Acer Therapeutics, Inc. (NASDAQ: ACER) was featured in a recent equity research report published by ROTH Capital Partners LLC. The report reads, “With yesterday's update that ACER-001 showed bioequivalence to the already approved Buphenyl for treatment of UCDs, ACER now has green lights ahead of a planned NDA submission for its taste-masked drug in early 2021. With NDA-bound ACER-001 development on the upswing and the FDRR for EDSIVO in review (submitted Dec. 2019), we believe the follow-through on execution has set ACER up for a strong 2020.”
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About Acer Therapeutics, Inc.
Acer is a pharmaceutical company focused on the acquisition, development and commercialization of therapies for serious rare and life-threatening diseases with significant unmet medical needs. Acer’s pipeline includes three clinical-stage candidates: EDSIVO™ (celiprolol), for the treatment of vascular Ehlers-Danlos syndrome (vEDS) in patients with a confirmed type III collagen (COL3A1) mutation; ACER-001 (a taste-masked, immediate release formulation of sodium phenylbutyrate), for the treatment of various inborn errors of metabolism, including urea cycle disorders (UCDs) and Maple Syrup Urine Disease (MSUD); and osanetant, for the treatment of induced Vasomotor Symptoms (iVMS) where Hormone Replacement Therapy (HRT) is likely contraindicated. Each of Acer’s product candidates is believed to present a comparatively de-risked profile, having one or more of a favorable safety profile, clinical proof-of-concept data, mechanistic differentiation and/or accelerated paths for development through specific programs and procedures established by the FDA.
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