ID

13900

Descripción

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

Palabras clave

  1. 15/3/16 15/3/16 -
Titular de derechos de autor

CC BY-NC 3.0

Subido en

15 de marzo de 2016

DOI

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Licencia

Creative Commons BY-NC 3.0

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VX-950HPC3006 NCT01571583 Enrollment Information

VX-950HPC3006 Enrollment Information

Enrollment Information
Descripción

Enrollment Information

Immunosuppressive regimen assigned to the subject
Descripción

Immunosuppressive regimen

Tipo de datos

integer

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

fibrosis stage

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3897040

Similar models

VX-950HPC3006 Enrollment Information

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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