ID
36099
Beschreibung
A Study of RO5024048 in Combination With Pegasys (Peginterferon Alfa-2a) and Copegus (Ribavirin) in Patients With Chronic Hepatitis C Genotype 1 or 4; ODM derived from: https://clinicaltrials.gov/show/NCT01057667
Link
https://clinicaltrials.gov/show/NCT01057667
Stichworte
Versionen (3)
- 16.01.19 16.01.19 -
- 14.04.19 14.04.19 -
- 15.04.19 15.04.19 -
Rechteinhaber
Hoffmann-La Roche
Hochgeladen am
15. April 2019
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY-NC 3.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
RO5024048 in Combination with Pegasys and Copegus in Chronic Hep C NCT01057667
Eligibility Criteria
- StudyEvent: Eligibility
Beschreibung
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Beschreibung
pregnant or breast feeding females or male partners of pregnant females (are to be included)
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
- UMLS CUI [3]
- C0919624
Beschreibung
Patients with previous interferon or ribavirin based therapy or investigational anti-hcv agent (are to be excluded)
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1514463
- UMLS CUI [1,2]
- C0035525
- UMLS CUI [2,1]
- C1514463
- UMLS CUI [2,2]
- C3652465
- UMLS CUI [3,1]
- C1514463
- UMLS CUI [3,2]
- C0019196
- UMLS CUI [3,3]
- C0013230
Beschreibung
systemic antiviral therapy with established or perceived activity against hcv </=3 months prior to first dose of study drug
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0280274
- UMLS CUI [1,2]
- C0205373
- UMLS CUI [1,3]
- C0441655
- UMLS CUI [1,4]
- C0521124
- UMLS CUI [1,5]
- C0524910
- UMLS CUI [1,6]
- C0332185
Beschreibung
Patients with hepatitis a or b, or hiv infection (are to be excluded)
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0019693
- UMLS CUI [2,1]
- C0019163
- UMLS CUI [2,2]
- C3714514
- UMLS CUI [3,1]
- C0019159
- UMLS CUI [3,2]
- C3714514
Beschreibung
Patients with history or evidence of medical condition associated with chronic liver disease other than hcv (are to be excluded)
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0012634
- UMLS CUI [1,3]
- C0332281
- UMLS CUI [1,4]
- C0341439
- UMLS CUI [2,1]
- C3887511
- UMLS CUI [2,2]
- C0012634
- UMLS CUI [2,3]
- C0332281
- UMLS CUI [2,4]
- C0341439
Ähnliche Modelle
Eligibility Criteria
- StudyEvent: Eligibility
C3532919 (UMLS CUI [1,2])
C0524910 (UMLS CUI [2,1])
C3532922 (UMLS CUI [2,2])
C0700589 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
C0919624 (UMLS CUI [3])
C0035525 (UMLS CUI [1,2])
C1514463 (UMLS CUI [2,1])
C3652465 (UMLS CUI [2,2])
C1514463 (UMLS CUI [3,1])
C0019196 (UMLS CUI [3,2])
C0013230 (UMLS CUI [3,3])
C0205373 (UMLS CUI [1,2])
C0441655 (UMLS CUI [1,3])
C0521124 (UMLS CUI [1,4])
C0524910 (UMLS CUI [1,5])
C0332185 (UMLS CUI [1,6])
C0019163 (UMLS CUI [2,1])
C3714514 (UMLS CUI [2,2])
C0019159 (UMLS CUI [3,1])
C3714514 (UMLS CUI [3,2])
C0012634 (UMLS CUI [1,2])
C0332281 (UMLS CUI [1,3])
C0341439 (UMLS CUI [1,4])
C3887511 (UMLS CUI [2,1])
C0012634 (UMLS CUI [2,2])
C0332281 (UMLS CUI [2,3])
C0341439 (UMLS CUI [2,4])