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Supernus Pharmaceuticals, Inc. (SUPN)

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Previous Close29.83
Open29.73
Bid29.50 x 800
Ask30.95 x 800
Day's Range29.45 - 30.62
52 Week Range17.20 - 32.31
Volume388,916
Avg. Volume586,731
Market Cap1.619B
Beta (5Y Monthly)1.25
PE Ratio (TTM)14.78
EPS (TTM)2.07
Earnings DateMay 05, 2021
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateN/A
1y Target Est35.00
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  • Supernus Pharmaceuticals Inc (SUPN) Q1 2021 Earnings Call Transcript
    Motley Fool

    Supernus Pharmaceuticals Inc (SUPN) Q1 2021 Earnings Call Transcript

    Image source: The Motley Fool. Supernus Pharmaceuticals Inc (NASDAQ: SUPN)Q1 2021 Earnings CallMay 5, 2021, 4:30 p.m. ETContents: Prepared Remarks Questions and Answers Call Participants Prepared Remarks: OperatorGood afternoon and welcome to Supernus Pharmaceuticals First Quarter 2021 Financial Results Conference Call.

  • Supernus Pharmaceuticals (SUPN) Q1 Earnings and Revenues Miss Estimates
    Zacks

    Supernus Pharmaceuticals (SUPN) Q1 Earnings and Revenues Miss Estimates

    Supernus (SUPN) delivered earnings and revenue surprises of -57.69% and -0.63%, respectively, for the quarter ended March 2021. Do the numbers hold clues to what lies ahead for the stock?

