción
[read-only]
Tipo de datos
partialDatetime
Alias
- UMLS CUI [1,1]
- C1264639
- UMLS CUI [1,2]
- C0013849
- UMLS CUI [1,3]
- C0205435
- UMLS CUI [1,4]
- C3899555
Descripción
[read-only]
Tipo de datos
partialDatetime
Alias
- UMLS CUI [1,1]
- C1264639
- UMLS CUI [1,2]
- C1710056
- UMLS CUI [1,3]
- C0023884
- UMLS CUI [1,4]
- C0443172
- UMLS CUI [1,5]
- C1518404
Descripción
Which liver chemistry result reached or exceeded protocol-defined investigational product stopping/interruption criteria?
Alias
- UMLS CUI-1
- C0023884
- UMLS CUI-2
- C0008000
- UMLS CUI-3
- C0304229
- UMLS CUI-4
- C2746065
- UMLS CUI-5
- C0243161
Descripción
It is particularly important to record any significant hypotension immediately prior to or concomitant with ALT elevation.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C2746065
- UMLS CUI [1,4]
- C0243161
Descripción
AST reached stopping criteria
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201899
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C2746065
- UMLS CUI [1,4]
- C0243161
Descripción
Total bilirubin reached stopping criteria
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201913
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C2746065
- UMLS CUI [1,4]
- C0243161
Descripción
Alkaline phosphatase reached stopping criteria
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0201850
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C2746065
- UMLS CUI [1,4]
- C0243161
Descripción
This item is conditional. Interruption may be removed if stopping/monitoring study only.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0202148
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C2746065
- UMLS CUI [1,4]
- C0243161
Descripción
This item is conditional. Interruption may be removed if stopping/monitoring study only.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0202035
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C2746065
- UMLS CUI [1,4]
- C0243161
Descripción
Other liver chemistry result reached stopping criteria
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C0023884
- UMLS CUI [1,3]
- C0008000
- UMLS CUI [1,4]
- C0304229
- UMLS CUI [1,5]
- C2746065
- UMLS CUI [1,6]
- C0243161
Descripción
Liver Events - Clinical
Alias
- UMLS CUI-1
- C0023884
- UMLS CUI-2
- C0877248
- UMLS CUI-3
- C0205210
Descripción
Age
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0001779
Descripción
If yes, ensure Pregnancy Notification Form has been completed.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0032961
Descripción
If Yes, answer whether the results were normal
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0011923
- UMLS CUI [1,2]
- C1711359
- UMLS CUI [2,1]
- C0011923
- UMLS CUI [2,2]
- C0023884
- UMLS CUI [3]
- C0412534
- UMLS CUI [4]
- C0412620
- UMLS CUI [5]
- C0412693
- UMLS CUI [6]
- C0008310
Descripción
If applicable If No, record the details on the Imaging form. Please ensure the overall diagnosis indicated by imaging is captured on the Non-serious Adverse Event form or Serious Adverse Event form.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0011923
- UMLS CUI [1,2]
- C1711359
- UMLS CUI [1,3]
- C0456984
- UMLS CUI [2,1]
- C0011923
- UMLS CUI [2,2]
- C0456984
- UMLS CUI [2,3]
- C0023884
Descripción
If yes, complete Liver Biopsy form.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0193388
- UMLS CUI [1,2]
- C1272695
Descripción
If yes, record on the appropriate Concomitant Medication form.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2347852
- UMLS CUI [2]
- C0025125
- UMLS CUI [3]
- C0242295
- UMLS CUI [4]
- C0086190
Descripción
Recent fasting or significant dietary change
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C3671772
- UMLS CUI [1,2]
- C0332185
- UMLS CUI [2,1]
- C0332185
- UMLS CUI [2,2]
- C0015663
Descripción
[hidden] Item will be calculated by InForm.
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2826267
Descripción
Investigational Product (Liver)
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0023884
Descripción
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.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0023884
- UMLS CUI [1,2]
- C0877248
- UMLS CUI [1,3]
- C2745955
- UMLS CUI [1,4]
- C0439564
- UMLS CUI [1,5]
- C2347804
Descripción
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.
