Cumberland Pharmaceuticals Reports First Quarter 2024 Financial Results & Company Update
Cumberland Pharmaceuticals Inc. reported $8.5 million in combined revenues for the first quarter of 2024. The company has $82 million in total assets, $54 million in total liabilities, and $27 million in shareholders' equity. Recent developments include a special report on Caldolor, eligibility for Medicare reimbursement under the NOPAIN Act, new manufacturing of Sancuso, and clinical studies on ifetroban. Financially, net revenue was $8.5 million, with a net loss of $1.9 million and adjusted earnings of a $0.6 million loss. Cumberland continues to focus on innovative products for hospital acute care, gastroenterology, and oncology segments.
Cumberland Pharmaceuticals reported a steady start to 2024 with combined revenues of $8.5 million for the first quarter.
The company has $82 million in total assets, showing financial stability and growth potential.
Cumberland's product portfolio includes FDA-approved brands like Caldolor, Sancuso, and Vibativ, offering a diverse range of treatments.
Recent developments, such as the special report on Caldolor and eligibility for Medicare reimbursement under the NOPAIN Act, highlight the company's commitment to innovation and growth.
Cumberland's clinical studies on ifetroban for various conditions demonstrate the company's focus on addressing unmet medical needs and expanding treatment options.
The company reported a net loss of $1.9 million for the first quarter of 2024, with adjusted earnings also showing a loss of $0.6 million.
Total operating expenses for the quarter were $10.4 million, indicating significant costs that impacted the company's financial performance.
Cumberland had $54 million in total liabilities, including $16 million outstanding on its revolving line of credit, which could affect its financial flexibility.
The need for ongoing clinical trials and research to bring ifetroban to market for various conditions represents potential future expenses and risks for the company.
Insights
"It has been a steady start to 2024 – and despite some challenges the biopharmaceutical sector is facing in the financial markets amid stubborn inflation and stalled interest rate cuts, we remain optimistic about our industry's fundamentals and future," said Cumberland's CEO, A.J. Kazimi. "We continue to build our portfolio of innovative and differentiated products here at Cumberland, and our resulting, diversified product line has enabled us to weather external challenges while our team remains responsive to the evolving market. We look forward to sharing an update on our brands, pipeline and partnerships, including a number of growth opportunities."
Recent company developments include:
Caldolor® Special Report
In March 2024, a Special Report was published in Anesthesiology News, General Surgery News and Pharmacy Practice News presenting the growing amount of clinical data supporting the use of Cumberland's Caldolor (ibuprofen) injection as a standard of care for the treatment of pain and fever in adults, children and infants as young as 3 months of age.
Takeaways from the Special Report include:
- Intravenous ibuprofen results in significant reduction in temperature compared with placebo in adults and with acetaminophen in pediatric patients.
- Administration of the product prior to surgery leads to patients waking up in significantly less postsurgical pain, while also lessening or even eliminating the need for opioids.
- The use of intravenous ibuprofen in the hospital emergency department for acute pain can minimize opioid requirements while achieving significant pain control.
- Caldolor should be considered a foundation for any multimodal pain regimen.
Pain management has become one of the most common health care problems. As this Special Report states, comprehensive multimodal pain regimens have become key in preventing pain and optimizing pain control, while minimizing the need for opioids. A non-steroidal anti-inflammatory drug, such as Caldolor, can provide a cornerstone for many treatment paradigms.
Federal NOPAIN Act
Cumberland expects Caldolor will be eligible for special Medicare reimbursement under the Non-Opioids Prevent Addiction in the Nation Act (the "NOPAIN Act"), which was enacted as part of the Consolidated Appropriations Act of 2023.
The NOPAIN Act requires Medicare to provide separate and more favorable reimbursement for non-opioid products used to manage pain during surgeries conducted in hospital outpatient departments or in ambulatory surgical centers. The NOPAIN Act applies, in part, to products that are indicated to provide analgesia without acting upon the body's opioid receptors.
The Centers for Medicare & Medicaid Services ("CMS") requested that manufacturers with potentially applicable non-opioid products submit comments and supporting clinical evidence regarding products that should be eligible for separate payment. Cumberland submitted a comment letter along with the requisite clinical information to the CMS in September 2023 explaining why Caldolor should be included and separately reimbursed. The company now awaits information from CMS regarding the reimbursement status and price for the product.
The Act is scheduled to go into effect in early 2025 and will initially apply to products that are furnished between January 1, 2025 and January 1, 2028.
