ID

13900

Beschrijving

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

Trefwoorden

  1. 15-03-16 15-03-16 -
Houder van rechten

CC BY-NC 3.0

Geüploaded op

15 maart 2016

DOI

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Licentie

Creative Commons BY-NC 3.0

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VX-950HPC3006 NCT01571583 Enrollment Information

VX-950HPC3006 Enrollment Information

Enrollment Information
Beschrijving

Enrollment Information

Immunosuppressive regimen assigned to the subject
Beschrijving

Immunosuppressive regimen

Datatype

integer

Alias
UMLS CUI [1]
C0021079
Does the subject have a fibrosis stage of F3?
Beschrijving

fibrosis stage

Datatype

boolean

Alias
UMLS CUI [1]
C3897040

Similar models

VX-950HPC3006 Enrollment Information

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Enrollment Information
Item
Immunosuppressive regimen assigned to the subject
integer
C0021079 (UMLS CUI [1])
Code List
Immunosuppressive regimen assigned to the subject
CL Item
Tacrolimus (1)
CL Item
Cyclosporin A (2)
fibrosis stage
Item
Does the subject have a fibrosis stage of F3?
boolean
C3897040 (UMLS CUI [1])

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