Atossa Therapeutics (ATOS) Receives Authorization from FDA t

Atossa Therapeutics (ATOS) Receives Authorization from FDA to Initiate its Phase 2 Study of Neoadjuvant (Z)-endoxifen in Premenopausal Women with ER+/HER2- Breast Cancer

Atossa Therapeutics (ATOS) Receives Authorization from FDA to Initiate its Phase 2 Study of Neoadjuvant (Z)-endoxifen in Premenopausal Women with ER+/HER2- Breast Cancer
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