Mission and Values

By curing pathologies that affect the minority, we solve the problems of the majority.

Our Mission

Atrema therapeutics is a gene therapy company that treats rare hereditary vision diseases in order to normalize the quality of life not only for patients themselves, but also their loved ones.

We understand that genetic loss of vision is a great tragedy for patients, as well as their families. By creating gene therapy drugs that can stop vision loss in patients with congenital eye pathologies, we not only make the patients happier, but also help the people around them. Thus, by curing pathologies that affect the minority, we solve the problems of the majority.

What we do

Gene Therapy

Development of genetic and cell therapies for ophthalmological hereditary disease.

rAAV viral vectors

We use recombinant AAV viral vectors for safe delivery of genetic material to specific eye tissues to minimize side effects.

Biotech advancement

Global development of safe and effective genetic technologies for the benefit of humanity.

Hereditary disease affects millions of people worldwide. We work to treat inherited rare diseases through gene therapy to save the vision of our patients, so that people with hereditary eye diseases can live full lives.

Dr. Pavel VolchkovChief Scientific Officer

Subscribe to our newsletter