ID

13832

Description

This is an open-label (all people know the identity of the intervention), multicenter study in genotype 1 chronic HCV infected liver transplant patients who will be treated for 12 weeks with telaprevir 750 mg every 8 hours given in combination with Peg-IFN-alfa-2a and ribavirin followed by 36 weeks of treatment with Peg-IFN-alfa-2a and ribavirin alone. The total treatment duration will be 48 weeks. Safety will be evaluated throughout the study and will include evaluations of adverse events, clinical laboratory tests, electrocardiogram, vital signs, and physical examination. NCT01571583

Keywords

Versions (2)
  1. 3/10/16 3/10/16 -
  2. 3/10/16 3/10/16 -
Copyright Holder

CC BY-NC 3.0

Uploaded on

March 10, 2016

DOI

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License

Creative Commons BY-NC 3.0
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VX-950HPC3006 NCT01571583 History Clinical Trials

English

VX-950HPC3006 History Clinical Trails

1 forms  
TMC114
Description

TMC114

CRF ID
Description

CRF ID

Data type

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Description

Date of first dose

Data type

date

Alias
UMLS CUI [1]
C3173309
TMC125
Description

TMC125

CRF ID
Description

CRF ID

Data type

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Description

Date of first dose

Data type

date

Alias
UMLS CUI [1]
C3173309
TMC278
Description

TMC278

CRF ID
Description

CRF ID

Data type

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Description

Date of first dose

Data type

date

Alias
UMLS CUI [1]
C3173309
TMC207
Description

TMC207

CRF ID
Description

CRF ID

Data type

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Description

Date of first dose

Data type

date

Alias
UMLS CUI [1]
C3173309
VX950
Description

VX950

CRF ID
Description

CRF ID

Data type

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Description

Date of first dose

Data type

date

Alias
UMLS CUI [1]
C3173309
TMC120
Description

TMC120

CRF ID
Description

CRF ID

Data type

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Description

Date of first dose

Data type

date

Alias
UMLS CUI [1]
C3173309
TMC 435
Description

TMC 435

CRF ID
Description

CRF ID

Data type

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Description

Date of first dose

Data type

date

Alias
UMLS CUI [1]
C3173309
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Similar models

VX-950HPC3006 History Clinical Trails

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
TMC114
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
TMC125
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
TMC278
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
TMC207
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
VX950
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
TMC120
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
TMC 435
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
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