- Second quarter 2019 revenue of $131 million
- Second quarter 2019 net loss of $44 million
- Second quarter 2019 Adjusted EBITDA1 of $60 million
- Generated cash flow from operating activities of $97 million in the first six months of 2019 and concluded the quarter with cash and cash equivalents of $224 million
MISSISSAUGA, ON, Aug. 7, 2019 /CNW/ - ADVANZ PHARMA Corp. ("ADVANZ PHARMA" or "the Company") (TSX:ADVZ), an international specialty pharmaceutical company focused on serving the needs of patients and healthcare providers around the world with enhanced access to high quality, niche-established medicines, today announced its financial and operational results for the three and six months ended June 30, 2019. All financial references are in U.S. dollars ("USD") unless otherwise noted.
"The Company generated second quarter financial results that are consistent with management's expectations," said Graeme Duncan, Chief Executive Officer of ADVANZ PHARMA. "We also made important progress with respect to our pipeline and M&A development during the reporting period."
Consolidated Second Quarter 2019 Financial and Operational Results
- Reported second quarter 2019 revenue of $131.1 million, compared to $139.5 million for the second quarter of 2018, and $135.6 million for the first quarter of 2019.
- Reported a net loss for the second quarter of 2019 of $44.3 million.
- Reported second quarter adjusted EBITDA1 of $59.7 million, compared to $66.8 million for the second quarter of 2018, and $65.1 million for the first quarter of 2019.
- Generated cash flows from operating activities of $97.4 million in the first six months of 2019, compared to $83.9 million during the same period in 2018.
- As of June 30, 2019, the Company had a cash and cash equivalents balance of $224.3 million compared to $224.4 million as of December 31, 2018.
- On April 1, 2019, announced the acquisition of the global rights to two established medicines, Salagen® tablets (pilocarpine hydrochloride) (excluding Japan) and Panretin® gel (alitretinoin), from Eisai Inc. for $30 million in cash plus approximately $3.3 million for purchased inventory and related prepayments. The Company funded the transaction using cash on hand on April 15, 2019. Since the transaction closed, the two medicines have performed in line with management's expectations.
Second Quarter 2019 Segment Results
ADVANZ PHARMA International segment revenue of $95.5 million for the quarter ended June 30, 2019, decreased by $11.2 million, or 11%, compared to the corresponding period in 2018.
The decline consisted of a $5.7 million decrease in baseline revenue, which was further compounded by a $5.5 million decrease in revenue as a result of the British pound (GBP) weakening against the USD, when compared against the second quarter of 2018.
Declines to revenue attributable to key products during the quarter, excluding the impact of foreign currency translation, included a $2.2 million decrease from Carbimazole; a $2.1 million decrease from Liothyronine Sodium; a $1.8 million decrease from Nitrofurantoin; a $1.5 million decrease from Levothyroxine Sodium; and a $1.2 million decrease from Cyclizine Hydrochloride.
These lower product volumes and revenues are primarily due to ongoing competitive market pressures resulting in market share erosion in the U.K.
These declines to revenue were partially offset by $4.4 million increase in revenue from Fusidic Acid as a result of product volume increases.
The remaining decrease was primarily due to general competitive market pressures across the segment's product portfolio.
North America Segment
ADVANZ PHARMA North America segment revenue of $35.6 million for the quarter ended June 30, 2019, increased by $2.8 million or 9%, compared to the corresponding period in 2018.
The increase was primarily due to a $2.6 million increase from Plaquenil® authorized generic due to the timing of shipments in 2019; a $1.0 million increase from recently acquired Salagen® and Panretin® brands in the U.S.; and a $0.9 million increase in revenue from Photofrin® as a result of higher volumes.
These increases were partially offset by a $3.6 million decrease from Donnatal® as a result of competitive pressures that have resulted in a loss of market share.
The Company continued to make progress with respect to the evaluation and advancement of its pipeline of medicines.
In the second quarter of 2019, ADVANZ PHARMA submitted for approval, or received approval, for 17 medicines.
