Lipella pharmaceuticals granted fda approval for expanded access program for lp-310 in oral lichen planus

Pittsburgh, feb. 06, 2025 (globe newswire) -- lipella pharmaceuticals inc. (nasdaq: lipo) (“lipella” or the “company”), a clinical-stage biotechnology company focused on developing innovative therapies for unmet medical needs, today announced that the u.s. food and drug administration (fda) has granted approval for an expanded access program (eap) for lp-310, an oral rinse formulation designed to treat oral lichen planus (olp). lp-310 is an innovative, localized therapy formulated to provide targeted relief for olp patients while minimizing systemic exposure.
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