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
European Organisation
for Rare Diseases



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

Monica Benson
Dystonia Europe

Every child with rare disease deserves a treatment.

Margie Frazier
Executive Director
Batten Disease Support
& Research Association