New Manufacturing & Supplies of Sancuso®
After acquiring
Vaprisol® Supply Update
Cumberland's new manufacturing and distribution partner for Vaprisol is providing a special supply of compounded product in support of critically ill patients. The companies await FDA approval for the facility in order to relaunch the brand.
Vaprisol is the first and only intravenously administered vasopressin receptor antagonist. It is used to raise serum sodium levels in hospitalized patients with hyponatremia, the most common electrolyte disorder among such patients.
Clinical Development Pipeline
Cumberland has been evaluating its ifetroban product candidate, a selective thromboxane-prostanoid receptor antagonist, in a series of clinical studies. It has now been dosed in nearly 1,400 subjects and has been found to be safe and well tolerated in healthy volunteers and various patient populations.
Cumberland has initiated its newest clinical program in medical centers across the country and enrollment has now begun in patients with Idiopathic Pulmonary Fibrosis, the most common form of progressive fibrosing interstitial lung disease. This FIGHTING FIBROSIS trial is designed to enroll 128 patients in over 20 medical centers of excellence across
Patient enrollment is already well underway in its two other company-sponsored Phase II clinical programs evaluating ifetroban in patients with: 1) Systemic Sclerosis, or scleroderma, a debilitating autoimmune disorder characterized by diffuse fibrosis of the skin and internal organs and 2) cardiomyopathy associated with Duchenne Muscular Dystrophy, a rare, fatal, genetic neuromuscular disease results in deterioration of the skeletal, heart and lung muscles.
Cumberland's plan going forward is to complete each of its company-sponsored studies, analyze their final data, announce top-line results and decide on the best development path for the registration of ifetroban, which the company continues to believe has the potential to benefit many patients with orphan diseases that represent unmet medical needs.
FINANCIAL RESULTS:
Net Revenue: For the three months ended March 31, 2024, net revenues were
Net revenue by product for the first quarter of 2024 included
Operating Expenses: Total operating expenses for the first quarter were
Net Income: The net loss for the first quarter of 2024 was
Adjusted Earnings: Adjusted earnings for the first quarter of 2024 were a loss of
Balance Sheet: At March 31, 2024, Cumberland had
Total liabilities were
EARNINGS REPORT CALL:
A conference call will be held on May 7, 2024, at 4:30 p.m. Eastern Time to provide a company update and discuss the financial results. To participate in the call, please register at: https://register.vevent.com/register/BIbb2d35bc9570474dabf8b2e3d2e4ca72.
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 Cumberland's website or by visiting https://edge.media-server.com/mmc/p/uqsbkw9t.
ABOUT CUMBERLAND PHARMACEUTICALS:
Cumberland Pharmaceuticals Inc. is the largest biopharmaceutical company founded and headquartered in
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) oral, a prescription laxative, for the treatment of constipation;
- Sancuso® (granisetron) transdermal, 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; and
- 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.
The company also has a series of Phase II clinical programs underway evaluating its ifetroban product candidate in patients with cardiomyopathy associated with Duchenne Muscular Dystrophy, Systemic Sclerosis and Idiopathic Pulmonary Fibrosis.
For more information on Cumberland's approved products, including full prescribing information, please visit links to the individual product websites, which can be found on the company's website www.cumberlandpharma.com.
About Acetadote® (acetylcysteine) Injection
Acetadote, administered intravenously within 8 to 10 hours after ingestion of a potentially hepatotoxic quantity of acetaminophen, is indicated to prevent or lessen hepatic injury. Used in the emergency department, Acetadote is approved in
About Caldolor® (ibuprofen) Injection
Caldolor is indicated in adults and pediatric patients for the management of mild to moderate pain and management of moderate to severe pain as an adjunct to opioid analgesics, as well as the reduction of fever. It was the first FDA-approved intravenous therapy for fever. Caldolor is contraindicated in patients with known hypersensitivity to ibuprofen or other NSAIDs, patients with a history of asthma or other allergic type reactions after taking aspirin or other NSAIDs. Caldolor is contraindicated for use during the peri-operative period in the setting of coronary artery bypass graft (CABG) surgery. For full prescribing and safety information, including boxed warning, visit www.caldolor.com.
