Incyte Reports 2019 Third Quarter Financial Results and Provides Updates on Key Clinical Programs

Total product and royalty revenues of $534 million (+24% vs. Q3 2018) and Jakafi® (ruxolitinib) revenues of $433 million (+25% vs. Q3 2018) for the quarter ended September 30, 2019; raising full year 2019 Jakafi revenue guidance to a new range of $1.65-1.68 billion Multiple positive developments within late-stage clinical portfolio, including New Drug Application (NDA) submission for pemigatinib, successful outcome of ruxolitinib REACH2 trial and updated data from ruxolitinib cream showing continued improvement in repigmentation of vitiligo lesions Conference Call and Webcast Scheduled Today at 8:00 a.m. EDT WILMINGTON, Del.--(BUSINESS WIRE)--Oct. 29, 2019-- Incyte Corporation (Nasdaq:INCY) today reports 2019 third quarter financial results and provides a status update on the Company’s development portfolio. “Revenue growth continues to be very strong, driven by robust demand for Jakafi (ruxolitinib) in all three approved indications and, as a result, we are raising guidance for full year Jakafi net sales,” stated Hervé Hoppenot, Chief Executive Officer, Incyte. “At the beginning of 2019, we laid out an ambitious set of development goals for our late-stage portfolio, and in the third quarter we have continued to execute against them. The recent clinical success in the REACH2 trial of ruxolitinib in steroid-refractory acute GVHD; the updated data from pemigatinib in cholangiocarcinoma and subsequent NDA submission; and the recently-presented 52-week data from the randomized Phase 2 trial of ruxolitinib cream in vitiligo are all illustrative of the significant progress we have made this year.” Portfolio Update Oncology – key highlights The positive result of REACH2, the Phase 3 study evaluating ruxolitinib in patients with steroid-refractory acute graft-versus-host disease (GVHD), was announced in October. The study met its primary endpoint of superior overall response rate (ORR) at Day 28 with ruxolitinib treatment compared to best available therapy. No new safety signals were observed, and the ruxolitinib safety profile in REACH2 was consistent with that seen in previously reported studies in steroid-refractory acute GVHD. A recent interim efficacy and safety analysis conducted by an Independent Data Monitoring Committee (IDMC) recommended that the Phase 3 REACH3 trial of ruxolitinib in patients with steroid-refractory chronic GVHD should continue without modification. The result of REACH3 is expected in 2020. The top-line result from GRAVITAS-301, the Phase 3 trial of itacitinib as a treatment for patients with newly diagnosed acute GVHD, is expected to be available at the end of 2019. GRAVITAS-309, a Phase 3 trial of itacitinib as a treatment for patients with newly diagnosed chronic GVHD, was initiated in January of this year with results expected in 2021. The NDA seeking approval for pemigatinib as a second-line treatment for cholangiocarcinoma patients with FGFR2 fusions or rearrangements was submitted to the U.S. Food and Drug Administration (FDA) under Breakthrough Therapy designation. Data from FIGHT-202, which supported the NDA, were presented at the recent European Society for Medical Oncology (ESMO) Congress. Enrollment in the continuous dosing cohort of FIGHT-201, the Phase 2 trial of pemigatinib in patients with bladder cancer, is expected to complete by the end of 2019 and FIGHT-207, a Phase 2 solid tumor-agnostic trial evaluating pemigatinib in patients with driver-activations of FGF/FGFR, has been initiated. Indication and status Ruxolitinib (JAK1/JAK2) Steroid-refractory acute GVHD: Phase 3 (REACH2) met primary endpoint1 Steroid-refractory chronic GVHD: Phase 3 (REACH3)1 Essential thrombocythemia: Phase 2 (RESET) Refractory myelofibrosis: Phase 2 with PI3Kδ, PIM or JAK1 inhibition Itacitinib (JAK1) Treatment-naïve acute GVHD: Phase 3 (GRAVITAS-301) Treatment-naïve chronic GVHD: Phase 3 (GRAVITAS-309) Pemigatinib (FGFR1/2/3) Cholangiocarcinoma: Phase 2 (FIGHT-202), Phase 3 (FIGHT-302) Bladder cancer: Phase 2 (FIGHT-201) 8p11 MPN: Phase 2 (FIGHT-203) Tumor agnostic: Phase 2 (FIGHT-207) Parsaclisib (PI3Kδ) Follicular lymphoma: Phase 2 (CITADEL-203) Marginal zone lymphoma: Phase 2 (CITADEL-204) Mantle cell lymphoma: