Acer therapeutics and relief therapeutics announce submission of a new drug application to the u.s. fda for acer-001 for treatment of urea cycle disorders

Newton, mass. and geneva, aug. 09, 2021 (globe newswire) -- acer therapeutics inc. (nasdaq: acer) (“acer”), a pharmaceutical company focused on the acquisition, development and commercialization of therapies for serious rare and life-threatening diseases with significant unmet medical needs, and relief therapeutics holding ag (six: rlf, otcqb: rlftf) (“relief”), a biopharmaceutical company seeking to provide patients therapeutic relief from serious diseases with high unmet need, today announced the submission of a new drug application (nda) to the u.s. food and drug administration (fda) for acer-001 (sodium phenylbutyrate) for the treatment of urea cycle disorders (ucds). acer-001 is a nitrogen-binding agent in development for use as adjunctive therapy in the chronic management of patients with ucds involving deficiencies of carbamylphosphate synthetase (cps), ornithine transcarbamylase (otc), or argininosuccinic acid synthetase (as).
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