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Cumberland Pharmaceuticals Reports Third Quarter 2020 Financial Results & Company Update

·22 min read

NASHVILLE, Tenn., Nov. 10, 2020 /PRNewswire/ -- Cumberland Pharmaceuticals Inc. (NASDAQ: CPIX), a specialty pharmaceutical company, today is providing a company update and third quarter 2020 financial results. Net revenues from continuing operations during the quarter were $9.3 million. The company also recorded an additional $750,000 in revenue during the third quarter associated with divested product rights for two brands it is no longer distributing.

Cumberland Pharmaceuticals Logo (PRNewsFoto/Cumberland Pharmaceuticals Inc.)
Cumberland Pharmaceuticals Logo (PRNewsFoto/Cumberland Pharmaceuticals Inc.)

The Company's financial position included $96 million in total assets – with $27 million in cash, $48 million of total liabilities, and $48 million of shareholders' equity at the end of the quarter.

"As we move to the close of 2020, we recognize that it has been a particularly difficult year with the pandemic impacting all our daily lives," said A.J. Kazimi, Chief Executive Officer of Cumberland Pharmaceuticals. "Overall, our third quarter was quite successful, given all the challenges of operating a business in the wake of the pandemic. We were able to generate solid financial performance and advance on important initiatives."

RECENT COMPANY DEVELOPMENTS:

Vibativ®

Cumberland's Vibativ product is being used to help COVID-19 patients who develop bacterial infections in their lungs. 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 that can result from COVID-19, flu, and other infections. It addresses a range of Gram-positive bacterial pathogens, including those that are considered difficult-to-treat and multidrug-resistant.

RediTrex® Launch

The Company is now finalizing plans for the launch of its newly FDA-approved RediTrex product line. Cumberland will initially implement a soft launch during the fourth quarter of 2020 and intends to follow with a full commercial launch of the brand next spring. The Company believes that RediTrex will be a valuable addition to the portfolio and help further diversify and grow its business.

RediTrex is approved for patients with severe, active rheumatoid arthritis and polyarticular juvenile idiopathic arthritis who have difficulty tolerating or responding to orally delivered methotrexate. It is also approved for symptomatic control of severe, recalcitrant, disabling psoriasis in adults who are not adequately responsive to other forms of therapy.

Caldolor® Clinical Manuscripts

During the third quarter, Cumberland announced a study published in the Journal of Orthopedic Trauma, evaluating the efficacy of Caldolor administration in the management of acute pain in orthopedic trauma patients. The study also measured Caldolor's ability in minimizing opioid use. This single-center, randomized, double-blind, placebo-controlled study found that Caldolor (ibuprofen) Injection reduced the quantity of opioids required to manage pain after a traumatic injury with fracture. In addition, the time to first narcotic medication was longer in the Caldolor group than with hospital standard of care. Pain was also managed better in the Caldolor group compared to standard of care narcotics.

Additionally, the results of a review of nine clinical studies evaluating Caldolor was announced. The comprehensive review was published in the journal, Clinical Therapeutics, and involved over 1,000 adult patients, with over 750 receiving Caldolor and another 300 receiving placebo or a comparator medication. The data noted that the use of Caldolor improved post-surgery recovery, decreased surgical stress, and reduced the use of opioids and over-the-counter medication. The study review determined that patients given Caldolor experienced less postoperative pain and decreased opioid use. Study authors also concluded that the rapid administration and preemptive use of Caldolor should be considered in Enhanced Recovery After Surgery protocols for the management of postoperative pain including that of traumatic origin.

Revolving Credit Loan Agreement

In October 2020, Cumberland entered into a Third Amendment to the Revolving Credit Note and Fourth Amendment ("Fourth Amendment") to the Revolving Credit Loan Agreement with Pinnacle Bank (the "Pinnacle Agreement"). The original Pinnacle Agreement was dated July 31, 2017. The Fourth Amendment provides for a principal available for borrowing of up to $15 million and Cumberland has the ability to request an increase of up to an additional $5 million, upon the satisfaction of certain conditions and approval by Pinnacle Bank. If fully expanded, the Fourth Amendment would provide a maximum principal available for borrowing of up to $20 million, which was also the maximum aggregate principal available for borrowing under the previously amended Pinnacle Agreement.

