Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Peking Union Medical College Hospital
This is a single arm, 24 weeks, pilot trial. All patients will be treated with standard of care plus Belimumab (at a dose of 10 mg per kilogram of body weight) .
The primary endpoint is the proportion of LLDAS in week 24.
Age
18–75
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Clinical diagnosis of SLE according to the 1997 American College of Rheumatology (ACR) classification criteria or 2019 EULAR/ACR classification criteria within three months, which is autoantibody-positive (antinuclear antibody titers ≥1:80, anti-double-stranded DNA antibodies, or both)
18-75 years of age
body weight 45-80kg
Disease duration of SLE ≤ 6months
SELENA-2K score ≥6 scores
Negative pregnancy test for child-bearing women at screening and baseline
Provide written informed consent
You may not be if
Known to be allergic to Prednisone Acetate, Meprednisone, Hydroxychloroquine, and Immunosuppressants including Mycophenolate Mofetil, Cyclophosphamide,et al
Active serious neuropsychiatric systemic lupus erythematosus or other severe situations of SLE who need pulse steroid treatment
Abnormal liver function (ALT or AST is 2 times higher than normal)
Pregnancy or breastfeeding women;
Have a history of malignant tumors;
Have any serious acute, chronic or recurrent infectious disease (such as pneumonia or active stage of pyelitis, recurrent pneumonia, chronic bronchiectasis and tuberculosis)
Chronic infections, such as Hepatitis B virus or hepatitis B and C and HIV;
Previous visual obstruction, monocular dysfunction and cataract;
Cardiac insufficiency with metabolic imbalance or severe high blood pressure (systolic pressure \> 160mmHg or diastolic pressure \> 100mmHg) or diabetics;
Active hemorrhage or peptic ulcer;
With other concommitant autoimmune disease;
Receipt of B-cell-targeted therapy (including belimumab) within 1 year before randomization.
Participated in other drugs clinical trials within 4 weeks.
