ID

21746

Beschreibung

A Multiple Dose Study to Evaluate Subcutaneous AMG 108 in Subjects With Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00293826

Link

https://clinicaltrials.gov/show/NCT00293826

Stichworte

  1. 27.04.17 27.04.17 -
Hochgeladen am

27. April 2017

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Rheumatoid Arthritis NCT00293826

Eligibility Rheumatoid Arthritis NCT00293826

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects with active rheumatoid arthritis as diagnosed by meeting acr classification criteria for at least 6 months.
Beschreibung

Criteria for Rheumatoid Arthritis

Datentyp

boolean

Alias
UMLS CUI [1]
C3273740
must be taking mtx consecutively for >/= 12 weeks and at a stable dose of methotrexate at 15-25 mg weekly for at least 4 weeks prior to screening
Beschreibung

MTX Dosage

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0025677
UMLS CUI [1,2]
C0178602
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
receipt of commercial or experimental biologic therapies for the treatment of inflammatory disease
Beschreibung

Pharmacotherapy for inflammatory diseases

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C1290884
presence of serious infection
Beschreibung

Infection

Datentyp

boolean

Alias
UMLS CUI [1]
C0009450
class iv rheumatoid arthritis
Beschreibung

Rheumatoid Arthritis Classification

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0003873
UMLS CUI [1,2]
C0008902
prior or current history of tuberculosis infection or exposure
Beschreibung

Tuberculosis

Datentyp

boolean

Alias
UMLS CUI [1]
C0041296
any other dmards other than methotrexate within 6 weeks of screening
Beschreibung

DMARD

Datentyp

boolean

Alias
UMLS CUI [1]
C0242708
pregnant or nursing
Beschreibung

Gynaecological Status

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
receipt of live vaccines within 3 months
Beschreibung

Live vaccine

Datentyp

boolean

Alias
UMLS CUI [1]
C0042211
felty's syndrome
Beschreibung

Felty Syndrome

Datentyp

boolean

Alias
UMLS CUI [1]
C0015773

Ähnliche Modelle

Eligibility Rheumatoid Arthritis NCT00293826

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Criteria for Rheumatoid Arthritis
Item
subjects with active rheumatoid arthritis as diagnosed by meeting acr classification criteria for at least 6 months.
boolean
C3273740 (UMLS CUI [1])
MTX Dosage
Item
must be taking mtx consecutively for >/= 12 weeks and at a stable dose of methotrexate at 15-25 mg weekly for at least 4 weeks prior to screening
boolean
C0025677 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Pharmacotherapy for inflammatory diseases
Item
receipt of commercial or experimental biologic therapies for the treatment of inflammatory disease
boolean
C0013216 (UMLS CUI [1,1])
C1290884 (UMLS CUI [1,2])
Infection
Item
presence of serious infection
boolean
C0009450 (UMLS CUI [1])
Rheumatoid Arthritis Classification
Item
class iv rheumatoid arthritis
boolean
C0003873 (UMLS CUI [1,1])
C0008902 (UMLS CUI [1,2])
Tuberculosis
Item
prior or current history of tuberculosis infection or exposure
boolean
C0041296 (UMLS CUI [1])
DMARD
Item
any other dmards other than methotrexate within 6 weeks of screening
boolean
C0242708 (UMLS CUI [1])
Gynaecological Status
Item
pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Live vaccine
Item
receipt of live vaccines within 3 months
boolean
C0042211 (UMLS CUI [1])
Felty Syndrome
Item
felty's syndrome
boolean
C0015773 (UMLS CUI [1])

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