Phase 2 (CITADEL-205) INCMGA0012 (PD-1)1 MSI-high endometrial cancer: Phase 2 (POD1UM-101) Merkel cell carcinoma: Phase 2 (POD1UM-201) Anal cancer: Phase 2 (POD1UM-202) Notes: 1) Clinical development of ruxolitinib in GVHD, including REACH2 and REACH3, conducted in collaboration with Novartis 2) INCMGA0012 licensed from MacroGenics Inflammation and autoimmunity (IAI) – key highlights Evidence of continued improvement with longer-term treatment was shown in the 52-week data from the randomized Phase 2 trial of ruxolitinib cream in patients with vitiligo, which were recently presented at the European Academy of Dermatology and Venereology (EADV) Congress. The Phase 3 TRuE-V development program of ruxolitinib cream in patients with vitiligo was initiated in September, with initial results expected in 2021. The Phase 3 TRuE-AD development program of ruxolitinib cream in patients with atopic dermatitis is ongoing, with initial results expected in the first half of 2020. Indication and status Ruxolitinib cream (JAK1/JAK2) Atopic dermatitis: Phase 3 (TRuE-AD) Vitiligo: Phase 3 (TRuE-V) INCB54707 (JAK1) Hidradenitis suppurativa: Phase 2 Itacitinib (JAK1) Ulcerative colitis: Phase 2 Parsaclisib (PI3Kδ) Autoimmune hemolytic anemia: Phase 2 Sjögren's syndrome: Phase 2 Discovery and early development – key highlights Incyte’s portfolio of earlier-stage clinical candidates is detailed below. Modality Candidates Small molecules INCB01158 (ARG)1, INCB81776 (AXL/MER), INCB62079 (FGFR4), epacadostat (IDO1), INCB59872 (LSD1), INCB53914 (PIM), INCB86550 (PD-L1) Monoclonal antibodies2 INCAGN1876 (GITR), INCAGN2385 (LAG-3), INCAGN1949 (OX40), INCAGN2390 (TIM-3) Bispecific antibodies MCLA-145 (PD-L1xCD137)3 Notes: 1) INCB01158 development in collaboration with Calithera 2) Discovery collaboration with Agenus 3) MCLA-145 development in collaboration with Merus Partnered – key highlights The status of Incyte’s partnered compounds is detailed below. Indication and status Baricitinib (JAK1/JAK2)1 Atopic dermatitis: Phase 3 (BREEZE-AD) Systemic lupus erythematosus: Phase 3 Severe alopecia areata: Phase 3 Capmatinib (MET)2 NSCLC (with MET exon 14 skipping mutations): NDA expected in Q4 2019 (by Novartis) Notes: 1) Worldwide rights to baricitinib licensed to Lilly: approved as Olumiant in multiple territories globally for certain patients with moderate to severe rheumatoid arthritis 2) Worldwide rights to capmatinib licensed to Novartis 2019 Third-Quarter and Year-to-Date Financial Results The financial measures presented in this press release for the three and nine months ended September 30, 2019 and 2018 have been prepared by the Company in accordance with U.S. Generally Accepted Accounting Principles (“GAAP”), unless otherwise identified as a Non-GAAP financial measure. Management believes that Non-GAAP information is useful for investors, when considered in conjunction with Incyte’s GAAP disclosures. Management uses such information internally and externally for establishing budgets, operating goals and financial planning purposes. These metrics are also used to manage the Company’s business and monitor performance. The Company adjusts, where appropriate, for expenses in order to reflect the Company’s core operations. The Company believes these adjustments are useful to investors by providing an enhanced understanding of the financial performance of the Company’s core operations. The metrics have been adopted to align the Company with disclosures provided by industry peers. Beginning in the first quarter of 2019, after reviewing our Reconciliation of GAAP Net Income to Selected Non-GAAP Adjusted Information with the U.S. Securities & Exchange Commission, we no longer adjust for upfront consideration and milestones that are part of collaboration agreements with new or existing partners. This revised methodology is reflected in this press release for the three and nine months ended September 30, 2019 and 2018. Non-GAAP information is not prepared under a comprehensive set of accounting rules and should only be used in conjunction with and to supplement Incyte’s operating results as reported under GAAP. Non-GAAP measures may be defined and calculated differently by other companies in our industry. The Company’s 2019 financial guidance related to research