  • Supernus Announces First Quarter 2021 Financial Results
    GlobeNewswire

    Supernus Announces First Quarter 2021 Financial Results

    First quarter 2021 total revenues of $130.9 million, a 38% increase compared to 2020Qelbree™ approved by FDA for pediatric ADHD and on track for a U.S. launch in Q2 2021Qelbree sNDA submission for adult ADHD anticipated in the third quarter of 2021SPN-830 (apomorphine infusion pump) NDA resubmission anticipated in the second half of 2021SPN-820 (mTORC1) has advanced towards a Phase II clinical program in treatment-resistant depression following successful completion of MAD study ROCKVILLE, Md., May 05, 2021 (GLOBE NEWSWIRE) -- Supernus Pharmaceuticals, Inc. (Nasdaq: SUPN), a biopharmaceutical company focused on developing and commercializing products for the treatment of central nervous system (CNS) diseases, today reported financial results for the first quarter of 2021, and associated Company developments. “The approval of Qelbree provides pediatric patients living with ADHD a therapy with proven efficacy and a tolerable safety profile, and that is not a controlled substance,” said Jack Khattar, President and CEO of Supernus Pharmaceuticals. “Our Qelbree commercial launch activities are ongoing and include engagement with both physicians and patient groups who have expressed great interest in this unique new alternative for the treatment of ADHD.” Net Product Sales First quarter 2021 net product sales were $128.4 million, 39% higher than the same period in 2020. Net Product Sales ($ in millions)Q1 2021 Q1 2020 Change %Trokendi XR®$71.8 $68.6 5%Oxtellar XR®27.4 23.9 14%APOKYN®21.7 — ** MYOBLOC®4.3 — ** XADAGO®3.2 — ** Net Product Sales$128.4 $92.5 39% Qelbree Launch Update In April 2021, the U.S. Food and Drug Administration (FDA) approved Qelbree for the treatment of attention-deficit hyperactivity disorder (ADHD) in pediatric patients 6 to 17 years of age. The Company plans to make Qelbree available in the U.S. during the second quarter of 2021.Supernus will conduct post-marketing commitment studies, including a new study of Qelbree in preschool aged children with ADHD, 4 to 5 years of age. The completion of these studies responds to a written request from the FDA and should therefore result in the FDA granting an additional 6 months of market exclusivity. Product Pipeline Update Qelbree (viloxazine, extended-release capsules) - Novel non-stimulant for the treatment of ADHD in adults In December 2020, the Company announced positive results from a Phase III trial in adult patients with ADHD and plans to submit a supplemental New Drug Application (sNDA) to the FDA for Qelbree in adults in the third quarter of 2021. SPN-830 (apomorphine infusion pump) - Continuous treatment of motor fluctuations (“on-off” episodes) in PD The company recently met with the FDA to discuss the path forward for resubmission of the SPN-830 NDA. The FDA provided additional clarity related to the contents of the November 2020 Refusal to File (RTF) letter and the requirements for resubmission. The Company now plans to resubmit the SPN-830 NDA in the second half of 2021. SPN-820 - Novel first-in-class activator of mTORC1 SPN-820 has advanced to a Phase II clinical program in treatment-resistant depression following the successful completion of a multiple-ascending dose (MAD) study in healthy volunteers. In the MAD study, SPN-820 exhibited a favorable safety and tolerability profile across a broad range of potentially therapeutic doses.The Company expects to initiate a randomized Phase II clinical study in treatment-resistant depression by the end of 2021. Financial Highlights First quarter 2021 operating earnings were $13.2 million, as compared to $29.0 million in the first quarter 2020. In the first quarter of 2021, the Company recorded non-cash research and development expense of $15 million related to the equity investment in Navitor as a result of the accounting impact of the March 2021 Navitor corporate restructuring and non-cash contingent consideration expense of $1 million associated with the 2020 USWM acquisition. Operating earnings for the first quarter of 2021 included amortization of intangible assets expense of $6.0 million, compared to $1.3 million in the first quarter of 2020. First quarter 2021 net earnings and diluted earnings per share were $5.7 million and $0.11, respectively, as compared to $21.5 million, or $0.40 per diluted share, in the same period last year. As of March 31, 2021, the Company had $807.7 million in cash, cash equivalents and marketable securities, compared to $772.9 million as of December 31, 2020. Full Year 2021 Financial Guidance For full year 2021, the Company reiterates its prior financial guidance and added full year 2021 effective tax rate guidance as set forth below: Full Year 2021 Guidance($ in millions)Total revenues1$550 - $580Combined R&D and SG&A expenses2$380 - $410Operating earnings3$65 - $90Amortization of intangible assets$24Effective Tax Rate428% - 31% ___________________________________________ 1) Total revenues includes net product sales and royalty revenue. Includes $10 million for Qelbree™ net product sales.2) Combined research and development and selling, general and administrative expenses.3) Operating earnings include amortization of intangible assets and contingent consideration expense.4) The full year 2021 effective tax rate guidance of 28% - 31% is above the normally expected range of 26% - 28% due to the effect of discrete tax items in the period. Conference Call Details The Company will hold a conference call hosted by Jack Khattar, President and Chief Executive Officer and Jim Kelly, Executive Vice President and Chief Financial Officer, to discuss these results at 4:30 p.m. Eastern Time, today, May 5, 2021. Please refer to the information below for conference call dial-in information and webcast registration. Callers should dial in approximately 10 minutes prior to the start of the call. Conference dial-in:(877) 288-1043International dial-in:(970) 315-0267Conference ID:9275942Conference Call Name:Supernus Pharmaceuticals First Quarter 2021 Results Conference Call Following the live call, a replay will