Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact
Recruiting Phase 3

A Phase 3 Clinical Study of MIL62 in Systemic Lupus Erythematosus

NCT07405970 · tracked via the Priya Life Science China tracker
Phase
Phase 3
Started
2026-04-10
Last updated
2026-05-05

Condition(s) studied

Systemic Lupus Erythematosus

Investigational drug(s) / intervention(s)

MIL62 →Placebo

MIL62: MIL62 will be administered by intravenous (IV) infusion at a dose of 1000 mg on Week (W) 1 Day (D) 1, W3D1, W25D1, W27D1.

Placebo: Placebo will be administered by intravenous (IV) infusion at a dose of 1000 mg on W1D1, W3D1, W25D1, W27D1.

Study summary

This study will evaluate the efficacy and safety of MIL62 compared with placebo in participants with systemic lupus erythematosus.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: 1. Age 18-80 ; 2. Diagnosis of systemic lupus erythematosus according to European League Against Rheumatism/American College of Rheumatology (EULAR/ACR) SLE classification criteria ; 3. Positive antinuclear antibodies (ANA) ≥ 1:80 at screening or positive anti- dsDNA ; 4. High disease activity at screening ,SLEDAI-2000 score ≥8 (excluding alopecia score); 5. On a stable dose of one or more standard treatments for SLE prior to the first administration; 6. Able and willing to provide written informed consent and to comply with the study protocol. Exclusion Criteria: 1. Unsufficient organ function; 2. Received rituximab or any B-cell depleting drug within 9 months prior to the first dose; 3. Subjects with CD4+ T lymphocyte count \< 200 cells/μL; 4. Received cyclophosphamide within 8 weeks prior to the first dose; received calcineurin inhibitors (cyclosporine, tacrolimus, etc., except for topical use) or plasma exchange therapy within 4 weeks prior to the first dose; 5. Received a B-cell stimulating factor inhibitor such as Belimumab, and Telitacicept within 8 weeks prior to the first administration; 6. TNF inhibitor, interleukin monoclonal antibody, JAK inhibitor, BTK inhibitor, TYK2 inhibitor, or thalidomide within 4 weeks prior to the first administration; 7. Received live or attenuated vaccination within 28 days prior to the first administration; 8. Participated in other clinical trials within 28 days prior to the first administration; 9. Concomitant with other serious diseases; 10. Positive for hepatitis B surface antigen (HBsAg) and/or hepatitis B core antibody (HBcAb) with HBV DNA titer above the normal range; positive for hepatitis C virus (HCV) antibody; positive for human immunodeficiency virus (HIV); 11. Subjects with known history of severe allergic reactions to humanized monoclonal antibodies MIL62; 12. Breastfeeding or pregnant women; 13. Childbearing potential and unwillingness or impossibility to comply with a scientifically acceptable birth-control method; 14. Other conditions unsuitable for participation in this study determined by the Investigator.

Primary outcome measure(s)

  • Percentage of participants achieving SRI-4 at Week 52 — at Week 52

Trial sites (1)

FacilityCityRegionStatus
Peking University People's Hospital Beijing China Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07405970 on ClinicalTrials.gov ↗ ← All trials in China