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临床试验/jRCT2033260131
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

发起方
未提供

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