The Fourth Amendment extends the maturity date of the Pinnacle Agreement through October 1, 2022.

Ifetroban Phase II Clinical Programs

Enrollment in Cumberland's clinical studies significantly slowed during 2020 due to the COVID-19 pandemic. While enrollment of new patients was limited, the Company ensured that patients already entered into a trial continued to receive their study drug.

During the third quarter, some of Cumberland's clinical study sites reopened and resumed screening of patients for potential enrollment into the Company's studies.

Cumberland has completed a pilot Phase II study involving ifetroban in patients suffering from aspirin-exacerbated respiratory disease, a severe form of asthma. A follow-up Phase II study is currently underway for this asthma indication.

The Company is also currently evaluating ifetroban in two pilot Phase II studies in 1) patients with systemic sclerosis or scleroderma, a debilitating autoimmune disorder characterized by diffuse fibrosis of the skin and internal organs and 2) patients with cardiomyopathy associated with Duchenne Muscular Dystrophy. This rare, fatal, genetic neuromuscular disease results in deterioration of the skeletal, heart and lung muscles.

Cumberland is awaiting further study results before deciding on the best path for approval for ifetroban, its first new chemical entity.

FINANCIAL RESULTS:

Net Revenues: For the three months ended September 30, 2020, net revenues from ongoing operations were $9.3 million, compared to $6.9 million for the prior year period. The company also recorded an additional $750,000 in revenue during the third quarter associated with divested product rights.

Net revenue by product for the three months ended September 30, 2020, included $3.6 million for Kristalose®, $2.8 million for Vibativ®, $1.4 million for Caldolor®, $0.2 million for Acetadote® (including the brand and Company's Authorized Generic), $0.5 million for Omeclamox®-Pak, and $0.4 million for Vaprisol®

For the nine months ended September 30, 2020, net revenues were $27.2 million, up 8.4% from $25.1 million for the prior year period.

Operating Expenses: Total operating expenses for the three months ended September 30, 2020 were $10.5 million, compared to $10.1 million during the prior year period.

Total operating expenses for the first nine months of 2020 were $31.8 million compared to $31.0 million for the nine months ended September 30, 2019.

Earnings: Net income (loss) for the third quarter 2020 was $(0.5) million or $(0.03) a share, compared to $(2.0) million or $(0.13) a share for the prior year period.

Adjusted Earnings (loss) for the third quarter were $0.2 million or $0.02 per diluted share, compared to $(1.7) million or $(0.11) per diluted share for the prior year period.

Balance Sheet: At September 30, 2020, Cumberland had $96.0 million in total assets including $26.6 million in cash and cash equivalents. Total liabilities were $48.2 million, including $17.0 million outstanding on the Company's revolving line of credit, resulting in total shareholders' equity of $47.9 million.

Conference Call and Webcast

A conference call and live internet webcast will be held on Tuesday, November 10, at 4:30 p.m. Eastern Time to discuss the results. To participate in the call, please dial 877-303-1298 (for U.S. callers) or 253-237-1032 (for international callers). A rebroadcast of the teleconference will be available for one week and can be accessed by dialing 855-859-2056 (for U.S. callers) or 404-537-3406 (for international callers). The Conference ID for the rebroadcast is 4484046. The live webcast and rebroadcast can be accessed via Cumberland's website at http://investor.shareholder.com/cpix/events.cfm.

About Cumberland Pharmaceuticals

Cumberland Pharmaceuticals Inc. is a specialty pharmaceutical company focused on the delivery of high quality prescription brands to improve patient care. The Company develops, acquires and commercializes brands for the hospital acute care, gastroenterology and oncology market segments. These medical specialties are categorized by moderately concentrated prescriber bases that the Company believes can be penetrated effectively by targeted sales forces. The Company's portfolio of FDA-approved brands includes:

  • Caldolor® (ibuprofen) Injection, for the treatment of pain and fever;

  • Kristalose® (lactulose) for Oral Solution, a prescription laxative, for the treatment of chronic and acute constipation;

  • 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;

  • RediTrex® (methotrexate) Injection, for the treatment of active rheumatoid, juvenile idiopathic and severe psoriatic arthritis, as well as disabling psoriasis;

  • Vaprisol® (conivaptan) Injection, to raise serum sodium levels in hospitalized patients with euvolemic and hypervolemic hyponatremia;

  • Omeclamox®-Pak, (omeprazole, clarithromycin, amoxicillin) for the treatment of Helicobacter pylori (H. pylori) infection and related duodenal ulcer disease;

  • Acetadote® (acetylcysteine) Injection, for the treatment of acetaminophen poisoning.

