ID
12560
Description
A Randomized, Double-blind, Placebo-controlled Clinical Study of the Oral IL-12/23 Inhibitor, STA-5326 Mesylate, Administered to Patients With Rheumatoid Arthritis to Determine Safety, Tolerability, Pharmacokinetic and Synovial Tissue Outcomes; ODM derived from: https://clinicaltrials.gov/show/NCT00642629
Lien
https://clinicaltrials.gov/show/NCT00642629
Mots-clés
Versions (1)
- 30/11/2015 30/11/2015 -
Téléchargé le
30 novembre 2015
DOI
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Licence
Creative Commons BY 4.0
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Eligibility Active, Moderate to Severe Rheumatoid Arthritis NCT00642629
Eligibility Active, Moderate to Severe Rheumatoid Arthritis NCT00642629
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
is taking any disease-modifying anti-rheumatic drug (dmard) other than mtx
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0242708
Description
positive (≥10 mm) tuberculin (ppd) skin test
Type de données
boolean
Alias
- UMLS CUI [1]
- C3161220
Description
has received any investigational drug or experimental procedure for the treatment of ra
Type de données
boolean
Alias
- UMLS CUI [1]
- C2348568
Description
(e.g., renal, hepatic, neurological, cardiovascular, pulmonary, endocrine, psychiatric, hematologic, urologic, or other acute or chronic illness)
Type de données
boolean
Alias
- UMLS CUI [1]
- C0525058
- UMLS CUI [2]
- C0439801
- UMLS CUI [3]
- C0009488
Similar models
Eligibility Active, Moderate to Severe Rheumatoid Arthritis NCT00642629
- StudyEvent: Eligibility
C0001779 (UMLS CUI [2])
C0750934 (UMLS CUI [2])
C0205360 (UMLS CUI [1,2])
C0006147 (UMLS CUI [1,2])
C0700589 (UMLS CUI [2])
C0242708 (UMLS CUI [1,2])
C0439801 (UMLS CUI [2])
C0009488 (UMLS CUI [3])