The following excerpt is from the company's SEC filing.
Royalties earned rose 28% to $55.8 million compared with the first quarter of 2017.
Net income attributable to Innoviva stockholders increased 76% from the first quarter of 2017 to $29.6 million, or $0.29 per basic share.
BRISBANE, Calif., April 26, 2018
Innoviva, Inc. (NASDAQ: INVA) (the Company) today reported financial results for the first quarter ended March 31, 2018.
Gross royalties earned on net sales of RELVAR
from Glaxo Group Limited (GSK) during the first quarter of 2018 were $55.8 million, up 28% from $43.7 million in the first quarter of 2017.
Income from operations for the first quarter of 2018 was $40.7 million, a 39% increase compared with $29.3 million for the same period in 2017. Adjusted EBITDA was $45.6 million for the first quarter of 2018, up from $35.4 million in the first quarter of 2017.
Net cash and cash equivalents, short-term investments and marketable securities totaled $56.5 million as of March 31, 2018, which reflects a $120.0 million prepayment made by the Company on its Term B loan in February 2018. Royalties receivable from GSK totaled $55.8 million at March 31, 2018.
I am pleased to report that both RELVAR
continued to achieve record TRx market share in the U.S., reaching 20.4% and 17.4%, respectively, for the quarter. First quarter 2018 net sales were unfavorably impacted by payor rebate adjustments related to prior periods and increased competitive pricing pressures, said Eric dEsparbes, interim Principal Executive Officer of Innoviva. In addition, during the quarter, we improved Innovivas capital structure through a substantial prepayment of our Term B Loan balance, which led to a reduction in our net cash interest expense.
GSK Net Sales:
First quarter 2018 net sales of RELVAR
by GSK were $307.7 million, up 19% from $257.9 million in the first quarter of 2017, with $137.0 million in net sales from the U.S. market and $170.7 million from non-U.S. markets.
First quarter 2018 net sales of ANORO
by GSK were $134.2 million, up 73% from $77.5 million in the first quarter of 2017, with $83.5 million net sales from the U.S. market and $50.7 million from non-U.S. markets.
First quarter 2018 net sales of TRELEGY
by GSK were $14.6 million.
Announced in March 2018 the positive European Commission approval for labelling update to RELVAR
in patients with asthma.
Made a partial prepayment in February 2018 of $120.0 million on the principal amount outstanding under the Companys outstanding senior secured first lien term loan debt.
Additional Financial Results for the First Quarter of 2018
Total net royalty revenue for the first quarter of 2018 was $52.4 million, up 30% compared with $40.3 million in the first quarter of 2017. Gross royalty revenues for the first quarter of 2018 included royalties of $46.1 million from global net sales of RELVAR
, royalties of $8.7 million from global net sales of ANORO
and $1.0 million from net sales of TRELEGY
in the U.S. market.
Total operating expenses for the first quarter of 2018 were $11.7 million (which includes $2.7 million payment to a related party pursuant to a settlement agreement, and $3.2 million in cash severance payments) compared with $11.1 million in the first quarter of 2017 (which included $4.2 million in proxy contest and related legal costs).
Net income attributable to Innoviva stockholders in the first quarter of 2018 was $29.6 million (or $0.29 per basic share), up 76% from the first quarter of 2017.
Adjusted EBITDA for the first quarter of 2018 was $45.6 million, up 29% from the first quarter of 2017. Adjusted earnings per share for the first quarter of 2018 was $0.35 per share, compared with $0.19 per share in the first quarter of 2017.
Non-GAAP Financial Measures
To supplement the consolidated financial statements presented in accordance with generally accepted accounting principles in the United States, or GAAP, Innoviva uses the non-GAAP financial measures of adjusted EBITDA and adjusted earnings per share. Generally, a non-GAAP financial measure is a numerical measure of a companys operating performance or financial position that either excludes or includes amounts that are not normally included or excluded in the most directly comparable measure calculated and presented in accordance with GAAP. A reconciliation of these non-GAAP financial measures to the closest GAAP financial measure is presented in the accompanying financial table under the headings Reconciliation of Non-GAAP Financial Measures to GAAP.
