ID

33841

Beschrijving

Study ID: 107032 Clinical Study ID: GLP107032 Study Title: An open-label study to evaluate the pharmacokinetics of an oral contraceptive containing Norethindrone and Ethinyl Estradiol when co-administered with GSK716155 in healthy adult female subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01077505 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

Trefwoorden

  1. 03-01-19 03-01-19 -
Houder van rechten

GSK group of companies

Geüploaded op

3 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Pharmacokinetics of an oral contraceptive co-administered with Albiglutide in women - 107032

Liver Event Assessments

Administrative data
Beschrijving

Administrative data

Site
Beschrijving

Site

Datatype

text

Subject
Beschrijving

Subject

Datatype

text

Visit Name
Beschrijving

Visit Name

Datatype

text

Status
Beschrijving

Status

Datatype

text

Document Number
Beschrijving

Document Number

Datatype

text

Liver Events Assessment
Beschrijving

Liver Events Assessment

Have liver chemistry results reached or exceeded protocol-defined stopping criteria?
Beschrijving

If Yes, stop investigational product, complete date stopped on Investigational Product form, contact GSK within 24 hours of occurrence, complete Liver Events Form and obtain the following test: 1.Blood sample for PK analysis, obtained within three half-lives(21 days) of last dose; 2.Hepatitis A: IgM antibody; 3, Hepatitis B surface antigen and Core Antibody (IgM); 4. Hepatitis C: RNA; 5.Hepatitis E IgM antibody (if subject resides or has travelled in past 3 month outside the USA or Canada); 6. Cytomegalovirus IgM antibody (CMV); 7. EBV (Epstein Barr Viral capsid antigen IgM antibody)or if unavailable, obtain heterophile antibody or monospot testing; 8.CPK (Serum creatine phosphokinase); 9. LDH (lactate dehydrogenase); 10. Bilirubin fractionation, if bilirubin >=1.5xULN (If ALT >=3xULN and bilirubin >1.5xULN(>35% direct), the following are needed: anti-nuclear antibody, anti-smooth muscle antibody, tape 1 anti-liver kidney microsomal antibodies, liver imaging).

Datatype

boolean

Liver Events
Beschrijving

Liver Events

SAE / AE reference number
Beschrijving

SAE / AE reference number

Datatype

integer

Date of assessment
Beschrijving

Date of assessment

Datatype

date

Which liver chemistry result or exceeded protocol-defined investigational product stopping criteria?
Beschrijving

check all that apply

Datatype

text

If Other, specify
Beschrijving

If Other, specify

Datatype

text

Is the subject 55 or older?
Beschrijving

Is the subject 55 or older?

Datatype

boolean

If female, is the subject pregnant?
Beschrijving

if Yes, complete the Pregnancy Notification Form

Datatype

text

Were any diagnostic imaging tests of the liver or hepatobiliary system performed (such as a liver ultrasound, computerized tomography or CAT scan, magnetic resonance imaging or MRI, or endoscopic retrograde cholangiopancreatography, or other)?
Beschrijving

Were any diagnostic imaging tests of the liver or hepatobiliary system performed (such as a liver ultrasound, computerized tomography or CAT scan, magnetic resonance imaging or MRI, or endoscopic retrograde cholangiopancreatography, or other)?

Datatype

boolean

If Yes, were the results normal?
Beschrijving

if No, record the details on the Non-Serious Adverse Events form or Serious Adverse Events form.

Datatype

boolean

Were any liver biopsies performed?
Beschrijving

Were any liver biopsies performed?

Datatype

boolean

Does the subject use herbals, complementary or alternative medicines?
Beschrijving

If Yes, record on the appropriate Concomitant Medication form

Datatype

boolean

Did the subject fast or undergo significant dietary change in the past week?
Beschrijving

Did the subject fast or undergo significant dietary change in the past week?

Datatype

boolean

Was a pharmacokinetic blood sample obtained?
Beschrijving

An unscheduled PK blood sample must be obtained within three half-lives (21 days) of last dose.

