Investors
Our Goal
Our goal is to advance at least one of our potential therapies to the clinic by 2024. We have yet to reach clinical trials and we’re actively seeking investors to accelerate development.
Our Opportunity
Both gene and cell therapy have the potential to provide long-term benefits for patients with muscular dystrophy by addressing the underlying causes of the disease. However, both approaches are still in the early stages of development and more research is needed to fully realize their potential. Nevertheless, the future of gene and cell therapy for muscular dystrophy is exciting, and further advancements hold promise for the development of effective treatments for these debilitating diseases.
Our Purpose
Our Request
We’ve spent more than 20 years researching these important potential therapies and people are depending on us.
If you know anyone interested in helping us move forward faster, contact us.