Accelerating affordable access to the most effective gene therapy treatments for children with ultra-rare diseases.
Accelerating affordable access to the most effective gene therapy treatments for children with ultra-rare diseases.
CCF is an international childhood rare disease fund aimed at accelerating the most effective cures for children with ultra-rare diseases. We use a nonprofit model to advance programs for small patient populations because pharmaceutical companies cannot justify the investment, yet there are clinically promising cures on the horizon. We aim to ensure equitable access to life-saving genetic medicine for children with ultra-rare diseases so no children are left behind when science can put a cure in reach.