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临床试验/DRKS00023867
DRKS00023867已完成不适用

A Multinational Observational Registry Collecting Data on safety and efficacy profile of Patients with Chronic Hepatitis D Virus Infection Receiving Treatment with Bulevirtide - MYR-Reg-02

MYR GmbH0 个研究点目标入组 45 人开始时间: 2021年2月4日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
MYR GmbH
入组人数
45

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • 1. HBsAg-positive, adult (=18 years) patients who have been diagnosed with chronic HDV infection according to current EASL/ AASLD treatment guidelines, confirmed by respective documentation in the patients’ medical records.
  • 2. Patients currently receiving treatment with bulevirtide (trade name: Hepcludex®) according to the current version of the SmPC; or for whom the decision to start treatment with BLV according to the current version of the SmPC has been taken and treatment initiation is planned; or patients who previously received treatment with BLV according to the previously valid version of the SmPC (not in the framework of a clinical trial).
  • 3. Patients who have provided written informed consent or non-opposition according to local requirements.

排除标准

  • Patients cannot be enrolled into the study if they are currently participating in a clinical trial with experimental treatment.

研究者

发起方
MYR GmbH

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