About Kristalose® (lactulose) Oral Solution
Kristalose is indicated for the treatment of acute and chronic constipation. It is a unique, proprietary, crystalline form of lactulose, with no restrictions on length of therapy or patient age. Kristalose is contraindicated in patients who require a low-galactose diet. Elderly, debilitated patients who receive lactulose for more than six months should have serum electrolytes (potassium, chloride, carbon dioxide) measured periodically. For full prescribing and safety information, visit www.kristalose.com.
About Sancuso® (granisetron) Transdermal System
Sancuso is the only skin patch approved by the
About Vaprisol® (conivaptan hydrochloride) Injection
Vaprisol is an intravenous treatment for hyponatremia used in the critical care setting. Hyponatremia is an electrolyte disturbance in which sodium ion concentration in blood plasma is lower than normal. This can be associated with a variety of critical care conditions including congestive heart failure, liver failure, kidney failure and pneumonia. The product is a vasopressin receptor antagonist that raises serum sodium levels and promotes free water secretion. Vaprisol is contraindicated in patients with hypovolemic hyponatremia. The coadministration of Vaprisol with potent CYP3A inhibitors, such as ketoconazole, itraconazole, clarithromycin, ritonavir and indinavir, is contraindicated. For full prescribing and safety information, including boxed warning, visit www.vaprisol.com.
About Vibativ® (telavancin) for Injection
Vibativ is a patented, FDA-approved injectable anti-infective for the treatment of certain serious bacterial infections, including hospital-acquired and ventilator-associated bacterial pneumonia, and complicated skin and skin structure infections. It addresses a range of Gram-positive bacterial pathogens, including those that are considered difficult-to-treat and multidrug-resistant. Intravenous unfractionated heparin sodium is contraindicated with Vibativ administration due to artificially prolonged activated partial thromboplastin time (aPTT) test results for up to 18 hours after Vibativ administration. Vibativ is contraindicated in patients with a known hypersensitivity to telavancin. For more information, please visit www.vibativ.com.
ABOUT CUMBERLAND EMERGING TECHNOLOGIES:
Cumberland Emerging Technologies, Inc. (www.cet-fund.com) is a joint initiative between Cumberland Pharmaceuticals Inc., Vanderbilt University, LaunchTN and WinHealth. The mission of CET is to advance biomedical technologies and products conceived at Vanderbilt University and other regional research centers toward the marketplace.
CET helps manage the development and commercialization process for select projects, and provides expertise on intellectual property, regulatory, manufacturing and marketing issues that are critical to successful new biomedical products. CET's Life Sciences Center provides laboratory space, equipment and infrastructure for CET's activities and other early-stage life sciences ventures.
FORWARD LOOKING STATEMENTS:
This press release contains forward-looking statements, which are subject to certain risks and reflect Cumberland's current views on future events based on what it believes are reasonable assumptions. No assurance can be given that these events will occur. Forward-looking statements include, among other things, statements regarding the company's intent, belief or expectations, and can be identified by the use of terminology such as "may," "will," "expect," "believe," "intend," "plan," "estimate," "should," "seek," "anticipate," "look forward" and other comparable terms or the negative thereof. As with any business, all phases of Cumberland's operations are subject to factors outside of its control, and any one or combination of these factors could materially affect Cumberland's operation results. These factors include macroeconomic conditions, including rising interest rates and inflation, competition, an inability of manufacturers to produce Cumberland's products on a timely basis, failure of manufacturers to comply with regulations applicable to pharmaceutical manufacturers, natural disasters, public health epidemics, maintaining an effective sales and marketing infrastructure, and other events beyond the company's control as more fully discussed in its most recent annual report on Form 10-K as filed with the
CUMBERLAND PHARMACEUTICALS INC. AND SUBSIDIARIES Condensed Consolidated Balance Sheets (Unaudited) | |||
March 31, 2024 | December 31, 2023 | ||
ASSETS | |||
Current assets: | |||
