Hologic Announces Financial Results for Second Quarter of Fiscal 2019

May 1, 2019 20:02 UTC
  • Revenue of $818.4 Million Grows 3.7%, 5.2% in Constant Currency
  • Company Posts GAAP Loss per Share of ($1.01) Due to Non-Cash Charges, Non-GAAP Diluted Earnings per Share (EPS) of $0.58
  • Company Raises Full-Year Guidance for Revenue and Non-GAAP EPS

MARLBOROUGH, Mass.--(BUSINESS WIRE)-- Hologic, Inc. (Nasdaq: HOLX) announced today the Company’s financial results for the fiscal second quarter ended March 30, 2019.

“We posted strong results in our second fiscal quarter, with both revenues and non-GAAP EPS exceeding our guidance ranges,” said Steve MacMillan, Hologic’s Chairman, President and Chief Executive Officer. “Growth was again driven by our largest businesses, Breast Health and Molecular Diagnostics. Our international franchises continued to perform well, our Surgical division strengthened, and our recent Breast Health acquisitions are off to a great start.”

Key Results

  • Total revenue of $818.4 million increased 3.7%, or 5.2% in constant currency, compared to the prior year period.
  • On a GAAP basis, the Company recorded a loss per share of ($1.01) due primarily to non-cash impairment charges totaling $443.8 million related to Medical Aesthetics. On a non-GAAP basis, the Company recorded diluted EPS of $0.58, an increase of 9.4% compared to the prior year period.
  • Global Molecular Diagnostics revenue of $167.8 million increased 11.4%, or 12.8% in constant currency, representing its highest growth rate in six quarters.
  • Global Breast Health revenue of $321.5 million increased 7.1%, or 8.4% in constant currency, continuing strong recent performance.
  • Global GYN Surgical revenue of $102.2 million increased 2.8%, or 4.1% in constant currency, representing its highest growth rate in seven quarters.
  • International revenue of $202.9 million increased 1.0%, or 6.9% in constant currency. All businesses grew solidly outside the United States except Medical Aesthetics, which declined.
  • Hologic’s innovation pipeline continued to be productive. Recent new product launches include the Aptima® Mycoplasma genitalium assay and the Unifi™ Analytics business intelligence tool for mammography centers in the United States, the Omni™ hysteroscope in Europe and Canada, and the LOCalizer™ wireless breast lesion localization system in Europe. In addition, the Aptima® HIV-1 Quant Dx Assay received two new CE marks in Europe – for early infant diagnosis and testing dried blood spots.
  • The Company opened a state-of-the-art Learning and Experience Centre in Zaventem, Belgium, to provide comprehensive training for customers, healthcare professionals and employees in the region.

Key financial results for the fiscal second quarter are shown in the table below.

        GAAP       Non-GAAP
        Q2’19       Q2’18      

Change

Increase
(Decrease)

      Q2’19       Q2’18      

Change

Increase

(Decrease)

Revenues       $818.4       $789.3       3.7%       $818.4       $789.3       3.7%
Gross Margin       5.2%       52.6%       (4,740 bps)       61.0%       62.7%       (170 bps)
Operating Expenses       $365.6       $1,019.3       (64.1%)       $272.8       $266.9       2.2%
Operating Margin       (39.5%)       (76.5%)       3,700 bps       27.7%       28.9%       (120 bps)
Net Margin       (33.3%)       (86.3%)       5,300 bps       19.0%       18.7%       30 bps
Diluted EPS       ($1.01)       ($2.46)       58.9%       $0.58       $0.53       9.4%
                                                 

Throughout this press release, all dollar figures are in millions, except EPS. Some totals may not foot due to rounding. Unless otherwise noted, all results are compared to the corresponding prior year period. Non-GAAP results exclude certain cash and non-cash items as discussed under “Use of Non-GAAP Financial Measures.” Constant currency percentage changes show current period revenue results as if the foreign exchange rates were the same as those in the prior year period.

Revenue Detail

                    Increase (Decrease)
$ in millions       Q2’19     Q2’18    

Global

Reported

Change

   

Global

Constant

Currency

Change

   

U.S.