and development and selling, general and administrative expenses does not include estimates associated with any potential future strategic transactions. Revenues For the quarter ended September 30, 2019, net product revenues of Jakafi were $433 million as compared to $348 million for the same period in 2018, representing 25 percent growth. For the nine months ended September 30, 2019, net product revenues of Jakafi were $1.2 billion as compared to $1.0 billion for the same period in 2018, representing 21 percent growth. For the quarter ended September 30, 2019, net product revenues of Iclusig® (ponatinib) were $21 million as compared to $20 million for the same period in 2018. For the nine months ended September 30, 2019, net product revenues of Iclusig were $66 million as compared to $61 million for the same period in 2018. For the quarter and nine months ended September 30, 2019, product royalties from sales of Jakavi® (ruxolitinib), which has been out-licensed to Novartis outside of the United States, were $58 million and $161 million, respectively, as compared to $51 million and $139 million, respectively, for the same periods in 2018. For the quarter and nine months ended September 30, 2019, product royalties from sales of Olumiant® (baricitinib), which has been out-licensed to Lilly globally, were $22 million and $57 million, respectively, as compared to $11 million and $26 million, respectively, for the same periods in 2018. For the quarter and nine months ended September 30, 2019, milestone and contract revenues earned from our collaborative partners were $18 million and $78 million, respectively, as compared to $20 million and $120 million, respectively, for the same periods in 2018. For the quarter and nine months ended September 30, 2019, total revenues were $552 million and $1.6 billion, respectively, as compared to $450 million and $1.4 billion, respectively, for the same periods in 2018. Year Over Year Revenue Growth (in thousands, unaudited) Three Months Ended Nine Months Ended September 30, % September 30, % 2019 2018 Change 2019 2018 Change Revenues: Jakafi net product revenue $ 433,387 $ 347,567 25% $ 1,218,504 $1,006,911 21% Iclusig net product revenue 20,611 20,148 2% 65,640 60,833 8% Jakavi product royalty revenues 58,440 50,923 15% 160,906 139,361 15% Olumiant product royalty revenues 21,643 11,000 97% 56,820 26,231 117% Product and royalty revenues 534,081 429,638 24% 1,501,870 1,233,336 22% Milestone and contract revenues 17,500 20,000 77,500 120,000 Other revenues - 45 - 145 Total GAAP revenues $ 551,581 $ 449,683 23% $ 1,579,370 $1,353,481 17% Cost of product revenues GAAP cost of product revenues for the quarter and nine months ended September 30, 2019 was $30 million and $82 million, respectively, as compared to $25 million and $68 million, respectively, for the same periods in 2018. Non-GAAP cost of product revenues for the quarter and nine months ended September 30, 2019 was $24 million and $65 million, respectively, as compared to $19 million and $52 million, respectively, for the same periods in 2018. Non-GAAP cost of product revenues excludes the amortization of licensed intellectual property for Iclusig relating to the acquisition of the European business of ARIAD Pharmaceuticals, Inc. and the cost of stock-based compensation. Research and development expenses GAAP research and development expenses for the quarter and nine months ended September 30, 2019 were $281 million and $841 million, respectively, as compared to $293 million and $894 million, respectively, for the same periods in 2018. The decrease in GAAP research and development expenses over the prior year quarter and prior year nine month period was driven primarily by our decision to no longer co-fund the development of baricitinib with Lilly and lower costs related to the epacadostat program, partially offset by costs to advance our other internal development programs. Non-GAAP research and development expenses for the quarter and nine months ended September 30, 2019 were $251 million and $756 million, respectively, including upfront and milestone expenses related to collaborative agreements of $0 million and $25 million, respectively. Non-GAAP research and development expenses for the quarter and nine months ended September 30, 