Going forward, the Company intends to expand its product portfolio in order to deliver mid-term value and long-term growth, through pipeline filling, optimization, licencing and development partnerships. These initiatives will be focussed on niche and differentiated generics, complex specialty and value-added medicines.
For 2019, the Company continues to believe that product launches from its pipeline will not generate a material amount of revenue.
Consolidated Financial Results
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(in $000's, except per share data)
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Jun 30, 2018
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Gross profit %
Total operating expenses
Operating income (loss) for the period
Income tax expense (recovery)
Net income (loss) for the period
Earnings (loss) per share
Adjusted EBITDA (2)
2018 amounts have been adjusted for the retrospective effect of the previously disclosed share consolidation.
Represents a non-IFRS measure. For the relevant definitions and reconciliation to reported results, see "Non-IFRS Financial Measures" section of this MD&A. Management believes non-IFRS measures, including Adjusted EBITDA, provide supplementary information to IFRS measures used in assessing the performance of the business.
Consolidated Results of Operations
Revenue for the second quarter of 2019 and year to date decreased by $8.4 million, or 6%, and $25.0 million, or 9%, respectively, compared to the corresponding periods in 2018.
These decreases were primarily due to lower sales from the ADVANZ PHARMA International segment, combined with lower foreign exchange rates impacting translated revenues from the ADVANZ PHARMA International segment, partially offset by higher sales from the ADVANZ PHARMA North America segment.
Gross profit for the second quarter of 2019 and year to date decreased by $9.6 million, or 10%, and $19.6 million, or 10%, respectively, compared to the corresponding periods in 2018, primarily due to segment revenue declines.
Gross profit percentage for the second quarter of 2019 and year to date decreased by 3% and 1%, respectively, compared to the corresponding periods in 2018, primarily due to a change in the mix of product sales within both segments.
Operating expenses for the second quarter of 2019 and year to date decreased by $42.8 million, or 31%, and $69.5 million, or 28%, respectively, compared to the corresponding periods in 2018.
The decrease in operating expenses for the second quarter of 2019 is primarily due to $24.7 million lower restructuring related, acquisition and other costs mainly associated with the Company's Recapitalization Transaction that was completed in 2018, $10.4 million lower amortization charges on intangible assets, and $7.9 million lower impairment charges.
Operating expenses were lower for the year to date compared to corresponding period in 2018, primarily due to $35.7 million lower restructuring related, acquisition and other costs mainly associated with the Company's Recapitalization Transaction that was completed in 2018, $22.9 million lower amortization charges on intangible assets, and $7.9 million lower impairment charges.
General and administrative expenses reflect costs related to salaries and benefits, professional and consulting fees, public company costs, travel and other administrative expenditures. General and administrative expenses for the second quarter of 2019 and year to date decreased by $0.3 million, or 3%, and $2.3 million, or 11%, respectively, compared to the corresponding periods in 2018. The decrease year to date is primarily due to $1.6 million lower costs associated with lease payments recorded in general and administrative expenses as a result of the revised accounting for these costs due to the adoption of IFRS 16 on January 1, 2019, combined with favourable foreign exchange rate movements impacting translation of general and administrative expenses from ADVANZ PHARMA International. The decrease was partially offset by increased legal costs within ADVANZ PHARMA North America associated with claims brought against the non-FDA approved competitors of Donnatal®.
Selling and marketing expenses reflect costs incurred by the Company for the marketing, promotion and sale of its portfolio of products across its segments. Selling and marketing costs for the second quarter of 2019 and year to date decreased by $1.7 million, or 16%, and $3.3 million, or 16%, respectively, compared to the corresponding periods in 2018. The decreases are primarily as a result of lower costs associated with sales promotion and advertising activities, as well as reduced salaries and benefits costs.