Datatype

boolean

Date of sample taken
Beschrijving

Date of sample taken

Datatype

date

Time of sample taken
Beschrijving

Time of sample taken

Datatype

time

Record date and time of last investigational product dose prior to PK sample (if administered at subject's home, please do not record the time)
Beschrijving

Record date and time of last investigational product dose prior to PK sample (if administered at subject's home, please do not record the time)

Datatype

datetime

Alcohol Intake
Beschrijving

Alcohol Intake

The average number of units of alcohol consumed per week:
Beschrijving

The average number of units of alcohol consumed per week:

Datatype

integer

Maateenheden
  • units per week
units per week
Liver Disease Medical Conditions
Beschrijving

Liver Disease Medical Conditions

1. Acute viral Hepatitis A
Beschrijving

1. Acute viral Hepatitis A

Datatype

text

2. Chronic Hepatitis B
Beschrijving

2. Chronic Hepatitis B

Datatype

text

3. Chronic Hepatitis C
Beschrijving

3. Chronic Hepatitis C

Datatype

text

4. Cytomegalovirus Hepatitis
Beschrijving

4. Cytomegalovirus Hepatitis

Datatype

text

5. Epstein Barr virus infectious mononucleosis
Beschrijving

5. Epstein Barr virus infectious mononucleosis

Datatype

text

6. Herpes Simplex Hepatitis
Beschrijving

6. Herpes Simplex Hepatitis

Datatype

text

7. Alcoholic liver disease
Beschrijving

7. Alcoholic liver disease

Datatype

text

8. Non-alcoholic steatohepatitis
Beschrijving

8. Non-alcoholic steatohepatitis

Datatype

text

9. Fatty Liver
Beschrijving

9. Fatty Liver

Datatype

text

10. Hepatic Cirrhosis
Beschrijving

10. Hepatic Cirrhosis

Datatype

text

11. Hemochromatosis
Beschrijving

11. Hemochromatosis

Datatype

text

12. Autoimmune Hepatitis
Beschrijving

12. Autoimmune Hepatitis

Datatype

text

13. Gallbladder disease or biliary disease
Beschrijving

13. Gallbladder disease or biliary disease

Datatype

text

Drug Related Liver Disease Conditions
Beschrijving

Drug Related Liver Disease Conditions

14. Specific condition:
Beschrijving

specify here

Datatype

text

Status of condition
Beschrijving

Status of condition

Datatype

text

15. Specific condition
Beschrijving

15. Specific condition

Datatype

text

Status of condition
Beschrijving

Status of condition

Datatype

text

15. Specific condition
Beschrijving

15. Specific condition

Datatype

text

Status of condition
Beschrijving

Status of condition

Datatype

text

Other Medical Conditions
Beschrijving

Other Medical Conditions

17. Drug allergies
Beschrijving

17. Drug allergies

Datatype

text

18. Rheumatoid Arthritis
Beschrijving

18. Rheumatoid Arthritis

Datatype

text

19. Psoriasis
Beschrijving

19. Psoriasis

Datatype

text

20. Thyroid disease
Beschrijving

20. Thyroid disease

Datatype

text

21. Inflammatory bowel disease
Beschrijving

21. Inflammatory bowel disease

Datatype

text

22. Lupus
Beschrijving

22. Lupus

Datatype

text

23. Sjoren's syndrome
Beschrijving

23. Sjoren's syndrome

Datatype

text

24. Vitiligo
Beschrijving

24. Vitiligo

Datatype

text

Similar models

Liver Event Assessments

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administrative data
Site
Item
Site
text
Subject
Item
Subject
text
Item
Visit Name
text
Code List
Visit Name
CL Item
Liver Event Assessment (1)
Status
Item
Status
text
Document Number
Item
Document Number
text
Item Group
Liver Events Assessment
Have liver chemistry results reached or exceeded protocol-defined stopping criteria?
Item
Have liver chemistry results reached or exceeded protocol-defined stopping criteria?
boolean
Item Group
Liver Events
SAE / AE reference number
Item
SAE / AE reference number
integer
Date of assessment
Item
Date of assessment
date
Item
Which liver chemistry result or exceeded protocol-defined investigational product stopping criteria?
text
Code List
Which liver chemistry result or exceeded protocol-defined investigational product stopping criteria?
CL Item
ALT (alanine aminotransferase) (1)
CL Item
AST (aspartate aminotransferase) (2)
CL Item
Total bilirubin (3)
CL Item
Other (4)
If Other, specify
Item
If Other, specify
text
Is the subject 55 or older?
Item
Is the subject 55 or older?
boolean
Item
If female, is the subject pregnant?
text
Code List
If female, is the subject pregnant?
CL Item
Yes (1)
CL Item
No (2)
CL Item
Not Applicable (3)
Were any diagnostic imaging tests of the liver or hepatobiliary system performed (such as a liver ultrasound, computerized tomography or CAT scan, magnetic resonance imaging or MRI, or endoscopic retrograde cholangiopancreatography, or other)?