2018 were $266 million and $818 million, respectively, including upfront and milestone expenses related to collaborative agreements of $15 million and $47 million, respectively. Non-GAAP research and development expenses exclude the cost of stock-based compensation. Selling, general and administrative expenses GAAP selling, general and administrative expenses for the quarter and nine months ended September 30, 2019 were $103 million and $333 million, respectively, as compared to $97 million and $326 million, respectively, for the same periods in 2018. Non-GAAP selling, general and administrative expenses for the quarter and nine months ended September 30, 2019 were $90 million and $294 million, respectively, as compared to $85 million and $291 million, respectively, for the same periods in 2018. Non-GAAP selling, general and administrative expenses exclude the cost of stock-based compensation. Change in fair value of acquisition-related contingent consideration GAAP change in fair value of acquisition-related contingent consideration for the quarter and nine months ended September 30, 2019 and was $3 million and $17 million, respectively, as compared to $5 million and $19 million, respectively, for the same periods in 2018. Unrealized gain (loss) on long term investments GAAP unrealized gain on long term investments for the quarter and nine months ended September 30, 2019 was $2 million and $19 million, respectively. GAAP unrealized loss on long term investments for the quarter and nine months ended September 30, 2018 was $10 million and $22 million, respectively. The unrealized gain (loss) on long term investments represents the fair market value adjustments of the Company’s investments in Agenus, Calithera, Merus and Syros. Net income GAAP net income for the quarter ended September 30, 2019 was $128 million, or $0.60 per basic and $0.59 per diluted share, as compared to net income of $29 million, or $0.14 per basic and diluted share for the same period in 2018. GAAP net income for the nine months ended September 30, 2019 was $336 million, or $1.57 per basic and $1.55 per diluted share, as compared to net income of $40 million, or $0.19 per basic and diluted share for the same period in 2018. Non-GAAP net income for the quarter ended September 30, 2019 was $179 million, or $0.83 per basic and $0.82 per diluted share, as compared to Non-GAAP net income of $87 million, or $0.41 per basic and diluted share for the same period in 2018. Non-GAAP net income for the nine months ended September 30, 2019 was $476 million, or $2.22 per basic and $2.19 per diluted share, as compared to Non-GAAP net income of $208 million, or $0.98 per basic and $0.97 per diluted share for the same period in 2018. Cash, cash equivalents and marketable securities position As of September 30, 2019 and December 31, 2018, cash, cash equivalents and marketable securities totaled $2.0 billion and $1.4 billion, respectively. 2019 Financial Guidance The Company has updated its full year 2019 financial guidance, as detailed below. Current Previous Jakafi net product revenues $1,650 - $1,680 million $1,610 - $1,650 million Iclusig net product revenues $90 - $100 million Unchanged GAAP Cost of product revenues $112 - $117 million Unchanged Non-GAAP Cost of product revenues(1) $90 - $95 million Unchanged GAAP Research and development expenses $1,145 - $1,195 million Unchanged Non-GAAP Research and development expenses(2) $1,020 - $1,070 million Unchanged GAAP Selling, general and administrative expenses $471 - $521 million Unchanged Non-GAAP Selling, general and administrative expenses(2) $420 - $470 million Unchanged GAAP Change in fair value of acquisition-related contingent consideration $30 million Unchanged Non-GAAP Change in fair value of acquisition-related contingent consideration(3) $0 million Unchanged (1) Adjusted to exclude the amortization of licensed intellectual property for Iclusig relating to the acquisition of the European business of ARIAD Pharmaceuticals, Inc. and the estimated cost of stock-based compensation. (2) Adjusted to exclude the estimated cost of stock-based compensation. (3) Adjusted to exclude the change in fair value of estimated future royalties relating to sales of Iclusig in the licensed territory relating to the acquisition of the