Atossa Therapeutics (ATOS) announced it has requested a Type C meeting with the U.S. Food and Drug Administration, FDA, to discuss a regulatory strategy aimed at accelerating development of low-dose (Z)-endoxifen for breast cancer risk reduction. Atossa is a clinical-stage biopharmaceutical company developing new approaches in breast cancer treatment and risk-reduction, commonly termed prevention of breast cancer.
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Read More on ATOS:
- Atossa Therapeutics Receives Nasdaq Non-Compliance Notice
- Atossa selects PSI for Z-endoxifen monotherapy study
- Buy Rating for Atossa Therapeutics: Strong Financials and Promising Endoxifen Developments
- Atossa Therapeutics Advances Breast Cancer Treatments
- Positive FDA Feedback and Promising Phase 2 Results Justify Buy Rating for Atossa Therapeutics