Reported

Change

   

International

Reported

Change

   

International

Constant

Currency

Change

Diagnostics                                            
Cytology & Perinatal       $ 115.5     $ 117.7     (1.9 %)     0.3 %     (2.5 %)     (0.7 %)     6.0 %
Molecular Diagnostics       $ 167.8     $ 150.7     11.4 %     12.8 %     10.6 %     14.8 %     22.8 %
Blood Screening       $ 13.4     $ 11.3     19.0 %     19.0 %     18.6 %    

-

     

-

 
Total Diagnostics       $ 296.7     $ 279.7     6.0 %     7.8 %     6.2 %     5.6 %     12.9 %
Total Diagnostics ex. Blood       $ 283.3     $ 268.4     5.6 %     7.3 %     5.5 %     5.6 %     12.9 %
                                             
Breast Health                                            
Breast Imaging       $ 265.9     $ 250.4     6.2 %     7.5 %     7.5 %     1.6 %     7.2 %
Interventional Breast Solutions       $ 55.6     $ 49.7     11.8 %     12.9 %     14.7 %     (1.5 %)     4.6 %
Total Breast Health       $ 321.5     $ 300.1     7.1 %     8.4 %     8.8 %     1.2 %     6.9 %
                                             
Medical Aesthetics       $ 73.8     $ 85.5     (13.7 %)     (12.1 %)     (15.3 %)     (11.9 %)     (8.2 %)
                                             
GYN Surgical       $ 102.2     $ 99.4     2.8 %     4.1 %     2.0 %     6.5 %     14.2 %
                                             
Skeletal Health       $ 24.2     $ 24.6     (1.4 %)     0.8 %     (10.7 %)     14.9 %     20.8 %
                                             
Total       $ 818.4     $ 789.3     3.7 %     5.2 %     4.6 %     1.0 %     6.9 %
Total Revenue ex. Blood       $ 805.0     $ 778.1     3.5 %     5.0 %     4.3 %     1.0 %     6.9 %
                                                           

Other Financial Highlights

  • U.S. revenue of $615.5 million increased 4.6%. International revenue of $202.9 million increased 1.0%, or 6.9% in constant currency. Excluding Medical Aesthetics, international growth was 4.4%, or 10.9% in constant currency.
  • The recently acquired Faxitron and Focal businesses contributed $14.6 million to Breast Health revenue, an increase of 40.4% compared to what the companies recorded as independent entities in the prior year period.
  • Gross margin was 5.2% on a GAAP basis, and 61.0% on a non-GAAP basis. GAAP gross margin decreased significantly primarily due to a $374.6 million non-cash impairment charge related to Medical Aesthetics intangible assets and equipment recorded within cost of goods sold. Non-GAAP gross margin decreased 170 basis points, primarily due to unfavorable product sales mix, manufacturing variances, one-time charges, and the negative impact of a stronger U.S. dollar.
  • The Company’s effective tax rate was a benefit of 22.9% on a GAAP basis, and a provision of 21.0% on a non-GAAP basis.
  • GAAP net loss was ($272.6) million, which included an aggregate $443.8 million of non-cash impairment charges related to intangible assets and equipment in Medical Aesthetics. This compares to a GAAP net loss of ($681.4) million in the prior year period, which included impairment charges related to goodwill and an in-process research and development asset in Medical Aesthetics.
  • Adjusted non-GAAP earnings before interest, taxes, depreciation and amortization (EBITDA) was $254.1 million, an increase of 2.4%.
  • GAAP EPS of ($1.01) increased 58.9% compared to the prior year period. Non-GAAP diluted EPS of $0.58 increased 9.4%.
  • Total debt outstanding at the end of the quarter was $3.1 billion. The Company ended the quarter with cash and equivalents of $401.0 million, and a net leverage ratio (net debt over adjusted EBITDA) of 2.6 times.
  • On a trailing 12 months basis, adjusted Return on Invested Capital (ROIC) of 12.3% declined 30 basis points compared to the prior year period.

Financial Guidance for Fiscal 2019

Based on its strong performance in the fiscal second quarter, Hologic is raising its full-year guidance for revenue and non-GAAP EPS.