Tipo de datos
partialDate
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Descripción
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.
Tipo de datos
partialDate
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Descripción
Pharmacokinetics (Liver PK)
Alias
- UMLS CUI-1
- C0005834
- UMLS CUI-2
- C0031328
- UMLS CUI-3
- C0023884
Descripción
An unscheduled PK sample must be obtained within obtained within 7 days of last dose. If yes, record date and time sample taken and date and time of last investigational product dose prior to PK sample
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0031328
Descripción
if applicable
Tipo de datos
datetime
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0031328
- UMLS CUI [1,3]
- C1264639
Descripción
if applicable
Tipo de datos
datetime
Alias
- UMLS CUI [1,1]
- C0945778
- UMLS CUI [1,2]
- C0013230
- UMLS CUI [1,3]
- C0332152
- UMLS CUI [1,4]
- C0005834
- UMLS CUI [1,5]
- C0031328
Descripción
Liver disease medical conditions
Alias
- UMLS CUI-1
- C0023895
Descripción
Acute type A viral hepatitis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0276434
Descripción
Hepatitis B, Chronic
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0524909
Descripción
Hepatitis C, Chronic
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0524910
Descripción
Cytomegalovirus Hepatitis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0276252
Descripción
Infectious Mononucleosis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0021345
Descripción
Herpes Simplex Hepatitis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1963747
Descripción
Alcoholic Liver Diseases
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0023896
Descripción
Non-alcoholic Steatohepatitis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C3241937
Descripción
Fatty Liver
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0015695
Descripción
Hepatic Cirrhosis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0023890
Descripción
Hemochromatosis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0018995
Descripción
Autoimmune Hepatitis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0241910
Descripción
It is particularly important to record any gallbladder or biliary disease, or pancreatitis, that occurred during the study.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0016977
Descripción
Drug related liver disease conditions
Alias
- UMLS CUI-1
- C0023895
- UMLS CUI-2
- C0041755
Descripción
Other Liver Disease
Alias
- UMLS CUI-1
- C0023895
- UMLS CUI-2
- C0205394
Descripción
[hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2348184
Descripción
Other liver disease
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0023895
- UMLS CUI [1,2]
- C0205394
Descripción
[hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C2826302
Descripción
[hidden]
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1140263
- UMLS CUI [1,2]
- C0871468
Descripción
[hidden]
Tipo de datos
text
Alias
- UMLS CUI [1]
- C3898442
Descripción
[hidden]
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0805701
- UMLS CUI [1,2]
- C0231175
Descripción
Other Liver Disease Conditions - Status
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0023895
- UMLS CUI [1,2]
- C0205394
- UMLS CUI [1,3]
- C0449438
Descripción
Other medical conditions
Alias
- UMLS CUI-1
- C0012634
- UMLS CUI-2
- C0205394
Descripción
Drug Allergies
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0013182
Descripción
Rheumatoid Arthritis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0003873
Descripción
Psoriasis
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0033860
Descripción
Thyroid Disease
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0040128
Descripción
Inflammatory Bowel Disease
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0021390
Descripción
Lupus
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0409974
Descripción
Sjogren's Syndrome
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C1527336
Descripción
Vitiligo
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C0042900
Descripción
Alcohol Intake at Onset of Liver Event
Alias
- UMLS CUI-1
- C0001948
- UMLS CUI-2
- C0023884
- UMLS CUI-3
- C0332162
- UMLS CUI-4
- C0877248
Descripción
If Yes, record the average number of units of alcohol consumed per week
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0001948
Descripción
if applicable
Tipo de datos
float
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C0560579
- UMLS CUI [1,3]
- C1510992
Descripción
[hidden] This item will be calculated by InForm.
