ID

13832

Beskrivning

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

Nyckelord

Versioner (2)
  1. 2016-03-10 2016-03-10 -
  2. 2016-03-10 2016-03-10 -
Rättsinnehavare

CC BY-NC 3.0

Uppladdad den

10 mars 2016

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

VX-950HPC3006 NCT01571583 History Clinical Trials

Engelsk

VX-950HPC3006 History Clinical Trails

1 Formulär  
TMC114
Beskrivning

TMC114

CRF ID
Beskrivning

CRF ID

Datatyp

text

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

Date of first dose

Datatyp

date

Alias
UMLS CUI [1]
C3173309
TMC125
Beskrivning

TMC125

CRF ID
Beskrivning

CRF ID

Datatyp

text

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

Date of first dose

Datatyp

date

Alias
UMLS CUI [1]
C3173309
TMC278
Beskrivning

TMC278

CRF ID
Beskrivning

CRF ID

Datatyp

text

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

Date of first dose

Datatyp

date

Alias
UMLS CUI [1]
C3173309
TMC207
Beskrivning

TMC207

CRF ID
Beskrivning

CRF ID

Datatyp

text

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

Date of first dose

Datatyp

date

Alias
UMLS CUI [1]
C3173309
VX950
Beskrivning

VX950

CRF ID
Beskrivning

CRF ID

Datatyp

text

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

Date of first dose

Datatyp

date

Alias
UMLS CUI [1]
C3173309
TMC120
Beskrivning

TMC120

CRF ID
Beskrivning

CRF ID

Datatyp

text

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

Date of first dose

Datatyp

date

Alias
UMLS CUI [1]
C3173309
TMC 435
Beskrivning

TMC 435

CRF ID
Beskrivning

CRF ID

Datatyp

text

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

Date of first dose

Datatyp

date

Alias
UMLS CUI [1]
C3173309
Tillbaka till toppen

Similar models

VX-950HPC3006 History Clinical Trails

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial