ID

14137

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. 31/3/16 31/3/16 -
Titular de derechos de autor

CC BY-NC 3.0

Subido en

31 de marzo de 2016

DOI

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Licencia

Creative Commons BY-NC 3.0

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VX-950HPC3006 NCT01571583 Trial Completion

VX-950HPC3006 NCT01571583 Trial Completion

Trial completion
Descripción

Trial completion

did the subject experience any Adverse Events during the trial?
Descripción

if yes, please ensure that all Adverse Events are recorded on the Adverse Event form

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0877248
did the subject take any concomitant medication during the trial?
Descripción

if yes, please ensure that all medications are recorded on the concomitant medication form

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2347852

Similar models

VX-950HPC3006 NCT01571583 Trial Completion

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Trial completion
adverse events during trial
Item
did the subject experience any Adverse Events during the trial?
boolean
C0877248 (UMLS CUI [1])
concomitant medication
Item
did the subject take any concomitant medication during the trial?
boolean
C2347852 (UMLS CUI [1])

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