Innoviva believes that the non-GAAP financial information provided in this release can assist investors, research analysts and others in understanding and assessing Innovivas on-going operations, financial performance and prospects for the future and provides an additional tool to use in comparing Innovivas financial results with other companies in Innovivas industry or with similar operating profiles, without regard to financing or capital structures. Adjusted EBITDA and adjusted earnings per share are used as supplemental financial operating measures by Innovivas management and frequently discussed with external users of its financial statements.
Adjusted EBITDA is determined by taking GAAP net income attributable to Innoviva stockholders and adding back interest expense (income), taxes, stock-based compensation expense, write off of debt issuance costs, depreciation expense and amortization of capitalized fees paid to a related party. Innoviva believes the non-GAAP measure of adjusted EBITDA is important as it measures the Companys ability to generate cash to pay interest costs and support its indebtedness, and it is also
used currently in the Companys annual performance review process. Innovivas method of computing adjusted EBITDA may not be the same method used to compute similar measures reported by other companies.
Adjusted earnings per share is determined by taking adjusted net income and dividing the total by the fully diluted number of shares outstanding used to calculate the GAAP diluted EPS. Adjusted net income is determined by taking GAAP net income attributable to Innoviva stockholders and adding back stock-based compensation expense, write off of debt issuance costs, amortization of debt discount, depreciation expense and amortization of capitalized fees paid to a related party. Innoviva believes the non-GAAP measure of adjusted earnings per share provides useful information about the Companys core operating performance, and enhances the overall understanding of the Companys past financial performance and its prospects for the future. Innovivas method of computing adjusted earnings per share may not be the same method used to compute similar measures reported by other companies.
Adjusted EBITDA, adjusted net income and adjusted earnings per share should not be considered in isolation or as a substitute to net income, income from operations, cash flows from operating activities, earnings per share or any other measure of financial performance presented in accordance with GAAP. Adjusted earnings per share is not intended to represent cash flow per share and does not represent a measure of liquidity or cash available for distribution. The principal limitation of these non-GAAP financial measures is that it excludes significant elements that are required by GAAP to be recorded in Innovivas consolidated financial statements. In addition, it is subject to inherent limitations as it reflects the exercise of judgments by management in determining these non-GAAP financial measures. In order to compensate for these limitations, management of Innoviva presents its non-GAAP financial measures in connection with its GAAP results. Investors are encouraged to review the reconciliation of Innovivas non-GAAP financial measures to their most directly comparable GAAP financial measure.
Innoviva is focused on bringing compelling new medicines to patients in areas of unmet need by leveraging its significant expertise in the development, commercialization and financial management of bio-pharmaceuticals. Innovivas portfolio is anchored by the respiratory assets partnered with Glaxo Group Limited (GSK), including RELVAR
, ANORO® ELLIPTA
, which were jointly developed by Innoviva and GSK. Under the agreement with GSK, Innoviva is eligible to receive associated royalty revenues from RELVAR
. In addition, Innoviva retains a 15 percent economic interest in royalty payments made by GSK for TRELEGY
and earlier-stage programs partnered with Theravance BioPharma, Inc. For more information, please visit Innovivas website at www.inva.com.
are trademarks of the GlaxoSmithKline group of companies.
