ID
13983
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
Versiones (1)
- 21/3/16 21/3/16 -
Titular de derechos de autor
CC BY-NC 3.0
Subido en
21 de marzo de 2016
DOI
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Licencia
Creative Commons BY-NC 3.0
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VX-950HPC3006 NCT01571583 Eligibility
VX-950HPC3006 NCT01571583 Eligibility
- StudyEvent: ODM
Descripción
Reason for withdrawal from study
Descripción
inclusion/exclusion criteria
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1512693
- UMLS CUI [2]
- C0680251
Descripción
(including death, abnormal lab values, intercurrent illness and pregnancy)
Tipo de datos
text
Alias
- UMLS CUI [1]
- C0877248
Descripción
Date of last contact with subject
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0805839
- UMLS CUI [1,2]
- C0681850
Descripción
date consent withdrawn
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0011008
Descripción
subject non-compliant
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0457432
- UMLS CUI [1,2]
- C0681850
Descripción
sponsor's decision
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2347796
- UMLS CUI [1,2]
- C0679006
Descripción
other reason
Tipo de datos
text
Alias
- UMLS CUI [1]
- C3840932
Similar models
VX-950HPC3006 NCT01571583 Eligibility
- StudyEvent: ODM
C2348563 (UMLS CUI [1,2])
C0220908 (UMLS CUI [2])
C0680095 (UMLS CUI [1,2])
C0680251 (UMLS CUI [2])
C0681850 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0681850 (UMLS CUI [1,2])
C0679006 (UMLS CUI [1,2])