Item
Were any diagnostic imaging tests of the liver or hepatobiliary system performed (such as a liver ultrasound, computerized tomography or CAT scan, magnetic resonance imaging or MRI, or endoscopic retrograde cholangiopancreatography, or other)?
boolean
If Yes, were the results normal?
Item
If Yes, were the results normal?
boolean
Were any liver biopsies performed?
Item
Were any liver biopsies performed?
boolean
Does the subject use herbals, complementary or alternative medicines?
Item
Does the subject use herbals, complementary or alternative medicines?
boolean
Did the subject fast or undergo significant dietary change in the past week?
Item
Did the subject fast or undergo significant dietary change in the past week?
boolean
Was a pharmacokinetic blood sample obtained?
Item
Was a pharmacokinetic blood sample obtained?
boolean
Date of sample taken
Item
Date of sample taken
date
Time of sample taken
Item
Time of sample taken
time
Record date and time of last investigational product dose prior to PK sample (if administered at subject's home, please do not record the time)
Item
Record date and time of last investigational product dose prior to PK sample (if administered at subject's home, please do not record the time)
datetime
Item Group
Alcohol Intake
The average number of units of alcohol consumed per week:
Item
The average number of units of alcohol consumed per week:
integer
Item Group
Liver Disease Medical Conditions
Item
1. Acute viral Hepatitis A
text
Code List
1. Acute viral Hepatitis A
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
2. Chronic Hepatitis B
text
Code List
2. Chronic Hepatitis B
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
3. Chronic Hepatitis C
text
Code List
3. Chronic Hepatitis C
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
4. Cytomegalovirus Hepatitis
text
Code List
4. Cytomegalovirus Hepatitis
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
5. Epstein Barr virus infectious mononucleosis
text
Code List
5. Epstein Barr virus infectious mononucleosis
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
6. Herpes Simplex Hepatitis
text
Code List
6. Herpes Simplex Hepatitis
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
7. Alcoholic liver disease
text
Code List
7. Alcoholic liver disease
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
8. Non-alcoholic steatohepatitis
text
Code List
8. Non-alcoholic steatohepatitis
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
9. Fatty Liver
text
Code List
9. Fatty Liver
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
10. Hepatic Cirrhosis
text
Code List
10. Hepatic Cirrhosis
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
11. Hemochromatosis
text
Code List
11. Hemochromatosis
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
12. Autoimmune Hepatitis
text
Code List
12. Autoimmune Hepatitis
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
13. Gallbladder disease or biliary disease
text
Code List
13. Gallbladder disease or biliary disease
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item Group
Drug Related Liver Disease Conditions
14. Specific condition:
Item
14. Specific condition:
text
Item
Status of condition
text
Code List
Status of condition
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
15. Specific condition
Item
15. Specific condition
text
Item
Status of condition
text
Code List
Status of condition
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
15. Specific condition
Item
15. Specific condition
text
Item
Status of condition
text
Code List
Status of condition
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item Group
Other Medical Conditions
Item
17. Drug allergies
text
Code List
17. Drug allergies
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
18. Rheumatoid Arthritis
text
Code List
18. Rheumatoid Arthritis
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
19. Psoriasis
text
Code List
19. Psoriasis
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
20. Thyroid disease
text
Code List
20. Thyroid disease
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
21. Inflammatory bowel disease
text
Code List
21. Inflammatory bowel disease
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
22. Lupus
text
Code List
22. Lupus
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
23. Sjoren's syndrome
text
Code List
23. Sjoren's syndrome
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)
Item
24. Vitiligo
text
Code List
24. Vitiligo
CL Item
Current (1)
CL Item
Past (2)
CL Item
No medical conditions (3)

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