be available on the Company's website, www.supernus.com, under “Investor Relations”. About Supernus Pharmaceuticals, Inc. Supernus Pharmaceuticals is a biopharmaceutical company focused on developing and commercializing products for the treatment of central nervous system (CNS) diseases. Our diverse neuroscience portfolio includes approved treatments for epilepsy, migraine, ADHD, hypomobility in Parkinson’s disease, cervical dystonia and chronic sialorrhea. We are developing a broad range of novel CNS product candidates including new potential treatments for hypomobility in Parkinson’s disease, epilepsy, depression, and rare CNS disorders. For more information, please visit www.supernus.com Forward-Looking Statements This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements do not convey historical information but relate to predicted or potential future events that are based upon management's current expectations. These statements are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. In addition to the factors mentioned in this press release, such risks and uncertainties include, but are not limited to, the Company’s ability to sustain and increase its profitability; the Company’s ability to raise sufficient capital to fully implement its corporate strategy; the implementation of the Company’s corporate strategy; the Company’s future financial performance and projected revenue and expenditures; the Company’s ability to increase the number of prescriptions written for each of its products; the Company’s ability to increase its revenues; the Company’s ability to commercialize its products including Qelbree; the Company’s ability to enter into future collaborations with pharmaceutical companies and academic institutions or to obtain funding from government agencies; the Company’s product research and development activities, including the timing and progress of the Company’s clinical trials; the Company’s ability to receive, and the timing of any receipt of, regulatory approvals to develop and commercialize the Company’s product candidates including SPN-830 and SPN-812 for adult ADHD patients; the Company’s ability to protect its intellectual property and operate its business without infringing upon the intellectual property rights of others; the Company’s expectations regarding federal, state and foreign regulatory requirements; the therapeutic benefits, effectiveness and safety of the Company’s product candidates; the accuracy of the Company’s estimates of the size and characteristics of the markets that may be addressed by its product candidates; the Company’s ability to increase its manufacturing capabilities for its products and product candidates; the Company’s projected markets and growth in markets; the Company’s product formulations and patient needs and potential funding sources; the Company’s staffing needs; and other risk factors set forth from time to time in the Company’s filings with the Securities and Exchange Commission made pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934, as amended. The Company undertakes no obligation to update the information in this press release to reflect events or circumstances after the date hereof or to reflect the occurrence of anticipated or unanticipated events. Supernus Pharmaceuticals, Inc.Condensed Consolidated Balance Sheets(in thousands, except share data) March 31, 2021 December 31, 2020 (unaudited) Assets Current assets Cash and cash equivalents$255,642 $288,640 Marketable securities135,459 133,893 Accounts receivable, net127,065 140,877 Inventories, net50,226 48,325 Prepaid expenses and other current assets17,631 18,682 Total current assets586,023 630,417 Long term marketable securities416,566 350,359 Property and equipment, net37,950 37,824 Intangible assets, net358,736 364,342 Goodwill77,911 77,911 Other assets30,257 43,249 Total assets$1,507,443 $1,504,102 Liabilities and stockholders’ equity Current liabilities Accounts payable and accrued liabilities$70,099 $78,934 Accrued product returns and rebates128,736 126,192 Contingent consideration, current portion31,520 30,900 Other current liabilities10,457 9,082 Total current liabilities240,812 245,108 Convertible notes, net366,038 361,751 Contingent consideration, long term46,200 45,800 Operating lease liabilities, long term28,532 28,579 Deferred income tax liabilities31,742 35,215 Other liabilities39,675 42,791 Total liabilities752,999 759,244 Stockholders’ equity Common stock, $0.001 par value; 130,000,000 shares authorized; 52,994,137 and 52,868,482 shares issued and outstanding as of March 31, 2021 and December 31, 2020, respectively53 53 Additional paid-in capital415,950 409,332 Accumulated other comprehensive earnings, net of tax6,249 8,975 Retained earnings332,192 326,498 Total stockholders’ equity754,444 744,858 Total liabilities and stockholders’ equity$1,507,443 $1,504,102 Supernus Pharmaceuticals, Inc.Condensed Consolidated Statements of Earnings(in thousands, except share and per share data) Three Months ended March 31, 2021 2020 (unaudited)Revenues Net product sales$128,381 $92,490 Royalty revenues2,551 2,486 Total revenues130,932 94,976 Costs and expenses Cost of goods sold (a)14,954 4,152 Research and development34,280 18,937 Selling, general and administrative61,457 41,614 Amortization of intangible assets6,007 1,261 Contingent consideration expense1,020 — Total costs and expenses117,718 65,964 Operating earnings13,214 29,012 Other income (expense) Interest expense(6,097) (5,755) Interest and other income, net3,812 5,777 Total other income (expense)(2,285) 22 Earnings before income taxes10,929 29,034 Income tax expense5,235 7,516 Net earnings$5,694 $21,518 Earnings per share Basic$0.11 $0.41 Diluted$0.11 $0.40 Weighted-average shares outstanding Basic52,927,467 52,534,787 Diluted54,196,971 53,581,051 ___________________________________________ (a) Excludes amortization of acquired intangible assets CONTACTS: Jack A. Khattar, President and CEOJim Kelly, Executive Vice President and CFOSupernus Pharmaceuticals, Inc.Tel: (301) 838-2591 or INVESTOR CONTACT:Peter VozzoWestwicke/ICROffice: (443) 213-0505Mobile: (443) 377-4767Email: peter.vozzo@westwicke.com