Hologic’s financial guidance for the third quarter and fiscal year 2019 is shown in the table below. The guidance is based on a full year non-GAAP tax rate of approximately 22%, lower than the Company’s previous estimate of 23%, and diluted shares outstanding of approximately 272 million for the full year. Constant currency guidance assumes that foreign exchange rates are the same in fiscal 2019 as in fiscal 2018. Current guidance assumes that recent foreign exchange rates persist for all of fiscal 2019.

        Current Guidance       Previous Guidance
       

Constant

Currency %

Increase

(Decrease)

     

Reported %

Increase

(Decrease)

      Guidance $      

Constant

Currency %

Increase

(Decrease)

     

Reported %

Increase

(Decrease)

     

Guidance $

Fiscal 2019

                                               
Revenue       4.3% to 4.9%       3.3% to 3.9%       $3,325 - $3,345       3.8% to 4.7%       2.7% to 3.6%       $3,305 - $3,335
GAAP EPS               N.M.       $0.06 - $0.09               N.M.       $1.39 – $1.43
Non-GAAP EPS               8.1% to 9.4%       $2.41 - $2.44               7.2% to 9.0%       $2.39 - $2.43
                                                 

Q3 2019

                                               
Revenue       1.2% to 3.0%       0.1% to 1.9%       $825 - $840                        
GAAP EPS               N.M.       $0.33 - $0.35                        
Non-GAAP EPS               3.4% to 6.9%       $0.60 - $0.62                        
                                                 

Use of Non-GAAP Financial Measures

The Company has presented the following non-GAAP financial measures in this press release: constant currency revenues; non-GAAP gross margin; non-GAAP operating expenses; non-GAAP operating margin; non-GAAP net income; non-GAAP EPS; and adjusted EBITDA. The Company defines its non-GAAP net income, EPS, and other non-GAAP financial measures to exclude, as applicable: (i) the amortization of intangible assets and impairment of goodwill, intangible assets and equipment; (ii) additional depreciation expense from acquired fixed assets and accelerated depreciation related to consolidation and closure of facilities; (iii) additional expenses resulting from the purchase accounting adjustment to record inventory at fair value; (iv) non-cash interest expense related to amortization of the debt discount from the equity conversion option of convertible notes; (v) restructuring and divestiture charges and facility closure and consolidation charges and costs incurred to integrate acquisitions (including retention, transaction bonuses, legal and professional consulting services) and separate divested businesses from existing operations; (vi) transaction related expenses for divestitures and acquisitions; (vii) debt extinguishment losses and related transaction costs; (viii) the unrealized (gains) losses on the mark-to-market of forward foreign currency contracts for which the Company has not elected hedge accounting; (ix) litigation settlement charges (benefits) and non-income tax related charges (benefits); (x) other-than-temporary impairment losses on investments and realized gains resulting from the sale of investments; (xi) the one-time discrete impact of tax reform primarily related to remeasuring net deferred tax liabilities; (xii) other one-time, non-recurring, unusual or infrequent charges, expenses or gains that may not be indicative of the Company's core business results; and (xiii) income taxes related to such adjustments. The Company defines adjusted EBITDA as its non-GAAP net income plus net interest expense, income taxes, and depreciation and amortization expense included in its non-GAAP net income.

These non-GAAP financial measures should be considered supplemental to, and not a substitute for, financial information prepared in accordance with GAAP. The company's definition of these non-GAAP measures may differ from similarly titled measures used by others.

The non-GAAP financial measures used in this press release adjust for specified items that can be highly variable or difficult to predict. The company generally uses these non-GAAP financial measures to facilitate management's financial and operational decision-making, including evaluation of Hologic's historical operating results, comparison to competitors' operating results and determination of management incentive compensation. These non-GAAP financial measures reflect an additional way of viewing aspects of the company's operations that, when viewed with GAAP results and the reconciliations to corresponding GAAP financial measures, may provide a more complete understanding of factors and trends affecting Hologic's business.

Because non-GAAP financial measures exclude the effect of items that will increase or decrease the company's reported results of operations, management strongly encourages investors to review the company's consolidated financial statements and publicly filed reports in their entirety. A reconciliation of the non-GAAP financial measures to the most directly comparable GAAP financial measures is included in the tables accompanying this release.

