• Skip to main content
  • Skip to footer
VIEW MENUMENU
  • Pachyonychia Congenita
        • What Is Pachyonychia Congenita?
          • Could I Have PC?
          • Getting Diagnosed
          • Genetics
          • Image Library
          • Glossary
          • Brochures
          • Patient Stories
        • Patient Registry (IPCRR)
          • Patient Registry Data
        • Understanding my Genetic Testing Results
          • K6a-pEDD-PC
          • K6b-pEDD-PC
          • K6c-pEDD-PC
          • K16-pEDD-PC
          • K17-pEDD-PC
          • Non-PC Palmoplantar EDDs
        • Managing and Caring For PC
          • Tips and Tools
          • Living With PC
          • PC & Children
          • Working With Medical Professionals
          • Family & Friends: How To Help
          • Video Library
  • For Professionals
        • For Professionals
          • International PC Consortium
          • Pharmaceutical Partners
          • Refer a Patient
          • Patient Registry (IPCRR)
            • Patient Registry Data
            • Non-PC Palmoplantar EDDs
          • Advocacy Partners
        • PC Research
          • Apply for a Grant
          • Awarded Grants
          • Published Research Articles
          • Clinical Trials
        • Patient Voices
          • Quality of Life
          • Patient Stories
          • Patient-Focused Drug Development Meeting
  • Ways To Give
        • Ways You Can Give
          • Donate
          • Donate Just Giving UK
          • Steady Relief Circle
          • Donor-Advised Fund
          • Giving Stock
          • Legacy Society
        • Raise Awareness
          • How You Can Help
          • Fundraising Ideas
          • Share Your Story
          • PC Advocates
          • Volunteer
        • 2025 Donor Gratitude Wall
  • News & Events
        • News
          • Current Newsletter
          • Newsletter Archives
          • Sign up for our Newsletter
        • Events
          • Patient Support Meetings
          • IPCC Meetings
          • Video Library
  • About Us
        • About PC Project
        • Medical and Scientific Advisory Board
        • Financial & Legal Information
        • Contact Us

Grants Awarded for Pachyonychia Congenita Research Projects

November 5, 2024

PC Project is pleased to announce the award recipients of the 2024 PC Research Grant cycle, with nearly $350,000 worth of proposals funded for PC-specific research projects.

Each submission was independently reviewed and scored by members of PC Project’s IPCC Research Committee, and then all were discussed at length in a group meeting for final recommendations to the PC Project Board of Trustees for funding.

Thank you to all the scientists who applied. Because PC is so rare, we sincerely appreciate the interest of researchers who are willing to dedicate time, labor, and expertise to advancing our knowledge of PC and to actively exploring avenues to find effective treatments and eventually a cure for PC and other conditions that cause painful PPKs. This includes all who are not funded, specifically by PC Project, but who still dedicate their efforts to finding solutions for our patients who suffer from so much pain.

Special thanks to the generous donors who are making these vital research projects possible.

Awarded a one-year, $100,000 grant from Pachyonychia Congenita Project. Project Title: Keratin 16 provides a new paradigm for keratin function in palmoplantar skinPrincipal…

Continue Reading Pierre Coulombe: 2025 PC Grant Award Recipient

Awarded a one-year, $19,950 grant from Pachyonychia Congenita Project. Pachyonychia congenita and palmoplantar disorders are rare, painful, and inherited skin and nail disorders.…

Continue Reading Sajid Malik: 2025 PC Grant Award Recipient

Awarded a one-year, $100,000 grant from Pachyonychia Congenita Project. To thoroughly understand pachyonychia congenita, this disease ought to be studied in models. A…

Continue Reading Jiang Chen: 2025 PC Grant Award Recipient

Awarded a two-year, $145,447 grant from Pachyonychia Congenita Project. Pachyonychia congenita (PC) is a rare genetic skin condition that causes thick, painful skin…

Continue Reading Alain Hovnanian: 2025 PC Grant Award Recipient

Footer

PC Project logo in white
PACHYONYCHIA CONGENITA PROJECT

P.O. Box 17850
Holladay, UT 84117

info@pachyonychia.org

801-987-8758

EIN 68-0567493

  • Facebook
  • Instagram
  • LinkedIn
  • Twitter
  • YouTube

Sign up for our Newsletter

Loading

Support PC Project

There are many ways you can help improve the lives of those who suffer from Pachyonychia Congenita.

Learn More
  • Contact Us
  • About Us
  • Donate
  • Patient Registry