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Business News | FDA Approves Direct Biologics to Proceed with a Landmark Phase 3 Acute Respiratory Distress Syndrome (ARDS) Trial

Get latest articles and stories on Business at LatestLY. Direct Biologics, a regenerative biotechnology company with a groundbreaking extracellular vesicle (EV) platform technology, announced today that the FDA has approved the company to proceed with its Phase 3 clinical trial using its investigational EV drug, ExoFlo, to treat Acute Respiratory Distress Syndrome (ARDS) due to Covid-19. Direct Biologics is the first and only EV company to receive FDA Phase 3 approval for an Investigational New Drug (IND) indication to date. Business News | FDA Approves Direct Biologics to Proceed with a Landmark Phase 3 Acute Respiratory Distress Syndrome (ARDS) Trial.

New Landmark Trial for Phase 3 Acute Respiratory Distress Syndrome

Direct Biologics announced today that the FDA has approved the company to proceed with its Phase 3 clinical trial using its investigational EV drug, | New Landmark Trial for Phase 3 Acute Respiratory Distress Syndrome

FDA approves Direct Biologics to proceed with a Landmark Phase 3 Acute Respiratory Distress Syndrome (ARDS) Trial

FDA approves Direct Biologics to proceed with a Landmark Phase 3 Acute Respiratory Distress Syndrome (ARDS) Trial
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FDA approves Direct Biologics to proceed with a Landmark Phase 3 Acute Respiratory Distress Syndrome (ARDS) Trial

FDA approves Direct Biologics to proceed with a Landmark Phase 3 Acute Respiratory Distress Syndrome (ARDS) Trial
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