Forward Looking Statements
This press release contains certain forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995 regarding, among other things, statements relating to goals, plans, objectives and future events. Innoviva intends such forward-looking statements to be covered by the safe harbor provisions for forward-looking statements contained in Section 21E of the
Securities Exchange Act of 1934 and the Private Securities Litigation Reform Act of 1995. The words anticipate, expect, goal, intend, objective, opportunity, plan, potential, target and similar expressions are intended to identify such forward-looking statements. Such forward-looking statements involve substantial risks, uncertainties and assumptions. These statements are based on the current estimates and assumptions of the management of Innoviva as of the date of this press release and are subject to risks, uncertainties, changes in circumstances, assumptions and other factors that may cause the actual results of Innoviva to be materially different from those reflected in the forward-looking statements. Important factors that could cause actual results to differ materially from those indicated by such forward-looking statements include, among others, risks related to: expected cost savings, lower than expected future royalty revenue from respiratory products partnered with GSK, the commercialization of RELVAR
in the jurisdictions in which these products have been approved; the strategies, plans and objectives of Innoviva (including Innovivas growth strategy and corporate development initiatives beyond the existing respiratory portfolio); the timing, manner, amount and planned growth of anticipated potential capital returns to shareholders; the status and timing of clinical studies, data analysis and communication of results; the potential benefits and mechanisms of action of product candidates; expectations for product candidates through development and commercialization; the timing of regulatory approval of product candidates; and projections of revenue, expenses and other financial items. Other risks affecting Innoviva are described under the headings Risk Factors and Managements Discussion and Analysis of Financial Condition and Results of Operations contained in Innovivas Annual Report on Form 10-K for the year ended December 31, 2017, which is on file with the Securities and Exchange Commission (SEC) and available on the SECs website at www.sec.gov. Additional factors may be described in those sections of Innovivas Quarterly Report on Form 10-Q for the quarter ended March 31, 2018, to be filed with the SEC in the second quarter of 2018. In addition to the risks described above and in Innovivas other filings with the SEC, other unknown or unpredictable factors also could affect Innovivas results. Past performance is not necessarily indicative of future results. No forward-looking statements can be guaranteed and actual results may differ materially from such statements. Given these uncertainties, you should not place undue reliance on these forward-looking statements. The information in this press release is provided only as of the date hereof, and Innoviva assumes no obligation to update its forward-looking statements on account of new information, future events or otherwise, except as required by law.
Interim Principal Executive Officer and Sr. Vice President and Chief Financial Officer
Condensed Consolidated Statements of Operations
(in thousands, except per share data)
Three Months Ended
Royalty revenue from a related party, net
Revenue from collaborative arrangements from a related party
Research and development
General and administrative
General and administrative - proxy contest and litigation costs
General and administrative - cash severance expenses
General and administrative - related party
Other income (expense), net
Net income attributable to noncontrolling interest
Net income attributable to Innoviva stockholders
Basic earnings per share
Diluted earnings per share
Shares used in computing basic earnings per share
Shares used in computing diluted earnings per share
(1) Revenue is comprised of the following (in thousands):
Royalties from a related party
Amortization of capitalized fees paid to a related party
Strategic alliance - MABA program
Total revenue from a related party
(2) Amounts include stock-based compensation expense as follows (in thousands):
Total stock-based compensation
Condensed Consolidated Balance Sheets
Cash, cash equivalents and marketable securities
Related party receivables from collaborative arrangements
Property and equipment, net
Capitalized fees paid to a related party, net
Liabilities and stockholders deficit
Other current liabilities
Accrued interest payable
Convertible subordinated notes, net
Convertible senior notes, net
Senior secured term loans, net
Other long-term liabilities
Innoviva stockholders deficit
Total liabilities and stockholders deficit
(1) The selected consolidated balance sheet amounts at December 31, 2017 are derived from audited financial statements.
Cash Flows Summary
Net cash provided by operating activities
Net cash provided by investing activities
Net cash provided by (used in) financing activities
Reconciliation from GAAP net income to adjusted EBITDA:
GAAP net income attributable to Innoviva stockholders
Interest expense (income), net
Write-off of debt issuance costs
Reconciliation from GAAP net income to adjusted net income for computing adjusted earnings per share:
Write off of debt issuance costs
Amortization of debt discount
The above information was disclosed in a filing to the SEC. To see the filing, click here.
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