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Atossa Therapeutics Reports Fourth Quarter and Year-End 2025 Financial Results and Provides a Corporate Update

Atossa's operating expenses rose 34% to $37.1 million driven by R&D and legal fees; FDA granted Rare Pediatric Disease and Orphan Drug designations for (Z)-endoxifen.

  • On Wednesday, March 25, 2026, Atossa Therapeutics Inc released its quarterly and annual figures. This report offers an update on corporate developments and clinical milestones achieved by the company.
  • Dr. Steven Quay, CEO, concluded, "We believe we are well-positioned to execute and advance our clinical programs toward key value-creating milestones." The company is developing -endoxifen for Duchenne Muscular Dystrophy and McCune-Albright Syndrome.
  • Financial disclosures show a consolidated net loss of $10.4 million for the year ended December 31, 2025. Total operating expenses reached $37.1 million during this period as the company executed its clinical development strategy.
  • Separately, COSCIENS Biopharma Inc filed an application on March 23, 2026, regarding insolvency proceedings for its German subsidiaries. This strategic decision follows the company's efforts to cease funding these international operations.
  • MediPharm Labs Corp will release its financial results on Monday, March 30, 2026. Management expects to host a conference call to discuss these performance metrics with investors and the public.
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Atossa Therapeutics Reports Fourth Quarter and Year-End 2025 Financial Results and Provides a Corporate Update

SEATTLE, March 25, 2026 /PRNewswire/ -- Atossa Therapeutics, Inc. (Nasdaq: ATOS) (Atossa or the Company), a clinical-stage biopharmaceutical company developing novel therapies in oncology and other areas of high unmet clinical need, today announces its financial results for the fourth…

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MSN broke the news in United States on Wednesday, March 25, 2026.
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