Medicure Reports Financial Results for 2014
10 September 2014
WINNIPEG, CANADA (September 10, 2014) Medicure Inc. ("Medicure" or the "Company") (TSXV:MPH, OTCQB:MCUJF), a specialty pharmaceutical company, today reported its results from operations for the fiscal year ended May 31, 2014.
- Recorded net revenue of $5.1 million during the year ended May 31, 2014, an increase of 94%, compared to $2.6 million for the previous fiscal year;
- Earnings before interest, taxes, depreciation and amortization (EBITDA)1 for the year ended May 31, 2014 was $726,000 compared to a loss of $1.5 million for the previous fiscal year;
- Net loss for the year ended May 31, 2014 was $1.6 million, compared to $2.6 million for the previous fiscal year.
Financial Results Net revenue from the sale of AGGRASTAT finished product for the year ended May 31, 2014 was $5.1 million compared to $2.6 million for the year ended May 31, 2013, an increase of 94%. Net revenue for the three months ended May 31, 2014 was $1.8 million compared to $768,000 for the three months ended May 31, 2013, an increase of 134%.
Hospital demand for AGGRASTAT increased significantly compared to the previous fiscal year. The increase in revenue is primarily attributable to an increase in the number of new hospital customers using AGGRASTAT. The number of new customers reviewing and implementing AGGRASTAT has increased sharply as a result of FDA approval of the new dosing regimen for AGGRASTAT as announced on October 11, 2013. Additionally, favourable fluctuations in the U.S. dollar exchange rate contributed to the increase in revenue.
The Company's commercial team continues to work on further expanding its customer base and the Company expects sales of AGGRASTAT to continue to increase over the coming quarters.
EBITDA for the year ended May 31, 2014 was $726,000 compared to a loss of $1.5 million for the year ended May 31, 2013. EBITDA for the three months ended May 31, 2014 was $538,000 compared to a loss of $458,000 for the three months ended May 31, 2013.
Net loss for the year ended May 31, 2014 was $1.6 million or $0.13 per share, compared to $2.6 million or $0.21 per share for the year ended May 31, 2013. The reduction in net loss is primarily a result of increased revenues and lower research and development expenses experienced during the year ended May 31, 2014, partially offset by higher finance expense and selling, general and administration expenses. The decrease in research and development expenses for the year ended May 31, 2014 is due to reduced costs from the Company's AGGRASTAT (tirofiban HCl) clinical trial entitled "Shortened Aggrastat Versus Integrilin in Percutaneous Coronary Intervention" (SAVI-PCI), as well as a renal dosing study that was completed as a part of the Company's sNDA filing during fiscal 2013. The increase in finance expense is primarily due to the revaluation of the Company's royalty obligation, a non-cash expense, which results from higher revenue estimates related to the October 2013 label change. The increase in selling, general and administration expenses is primarily due to higher personnel expenses, higher selling costs associated with the growth in AGGRASTAT revenues as well as business development expenses incurred during the year ended May 31, 2014.
Net loss for the three months ended May 31, 2014 was $737,000 or $0.06 per share, compared to $706,000, also $0.06 per share, for the three months ended May 31, 2013. The loss is consistent between the two quarters, however there were significantly higher revenues for the three months ended May 31, 2014, offset by higher finance expense due to the revaluation of the Company's royalty obligation, a non-cash expense and selling, general and administration expenses, when compared to the three months ended May 31, 2013.
At May 31, 2014, the Company had cash totaling $234,000 compared to $127,000 as of May 31, 2013. The increase in cash is primarily due to the lower net loss after adjusting for non-cash items and higher accounts payable and accrued liabilities at May 31, 2014, partially offset by higher accounts receivable. Cash flows from operating activities for the year ended May 31, 2014 were $111,000 compared to cash used in operating activities of $1.0 million for the year ended May 31, 2013.
All amounts referenced herein are in Canadian dollars unless otherwise noted.
On October 11, 2013 the Company announced that the United States Food and Drug Administration (FDA) has approved the AGGRASTAT high-dose bolus (HDB) regimen, as requested under Medicure's supplemental New Drug Application (sNDA).
Conference Call Information
Conference call details are as follows:
Topic: Medicure's Fiscal Year Ended May 31, 2014 Results Call
Time: 8:00 am, Central Time (9:00 am, Eastern Time)
Date: Thursday, September 11, 2014
To access the call within Canada and the United States dial toll free 1-800-920-7487/Passcode 2473365#.
International callers may access the call at 1-404-920-1710/Passcode 2473365# or you may request country specific international access info by emailing us in advance at email@example.com.
Management will accept and answer questions related to the financial results and its operations during the Q&A period at the end of the conference call. Questions may be forwarded in advance or during the presentation to firstname.lastname@example.org.