Research and development expenses reflect costs for clinical trial activities, product development, professional and consulting fees and services associated with the activities of the medical, clinical and scientific affairs, quality assurance costs, regulatory compliance and drug safety costs (Pharmacovigilence) of the Company. Research and development costs for the second quarter of 2019 increased by $0.6 million, or 8%, compared to the corresponding period in 2018 primarily due to lower clinical trial costs, combined with favourable foreign exchange rate movements impacting translation of research and development costs from ADVANZ PHARMA International. Research and development costs for the year to date 2019, compared to the same period in 2018, were essentially flat.
Adjusted EBITDA for the second quarter of 2019 and year to date decreased by $7.0 million, or 11% and $14.0 million, or 10%, compared to the corresponding periods in 2018. These declines were primarily due to lower sales and gross profits from the ADVANZ PHARMA International segment, combined with lower foreign exchange rates impacting translated results. Adjusted EBITDA by segment for the second quarter of 2019 and year to date was $41.1 million and $87.9 million, respectively from ADVANZ PHARMA International and $21.8 million and $43.3 million from ADVANZ PHARMA North America.
In addition, during the second quarter of 2019 and year to date, the Company incurred $3.1 million, and $6.4 million, respectively, of corporate costs. Corporate expenses for the second quarter of 2019 and year to date increased by $0.5 million and decreased by $0.1 million, respectively, compared to the corresponding periods in 2018.
As of June 30, 2019, the Company had cash and cash equivalents of $224.3 million and 48,913,490 limited voting shares issued and outstanding.
Conference Call Notification
The Company will hold a conference call on Wednesday, August 7, 2019, at 8:30 a.m. ET hosted by senior management. A question-and-answer session will follow the corporate update.
CONFERENCE CALL DETAILS
Wednesday, August 7, 2019
8:30 a.m. ET
(647) 427-7450 or (888) 231-8191
(416) 849-0833 or (855) 859-2056
This call is being webcast and can be accessed by going to:
An archived replay of the webcast will be available by clicking the link above.
About ADVANZ PHARMA
ADVANZ PHARMA operates an international specialty pharmaceutical business with a diversified portfolio of more than 200 patented and off-patent products, and sales in more than 90 countries, and going forward, is focused on becoming the leading platform for niche-established medicines, with advanced commercial capabilities throughout Western Europe.
ADVANZ PHARMA operates out of facilities in Mississauga, Ontario and, through its subsidiaries, operates out of facilities in Sydney, Australia; Bridgetown, Barbados; London, England; Mumbai, India; Dublin, Ireland; St. Helier, Jersey; and in Helsingborg, Sweden.
Non-IFRS Financial Measures
This press release makes reference to certain measures that are not recognized measures under International Financial Reporting Standards ("IFRS"). These non-IFRS measures are not recognized measures under IFRS and do not have a standardized meaning prescribed by IFRS, and are therefore unlikely to be comparable to similar measures presented by other companies. When used, these measures are defined in such terms to allow the reconciliation to the closest IFRS measure. These measures are provided as additional information to complement those IFRS measures by providing further understanding of the Company's results of operations from management's perspective. Accordingly, they should not be considered in isolation nor as a substitute to the Company's financial information reported under IFRS. Management uses non-IFRS measures such as EBITDA, and Adjusted EBITDA, to provide investors with supplemental information of the Company's operating performance and thus highlight trends in the Company's core business that may not otherwise be apparent when relying solely on IFRS financial measures. Management believes that securities analysts, investors and other interested parties frequently use non-IFRS measures in the evaluation of issuers. Management also uses non-IFRS measures in order to facilitate operating performance comparisons from period to period, prepare annual operating budgets, to assess its ability to meet future debt service requirements, in making capital expenditures, and to consider the business's working capital requirements. Readers are cautioned that the non-IFRS measures contained herein may not be appropriate for any other purpose.
EBITDA is defined as net income (loss) adjusted for interest and accretion expense, interest income, income taxes, depreciation and amortization of intangible assets. Management uses EBITDA to assess the Company's operating performance.
