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临床试验/EUCTR2020-000713-32-BE
EUCTR2020-000713-32-BE进行中(未招募)1 期

A Phase 3, Double-Blind, Multicenter Study to Evaluate the Efficacy and Safety of CAEL-101 and Plasma Cell Dyscrasia Treatment Versus Placebo and Plasma Cell Dyscrasia Treatment in Plasma Cell Dyscrasia Treatment-Naïve Patients with Mayo Stage IIIa AL Amyloidosis

Caelum Biosciences, Inc.0 个研究点目标入组 267 人开始时间: 2020年11月9日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
267

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

  • Key Inclusion Criteria:
  • 1. AL amyloidosis stage IIIa based on the 2013 European Modification of the 2004 Standard Mayo Clinic Staging in patients with advanced cardiac involvement at the time of
  • 2. Measurable hematologic disease at Screening as defined by at least one of the following:
  • a. Involved/uninvolved free light chain difference (dFLC) > 4 mg/dL or
  • b. Involved free light chain (iFLC)> 4 mg/dL with abnormal ratio or
  • c. Serum protein electrophoresis (SPEP) m-spike > 0.5 g/dL
  • 3. Histopathological diagnosis of amyloidosis based on polarizing light microscopy of green bi-refringent material in Congo red stained tissue specimens AND confirmation of
  • AL derived amyloid deposits by at least one of the following:
  • a. Immunohistochemistry or
  • b. Mass spectrometry or
  • c. Characteristic electron microscopy appearance
  • 4. Cardiac involvement as defined by:
  • a. Documented clinical signs and symptoms supportive of a diagnosis of heart failure in the setting of a confirmed diagnosis of AL amyloidosis in the absence
  • of an alternative explanation for heart failure
  • b. At least one of the following:
  • i. Endomyocardial biopsy demonstrating AL cardiac amyloidosis or
  • ii. Echocardiogram demonstrating a mean left ventricular wall thickness (calculated as [IVSd+LPWd]/2) of > 12 mm at diastole in the absence of other
  • causes (e.g., severe hypertension, aortic stenosis), which would adequately explain the degree of wall thickening or
  • iii. Cardiac magnetic resonance imaging (MRI) with gadolinium contrast agent diagnostic of cardiac amyloidosis
  • 5. Planned first-line treatment for plasma cell dyscrasia is cyclophosphamide-bortezomibdexamethasone (CyBorD)-based regimen administered as SoC.
  • 6. WOCBP must have a negative pregnancy test during Screening and must agree to use highly effective physician approved contraception (Section 6.9) from Screening to 90 days at
  • least 5 months following the last study drug administration or 12 months following the last dose of her PCD therapy, whichever is longer
  • 7. Men must be surgically sterile or must agree to use effective physician approved contraception (Section 6.9) and refrain from donating sperm from Screening to 90 days
  • at least 5 months following the last study drug administration or 12 months following the last dose of his PCD therapy, whichever is longer
  • 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 160
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 107

排除标准

  • Key Exclusion Criteria:
  • 1. Have any other form of amyloidosis other than AL amyloidosis
  • 2. Received prior therapy for AL amyloidosis or multiple myeloma. A maximum exposure of 160 mg dexamethasone (or equivalent corticosteroid) since diagnosis of AL amyloidosis
  • and prior to randomization is allowed.
  • 3. Meets the International Myeloma Working Group (IMWG) definition of multiple myeloma or POEMS syndrome (plasma cell dyscrasia with polyneuropathy, organomegaly,
  • endocrinopathy, monoclonal protein and skin changes) (Appendix A)
  • 4. Have supine systolic blood pressure < 90 mmHg or symptomatic orthostatic hypotension, defined as a decrease in systolic blood pressure upon standing of > 30 mmHg despite
  • medical management (e.g., midodrine, fludrocortisones) in the absence of volume depletion.

研究者

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