ID

39644

Description

Part A: Drug Interaction Study of Sofosbuvir and Antiretroviral Therapy (ART) Combinations in HIV and Hepatitis C Virus (HCV) Co-infected Patients. Part B: Efficacy and Safety of Sofosbuvir for 12 Weeks in HIV/HCV Co-infected Patients.; ODM derived from: https://clinicaltrials.gov/show/NCT01565889

Link

https://clinicaltrials.gov/show/NCT01565889

Keywords

  1. 2/7/20 2/7/20 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

February 7, 2020

DOI

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License

Creative Commons BY 4.0

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Eligibility Hepatitis C NCT01565889

Eligibility Hepatitis C NCT01565889

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
healthy according to medical history and physical examination with exception of hcv and hiv diagnoses
Description

Healthy Medical History | Healthy Physical Examination | Exception Hepatitis C | Exception HIV Infection

Data type

boolean

Alias
UMLS CUI [1,1]
C3898900
UMLS CUI [1,2]
C0262926
UMLS CUI [2,1]
C3898900
UMLS CUI [2,2]
C0031809
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0019196
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C0019693
confirmation of chronic hcv infection
Description

Hepatitis C, Chronic

Data type

boolean

Alias
UMLS CUI [1]
C0524910
confirmation of chronic hiv-1 infection
Description

HIV-1 infection chronic

Data type

boolean

Alias
UMLS CUI [1,1]
C2363741
UMLS CUI [1,2]
C0205191
on a stable protocol approved hiv antiretroviral (arv) regimen with undetectable hiv-rna
Description

HIV Antiretroviral therapy Stable | HIV RNA undetectable

Data type

boolean

Alias
UMLS CUI [1,1]
C0019682
UMLS CUI [1,2]
C1963724
UMLS CUI [1,3]
C0205360
UMLS CUI [2]
C0877598
agree to use two forms of highly effective contraception for the duration of the study and 6 months after the last dose of study medication
Description

Contraceptive methods Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C1265611
subjects must be naive to treatment for chronic hcv infection
Description

Therapy naive Chronic Hepatitis C

Data type

boolean

Alias
UMLS CUI [1,1]
C0919936
UMLS CUI [1,2]
C0524910
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known or suspected cirrhosis
Description

Liver Cirrhosis | Liver Cirrhosis Suspected

Data type

boolean

Alias
UMLS CUI [1]
C0023890
UMLS CUI [2,1]
C0023890
UMLS CUI [2,2]
C0750491
history of any other clinically significant chronic liver disease
Description

Chronic liver disease Other

Data type

boolean

Alias
UMLS CUI [1,1]
C0341439
UMLS CUI [1,2]
C0205394
a history consistent with decompensated liver disease.
Description

Medical History Consistent with Decompensated liver disease

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0332290
UMLS CUI [1,3]
C4075847
use of any prohibited medications as defined by the protocol
Description

Illicit medication use

Data type

boolean

Alias
UMLS CUI [1]
C0281875
pregnant or nursing female or male with pregnant female partner
Description

Pregnancy | Breast Feeding | Gender Partner Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3,1]
C0079399
UMLS CUI [3,2]
C0682323
UMLS CUI [3,3]
C0032961
contraindication to peg or rbv therapy (for part b)
Description

Medical contraindication PEGINTERFERON Therapy | Medical contraindication Ribavirin Therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0982327
UMLS CUI [1,3]
C0087111
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0035525
UMLS CUI [2,3]
C0087111
clinically relevant drug or alcohol abuse
Description

Substance Use Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0038586

Similar models

Eligibility Hepatitis C NCT01565889

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Healthy Medical History | Healthy Physical Examination | Exception Hepatitis C | Exception HIV Infection
Item
healthy according to medical history and physical examination with exception of hcv and hiv diagnoses
boolean
C3898900 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
C3898900 (UMLS CUI [2,1])
C0031809 (UMLS CUI [2,2])
C1705847 (UMLS CUI [3,1])
C0019196 (UMLS CUI [3,2])
C1705847 (UMLS CUI [4,1])
C0019693 (UMLS CUI [4,2])
Hepatitis C, Chronic
Item
confirmation of chronic hcv infection
boolean
C0524910 (UMLS CUI [1])
HIV-1 infection chronic
Item
confirmation of chronic hiv-1 infection
boolean
C2363741 (UMLS CUI [1,1])
C0205191 (UMLS CUI [1,2])
HIV Antiretroviral therapy Stable | HIV RNA undetectable
Item
on a stable protocol approved hiv antiretroviral (arv) regimen with undetectable hiv-rna
boolean
C0019682 (UMLS CUI [1,1])
C1963724 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0877598 (UMLS CUI [2])
Contraceptive methods Quantity
Item
agree to use two forms of highly effective contraception for the duration of the study and 6 months after the last dose of study medication
boolean
C0700589 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
Therapy naive Chronic Hepatitis C
Item
subjects must be naive to treatment for chronic hcv infection
boolean
C0919936 (UMLS CUI [1,1])
C0524910 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Liver Cirrhosis | Liver Cirrhosis Suspected
Item
known or suspected cirrhosis
boolean
C0023890 (UMLS CUI [1])
C0023890 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
Chronic liver disease Other
Item
history of any other clinically significant chronic liver disease
boolean
C0341439 (UMLS CUI [1,1])
C0205394 (UMLS CUI [1,2])
Medical History Consistent with Decompensated liver disease
Item
a history consistent with decompensated liver disease.
boolean
C0262926 (UMLS CUI [1,1])
C0332290 (UMLS CUI [1,2])
C4075847 (UMLS CUI [1,3])
Illicit medication use
Item
use of any prohibited medications as defined by the protocol
boolean
C0281875 (UMLS CUI [1])
Pregnancy | Breast Feeding | Gender Partner Pregnancy
Item
pregnant or nursing female or male with pregnant female partner
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0079399 (UMLS CUI [3,1])
C0682323 (UMLS CUI [3,2])
C0032961 (UMLS CUI [3,3])
Medical contraindication PEGINTERFERON Therapy | Medical contraindication Ribavirin Therapy
Item
contraindication to peg or rbv therapy (for part b)
boolean
C1301624 (UMLS CUI [1,1])
C0982327 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C1301624 (UMLS CUI [2,1])
C0035525 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,3])
Substance Use Disorders
Item
clinically relevant drug or alcohol abuse
boolean
C0038586 (UMLS CUI [1])

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