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Two female EB researchers working in a lab.

Welcome to the EB-Research Network

The EB-Research Network is a network of patient organisations working together and in cooperation with partners to develop and deliver effective therapies for all people living with Epidermolysis Bullosa (EB).

About the network Funding possibilities

You can find an overview of ongoing and completed EB research projects, most funded by EB-ResNet members, here.

See our project list

EB-ResNet funds research via its member organisations and in collaboration with partners. Last research call closed 6. April 2020.

Upcoming calls
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EB 2020 – London, UK

From 19 - 23 January 2020 the first Global Congress on Epidermolysis Bullosa, the EB 2020 Congress, took place in London. Together we can do more!

More details.

Our network & partners

Collaborating to focus resources and expertise in EB research and its clinical translation to create effective treatments for people with EB. EB-ResNet works on behalf of its members, including DEBRA and other member patient organisations. EB-ResNet also works with other charities and individuals and in partnership with industry and healthcare providers to expedite the development and delivery of effective therapies.


Our network & partners

EB-ResNet provides a portal for information on unmet needs in fundamental and clinical EB research, ongoing clinical trials, and research funding opportunities. We welcome your interest in joining us in tackling the challenges and exciting opportunities of EB research and clinical translation.

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