Postmarketing Safety Study of Hemoporfin in Patients With Port Wine Stain

Status Completed

Clinical Trial Summary

This study is to provide safety information of hemoporfin during the post-marketing period as required by China Food and Drug Administration (CFDA) regulations in order to identify any potential drug related treatment factors in the Chinese population, such as unknown/unexpected adverse reactions, the incidence of adverse reactions under the routine drug uses.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03181984
Study type	Interventional
Source	Shanghai Fudan-Zhangjiang Bio-Pharmaceutical Co., Ltd.
Contact
Status	Completed
Phase	Phase 4
Start date	August 31, 2017
Completion date	April 19, 2023

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See also
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