European business of ARIAD Pharmaceuticals, Inc. Future Non-GAAP financial measures may also exclude impairment of goodwill or other assets, changes in the fair value of equity investments in our collaboration partners, non-cash interest expense related to the amortization of the initial discount on our 2020 Senior Notes and the impact on our tax provision of discrete changes in our valuation allowance position on deferred tax assets. Conference Call and Webcast Information Incyte will hold a conference call and webcast this morning at 8:00 a.m. EDT. To access the conference call, please dial 877-407-3042 for domestic callers or 201-389-0864 for international callers. When prompted, provide the conference identification number, 13695247. If you are unable to participate, a replay of the conference call will be available for 30 days. The replay dial-in number for the United States is 877-660-6853 and the dial-in number for international callers is 201-612-7415. To access the replay you will need the conference identification number, 13695247. The conference call will also be webcast live and can be accessed at www.incyte.com in the Investors section under “Events and Presentations”. About Incyte Incyte Corporation is a Wilmington, Delaware-based biopharmaceutical company focused on the discovery, development and commercialization of proprietary therapeutics. For additional information on Incyte, please visit the Company’s website at www.incyte.com. Follow @Incyte on Twitter at https://twitter.com/Incyte. About Jakafi® (ruxolitinib) Jakafi is a first-in-class JAK1/JAK2 inhibitor approved by the U.S. FDA for treatment of steroid-refractory acute GVHD in adult and pediatric patients 12 years and older. Jakafi is also indicated for treatment of polycythemia vera (PV) in adults who have had an inadequate response to or are intolerant of hydroxyurea as well as adults with intermediate or high-risk myelofibrosis (MF), including primary MF, post-polycythemia vera MF and post-essential thrombocythemia MF. Jakafi is marketed by Incyte in the United States and by Novartis as Jakavi® (ruxolitinib) outside the United States. Jakafi is a registered trademark of Incyte Corporation. Jakavi is a registered trademark of Novartis AG in countries outside the United States. About Iclusig® (ponatinib) tablets Iclusig targets not only native BCR-ABL but also its isoforms that carry mutations that confer resistance to treatment, including the T315I mutation, which has been associated with resistance to other approved TKIs. In the EU, Iclusig is approved for the treatment of adult patients with chronic phase, accelerated phase or blast phase chronic myeloid leukemia (CML) who are resistant to dasatinib or nilotinib; who are intolerant to dasatinib or nilotinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the T315I mutation, or the treatment of adult patients with Philadelphia-chromosome positive acute lymphoblastic leukemia (Ph+ ALL) who are resistant to dasatinib; who are intolerant to dasatinib and for whom subsequent treatment with imatinib is not clinically appropriate; or who have the T315I mutation. Incyte has an exclusive license from ARIAD Pharmaceuticals, Inc., since acquired by Takeda Pharmaceutical Company Limited, to develop and commercialize Iclusig in the European Union and 22 other countries, including Switzerland, Norway, Turkey, Israel and Russia. Forward-Looking Statements Except for the historical information set forth herein, the matters set forth in this release contain predictions, estimates and other forward-looking statements, including without limitation statements regarding: the revision to the Company’s 2019 Jakafi revenue guidance range; the expected timing of results of the trials evaluating ruxolitinib and itacitinib in GVHD; the expected date of completion of enrollment in the Phase 2 trial of pemigatinib in patients with bladder cancer; expectations of the Company’s collaboration partner for the submission of an NDA for capmatinib; the expected timing of the receipt of data from the Phase 3 trials of ruxolitinib cream in vitiligo and atopic dermatitis; and the Company’s updated financial guidance for 2019 and the expectations underlying such guidance. These forward-looking statements are based on the Company’s current