ID

13832

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 (2)
  1. 10/3/16 10/3/16 -
  2. 10/3/16 10/3/16 -
Titular de derechos de autor

CC BY-NC 3.0

Subido en

10 de marzo de 2016

DOI

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Licencia

Creative Commons BY-NC 3.0
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VX-950HPC3006 NCT01571583 History Clinical Trials

Inglés

VX-950HPC3006 History Clinical Trails

1 formularios  
TMC114
Descripción

TMC114

CRF ID
Descripción

CRF ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Descripción

Date of first dose

Tipo de datos

date

Alias
UMLS CUI [1]
C3173309
TMC125
Descripción

TMC125

CRF ID
Descripción

CRF ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Descripción

Date of first dose

Tipo de datos

date

Alias
UMLS CUI [1]
C3173309
TMC278
Descripción

TMC278

CRF ID
Descripción

CRF ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Descripción

Date of first dose

Tipo de datos

date

Alias
UMLS CUI [1]
C3173309
TMC207
Descripción

TMC207

CRF ID
Descripción

CRF ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Descripción

Date of first dose

Tipo de datos

date

Alias
UMLS CUI [1]
C3173309
VX950
Descripción

VX950

CRF ID
Descripción

CRF ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Descripción

Date of first dose

Tipo de datos

date

Alias
UMLS CUI [1]
C3173309
TMC120
Descripción

TMC120

CRF ID
Descripción

CRF ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Descripción

Date of first dose

Tipo de datos

date

Alias
UMLS CUI [1]
C3173309
TMC 435
Descripción

TMC 435

CRF ID
Descripción

CRF ID

Tipo de datos

text

Alias
UMLS CUI [1]
C2348585
In case subject has only participated in a non clinial trial please provide date of first dosing
Descripción

Date of first dose

Tipo de datos

date

Alias
UMLS CUI [1]
C3173309
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Similar models

VX-950HPC3006 History Clinical Trails

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
TMC114
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
TMC125
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
TMC278
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
TMC207
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
VX950
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
TMC120
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Item Group
TMC 435
CRF ID
Item
CRF ID
text
C2348585 (UMLS CUI [1])
Date of first dose
Item
In case subject has only participated in a non clinial trial please provide date of first dosing
date
C3173309 (UMLS CUI [1])
Volver a la parte superior de la página 

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