Cash and cash equivalents | $ 18,548,485 | $ 18,321,624 | |
Accounts receivable, net | 10,647,267 | 9,758,176 | |
Inventories, net | 4,327,526 | 4,609,362 | |
Prepaid and other current assets | 2,682,673 | 3,025,248 | |
Total current assets | 36,205,951 | 35,714,410 | |
Non-current inventories | 12,915,896 | 12,804,529 | |
Property and equipment, net | 369,499 | 367,903 | |
Intangible assets, net | 21,522,441 | 22,607,918 | |
Goodwill | 914,000 | 914,000 | |
Operating lease right-of-use assets | 6,521,088 | 6,674,394 | |
Other assets | 3,060,643 | 2,692,921 | |
Total assets | $ 81,509,518 | $ 81,776,075 | |
LIABILITIES AND EQUITY | |||
Current liabilities: | |||
Accounts payable | $ 13,075,764 | $ 14,037,629 | |
Operating lease current liabilities | 362,244 | 348,092 | |
Other current liabilities | 12,987,372 | 13,596,528 | |
Total current liabilities | 26,425,380 | 27,982,249 | |
Revolving line of credit | 16,084,144 | 12,784,144 | |
Operating lease non-current liabilities | 5,200,148 | 5,296,247 | |
Other long-term liabilities | 6,610,294 | 6,453,566 | |
Total liabilities | 54,319,966 | 52,516,206 | |
Equity: | |||
Shareholders' equity: | |||
Common stock—no par value; 100,000,000 shares authorized; 14,159,954 and 14,121,833 shares issued and outstanding as of March 31, 2024 and December 31, 2023, respectively | 46,923,757 | 47,091,602 | |
Accumulated deficit | (19,434,424) | (17,488,161) | |
Total shareholders' equity | 27,489,333 | 29,603,441 | |
Noncontrolling interests | (299,781) | (343,572) | |
Total equity | 27,189,552 | 29,259,869 | |
Total liabilities and equity | $ 81,509,518 | $ 81,776,075 | |
CUMBERLAND PHARMACEUTICALS INC. AND SUBSIDIARIES Condensed Consolidated Statements of Operations (Unaudited) | |||
Three months ended March 31, | |||
2024 | 2023 | ||
Net revenues | $ 8,497,701 | $ 9,224,638 | |
Costs and expenses: | |||
Cost of products sold | 1,575,542 | 1,250,264 | |
Selling and marketing | 4,154,588 | 4,277,318 | |
Research and development | 1,158,253 | 1,499,670 | |
General and administrative | 2,367,907 | 2,498,993 | |
Amortization | 1,110,661 | 1,230,071 | |
Total costs and expenses | 10,366,951 | 10,756,316 | |
Operating loss | (1,869,250) | (1,531,678) | |
Interest income | 96,746 | 50,190 | |
Other income | — | 1,847,065 | |
Interest expense | (118,526) | (186,353) | |
Income (loss) before income taxes | (1,891,030) | 179,224 | |
Income tax expense | (11,442) | (6,938) | |
Net income (loss) | (1,902,472) | 172,286 | |
Net loss at subsidiary attributable to noncontrolling interests | (43,791) | 19,898 | |
Net income (loss) attributable to common shareholders | $ (1,946,263) | $ 192,184 | |
Earnings (loss) per share attributable to common shareholders | |||
- basic | $ (0.14) | $ 0.01 | |
- diluted | $ (0.14) | $ 0.01 | |
Weighted-average shares outstanding | |||
- basic | 14,098,022 | 14,359,322 | |
- diluted | 14,098,022 | 14,587,843 | |
CUMBERLAND PHARMACEUTICALS INC. AND SUBSIDIARIES Condensed Consolidated Statements of Cash Flows (Unaudited) | |||
Three months ended March 31, | |||
2024 | 2023 | ||
Cash flows from operating activities: | |||
Net income (loss) | $ (1,902,472) | $ 172,286 | |
Adjustments to reconcile net loss to net cash provided by operating activities: | |||
Depreciation and amortization expense | 1,150,685 | 1,255,675 | |
Amortization of operating lease right-of-use assets | 285,184 | 172,209 | |
Share-based compensation | 78,754 | 90,156 | |
Decrease in non-cash contingent consideration | (230,430) | (267,637) | |
Increase in cash surrender value of life insurance policies over premiums paid | (129,217) | (30,799) | |
Increase in noncash interest expense | 3,810 | 4,296 | |
Gain on receivable of FDA fees | — | (1,847,065) | |
Net changes in assets and liabilities affecting operating activities: | |||
Accounts receivable | (1,066,410) | 481,613 | |
Inventories | 170,469 | (323,557) | |
Other current assets and other assets | 205,619 | 383,612 | |
Operating lease liabilities | (213,825) | 127,137 | |
Accounts payable and other current liabilities | (645,542) | (1,105,263) | |
Other long-term liabilities | 156,728 | (530,872) | |
Net cash used in operating activities | (2,136,647) | (1,418,209) | |
Cash flows from investing activities: | |||
Additions to property and equipment | (41,621) | (107,260) | |
Additions to intangible assets | (16,565) | (67,193) | |
Net cash used in investing activities | (58,186) | (174,453) | |
Cash flows from financing activities: | |||
Borrowings on line of credit | 11,000,000 | 8,000,000 | |
Payments on line of credit | (7,700,000) | (8,127,714) | |