expectations and subject to risks and uncertainties that may cause actual results to differ materially, including unanticipated developments in and risks related to: unanticipated delays; further research and development and the results of clinical trials possibly being unsuccessful or insufficient to meet applicable regulatory standards or warrant continued development; the ability to enroll sufficient numbers of subjects in clinical trials; determinations made by the FDA; the Company's dependence on its relationships with and changes in the plans of its collaboration partners; the efficacy or safety of the Company’s products and the products of the Company’s collaboration partners; the acceptance of the Company’s products and the products of the Company’s collaboration partners in the marketplace; market competition; unexpected variations in the demand for the Company’s products; sales, marketing, manufacturing and distribution requirements; greater than expected expenses, including expenses relating to litigation or strategic activities; and other risks detailed from time to time in the Company’s reports filed with the Securities and Exchange Commission, including its quarterly report on Form 10-Q for the quarter ended June 30, 2019. The Company disclaims any intent or obligation to update these forward-looking statements. INCYTE CORPORATION CONSOLIDATED STATEMENTS OF OPERATIONS (unaudited, in thousands, except per share amounts) Three Months Ended Nine Months Ended September 30, September 30, 2019 2018 2019 2018 GAAP GAAP Revenues: Product revenues, net $ 453,998 $ 367,715 $ 1,284,144 $ 1,067,744 Product royalty revenues 80,083 61,923 217,726 165,592 Milestone and contract revenues 17,500 20,000 77,500 120,000 Other revenues - 45 - 145 Total revenues 551,581 449,683 1,579,370 1,353,481 Costs and expenses: Cost of product revenues (including definite-lived intangible amortization) 30,040 24,795 82,034 67,757 Research and development 281,336 292,527 841,244 893,719 Selling, general and administrative 102,608 96,522 332,534 326,049 Change in fair value of acquisition-related contingent consideration 3,281 4,720 16,560 18,708 Total costs and expenses 417,265 418,564 1,272,372 1,306,233 Income from operations 134,316 31,119 306,998 47,248 Other income (expense), net 11,961 10,211 36,334 20,481 Interest expense (597 ) (405) (1,248) (1,188) Unrealized gain (loss) on long term investments 2,339 (9,949) 18,703 (21,911) Income before provision for income taxes 148,019 30,976 360,787 44,630 Provision for income taxes 19,748 1,800 24,886 4,200 Net income $ 128,271 $ 29,176 $ 335,901 $ 40,430 Net income per share: Basic $ 0.60 $ 0.14 $ 1.57 $ 0.19 Diluted $ 0.59 $ 0.14 $ 1.55 $ 0.19 Shares used in computing net income per share: Basic 215,199 212,627 214,628 212,172 Diluted 217,791 215,964 217,393 215,516 INCYTE CORPORATION CONDENSED CONSOLIDATED BALANCE SHEETS (unaudited, in thousands) September 30, December 31, 2019 2018 ASSETS Cash, cash equivalents and marketable securities $ 1,986,218 $ 1,438,323 Accounts receivable 276,116 307,598 Property and equipment, net 347,250 319,751 Finance lease right-of-use assets, net 29,690 - Inventory 13,318 10,405 Prepaid expenses and other assets 89,519 99,529 Long term investments 117,902 99,199 Other intangible assets, net 199,212 215,364 Goodwill 155,593 155,593 Total assets $ 3,214,818 $ 2,645,762 LIABILITIES AND STOCKHOLDERS’ EQUITY Accounts payable, accrued expenses and other liabilities $ 492,211 $ 415,360 Convertible senior notes 18,080 17,434 Acquisition-related contingent consideration 282,000 287,001 Stockholders’ equity 2,422,527 1,925,967 Total liabilities and stockholders’ equity $ 3,214,818 $ 2,645,762 INCYTE CORPORATION RECONCILIATION OF GAAP NET INCOME TO SELECTED NON-GAAP ADJUSTED INFORMATION (unaudited, in thousands, except per share amounts) Three Months Ended Nine Months Ended September 30, September 30, 2019 2018 2019 2018 GAAP Net Income $ 128,271 $ 29,176 $ 335,901 $ 40,430 Adjustments1: Non-cash stock compensation from equity awards (R&D)2 30,426 26,266 85,464 75,283 Non-cash stock compensation from equity awards (SG&A)2 12,758 11,687 38,575 35,500 Non-cash stock compensation from equity awards (COGS)5 173 - 525 - Non-cash interest expense related to convertible notes3 