EB Research Partnership
  • Epidermolysis Bullosa
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EB Research Partnership is dedicated to finding a cure, and finding it quickly.
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OUR STORY

At EBRP, we have one bold audacious goal: heal and cure EB by 2030. In the process, we’re pioneering a model that can benefit the more than 400 million people affected by a rare disease. We are proud of the progress being made towards achieving that goal and more inspired than ever to continue advancing life-saving treatments and cures for EB families across the globe.
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OUR IMPACT

Epidermolysis Bullosa (EB) is a rare and life-threatening genetic skin disorder that affects children from birth.
About eb
We're building a faster path to heal EB. Our innovative model puts speed in the system to find cures quickly.
OUR MODEL
Committed to financial responsibility. With the highest charity ratings, we ensure your dollars  make an impact.
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LIFE WITH EB
Click on the photos to read each child's story.
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SALIM: DYSTROPHIC EB
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CLARA: EB SIMPLEX
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RYAN: JUNCTIONAL EB
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EB Research Partnership

244 Madison Ave Ste 104
New York, NY 10016 
[email protected]
646-844-0902
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COPYRIGHT @2025 EB RESEARCH PARTNERSHIP. ALL RIGHTS RESERVED. EB RESEARCH PARTNERSHIP IS A 501(C)(3) NON PROFIT.

  • Epidermolysis Bullosa
    • What is EB?
    • Life with EB
    • Resources
  • Research
    • Our Impact
    • Scientific Advisory Board
    • Clinical Trials >
      • Filsuvez
      • Vyjuvek
      • ZEVASKYN
    • Town Halls
    • Apply for a Grant
  • Get Involved
    • Donate
    • Sponsor
    • EB Active
    • Events
    • The Effect
    • Shop
    • Give Cryptocurrency
    • Give Stocks
    • Give through Donor Advised Funds (DAF)
    • Accelerator Fund
  • Media
    • Matter of Time Film
    • Press
    • Videos
  • About Us
    • Our Mission
    • Financials
    • Venture Philanthropy
    • Supporter Spotlights
    • Leadership >
      • Board of Directors
      • Staff
  • Donate