Phase
Condition
Cutaneous Lupus Erythematosus
Musculoskeletal Diseases
Bone Diseases
Treatment
Placebo
Telitacicept
Clinical Study ID
Ages 12-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age 12-70 years at screening.
Has a diagnosis of SLE for at least 6 months prior to the screening visit.
Meets the 2019 EULAR/ACR Classification criteria for SLE.
Moderately to severely active SLE definined by the following:
SELENA SLEDAI total score ≥6 points with clinical SLEDAI score ≥4 points atscreening;
BILAG organ system scores of at least 1A or 2B at screening.
Clinical SLEDAI score of ≥4 at Day 0 prior to randomization.
At least one positive serologic parameter within the screening period.
Currently receiving at least one of the SOC SLE medications: oral corticosteroid,antimalarial and/or immunosuppressive agent.
Exclusion
Exclusion Criteria:
Active lupus nephritis undergoing induction therapy or unstable renal diseaseswithin 12 weeks prior to screening.
Active or unstable neuropsychiatric SLE.
Autoimmune or rheumatic disease other than SLE.
History of arterial or venous thromboembolism or microangiopathy within 12 monthsprior to screening.
History of non-SLE disease requiring treatment with oral or parenteral.glucocorticosteroids for more than a total of 2 weeks within the last 24 weeks priorto screening.
Study Design
Study Description
Connect with a study center
Hemet site
Hemet, California 92543
United StatesSite Not Available
Menifee site
Menifee, California 92586
United StatesSite Not Available
Hemet site
Hemet 5356277, California 5332921 92543
United StatesSite Not Available
Menifee site
Menifee 5372205, California 5332921 92586
United StatesSite Not Available
Rockford site
Rockford, Illinois 61114
United StatesSite Not Available
Rockford site
Rockford 4907959, Illinois 4896861 61114
United StatesSite Not Available
Stafford site
Stafford, Texas 77477
United StatesSite Not Available
Stafford site
Stafford 4734005, Texas 4736286 77477
United StatesSite Not Available

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