跳至主要内容
临床试验/JPRN-jRCT2080224805
JPRN-jRCT2080224805已完成3 期

A Phase 3, open-label study to evaluate NS-32 in subjects with iron deficiency anemia associated with postpartum hemorrhage

ippon Shinyaku Co., Ltd.0 个研究点目标入组 21 人开始时间: 2019年7月29日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
21

研究概览

简要总结

There was a significant difference in the maximum change in hemoglobin concentration from baseline for the primary endpoint. All TEAEs were mild except for the moderate jaundice neonatal reported in 1 neonate and no serious related SAEs were reported.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 39age old(—)
性别
Female

入选标准

  • Patients diagnosed with IDA associated with postpartum heamorrhage

排除标准

  • Patients with anemia due to causes other than iron deficiency

研究者

发起方
ippon Shinyaku Co., Ltd.

相似试验