ID

34563

Beschreibung

A Study Of PF-06410293 (Adalimumab-Pfizer) And Adalimumab (Humira) In Combination With Methotrexate In Subjects With Active Rheumatoid Arthritis (REFLECTIONS B538-02).; ODM derived from: https://clinicaltrials.gov/show/NCT02480153

Link

https://clinicaltrials.gov/show/NCT02480153

Stichworte

  1. 19.01.19 19.01.19 -
Rechteinhaber

see on clinicaltrials.gov

Hochgeladen am

19. Januar 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Rheumatoid Arthritis NCT02480153

Eligibility Rheumatoid Arthritis NCT02480153

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of rheumatoid arthritis based on 2010 acr/eular criteria for at least 4 months.
Beschreibung

ID.1

Datentyp

boolean

at least 6 tender (of 68 assessed) and 6 swollen (of 66 assessed) joints at screening and baseline.
Beschreibung

ID.2

Datentyp

boolean

hs-crp equal or greater than 8 mg/l.
Beschreibung

ID.3

Datentyp

boolean

must have received methotrexate for at least 12 weeks and been on a stable dose for at least 4 weeks prior to the first study dose.
Beschreibung

ID.4

Datentyp

boolean

Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
evidence of untreated or inadequately treated latent or active tb.
Beschreibung

ID.5

Datentyp

boolean

evidence of uncontrolled, clinically significant diseases, including moderate or severe heart failure (nyha class iii/iv) or malignancy in the previous 5 years.
Beschreibung

ID.6

Datentyp

boolean

history of infection requiring hospitalization or parenteral antimicrobial therapy within 6 months prior to first dose of study drug.
Beschreibung

ID.7

Datentyp

boolean

may have received no more than 2 doses of one biologic therapy (other than adalimumab or lymphocyte depleting therapy).
Beschreibung

ID.8

Datentyp

boolean

any second dmard must be washed out prior to the first study dose.
Beschreibung

ID.9

Datentyp

boolean

Ähnliche Modelle

Eligibility Rheumatoid Arthritis NCT02480153

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
diagnosis of rheumatoid arthritis based on 2010 acr/eular criteria for at least 4 months.
boolean
ID.2
Item
at least 6 tender (of 68 assessed) and 6 swollen (of 66 assessed) joints at screening and baseline.
boolean
ID.3
Item
hs-crp equal or greater than 8 mg/l.
boolean
ID.4
Item
must have received methotrexate for at least 12 weeks and been on a stable dose for at least 4 weeks prior to the first study dose.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
evidence of untreated or inadequately treated latent or active tb.
boolean
ID.6
Item
evidence of uncontrolled, clinically significant diseases, including moderate or severe heart failure (nyha class iii/iv) or malignancy in the previous 5 years.
boolean
ID.7
Item
history of infection requiring hospitalization or parenteral antimicrobial therapy within 6 months prior to first dose of study drug.
boolean
ID.8
Item
may have received no more than 2 doses of one biologic therapy (other than adalimumab or lymphocyte depleting therapy).
boolean
ID.9
Item
any second dmard must be washed out prior to the first study dose.
boolean

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