Adjusted EBITDA is defined as EBITDA adjusted for certain charges including costs associated with acquisitions, restructuring initiatives, and other costs (which includes onerous contract costs and direct costs associated with contractual terminations), management retention costs, non-operating gains / losses, integration costs, legal settlements (net of insurance recoveries) and related legal costs, non-cash items such as unrealized gains / losses on derivative instruments, share based compensation expense/recovery, fair value changes including purchase consideration and derivative financial instruments, asset impairments, fair value increases to inventory arising from purchased inventory from a business combination, gains / losses from the sale of assets and unrealized gains / losses related to foreign exchange. Management uses Adjusted EBITDA, among other non-IFRS financial measures, as the key metric in assessing business performance when comparing actual results to budgets and forecasts. Management believes Adjusted EBITDA is an important measure of operating performance and cash flow, and provides useful information to investors because it highlights trends in the underlying business that may not otherwise be apparent when relying solely on IFRS measures.
The table below sets forth the reconciliation of net income (loss) to EBITDA and to Adjusted EBITDA for the three and six month periods ended June 30, 2019, and June 30, 2018.
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Jun 30, 2019
Jun 30, 2018
Jun 30, 2019
Jun 30, 2018
Net income (loss) for the period
Interest and accretion expense
Amortization of intangible assets
Restructuring related, acquisition and other
Share-based compensation (recovery) expense
Fair value loss on purchase consideration and derivatives
Foreign exchange (gain) loss
Unrealized foreign exchange (gain) loss
Gain on debt and purchase consideration settlement
Notice Regarding Trademarks
This press release includes trademarks that are protected under applicable intellectual property laws and are the property of ADVANZ PHARMA or its affiliates or its licensors. Solely for convenience, the trademarks of ADVANZ PHARMA, its affiliates and/or its licensors referred to in this press release may appear with or without the ® or TM symbol, but such references or the absence thereof are not intended to indicate, in any way, that the Company or its affiliates or licensors will not assert, to the fullest extent under applicable law, their respective rights to these trademarks. Any other trademarks used in this press release are the property of their respective owners.
Notice regarding future-oriented financial information:
To the extent any forward-looking statements or forward-looking information in this press release or in statements made during the corresponding earnings conference call constitute future-oriented financial information or financial outlooks within the meaning of applicable securities laws, such information is being provided to demonstrate the potential financial performance of the Company and readers are cautioned that this information may not be appropriate for any other purpose and that they should not place undue reliance on such future-oriented financial information and financial outlooks.
Future-oriented financial information and financial outlooks (collectively, "FOFI"), as with forward-looking statements and forward-looking information generally, are, without limitation, based on the assumptions and subject to the risks set out below under "Notice Regarding Forward-Looking Statements", a number of which are beyond the Company's control. In addition, the following is summary of the significant assumptions underlying the FOFI contained in the Company's earnings disclosure:
- prescription trends;
- pricing for the Company's products;
- future market demand trends;
- mix of sales to government and non-government customers;
- gross profits for each product;
- foreign currency rates, including translation between the U.S. dollar and the British pound;
- inventory levels;
- operating cost estimates;
- ability to develop and market future product launches;
- anticipated timing of future product launches;
- cost to develop future products;
- anticipated timing to exit markets;
- operating cost synergies realized; and
- annual cost of current tax by jurisdiction
The FOFI do not purport to present the Company's financial condition in accordance with IFRS, and there can be no assurance that the assumptions made in preparing the FOFI will prove accurate. It is expected that there will be differences between actual and forecasted results, and the differences may be material, including due to the occurrence of unforeseen events occurring subsequent to the preparation of the FOFI. The inclusion of the FOFI in the earnings disclosure should not be regarded as an indication that ADVANZ PHARMA considers the FOFI to be a reliable prediction of future events, and the FOFI should not be relied upon as such.
Risks and other factors related to FOFI include those risks and other factors referenced in this press release as well as in ADVANZ PHARMA's filings with the Canadian Securities Administrators, including (a) the factors described under the heading "Forward-looking Statements" in ADVANZ PHARMA's Management's Discussion and Analysis dated August 7, 2019, for the period ended June 30, 2019.