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0038586
- UMLS CUI [1,2]
- C0332307
Similar models
Liver Events incl. Pharmacokinetics, Medical Conditions, Alcohol
- StudyEvent: ODM
C1264639 (UMLS CUI [1,2])
C0023884 (UMLS CUI-2)
C0877248 (UMLS CUI [1,2])
C1519255 (UMLS CUI [1,3])
C0013849 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C1708968 (UMLS CUI [1,4])
C0205435 (UMLS CUI [1,2])
C0013849 (UMLS CUI [1,3])
C1708968 (UMLS CUI [1,4])
C0013849 (UMLS CUI [1,2])
C1517741 (UMLS CUI [1,3])
C3899555 (UMLS CUI [1,4])
C0013849 (UMLS CUI [1,2])
C0205435 (UMLS CUI [1,3])
C3899555 (UMLS CUI [1,4])
C1710056 (UMLS CUI [1,2])
C0023884 (UMLS CUI [1,3])
C0443172 (UMLS CUI [1,4])
C1518404 (UMLS CUI [1,5])
C0008000 (UMLS CUI-2)
C0304229 (UMLS CUI-3)
C2746065 (UMLS CUI-4)
C0243161 (UMLS CUI-5)
C0304229 (UMLS CUI [1,2])
C2746065 (UMLS CUI [1,3])
C0243161 (UMLS CUI [1,4])
C0304229 (UMLS CUI [1,2])
C2746065 (UMLS CUI [1,3])
C0243161 (UMLS CUI [1,4])
C0304229 (UMLS CUI [1,2])
C2746065 (UMLS CUI [1,3])
C0243161 (UMLS CUI [1,4])
C0304229 (UMLS CUI [1,2])
C2746065 (UMLS CUI [1,3])
C0243161 (UMLS CUI [1,4])
C0304229 (UMLS CUI [1,2])
C2746065 (UMLS CUI [1,3])
C0243161 (UMLS CUI [1,4])
C0304229 (UMLS CUI [1,2])
C2746065 (UMLS CUI [1,3])
C0243161 (UMLS CUI [1,4])
C0023884 (UMLS CUI [1,2])
C0008000 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,4])
C2746065 (UMLS CUI [1,5])
C0243161 (UMLS CUI [1,6])
C0877248 (UMLS CUI-2)
C0205210 (UMLS CUI-3)
C1711359 (UMLS CUI [1,2])
C0011923 (UMLS CUI [2,1])
C0023884 (UMLS CUI [2,2])
C0412534 (UMLS CUI [3])
C0412620 (UMLS CUI [4])
C0412693 (UMLS CUI [5])
C0008310 (UMLS CUI [6])
C1711359 (UMLS CUI [1,2])
C0456984 (UMLS CUI [1,3])
C0011923 (UMLS CUI [2,1])
C0456984 (UMLS CUI [2,2])
C0023884 (UMLS CUI [2,3])
C1272695 (UMLS CUI [1,2])
C0025125 (UMLS CUI [2])
C0242295 (UMLS CUI [3])
C0086190 (UMLS CUI [4])
C0332185 (UMLS CUI [1,2])
C0332185 (UMLS CUI [2,1])
C0015663 (UMLS CUI [2,2])
C0023884 (UMLS CUI-2)
C0877248 (UMLS CUI [1,2])
C2745955 (UMLS CUI [1,3])
C0439564 (UMLS CUI [1,4])
C2347804 (UMLS CUI [1,5])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0031328 (UMLS CUI-2)
C0023884 (UMLS CUI-3)
C0031328 (UMLS CUI [1,2])
C0031328 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C0013230 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])
C0005834 (UMLS CUI [1,4])
C0031328 (UMLS CUI [1,5])
C0041755 (UMLS CUI-2)
C0041755 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0871468 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,2])
C0449438 (UMLS CUI [1,3])
C0205394 (UMLS CUI-2)
C0023884 (UMLS CUI-2)
C0332162 (UMLS CUI-3)
C0877248 (UMLS CUI-4)
C0560579 (UMLS CUI [1,2])
C1510992 (UMLS CUI [1,3])
C0332307 (UMLS CUI [1,2])