jRCT2033260131尚未招募不适用
A Phase 3, Randomized, Open-label, Multicenter Study to Compare the Efficacy and Safety of BMS-986353, CD19-targeted NEX-T CAR T Cells, Versus Standard of Care in Participants With Active Systemic Sclerosis (Breakfree-SSc)
未提供0 个研究点目标入组 92 人开始时间: 待定
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 92
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
入排标准
- 年龄范围
- 16age old over 至 No limit(—)
- 性别
- All
入选标准
- •Participants must fulfill the 2013 American College of Rheumatology (ACR) / European League Against Rheumatism (EULAR) classification criteria for Systemic Sclerosis (SSc), and additionally have the following:.
- •i) Positive Antinuclear Antibodies (ANA) with nucleolar pattern and/or anti-Topoisomerase I (anti-Scl-70) antibodies.
- •ii) Confirmation of Interstitial Lung Disease (ILD) on centrally read High-Resolution Computed Tomography (HRCT) with >= 10% total lung involvement, with at least one of the following attributed to active SSc:
- •A. Arthritis.
- •B. Myositis.
- •C. Carditis.
- •D. Progressive skin disease.
- •E. Elevated inflammatory markers.
- •Participants must have a non-response or intolerance despite >= 6 months of treatment with at least one immunomodulatory drug. Non-response is defined as a patient, who in the opinion of the investigator, is not adequately controlled/treated and requires treatment escalation.
排除标准
- •Participants must not have a requirement for supplemental oxygen therapy and/or Diffusing Capacity of the Lungs for Carbon Monoxide (DLCO) =<40% (Hemoglobin (Hgb) corrected) at screening.
- •Participants must not have moderate to severe Pulmonary Arterial Hypertension (PAH) requiring PAH-specific combination treatment.
- •Participants must not have pulmonary comorbidity including chronic obstructive pulmonary disease or asthma requiring daily oral corticosteroids, cigarette smoking (including e-cigarettes) within 3 months before screening or unwilling to avoid smoking throughout the study, and/or clinically significant abnormalities on HRCT not attributable to SSc assessed by the central reader at screening.
- •Participants must not have gastrointestinal (GI) dysmotility requiring Total Parenteral Nutrition (TPN).
- •Participants must not have current gangrene of a digit.
- •Other protocol-defined Inclusion/Exclusion criteria apply.
研究者
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