The study is a multicenter, randomized, double-blind, placebo-controlled study to evaluate the safety and efficacy of 12 weeks daily treatment with 100 mg AP1189 in RA patients who are to start up-titration with methotrexate (MTX).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
127
AP1189 tablets for oral use
Matching placebo for oral use
Timofei Mosneaga Republican Clinical Hospital
Chisinau, Moldova
Number of reported AEs
Evaluation of the safety and tolerability of AP1189 on the number and severity of reported Adverse Events, compared with placebo
Time frame: 12 weeks
Change in ACR20
The change in American College of Rheumatology 20% (ACR20) compared to baseline
Time frame: 12 weeks
Change in ACR50
The change in American College of Rheumatology 50% (ACR50) compared to baseline
Time frame: 12 weeks
Change in ACR70
The change in American College of Rheumatology 70% (ACR70) compared to baseline
Time frame: 12 weeks
Change in (CDAI)
The change Clinical Disease Activity Index (CDAI) compared to baseline
Time frame: 12 weeks
Change in DAS-28
The change in DAS-28, based on a CRP value, compare to baseline
Time frame: 12 weeks
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