The Company anticipates that its Management's Discussion and Analysis will be available online at www.sedar.com on August 7, 2019.
1 Management uses non-IFRS measures such as EBITDA and Adjusted EBITDA to provide a supplemental measure of operating performance. Please refer to the "Non-IFRS Measures" section of this press release for further information.
Notice Regarding Forward-looking Statements and Information:
This news release includes forward‐looking statements within the meaning of the United States Private Securities Litigation Reform Act of 1995 and forward‐looking information within the meaning of Canadian securities laws, regarding ADVANZ PHARMA and its business, which may include, but are not limited to, statements with respect to ADVANZ PHARMA's focus on serving the needs of patients and healthcare providers around the world with niche-established medicines, statements with respect to ADVANZ PHARMA's long-term growth strategy and refined strategic direction, ADVANZ PHARMA's outlook for 2019, ADVANZ PHARMA's intention to expand its product portfolio in order to deliver mid-term value and long-term growth through pipeline filling, optimization, licencing and development partnerships, its focus on niche and differentiated generics, complex speciality and value-added medicines, ADVANZ PHARMA's financial performance (including the performance of its operating segments), and the Company's belief that product launches from its pipeline will not generate a material amount of revenue. Often, but not always, forward‐looking statements and forward‐looking information can be identified by the use of words such as "plans", "is expected", "expects", "scheduled", "intends", "contemplates", "anticipates", "believes", "proposes" or variations (including negative and grammatical variations) of such words and phrases, or state that certain actions, events or results "may", "could", "would", "might" or "will" be taken, occur or be achieved. Such statements are based on the current expectations of ADVANZ PHARMA's management, and are based on assumptions and subject to risks and uncertainties. Although ADVANZ PHARMA's management believes that the assumptions underlying these statements are reasonable, they may prove to be incorrect. The forward‐looking events and circumstances discussed in this news release may not occur by certain dates or at all and could differ materially as a result of known and unknown risk factors and uncertainties affecting ADVANZ PHARMA, including risks associated with ADVANZ PHARMA's securities, increased indebtedness and leverage, ADVANZ PHARMA's growth, risks associated with the use of ADVANZ PHARMA's products, the inability to generate cash flows, revenues and/or stable margins, the inability to repay debt and/or satisfy future obligations, risks associated with a delay in releasing ADVANZ PHARMA's financial statements (which could result in a default under ADVANZ PHARMA's debt agreements and a violation of applicable laws), ADVANZ PHARMA's outstanding debt, risks associated with the geographic markets in which ADVANZ PHARMA operates and/or distributes its products, risks associated with distribution agreements, the pharmaceutical industry and the regulation thereof, regulatory investigations, the failure to comply with applicable laws, economic factors, market conditions, risks associated with growth and competition, the failure to obtain regulatory approvals, the equity and debt markets generally, general economic and stock market conditions, risks associated with fluctuations in exchange rates (including, without limitation, fluctuations in currencies), political risks (including changes to political conditions), risks associated with the United Kingdom's exit from the European Union (including, without limitation, risks associated with regulatory changes in the pharmaceutical industry, changes in cross‐border tariff and cost structures and the loss of access to the European Union global trade markets), risks related to patent infringement actions, the loss of intellectual property rights, risks and uncertainties detailed from time to time in ADVANZ PHARMA's filings with the Canadian Securities Administrators, and many other factors beyond the control of ADVANZ PHARMA. Although ADVANZ PHARMA has attempted to identify important factors that could cause actual actions, events or results to differ materially from those described in forward‐looking statements and information, there may be other factors that cause actions, events or results to differ from those anticipated, estimated or intended. No forward‐looking statement or information can be guaranteed. Except as required by applicable securities laws, forward‐looking statements and information speak only as of the date on which they are made and ADVANZ PHARMA undertakes no obligation to publicly update or revise any forward‐looking statement or information, whether as a result of new information, future events, or otherwise.
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