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临床试验/JPRN-UMIN000025368
JPRN-UMIN000025368已完成4 期

A postmarketing all-case surveillance of mogamulizumab in patients with CCR4 positive relapsed or refractory adult T cell lymphoma-leukemia - A postmarketing all-case surveillance of mogamulizumab

Kyowa Kirin Co., Ltd.0 个研究点目标入组 597 人开始时间: 2016年12月22日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
597

研究概览

简要总结

In the safety analysis population, adverse drug reactions (ADRs) were reported in 73.4% (38.6% serious cases) of patients. The most common ADRs were skin disorders (33.2% [10.8% serious cases]), infusion-related reactions (30.1% [4.7% serious cases]), and infections (22.0% [14.7% serious cases]). In the effectiveness analysis population, the best overall response rate and the response rate at the end of therapy were 57.9% and 42.0%, respectively. The median overall survival was 5.5 months.

研究设计

研究类型
Observational

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 未提供

研究者

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