EUCTR2021-001671-16-IT进行中（未招募）1 期
A multicenter, open-label, Phase IIb study to evaluate the efficacy, safety and pharmacokinetics of rilzabrutinib in patients with warm autoimmune hemolytic anemia - .
SANOFI-AVENTIS RECHERCHE E DEVELOPPEMENT0 个研究点目标入组 25 人开始时间: 2021年10月12日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 25
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
- •- Male and female patients with a confirmed diagnosis of primary wAIHA or systemic lupus erythematosus (SLE)-associated wAIHA (without other SLE-related manifestations apart from cutaneous and musculoskeletal manifestations)
- •- Participants who have previously failed to maintain a sustained response after treatment with corticosteroids.
- •- Eastern Cooperative Oncology Group (ECOG) performance status grade 2 or lower.
- •- Up-to-date vaccination status as per local guidelines.
- •- Body mass index (BMI) >17.5 and <40 kg/m2
- •- All contraceptive use by men and women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
- •Part B only
- •- Evidence of treatment efficacy to rilzabrutinib as defined by achieving overall response during Part A.
- •- Completion of Part A treatment period (24 weeks).
- •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 15
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 10
排除标准
- •- Clinically significant medical history or ongoing chronic illness that would jeopardize the safety of the participant or compromise the quality of the data derived from his or her participation in the study as determined by the Investigator.
- •- Participants with medical history of lymphoma, leukemia, or any malignancy within the past 5 years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of metastatic disease for the past 3 years.
- •- Secondary wAIHA from any cause including drugs, lymphoproliferative disorders (low-count monoclonal B-cell lymphocytosis is allowed), infectious or autoimmune disease, or active hematologic malignancies.
- •Participants with positive antinuclear antibodies but without a definitive diagnosis of an autoimmune disease are allowed.
- •- Myelodysplastic syndrome.
- •- Uncontrolled or active HBV infection: Patients with positive HBsAg and/or HBV DNA.
- •- HIV infection.
- •- Concurrent treatment with other experimental drugs or participation in another clinical trial with any investigational drug within 30 days or 5 half-lives, whichever is greater, prior to treatment start.
- •- Known allergy to any of the study medications, their analogues, or excipients in the various formulations of any agent.
- •Part B only
- •- Participants who receive any therapy during Part A known to be active in wAIHA.
- •- Presence of unacceptable side effect(s) or toxicity associated with rilzabrutinib such that there is an unfavorable risk-benefit assessment for continued treatment with rilzabrutinib in the opinion of the Investigator and/or Sponsor.
研究者
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