DMD is caused by pathogenic variants in the DMD gene that result in absent or deficient dystrophin. Progressive muscle damage leads to weakness and, over time, cardiac and respiratory complications. Advances in multidisciplinary care have improved outcomes, but DMD remains a serious, life-limiting disease with substantial unmet need.
Atossa is evaluating (Z)-endoxifen as a potential mutation-agnostic therapy—that is, an approach whose activity would not depend on a specific DMD genetic variant.
Estimated people living with DMD worldwide
Estimate people living with DMD in the U.S
Many children with DMD use wheelchairs by the age of 12
Most patients experience shortened lifespans and may pass away in their 20s

Infographic ©2025 CureDuchenne
Current DMD Treatments VS Atossa Therapeutics’ Endoxifen Program
Currently available treatments:
The program currently includes:
In preclinical DMD models, Atossa has reported improvements in measures including muscle strength and markers of muscle injury. These findings have not yet established clinical benefit in patients.