Study identifier:D1520C05287
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Randomised, Double-Blind, Placebo-Controlled, Parallel Group, Ascending Dose Study to Assess the Activity, Safety and Tolerability of 2 Doses of AZD9056 for 4 Weeks in Patients with Active Rheumatoid Arthritis Receiving Methotrexate and/or Sulphasalazine
Rheumatoid Arthritis
Phase 1
-
-
-
-
Interventional
-
Allocation: -
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -
Verified 01 Nov 2013 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|