The potential is huge…for all those suffering with a rare disease.

Lindsay Groff
Executive Director
Barth Syndrome Foundation


BioPontis… will form a novel and powerful development machine, hitherto non-existent in the field.

Yann le Cam
CEO
European Organisation
for Rare Diseases


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bridge

We support the nonprofit BioPontis Alliance and its very unique and innovative approach [to] therapy development and building alliances.

Monica Benson
President
Dystonia Europe


Every child with rare disease deserves a treatment.

Margie Frazier
Executive Director
Batten Disease Support
& Research Association