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.

The Company has Phase II clinical programs underway evaluating its ifetroban product candidates in patients with cardiomyopathy associated with Duchenne Muscular Dystrophy ("DMD"), Systemic Sclerosis ("SSc"), and Aspirin-Exacerbated Respiratory Disease ("AERD").

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 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 RediTrex® (methotrexate) Injection

RediTrex is a single-dose prefilled syringe containing prescription methotrexate. RediTrex is used to treat adults with severe, active rheumatoid arthritis and children with active polyarticular juvenile idiopathic arthritis, after treatment with other medicines including non-steroidal anti-inflammatory drugs (NSAIDS) have been used and did not work well. Methotrexate can control the symptoms of severe, resistant, disabling psoriasis in adults when other types of treatment have failed. For full prescribing and safety information, visit www.reditrex.com.

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 Omeclamox®-Pak (omeprazole, clarithromycin, amoxicillin)

Omeprazole is an antisecretory drug, which works by decreasing the amount of acid the stomach produces. Clarithromycin and amoxicillin are antibacterial drugs, which inhibit the growth of bacteria allowing the stomach lining to heal. Omeclamox-Pak is contraindicated in patients with a history of hypersensitivity to omeprazole, any macrolide antibiotic or penicillin. For full prescribing and safety information, visit www.omeclamox.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 the United States to treat overdose of acetaminophen, a common ingredient in many over-the-counter medications. Acetadote is contraindicated in patients with hypersensitivity or previous anaphylactoid reactions to acetylcysteine or any components of the preparation. For full prescribing and safety information, visit www.acetadote.com.

About Cumberland Emerging Technologies (CET)

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 towards 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 may contain statements that are "forward-looking" within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.

Forward-looking statements are based on certain assumptions and can include future expectations, future plans and strategies, financial and operating projections or other information. Such forward-looking statements reflect management's current beliefs and are based on information currently available to management. Because forward-looking statements relate to future events, they are subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which are outside of Cumberland's control.

Thus, Cumberland's actual results and financial condition may differ materially due to: market conditions, competition, an inability of manufacturers to supply Cumberland's products, maintaining an effective sales and marketing infrastructure, availability of additional debt and equity capital required to finance the business, our ability to continue to acquire brands, management of our growth and integration of our acquisitions, impacts on our business, as well as national and international markets and economies resulting from the 2020 COVID-19 pandemic, and the other factors described in the section entitled "Risk Factors" in the Company's Annual Report on Form 10-K for the year ended December 31, 2019, the Company's Quarterly Reports on Form 10-Q for the quarters ended March 31, 2020, and September 30, 2020, respectively, and the Company's other filings with the SEC. Readers are cautioned not to place undue reliance on any forward-looking statements, and Cumberland undertakes no obligation to update them, whether as a result of new information, future developments, or otherwise, except as may be required by law.

CUMBERLAND PHARMACEUTICALS INC. AND SUBSIDIARIES

Condensed Consolidated Balance Sheets

(Unaudited)



September 30,
2020


December 31,
2019

ASSETS




Current assets:




Cash and cash equivalents

$

26,646,530



$

28,212,635


Accounts receivable, net

9,661,407



7,843,917


Inventories

10,080,394



8,871,254


Current assets of discontinued operations

727,670



2,477,813


Prepaid and other current assets

1,778,078



2,757,456


Total current assets

48,894,079



50,163,075


Non-current inventories

12,649,184



15,554,992


Property and equipment, net

602,911



747,796


Intangible assets, net

28,180,090



30,920,324


Goodwill

882,000



882,000


Deferred tax assets, net

21,802



21,802


Operating lease right-of-use assets

2,267,669



2,960,569


Other assets

2,511,894



3,298,725


Total assets

$

96,009,629



$

104,549,283


LIABILITIES AND EQUITY




Current liabilities:




Accounts payable

$

10,833,972



$

9,993,578


Current liabilities of discontinued operations



1,918,868


Operating lease current liabilities

991,969



920,431


Current portion of revolving line of credit

2,000,000




Other current liabilities

10,112,100



11,317,358


Total current liabilities

23,938,041



24,150,235


Revolving line of credit

15,000,000



18,500,000


Operating lease noncurrent liabilities

1,323,792



2,076,472


Other long-term liabilities

7,904,419



8,737,323


Total liabilities

48,166,252



53,464,030


Commitments and contingencies




Equity:




Shareholders' equity:




Common stock—no par value; 100,000,000 shares authorized; 15,084,372 and 15,263,555 shares issued and outstanding as of September 30, 2020 and December 31, 2019, respectively

49,176,040



49,914,478


Retained earnings (deficit)

(1,247,237)



1,208,395


Total shareholders' equity

47,928,803



51,122,873


Noncontrolling interests

(85,426)



(37,620)


Total equity

47,843,377



51,085,253


Total liabilities and equity

$

96,009,629



$

104,549,283


CUMBERLAND PHARMACEUTICALS INC. AND SUBSIDIARIES

Condensed Consolidated Statements of Operations

(Unaudited)



Three months ended September 30,


Nine months ended September 30,


2020


2019


2020


2019

Net revenues

$

9,250,689



$

6,935,439



$

27,179,600



$

25,082,742


Costs and expenses:








Cost of products sold

2,142,839



1,580,650



6,387,002



5,031,732


Selling and marketing

3,587,842



3,812,467



11,160,924



11,231,778


Research and development

1,230,335



1,672,843



4,374,392



4,788,698


General and administrative

2,381,273



2,032,129



6,608,322



6,839,187


Amortization

1,117,086



1,033,786



3,284,610



3,085,139


Total costs and expenses

10,459,375



10,131,875



31,815,250



30,976,534


Operating income (loss)

(1,208,686)



(3,196,436)



(4,635,650)



(5,893,792)


Interest income

12,004



(50,511)



70,553



195,915


Interest expense

(75,210)



(64,877)



(227,730)



(216,988)


Income (loss) from continuing operations before income taxes

(1,271,892)



(3,311,824)



(4,792,827)



(5,914,865)


Income tax (expense) benefit

(3,728)



(4,462)



(45,423)



72,504


Net income (loss) from continuing operations

(1,275,620)



(3,316,286)



(4,838,250)



(5,842,361)


Discontinued operations

777,916



1,349,351



2,334,811



3,268,196


Net income (loss)

(497,704)



(1,966,935)



(2,503,439)



(2,574,165)


Net (income) loss at subsidiary attributable to noncontrolling interests

15,967



13,267



47,806



(2,888)


Net income (loss) attributable to common shareholders

$

(481,737)



$

(1,953,668)



$

(2,455,633)



$

(2,577,053)


Earnings (loss) per share attributable to common shareholders








- Continuing operations - basic

$

(0.08)



$

(0.22)



$

(0.31)



$

(0.38)


- Discontinued operations - basic

0.05



0.09



0.15



0.21



$

(0.03)



$

(0.13)



$

(0.16)



$

(0.17)










- Continuing operations - diluted

$

(0.08)



$

(0.22)



$

(0.31)



$

(0.38)


- Discontinued operations - diluted

0.05



0.09



0.15



0.21



$

(0.03)



$

(0.13)



$

(0.16)



$

(0.17)


Weighted-average shares outstanding








- basic

15,134,583



15,368,027



15,206,179



15,454,159


- diluted

15,134,583



15,368,027



15,206,179



15,454,159


CUMBERLAND PHARMACEUTICALS INC. AND SUBSIDIARIES

Condensed Consolidated Statements of Cash Flows

(Unaudited)



Nine months ended September 30,


2020


2019

Cash flows from operating activities:




Net income (loss)

$

(2,503,438)



$

(2,574,165)


Discontinued operations

2,334,811



$

3,268,196


Net income(loss) from continuing operations

(4,838,249)



$

(5,842,361)


Adjustments to reconcile net income (loss) from continuing operations to net cash provided by (used in) operating activities:




Depreciation and amortization expense

3,524,684



3,278,958


Deferred tax expense



43,605


Share-based compensation

805,338



1,107,817


Decrease in non-cash contingent consideration

(806,390)



(681,577)


Noncash interest expense

36,197



36,292


Noncash investment gains



(34,303)


