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Cumberland Pharmaceuticals Reports 11.6% Fourth Quarter 2024 Revenue Growth
CPIXCumberland Pharmaceuticals(CPIX) Prnewswire·2025-03-04 21:05

Core Insights - Cumberland Pharmaceuticals Inc. reported a net revenue of 10.4millionforQ42024,markingan11.610.4 million for Q4 2024, marking an 11.6% increase year-over-year, with total annual revenues reaching 38 million [1][9] - The company ended 2024 with total assets of 76million,including76 million, including 18 million in cash and 53millioninliabilities[2][12]CEOA.J.Kazimihighlighted2024asatransformativeyearwithexpandedproductlabeling,keyFDAdesignations,andnewstudypublications[3]FinancialPerformanceForthefullyear2024,netrevenueswere53 million in liabilities [2][12] - CEO A.J. Kazimi highlighted 2024 as a transformative year with expanded product labeling, key FDA designations, and new study publications [3] Financial Performance - For the full year 2024, net revenues were 38 million, with significant contributions from Kristalose® (15.3million),Sancuso®(15.3 million), Sancuso® (9 million), Vibativ® (7.2million),andCaldolor®(7.2 million), and Caldolor® (5 million) [9] - Total operating expenses for 2024 were 44million,resultinginanetlossofapproximately44 million, resulting in a net loss of approximately 6.4 million for the year [9][11] - The adjusted loss for the year was $1 million, excluding certain costs related to product acquisitions [11] Product Developments - The FDA granted Orphan Drug and Rare Pediatric Disease designations for ifetroban, aimed at treating cardiomyopathy in Duchenne muscular dystrophy [3] - New research published demonstrated Caldolor's safety and healthcare resource advantages over ketorolac in both adult and pediatric populations [4] - A simplified dosing regimen for Acetadote® was approved by the FDA, enhancing the efficiency of administration [6] Clinical Trials and Studies - Cumberland made significant progress in Phase II clinical trials for ifetroban, closing studies in Duchenne muscular dystrophy and nearing completion in systemic sclerosis and pulmonary fibrosis [8] - The company provided 3.9 million doses of FDA-approved products to patients in 2024 and reported no product recalls [7] Market Expansion - Vibativ® received approval in China, expanding Cumberland's international business, alongside shipments to Saudi Arabia [10]