Eligibility Rheumatoid Arthritis NCT02480153

Inclusion Criteria
Descripción

Inclusion Criteria

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

ID.1

Tipo de datos

boolean

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

ID.2

Tipo de datos

boolean

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

ID.3

Tipo de datos

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.
Descripción

ID.4

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

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

ID.5

Tipo de datos

boolean

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

ID.6

Tipo de datos

boolean

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

ID.7

Tipo de datos

boolean

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

ID.8

Tipo de datos

boolean

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

ID.9

Tipo de datos

boolean

Similar models

Eligibility Rheumatoid Arthritis NCT02480153

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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