SC12267 (4SC-101)
Drugoral administration
NCT Number: NCT01010581
The purpose of the study is to determine the efficacy, safety and pharmacokinetics of SC12267 (4SC-101, 35 mg) in combination with methotrexate in comparison to methotrexate alone in the treatment of patients suffering from Rheumatoid Arthritis.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
MHAT "Kaspela" Department of Rheumatology, Plovdiv, Bulgaria
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Main Inclusion Criteria:
Main Exclusion Criteria:
oral administration
oral administration
oral administration
oral administration
Time frame: 13 weeks
Time frame: 13 weeks
Time frame: 13 weeks
4SC AG
Industry
A Randomized, Double Blind, Placebo-Controlled, Phase II Study to Evaluate Efficacy, Safety, and Pharmacokinetics of SC12267 (35 mg) in Combination With Methotrexate Compared to Methotrexate Alone in Patients With Rheumatoid Arthritis
Acronym: COMPONENT
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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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