EUCTR2012-003364-51-PL进行中（未招募）1 期
A Randomized, Controlled Double-blind Study Comparing the Efficacy and Safety of Voclosporin (23.7 mg BID, or 39.5 mg BID) with Placebo in Achieving Remission in Patients with Active Lupus Nephritis - Aurinia Urinary protein Reduction Active - Lupus with Voclosporin
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 258
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1. Written informed consent (by subject or legally acceptable representative) before any study-specific procedures are performed.
- •2. Male or female subjects aged 18 to 75 years inclusive at the time of consent.
- •3. Diagnosis of systemic lupus erythematosus (SLE) according to the American College of Rheumatology criteria (1997; see Appendix 7).
- •4. Kidney biopsy within 6 months prior to screening (Visit 1) with a histologic
- •diagnosis of lupus nephritis (International Society of Nephrology/Renal
- •Pathology Society 2003 classification of lupus nephritis) Classes III, IV-S or
- •IV-G, (A) or (A/C); or Class V, alone or in combination with Class III or IV;
- •see Appendix 5. If a subject has not had a recent kidney biopsy, one may be
- •performed to assess eligibility into the study provided consent is in place and
- •provided results are received before randomization.
- •5. Subjects with laboratory evidence of active nephritis at screening, defined as
- •Class III, IV-S or IV-G
- •Confirmed proteinuria =1,500 mg/24 hours when assessed by 24-hour urine
- •collection, defined by a urine protein/creatinine ratio (UPCR) of
- •=1.5 mg/mg assessed in a first morning void urine specimen (2 samples).
- •Class V (alone or in combination with Class III or IV)
- •Confirmed proteinuria =2,000 mg/24 hours when assessed by 24-hour urine
- •collection, defined by a UPCR of =2 mg/mg assessed in a first morning
- •void urine specimen (2 samples)
- •6. In the opinion of the Investigator, subject requires high dose corticosteroids and immunosuppressive therapy.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 228
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 30
排除标准
- •1. Subjects unable or unwilling to give written informed consent and/or to comply with study procedures.
- •2. Estimated glomerular filtration rate (eGFR) as calculated by the Chronic Kidney Disease Epidemiology Collaboration equation of =45 mL/min/1.73 m2 at screening (Visit 1)
- •3. Currently taking or known need for any of the medications listed in Section 7.8, Prohibited Therapy and Concomitant Treatment.
- •4. Serum potassium >5.5 mmol/L at screening confirmed before randomization.
- •5. Currently requiring renal dialysis (hemodialysis or peritoneal dialysis) or expected to require dialysis during the study period.
- •6. A previous kidney transplant or planned transplant within study treatment period.
- •7. In the opinion of the Investigator, subject does not require long-term immunosuppressive treatment (in addition to corticosteroids).
- •8. Any known hypersensitivity or contraindication to MMF, mycophenolic acid, cyclosporine, corticosteroids or any components of these drug products.
- •9. Current or medical history of:
- •Pancreatitis or gastrointestinal hemorrhage within 6 months prior to screening.
- •Active unhealed peptic ulcer within 3 months prior to screening. If an ulcer has healed and the subject is on adequate therapy, the subject may be randomized.
- •Congenital or acquired immunodeficiency.
- •In the opinion of the Investigator, clinically significant drug or alcohol abuse 2 years prior to screening.
- •Malignancy within 5 years of screening, with the exception of basal and squamous cell carcinomas treated by complete excision. Subjects with cervical dysplasia that is cervical intraepithelial neoplasia 1, but have been treated with conization or loop electrosurgical excision procedure, and have had a normal repeat PAP are allowed.
- •Lymphoproliferative disease or previous total lymphoid irradiation.
- •Severe viral infection (such as CMV, HBV, HCV) within 3 months of screening; or known human immunodeficiency virus infection.
- •Active tuberculosis (TB), or known history of TB/evidence of old TB if not taking prophylaxis with isoniazid.
- •10. Other known clinically significant active medical conditions, such as:
- •Severe cardiovascular disease including congestive heart failure, history of cardiac dysrhythmia or congenital long QT syndrome. QTcF (QT interval duration corrected for heart rate using method of Fridericia) exceeding 480 msec in the presence of a normal QRS interval (<110 msec) at time of screening will result in exclusion.
- •Liver dysfunction (aspartate aminotransferase, alanine aminotransferase, or bilirubin greater than 2.5 times the upper limit of normal) at screening and confirmed before randomization.
- •Chronic obstructive pulmonary disease or asthma requiring oral steroids.
- •Bone marrow insufficiency unrelated to active SLE (according to Investigator judgment) with white blood cell count <2,500/mm3; absolute neutrophil count <1.3 × 103/µL; thrombocytopenia (platelet count <50,000/mm3).
- •Active bleeding disorders.
- •Current infection requiring IV antibiotics.
- •11. Any overlapping autoimmune condition for which the condition or the treatment of the condition may affect the study assessments or outcomes (e.g., scleroderma with significant pulmonary hypertension; any condition for
- •which additional immunosuppression is indicated). Overlapping conditions for which the condition or treatment is not expected to affect assessments or outcomes (e.g., Sjogren’s syndrome) are not excluded.
- •12. Other major physical
研究者
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