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FDA Grants Fast Track Status to Aegle Therapeutics’ AGLE-102 for the Treatment of Dystrophic Epidermolysis Bullosa

10/01/20 The U.S. Food and Drug Administration (FDA) has granted Fast Track designation to AGLE-102™ for the treatment of patients with DEB. Evangelos Badiavas, MD, PhD, Chief Scientific Officer at Aegle Therapeutics said, “This designation will expedite the development and regulatory review of AGLE-102 and highlights the importance…

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