CUMBERLAND PHARMACEUTICALS TO ANNOUNCE 2025 ANNUAL FINANCIAL RESULTS & COMPANY UPDATE
Rhea-AI Summary
Cumberland Pharmaceuticals (Nasdaq: CPIX) will report its 2025 annual financial results and provide a company update after market close on March 3, 2026. A conference call is scheduled for March 3 at 4:30 p.m. ET with a replay available for one year.
The company highlighted its FDA-approved hospital, gastroenterology and oncology portfolio and noted ongoing Phase II trials for ifetroban in systemic sclerosis, DMD cardiomyopathy and idiopathic pulmonary fibrosis.
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Negative
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Key Figures
Market Reality Check
Peers on Argus
CPIX was down 1.54% ahead of its earnings-date news, while key peers were mixed: DRRX (-1.04%), RMTI (-3.06%), CRDL (-3.32%), INCR (-3.41%), and ASRT (+2.56%). Momentum scanner only flagged SCYX (+10.36%), indicating stock-specific rather than broad sector-driven action.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| 2026-02-04 | Fast Track designation | Positive | +4.0% | FDA Fast Track Designation for ifetroban in DMD heart disease. |
| 2025-12-08 | Reimbursement update | Positive | -9.2% | Caldolor J-code linked to reimbursement price for non-opioid pain management. |
| 2025-11-04 | Revenue update | Positive | -3.6% | Reported Q3 and YTD 2025 revenue growth and asset/liability position. |
| 2025-10-28 | Earnings date notice | Neutral | -1.5% | Announcement of Q3 2025 results release and conference call timing. |
| 2025-10-20 | Portfolio expansion | Positive | +3.5% | Talicia co-commercialization joint venture and long-dated IP protections. |
Recent CPIX news often produced mixed or negative next-day moves, even on operationally positive updates, indicating a tendency toward price divergence from headline tone.
Over the last several months, Cumberland reported Q3 2025 revenues of $8.3M and year‑to‑date revenues of $30.8M, reflecting 12% growth versus the prior year’s first nine months. It expanded its portfolio via a Talicia co‑commercialization deal effective Oct 20, 2025 and secured a reimbursement‑linked J‑code for Caldolor on Dec 8, 2025. More recently, oral ifetroban for DMD heart disease received FDA Fast Track designation on Feb 4, 2026. Today’s earnings‑date announcement follows this steady stream of clinical and commercial developments.
Market Pulse Summary
This announcement schedules release of Cumberland’s 2025 annual financial results and a company update for March 3, 2026, along with a conference call and one‑year replay. It follows prior milestones like FDA Fast Track designation for ifetroban and expansion via Talicia and Caldolor initiatives. Investors may focus on revenue trends, cash levels, and progress in Phase II ifetroban programs as key markers of execution and future optionality.
Key Terms
transdermal system medical
euvolemic medical
hypervolemic medical
hyponatremia medical
Systemic Sclerosis medical
Idiopathic Pulmonary Fibrosis medical
H. pylori infection medical
AI-generated analysis. Not financial advice.
A conference call will be held on March 3 at 4:30 p.m. Eastern Time to discuss the results and update.
The link to register is https://register-conf.media-server.com/register/BI6effc1a9cae9445f9bb0d60817870ffa.
Once registered, participants can dial in from their phone using a dial-in and PIN number that will be provided to them. Alternatively, they can choose a "Call Me" option to have the system automatically
call them at the start of the conference.
A replay of the call will be available for one year and can be accessed via the Investor Relations page of Cumberland's website or by visiting https://edge.media-server.com/mmc/p/w5m9usns.
Cumberland Pharmaceuticals is a specialty pharmaceutical company dedicated to providing unique
products that improve patient care. The company develops, acquires, and commercializes products for the hospital acute care, gastroenterology and oncology market segments.
The company's portfolio of FDA-approved brands includes:
- Acetadote® (acetylcysteine) injection, for the treatment of acetaminophen poisoning;
- Caldolor® (ibuprofen) injection, for the treatment of pain and fever;
- Kristalose® (lactulose) for oral solution, a prescription laxative, for the treatment of constipation;
- Sancuso® (granisetron) transdermal system, for the prevention of nausea and vomiting in patients receiving certain types of chemotherapy treatment;
- Vaprisol® (conivaptan) injection, to raise serum sodium levels in hospitalized patients with euvolemic and hypervolemic hyponatremia;
- Vibativ® (telavancin) injection, for the treatment of certain serious bacterial infections including hospital-acquired and ventilator-associated bacterial pneumonia, as well as complicated skin and skin structure infections; and
- Talicia® (omeprazole, amoxicillin and rifabutin) oral capsule, for the treatment of H. pylori infection.
The Company also has a series of Phase II clinical programs underway evaluating its ifetroban product candidate in patients with Systemic Sclerosis, the cardiomyopathy associated with Duchenne Muscular Dystrophy and Idiopathic Pulmonary Fibrosis.
For more information on Cumberland's approved products, including full prescribing information, please visit links to the individual product websites, found on the company's website at www.cumberlandpharma.com.
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SOURCE Cumberland Pharmaceuticals Inc.