ID
13983
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
Versies (1)
- 21-03-16 21-03-16 -
Houder van rechten
CC BY-NC 3.0
Geüploaded op
21 maart 2016
DOI
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Licentie
Creative Commons BY-NC 3.0
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VX-950HPC3006 NCT01571583 Eligibility
VX-950HPC3006 NCT01571583 Eligibility
- StudyEvent: ODM
Beschrijving
Reason for withdrawal from study
Beschrijving
inclusion/exclusion criteria
Datatype
boolean
Alias
- UMLS CUI [1]
- C1512693
- UMLS CUI [2]
- C0680251
Beschrijving
(including death, abnormal lab values, intercurrent illness and pregnancy)
Datatype
text
Alias
- UMLS CUI [1]
- C0877248
Beschrijving
Date of last contact with subject
Datatype
date
Alias
- UMLS CUI [1,1]
- C0805839
- UMLS CUI [1,2]
- C0681850
Beschrijving
date consent withdrawn
Datatype
date
Alias
- UMLS CUI [1,1]
- C1707492
- UMLS CUI [1,2]
- C0011008
Beschrijving
subject non-compliant
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0457432
- UMLS CUI [1,2]
- C0681850
Beschrijving
sponsor's decision
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2347796
- UMLS CUI [1,2]
- C0679006
Beschrijving
other reason
Datatype
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])