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Atossa Therapeutics Receives Approval From Swedish Regulators To Initiate Phase 2 Clinical Study Of Oral Endoxifen To Reduce Mammographic Breast Density


Benzinga | Jun 11, 2021 09:03AM EDT

Atossa Therapeutics Receives Approval From Swedish Regulators To Initiate Phase 2 Clinical Study Of Oral Endoxifen To Reduce Mammographic Breast Density

Atossa Therapeutics, Inc. (NASDAQ:ATOS), a clinical-stage biopharmaceutical company seeking to discover and develop innovative medicines in oncology and infectious disease with a current focus on breast cancer and COVID-19, announces that it has received approval from the Swedish Medical Product Agency (MPA) to initiate a Phase 2 clinical study of its oral Endoxifen for the reduction of mammographic breast density (MBD). MBD is an emerging public health issue affecting more than 10 million women in the United States and many more worldwide. Studies conducted by others have shown that MBD reduces the ability of mammograms to detect cancer (sensitivity) and increases the risk of developing breast cancer. Additional studies show a correlation between reducing MBD and a reduction in the incidence of breast cancer.






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