Net changes in assets and liabilities affecting operating activities:




Accounts receivable

(1,817,490)



1,026,633


Inventories

1,696,668



1,332,140


Other current assets and other assets

1,962,024



195,529


Accounts payable and other current liabilities

3,417,856



(539,525)


Other long-term liabilities

(1,585,584)



(207,648)


Net cash provided by (used in) operating activities from continuing operations

2,395,054



(284,440)


Discontinued operations

2,166,086



2,483,796


Net cash provided by operating activities

4,561,140



2,199,356


Cash flows from investing activities:




Additions to property and equipment

(95,189)



(166,407)


Purchases of marketable securities



(9,627,191)


Proceeds from sale of marketable securities



15,686,334


Proceeds from surrender of life insurance policies

460,888




Cash paid for acquisitions



(5,000,000)


Additions to intangibles

(1,807,467)



(498,003)


Net cash provided by (used in) investing activities

(1,441,768)



394,733


Cash flows from financing activities:




Borrowings on line of credit

44,000,000



56,000,000


Repayments on line of credit

(45,500,000)



(56,000,000)


Payments of financing costs



(52,500)


Cash payment of contingent consideration

(834,014)



(908,347)


Repurchase of subsidiary shares to noncontrolling interest

(800,000)




Repurchase of common shares

(1,551,463)



(2,593,778)


Net cash used in financing activities

(4,685,477)



(3,554,625)


Net decrease in cash and cash equivalents

(1,566,105)



(960,536)


Cash and cash equivalents at beginning of period

28,212,635



27,938,960


Cash and cash equivalents at end of period

$

26,646,530



$

26,978,424


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
September 30, 2020


Three months ended
September 30, 2019



Earnings
impact


Earnings per
share impact


Earnings
impact


Earnings per
share impact

Net income (loss) attributable to common shareholders


$

(481,737)



$

(0.03)



$

(1,953,668)



$

(0.13)


Less: Net (income) loss at subsidiary attributable to noncontrolling interests


15,967





13,267




Net income (loss)


(497,704)



(0.03)



(1,966,935)



(0.13)


Discontinued operations


777,916



0.05



1,349,351



0.09


Net income (loss) from continuing operations


(1,275,620)



(0.08)



(3,316,286)



(0.22)


Adjustments to net income (loss) from continuing operations









Income tax expense (benefit)


3,728





4,462




Depreciation and amortization


1,190,015



0.08



1,104,561



0.07


Share-based compensation (a)


262,415



0.02



346,835



0.02


Interest income


(12,004)





50,511




Interest expense


75,210





64,877




Adjusted Earnings (loss) from continuing operations and Adjusted Diluted Earnings (loss) from continuing operations Per Share


$

243,744



$

0.02



$

(1,745,040)



$

(0.11)











Diluted weighted-average common shares outstanding:




15,134,583





15,368,027






Nine months ended
September 30, 2020


Nine months ended
September 30, 2019



Earnings
impact


Earnings per
share impact


Earnings
impact


Earnings per
share impact

Net income (loss) attributable to common shareholders


$

(2,455,633)



$

(0.16)



$

(2,577,053)



$

(0.17)


Less: Net (income) loss at subsidiary attributable to noncontrolling interests


47,806





(2,888)




Net income (loss)


(2,503,439)



(0.16)



(2,574,165)



(0.17)


Discontinued operations


2,334,811



0.15



3,268,196



0.21


Net income (loss) from continuing operations


(4,838,250)



(0.31)



(5,842,361)



(0.38)


Adjustments to net income (loss) from continuing operations









Income tax expense (benefit)


45,423





(72,504)




Depreciation and amortization


3,524,684



0.23



3,278,958



0.21


Share-based compensation (a)


805,338



0.05



1,107,817



0.07


Interest income


(70,553)





(195,915)



(0.01)


Interest expense


227,730



0.01



216,988



0.01


Adjusted Earnings (loss) from continuing operations and Adjusted Diluted Earnings (loss) from continuing operations Per Share


$

(305,628)



$

(0.02)



$

(1,507,017)



$

(0.10)











Diluted weighted-average common shares outstanding:




15,206,179





15,454,159


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 and interest income and interest expense.

(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.

Cision
Cision

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SOURCE Cumberland Pharmaceuticals Inc.