Cash settlement of contingent consideration | (630,701) | (1,464,311) | |
Payments made in connection with repurchase of common shares | (247,605) | (187,117) | |
Net cash provided by (used in) financing activities | 2,421,694 | (1,779,142) | |
Net increase (decrease) in cash and cash equivalents | 226,861 | (3,371,804) | |
Cash and cash equivalents at beginning of period | $ 18,321,624 | $ 19,757,970 | |
Cash and cash equivalents at end of period | $ 18,548,485 | $ 16,386,166 | |
CUMBERLAND PHARMACEUTICALS INC. AND SUBSIDIARIES Reconciliation of Net Income (loss) Attributable to Common Shareholders to Adjusted Earnings (loss) and Adjusted Diluted Earnings (loss) Per Share (Unaudited) | ||||||||
Three months ended March 31, | Three months ended March 31, | |||||||
2024 | 2024 | 2023 | 2023 | |||||
Earnings impact | Earnings per share impact | Earnings impact | Earnings per share impact | |||||
Net income (loss) attributable to common shareholders | $ (1,946,263) | $ (0.14) | $ 192,184 | $ 0.01 | ||||
Less: Net loss at subsidiary attributable to noncontrolling interests | (43,791) | — | 19,898 | — | ||||
Net income (loss) | (1,902,472) | (0.13) | 172,286 | 0.01 | ||||
Adjustments to net loss | ||||||||
Income tax expense | 11,442 | — | 6,938 | — | ||||
Depreciation and amortization | 1,150,685 | 0.08 | 1,255,675 | 0.09 | ||||
Share-based compensation (a) | 78,754 | 0.01 | 90,156 | 0.01 | ||||
Interest income | (96,746) | (0.01) | (50,190) | — | ||||
Interest expense | 118,526 | 0.01 | 186,353 | 0.01 | ||||
Adjusted Earnings (Loss) and Adjusted Diluted Earnings (Loss) Per Share | $ (639,811) | $ (0.05) | $ 1,661,218 | $ 0.11 | ||||
Diluted weighted-average common shares outstanding: | 14,098,022 | 14,587,843 | ||||||
The Company provided the above adjusted supplemental financial performance measures, which are considered "non-GAAP" financial measures under applicable SEC rules and regulations. These financial measures should be considered supplemental to, and not as a substitute for, financial information prepared in accordance with Generally Accepted Accounting Principles ("GAAP"). The definition of these supplemental measures may differ from similarly titled measures used by others.
Because these supplemental financial measures exclude the effect of items that will increase or decrease the Company's reported results of operations, management encourages investors to review the Company's consolidated financial statements and publicly filed reports in their entirety. A reconciliation of the supplemental financial measures to the most directly comparable GAAP financial measures is included in the tables accompanying this release.
Cumberland's management believes these supplemental financial performance measures are important as they are used by management, along with financial measures in accordance with GAAP, to evaluate the Company's operating performance. In addition, Cumberland believes that they will be used by certain investors to measure the Company's operating results. Management believes that presenting these supplemental measures provides useful information about the Company's underlying performance across reporting periods on a consistent basis by excluding items that Cumberland does not believe are indicative of its core business performance or reflect long-term strategic activities. Certain of these items are not settled through cash payments and include: depreciation, amortization, share-based compensation expense and income taxes. Cumberland utilizes its net operating loss carryforwards to pay minimal income taxes. In addition, the use of these financial measures provides greater transparency to investors of supplemental information used by management in its financial and operational decision-making, including the evaluation of the Company's operating performance.
The Company defines these supplemental financial measures as follows:
- Adjusted Earnings (loss): net income (loss) adjusted for the impact of income taxes, depreciation and amortization expense, share-based compensation, interest income and interest expense. The definition of Adjusted Earnings has been changed to include all gains and losses, as gains are occurring more frequently for the Company.
(a) Represents the share-based compensation of Cumberland.
- Adjusted Diluted Earnings (loss) Per Share: Adjusted Earnings (loss) divided by diluted weighted-average common shares outstanding.
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SOURCE Cumberland Pharmaceuticals Inc.
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