跳至主要内容
临床试验/CTIS2024-511164-92-00
CTIS2024-511164-92-00招募中1 期

A Phase 2/3, Multicenter, randOmized, Double-blind, placebo-controlled, stUdy to evaLuate the safety and efficacy of Alpha-1 AntiTrypsin for the prEvention of graft versus-host disease in patients receiving hematopoietic cell transplant (MODULAATE Study) - CSL964_2001

CSL Behring LLC0 个研究点目标入组 310 人开始时间: 2024年4月29日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
入组人数
310

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
0 至 65+(—)
性别
All

入选标准

  • Male or female subjects, =12 years of age (= 18 years of age for subjects at German sites only), undergoing HCT for hematological malignancies, including leukemia, lymphoma multiple myeloma, myelodysplastic syndrome and myeloproliferative neoplasms., Planned myeloablative conditioning regimen.

排除标准

  • Prior autologous or allogeneic HCT., T-cell depleted transplant or planned use of anti-T cell antibody therapy either ex vivo or in vivo (ie, anti-thymocyte globulin [ATG], alemtuzumab) for GVHD prophylaxis., Planned umbilical cord blood transplant.

研究者

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