Timofei Mosneaga Republican Clinical Hospital
Chisinau, Moldova
NCT Number: NCT05516979
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).
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Notify Me18 year–85 year
All sexes
Interventional
Phase 2
Chisinau, Moldova
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
Main Exclusion Criteria:
AP1189 tablets for oral use
Other names: AP1189 tablets for oral use
Matching placebo for oral use
Time frame: 12 weeks
Evaluation of the safety and tolerability of AP1189 on the number and severity of reported Adverse Events, compared with placebo
Time frame: 12 weeks
The change in American College of Rheumatology 20% (ACR20) compared to baseline
Time frame: 12 weeks
The change in American College of Rheumatology 50% (ACR50) compared to baseline
Time frame: 12 weeks
The change in American College of Rheumatology 70% (ACR70) compared to baseline
Time frame: 12 weeks
The change Clinical Disease Activity Index (CDAI) compared to baseline
Time frame: 12 weeks
The change in DAS-28, based on a CRP value, compare to baseline
SynAct Pharma Aps
Industry
A Double-blind, Multi-center, Randomized, Placebo-controlled Study of the Safety and Efficacy of 12 Weeks Extended Treatment With AP1189 in Early Rheumatoid Arthritis (RA) Patients naïve to DMARD Treatment
Acronym: EXPAND
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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