Abbvie Inc. quarterly report, Q1 FY2015

AbbVie Inc. — Q1 2015 Form 10-Q

Reporting period: Three months ended March 31, 2015. AbbVie is a global biopharmaceutical company operating in one pharmaceutical-products segment. Financial amounts are in U.S. dollars; dollar figures below are in millions unless stated otherwise.

Financial performance

MetricQ1 2015Q1 2014Change or context
Net sales$5,040$4,563Up 10% at reported exchange rates; up 18% at constant currency
Gross profit / margin$4,098 / 81%$3,463 / 76%Margin improved 5 percentage points
Operating earnings$1,687$1,351Up 25%
Net earnings$1,022$980Up 4%
Diluted EPS$0.63$0.61Up 3%
Operating cash flow$1,585$624Increase attributed primarily to stronger operating results and lower pension contributions
Cash and equivalents$7,906$8,348 at Dec. 31, 2014Down $442 million during the quarter
Debt and lease obligations, including short-term borrowings$15,273—Includes $569 million of short-term borrowings; no borrowings under the $3.0 billion revolving facility
Current assets / current liabilities$15,408 / $11,050$16,088 / $11,400 at Dec. 31, 2014Current ratio approximately 1.39 at quarter-end
Dividends declared per share$0.51$0.42Quarterly rate increased; cash dividends paid were $786 million versus $641 million

Gross-margin improvement reflected product mix, operational efficiencies, foreign-exchange effects, and lower intangible amortization. SG&A rose 10% to $1,473 million, while R&D rose 5% to $811 million. The effective tax rate increased to 27% from 24%.

Material changes and business drivers

  • HUMIRA sales increased 18% reported and 26% at constant currency to $3,111 million, representing approximately 62% of total sales.
  • VIEKIRA generated $231 million in sales following launches in the United States and Europe. Management expected the hepatitis C regimen to contribute significantly to 2015 sales growth.
  • AndroGel sales fell 40% to $153 million, reflecting market weakness and generic competition for the 1% formulation. Dyslipidemia product sales fell 54% to $43 million.
  • Other sales increases included Synthroid (+19%), Creon (+19%), and Duodopa (+19% at constant currency). International sales grew 2% reported but 17% at constant currency, with currency weakness materially affecting reported results.
  • Q1 operating cash flow was substantially higher year over year, in part because voluntary contributions to the main domestic defined-benefit pension plan were $150 million versus $370 million in Q1 2014.

Outlook, transactions, risks, and unusual items

  • Management expected 2015 sales growth from HUMIRA, the HCV launch, Creon, and Duodopa, partly offset by generic competition and declines in selected products. It also expected operating-margin improvement and operating-cash-flow growth while continuing pipeline investment. No full-year numerical guidance is provided in this filing text.
  • AbbVie agreed to acquire Pharmacyclics for approximately $21 billion, with the transaction expected to close in Q2 2015 subject to tender and regulatory conditions. It arranged an undrawn $18 billion, 364-day bridge facility and intended to issue approximately $17 billion of senior notes. Acquisition-related financing costs of $59 million were expensed in Q1.
  • The board expanded the share-repurchase authorization by $5 billion to support an accelerated repurchase intended to offset at least half of the equity issued for Pharmacyclics. Remaining authorization was approximately $9.4 billion at March 31.
  • AbbVie recorded $127 million of acquired in-process R&D charges, including a $100 million upfront payment for an exclusive anti-tau antibody license from C2N; potential additional milestone payments were up to $685 million plus royalties. Cash outflows for acquisitions, collaborations, and other arrangements totaled $736 million, including a $500 million Calico payment.
  • Net foreign-exchange loss was $164 million; management said it included $170 million of losses on liquidation of currency positions related to the terminated proposed Shire combination. The quarter also had a $549 million foreign-currency translation loss in other comprehensive income, principally associated with the weaker euro.
  • Venezuela is a significant currency uncertainty: AbbVie used the official rate of 6.3 bolivars per U.S. dollar for $265 million of net monetary assets. Using a rate of 12 would have produced a $126 million devaluation loss, according to the filing.
  • Pharmacyclics prompted negative outlook revisions from Moody’s and S&P, although their cited ratings were affirmed. AbbVie reported compliance with its revolving-credit covenants and said the facility had no amounts outstanding.
  • Three U.S. wholesalers accounted for 48% of net receivables, and substantially all U.S. sales were to those wholesalers. Government receivables in Greece, Portugal, Italy, and Spain totaled $479 million; the company noted collection risk if funding or reimbursement conditions worsen.
  • Legal matters include antitrust and product-related claims, securities litigation concerning the terminated Shire transaction, and other proceedings. Accrued litigation balances were not significant; management did not expect ultimate dispositions to materially adversely affect consolidated financial position, results, or cash flows, while acknowledging outcomes are uncertain.
  • Disclosure controls were assessed as effective. A phased ERP and infrastructure implementation was expected to continue through 2015 and would involve changes to financial-reporting controls.

Key investor verification points

  • Confirm Pharmacyclics closing, final consideration mix, funding terms, resulting leverage, and any further credit-rating changes.
  • Track HUMIRA concentration and growth, VIEKIRA adoption, and generic or market-driven declines in AndroGel and the lipid franchise.
  • Assess whether operating cash-flow growth persists after considering pension contributions, working-capital movements, and acquisition and collaboration spending.
  • Monitor foreign-exchange exposure, especially the euro and Venezuela’s official exchange rate, and distinguish earnings effects from translation adjustments.
  • Review collection trends for concentrated wholesaler and Southern European government receivables, as well as developments in material litigation and patent challenges.