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Soligenix Announces Submission of New Drug Application to the FDA for HyBryteTM in the Treatment of Cutaneous T-cell Lymphoma. #soligenix #hybryte #richtvlive #richtv #lymphoma #stocks #news #business #finance #education #trading #pennystocks

Soligenix, Inc. (Nasdaq: SNGX) (Soligenix or the Company), a late-stage biopharmaceutical company focused on developing and commercializing
products to treat rare diseases where there is an unmet medical need, announced today that it submitted a new drug application (NDA) to the United States (U.S.) Food and Drug Administration (FDA) for HyBryteTM (synthetic hypericin) in the treatment of early stage cutaneous T-cell lymphoma (CTCL), a rare cancer and area of unmet medical need affecting over 25,000 patients in the U.S. The Company estimates the potential worldwide market for HyBryteTM to be in excess of $250 million for the treatment of CTCL.

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