Indications and Usage
AGGRASTAT is indicated to reduce the rate of thrombotic cardiovascular events (combined endpoint of death, myocardial infarction, or refractory ischemia/repeat cardiac procedure) in patients with non-ST elevation acute coronary syndrome (NSTE-ACS).
Dosage and Administration
Administer intravenously 25 mcg/kg over 3 minutes and then 0.15 mcg/kg/min for up to 18 hours. In patients with creatinine clearance ≤60 mL/min, give 25 mcg/kg over 3 minutes and then 0.075 mcg/kg/min.
Warnings and Precautions
Bleeding is the most common complication encountered during therapy with AGGRASTAT. Most bleeding associated with AGGRASTAT occurs at the arterial access site for cardiac catheterization. Minimize the use of traumatic or potentially traumatic procedures such arterial and venous punctures, intramuscular injections, nasotracheal intubation, etc. Fatal bleeding events have been reported. Concomitant use of fibrinolytics, oral anticoagulants and antiplatelet drugs increases the risk of bleeding.
Profound thrombocytopenia has been reported with AGGRASTAT. Monitor platelet counts beginning about 6 hours after treatment initiation and daily thereafter. If the platelet count decreases to 90,000/mm3, monitor platelet counts to exclude pseudothrombocytopenia. If thrombocytopenia is confirmed, discontinue AGGRASTAT and heparin. Previous exposure to a glycoprotein (GP) IIb/IIIa receptor antagonist may increase the risk of developing thrombocytopenia.
AGGRASTAT® (tirofiban HCl) is a registered trademark of Medicure International, Inc.
Please refer to Full Prescribing Information.
Neither the TSX Venture Exchange nor its Regulation Services Provider (as that term is defined in policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.
About Medicure Inc.
Medicure is a specialty pharmaceutical company focused on the development and commercialization of novel small molecule therapeutics. The primary focus of the Company and its subsidiaries is the marketing and distribution of AGGRASTAT (tirofiban HCl) for non-ST elevation acute coronary syndrome in the United States, where it is sold through the Company's U.S. subsidiary, Medicure Pharma, Inc. For more information on Medicure please visit www.medicure.com.
Neither the TSX Venture Exchange nor its Regulation Services Provider )as that term is defined in policies of the TSX Venture Exchange) accepts responsibility for the adequacy or accuracy of this release.
Forward Looking Information: Statements contained in this press release that are not statements of historical fact, including, without limitation, statements containing the words "believes", "may", "plans", "will", "estimates", "continues", "anticipates", "intends", "expects" and similar expressions, may constitute "forward-looking information" within the meaning of applicable Canadian and U.S. federal securities laws (such forward-looking information and forward-looking statements are hereinafter collectively referred to as "forward-looking statements"). Forward-looking statements, including the expectation of continued revenue growth, are based on the current assumptions, estimates, analysis and opinions of management of the Company made in light of its experience and its perception of trends, current conditions and expected developments, as well as other factors which the Company believes to be relevant and reasonable in the circumstances. Inherent in forward-looking statements are known and unknown risks, uncertainties and other factors beyond the Company's ability to predict or control that may cause the actual results, events or developments to be materially different from any future results, events or developments expressed or implied by such forward-looking statements, and as such, readers are cautioned not to place undue reliance on forward-looking statements. Such risk factors include, among others, the Company's future product revenues, stage of development, additional capital requirements, risks associated with the completion and timing of clinical trials and obtaining regulatory approval to market the Company's products, the ability to protect its intellectual property, dependence upon collaborative partners, changes in government regulation or regulatory approval processes, and rapid technological change in the industry. Such statements are based on a number of assumptions which may prove to be incorrect, including, but not limited to, assumptions about: general business and economic conditions; the impact of changes in Canadian-US dollar and other foreign exchange rates on the Company's revenues, costs and results; the timing of the receipt of regulatory and governmental approvals for the Company's research and development projects; the availability of financing for the Company's commercial operations and/or research and development projects, or the availability of financing on reasonable terms; results of current and future clinical trials; the uncertainties associated with the acceptance and demand for new products and market competition. The foregoing list of important factors and assumptions is not exhaustive. The Company undertakes no obligation to update publicly or otherwise revise any forward-looking statements or the foregoing list of factors, other than as may be required by applicable legislation. Additional discussion regarding the risks and uncertainties relating to the Company and its business can be found in the Company's other filings with the applicable Canadian securities regulatory authorities or the US Securities and Exchange Commission, and in the "Risk Factors" section of its Form 20F for the year ended May 31, 2014.
(1) The Company defines EBITDA as "earnings before interest, taxes, depreciation and amortization". The term "EBITDA", as it relates to 2014 and 2013 results prepared using International Financial Reporting Standards ("IFRS"), does not have any standardized meaning according to IFRS. It is therefore unlikely to be comparable to similar measures presented by other companies.
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