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Cumberland Pharmaceuticals (CPIX) investor relations material
Cumberland Pharmaceuticals Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Year-to-date revenue grew 12% to $30.9 million for the first nine months of 2025, with Q3 net revenues at $8.3 million and a net loss of $1.9 million for the quarter.
Added Talicia, an FDA-approved H. pylori treatment, to the portfolio via a joint venture with RedHill Biopharma, forming Talicia Holdings, Inc. and investing up to $4 million.
Launched Vibativ in Saudi Arabia, secured regulatory approvals in China and Mexico, and expanded access through Premier and Vizient agreements.
Advanced clinical pipeline, notably ifetroban for Duchenne muscular dystrophy, systemic sclerosis, and idiopathic pulmonary fibrosis, with positive Phase II DMD results.
Sancuso and Vibativ were key growth drivers, offsetting declines in Kristalose and Caldolor.
Financial highlights
Q3 2025 net revenues were $8.3 million; year-to-date revenues reached $30.9 million, up 12% year-over-year.
Adjusted Q3 loss was $0.8 million ($0.06/share); adjusted nine-month earnings were $1.9 million ($0.13/share).
Net loss for Q3 was $1.9 million; year-to-date net loss was $1.4 million.
Cash flow from operations for 2025 was $5 million; cash and cash equivalents at quarter-end were $15.2 million.
Q3 product revenue: Sancuso $3.2M, Vibativ $2.6M, Kristalose $1.2M, Caldolor $0.9M.
Outlook and guidance
Management anticipates continued momentum from new product launches, expanded international partnerships, and clinical progress.
Expects Q4 to be the strongest quarter due to customer purchasing patterns.
Focus remains on expanding the commercial portfolio and advancing clinical programs for orphan diseases.
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