Date of subject completion or withdrawal
Item
Date of subject completion or withdrawal
date
C2983670 (UMLS CUI [1])
Was the subject withdrawn from the study?
Item
Was the subject withdrawn from the study?
boolean
C0422727 (UMLS CUI [1])
1. Adverse event
Item
1. Adverse event
boolean
C0877248 (UMLS CUI [1])
Item
2. Lack of efficacy
text
C0235828 (UMLS CUI [1])
Code List
2. Lack of efficacy
CL Item
No subreasons (1)
Item
3. Protocol Deviation
text
C1705236 (UMLS CUI [1])
Code List
3. Protocol Deviation
CL Item
No subreasons (1)
CL Item
Lack of adherence (3)
CL Item
Prohibited medication use (4)
Item
4. Subject reached protocol defined stopping criteria
text
C2746065 (UMLS CUI [1,1])
C0243161 (UMLS CUI [1,2])
Code List
4. Subject reached protocol defined stopping criteria
CL Item
Liver function test abnormality (3)
5. Study closed/terminated
Item
5. Study closed/terminated
boolean
C2348570 (UMLS CUI [1])
6. Lost to Follow-Up
Item
6. Lost to Follow-Up
boolean
C1302313 (UMLS CUI [1])
7. Investigator discretion, specify
Item
7. Investigator discretion, specify
text
C0008961 (UMLS CUI [1,1])
C0022423 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
8. Withdrew consent, specify
Item
8. Withdrew consent, specify
text
C1707492 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])