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临床试验/CTIS2023-504975-25-00
CTIS2023-504975-25-00进行中(未招募)1 期

A phase IV, open, non-randomised, low-intervention clinical trial to evaluate the subjective user experience of Zeqmelit™ 6 mg mouth dissolving film for treatment of acute allergic reaction - ZEQ-001

AcuCort AB0 个研究点目标入组 50 人开始时间: 2023年4月20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
50

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
18 至 65+(—)
性别
All

入选标准

  • Male or female patients = 18 years of age, willing and able to give written informed consent for participating in the trial who previously have experienced acute allergic reactions and who is currently prescribed betamethasone tablets for treatment of such reactions.

排除标准

  • Patient who cannot handle a web-based eDiary via their own electronic device (phone, tablet)., Patients with other medical conditions that in the opinion of the Investigator would exclude the patient from trial participation., Patients who are pregnant, currently breastfeeding, or intend to become pregnant during the course of the trial.

研究者

发起方
AcuCort AB

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