218 305 646 902 Changes in fair value of equity investments4 (2,339) 9,949 (18,703) 21,911 Amortization of acquired product rights5 5,384 5,384 16,152 16,152 Change in fair value of contingent consideration6 3,281 4,720 16,560 18,708 Tax effect of Non-GAAP adjustments7 847 (10) 910 (400) Non-GAAP Net Income $ 179,019 $ 87,477 $ 476,030 $ 208,486 Non-GAAP net income per share: Basic $ 0.83 $ 0.41 $ 2.22 $ 0.98 Diluted $ 0.82 $ 0.41 $ 2.19 $ 0.97 Shares used in computing Non-GAAP net income per share: Basic 215,199 212,627 214,628 212,172 Diluted 217,791 215,964 217,393 215,516 1 Beginning in the first quarter of 2019, after reviewing our Reconciliation of GAAP Net Income to Selected Non-GAAP Adjusted Information with the U.S. Securities & Exchange Commission, we no longer adjust for milestones received from new or existing partners and upfront consideration and milestones paid to new or existing partners, which is reflected above for the three and nine months ended September 30, 2019 and 2018. Included within the Milestone and contract revenues line item in the Consolidated Statements of Operations (in thousands) for the three and nine months ended September 30, 2019 are upfront consideration and milestones of $17,500 and $77,500, respectively, earned from our collaborative partners. Also included within the Milestone and contract revenues line item in the Consolidated Statements of Operations (in thousands) for the three and nine months ended September 30, 2018 are milestones of $20,000 and $120,000, respectively, earned from our collaborative partners. Included within the Research and development expenses line item in the Consolidated Statements of Operations (in thousands) for the nine months ended September 30, 2019 are upfront and milestone expenses of $25,000 related to our collaborative agreements. Also included within the Research and development expenses line item in the Consolidated Statements of Operations (in thousands) for the three and nine months ended September 30, 2018 are upfront and milestone expenses of $15,000 and $47,444, respectively, related to our collaborative agreements. 2 As included within the Research and development expenses line item in the Consolidated Statements of Operations, and within the Selling, general and administrative expenses line item in the Consolidated Statements of Operations. 3 As included within the Interest expense line item in the Consolidated Statements of Operations. 4 As included within the Unrealized gain (loss) on long term investments line item in the Consolidated Statements of Operations. 5 As included within the Cost of product revenues (including definite-lived intangible amortization) line item in the Consolidated Statements of Operations. Acquired product rights of licensed intellectual property for Iclusig is amortized utilizing a straight-line method over the estimated useful life of 12.5 years. 6 As included within the Change in fair value of acquisition-related contingent consideration line item in the Consolidated Statements of Operations. 7 As included within the Provision for income taxes line item in the Consolidated Statements of Operations. Income tax effects of Non-GAAP adjustments are calculated using the applicable statutory tax rate for the jurisdictions in which the charges are incurred, while taking into consideration any valuation allowances. View source version on businesswire.com: https://www.businesswire.com/news/home/20191029005365/en/ Source: Incyte Corporation Media Catalina Loveman +1 302 498 6171 [email protected] Investors Michael Booth, DPhil +1 302 498 5914 [email protected] Investor Relations Inquiries [email protected] Our Company Our Leadership What We Do Portfolio Hematology and Oncology Inflammation and Autoimmunity Partnerships Careers Join Our Team Life at Incyte How We Hire Incyte Involved Patient Resources HCP Resources Our Stories News Press Releases Company Statements Media Contact Email Alerts Investors Events & Presentations Financials Stock Information Governance Resources Responsibility Compliance & Transparency Contact Us Our Locations Medical Information Legal Notice Suppliers Site Map Privacy Policy Cookie Policy Consumer Health Data Privacy Policy © 2012-2026 Incyte.

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