ISRCTN78423540已完成1 期
Serologic response to a new recombinant, adjuvanted herpes zoster vaccine in patients with chronic lymphocytic leukemia and Waldenstrom macroglobulinemia treated with first-line BTK inhibitors
niversity of Rochester0 个研究点目标入组 32 人开始时间: 2023年11月16日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 32
研究概览
简要总结
2023 Results article in https://pubmed.ncbi.nlm.nih.gov/37483138/ (added 16/11/2023)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Patients diagnosed with chronic lymphocytic leukemia (CLL) OR Waldenström macroglobulinemia (WM)
- •2. 50 years of age or older
- •3. Receiving first-line treatment with BTK inhibitor for at least 3 months; prior treatment with single-agent rituximab is permitted if the last dose was administered more than 1 year ago
- •4. Have at least a 1-year life expectancy
- •5. Have a history of varicella (chickenpox) OR lived in the US or any endemic country for >30 years
排除标准
- •1. Known hypersensitivity to a vaccine component
- •2. Herpes zoster reactivation within the past year
- •3. Received or were scheduled to receive a live virus vaccine in the period from 4 weeks prior to Dose 1 through 28 days post-second dose
- •4. Received or were scheduled to receive an inactivated vaccine in the period ranging from 7 days prior to Dose 1 through 7 days post-second dose
- •5. Are unable to give informed consent;
- •6. An absolute lymphocyte count greater than 20,000 x 10e9/L
- •7. Receiving treatment for CLL or WM with an additional agent other than a BTK inhibitor
- •8. Rituximab treatment less than one year prior to study start
- •9. Prior chemotherapy
研究者
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