Future Non-GAAP Adjustments

Future GAAP EPS may be affected by changes in ongoing assumptions and judgments, and may also be affected by non-recurring, unusual or unanticipated charges, expenses or gains, which are excluded in the calculation of the Company's non-GAAP EPS guidance as described in this press release.

Conference Call and Webcast

Hologic’s management will host a conference call at 4:30 p.m. ET today to discuss its financial results for the second quarter of fiscal 2019. Approximately 10 minutes before the call, dial 888-254-3590 (in the U.S.) or +1 323-994-2093 (international) and enter access code 5259693. A replay will be available approximately two hours after the call ends through Friday, May 24, 2019. The replay numbers are 888-203-1112 (U.S.) or +1 719-457-0820 (international), access code 5259693, PIN 2953. The Company will also provide a live webcast of the call at http://investors.hologic.com.

About Hologic, Inc.

Hologic, Inc. is an innovative medical technology company primarily focused on improving women's health and well-being through early detection and treatment. For more information on Hologic, visit www.hologic.com.

Hologic, Aptima, Cynosure, LOCalizer, Unifi, and associated logos are trademarks and/or registered trademarks of Hologic, Inc. and/or its subsidiaries in the United States and/or other countries.

Forward-Looking Statements

This news release contains forward-looking information that involves risks and uncertainties, including statements about the Company’s plans, objectives, expectations and intentions. Such statements include, without limitation: financial or other information included herein based upon or otherwise incorporating judgments or estimates relating to future performance, events or expectations; the Company’s strategies, positioning, resources, capabilities, and expectations for future performance; and the Company's outlook and financial and other guidance. These forward-looking statements are based upon assumptions made by the Company as of the date hereof and are subject to known and unknown risks and uncertainties that could cause actual results to differ materially from those anticipated.

Risks and uncertainties that could adversely affect the Company’s business and prospects, and otherwise cause actual results to differ materially from those anticipated, include without limitation: the ability of the Company to successfully manage leadership and organizational changes, including the ability of the Company to attract, motivate and retain key employees; U.S., European and general worldwide economic conditions, trade relations, and related uncertainties; the Company’s reliance on third-party reimbursement policies to support the sales and market acceptance of its products, including the possible adverse impact of government regulation and changes in the availability and amount of reimbursement and uncertainties for new products or product enhancements; changes to applicable laws and regulations, including tax laws, global health care reform, and import/export trade laws; changes in guidelines, recommendations and studies published by various organizations that could affect the use of the Company’s products; uncertainties inherent in the development of new products and the enhancement of existing products, including FDA approval and/or clearance and other regulatory risks, technical risks, cost overruns and delays; the risk that products may contain undetected errors or defects or otherwise not perform as anticipated; risks associated with strategic alliances and the ability of the Company to realize anticipated benefits of those alliances; risks associated with acquisitions, including, without limitation, the Company’s ability to successfully integrate acquired businesses, the risks that the acquired businesses may not operate as effectively and efficiently as expected even if otherwise successfully integrated, and the risks that acquisitions may involve unexpected costs or unexpected liabilities; the risks of conducting business internationally; the risk of adverse exchange rate fluctuations on the Company’s international activities and businesses; manufacturing risks, including the Company’s reliance on a single or limited source of supply for key components, the need to comply with especially high standards for the manufacture of many of its products and risks associated with utilizing third party manufacturers; the Company’s ability to predict accurately the demand for its products, and products under development, and to develop strategies to address its markets successfully; the early stage of market development for certain of the Company’s products; the Company’s leverage risks, including the Company’s obligation to meet payment obligations and financial covenants associated with its debt; cybersecurity risks; risks related to the use and protection of intellectual property; expenses, uncertainties and potential liabilities relating to litigation, including, without limitation, commercial, intellectual property, employment and product liability litigation; technical innovations that could render products marketed or under development by the Company obsolete; and competition.

The risks included above are not exhaustive. Other factors that could adversely affect the Company's business and prospects are described in the filings made by the Company with the SEC. The Company expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any such statements presented herein to reflect any change in expectations or any change in events, conditions or circumstances on which any such statements are based.

SOURCE: Hologic, Inc.

Contacts

Michael Watts
Vice President, Investor Relations and Corporate Communications
858-410-8588
Michael.watts@hologic.com

Source: Hologic, Inc.

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