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8-K - 8-K - SUPERNUS PHARMACEUTICALS, INC.supn-20210804.htm


Exhibit 99.1
supernuslogoa.jpg
 
Supernus Announces Second Quarter 2021 Financial Results

Second quarter 2021 total revenues of $141.3 million, a 12% increase compared to 2020
Qelbree™ launched in the U.S. for pediatric ADHD at the end of May 2021
Qelbree sNDA for adult ADHD submitted to the FDA
SPN-830 (apomorphine infusion pump) NDA resubmission anticipated in the second half of 2021
ROCKVILLE, MD, August 4, 2021 – 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 second quarter of 2021, and associated Company developments.
“The approval and commercial launch of Qelbree for pediatric patients with ADHD mark an important milestone for children and families searching for new treatment options for ADHD,” said Jack Khattar, President and CEO of Supernus Pharmaceuticals. “As a non-controlled substance that has a unique profile of proven efficacy, safety and tolerability, Qelbree provides patients living with ADHD a novel treatment option like no other ADHD medication.”
Net Product Sales
Second quarter 2021 net product sales were $138.6 million, 12% higher than the same period in 2020.
Net Product Sales
($ in millions)Q2 2021
Q2 2020 (1)
Change %
Trokendi XR®
$78.8 $89.7 (12)%
Oxtellar XR®
25.0 23.7 %
APOKYN®
27.0 8.6 **
MYOBLOC®
4.6 1.2 **
XADAGO®
2.9 0.8 **
Qelbree0.3 — **
Net Product Sales$138.6 $124.0 12 %
___________________________________________
(1) Net product sales of APOKYN, MYOBLOC and XADAGO from June 9, 2020 to June 30, 2020.
Qelbree Launch Update
At the end of May 2021, Supernus launched Qelbree for the treatment of attention-deficit hyperactivity disorder (ADHD) in pediatric patients 6 to 17 years of age. Net product sales for the second quarter of 2021 were $0.3 million.
The early performance of Qelbree is on track with our expectations. Current trends in prescriptions reflect the heavy sampling programs with patients. Over 25,000 starter kits have been distributed to physicians since the launch and in preparation for the back-to-school season.
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Early clinical feedback about the performance of Qelbree in patients is positive and in line with the Phase III clinical results.

Product Pipeline Update
Qelbree (viloxazine, extended-release capsules) - Novel non-stimulant for the treatment of ADHD in adults
The Company recently submitted a supplemental New Drug Application (sNDA) to the U.S. Food and Drug Administration (FDA) for Qelbree for adult patients with ADHD.
SPN-830 (apomorphine infusion pump) - Continuous treatment of motor fluctuations (“on-off” episodes) in Parkinson's disease (PD)
The Company continues to plan to resubmit the SPN-830 NDA in the second half of 2021.
SPN-820 - Novel first-in-class activator of mTORC1
A randomized Phase II clinical study of SPN-820 in treatment-resistant depression is expected to start by the end of 2021.
Financial Highlights
Second quarter 2021 operating earnings were $34.1 million, as compared to $45.5 million in the second quarter of 2020. Operating earnings for the second quarter of 2021 included amortization of intangible assets expense of $5.9 million, compared to $2.4 million in the second quarter of 2020.
Second quarter 2021 net earnings and diluted earnings per share were $23.7 million and $0.43, respectively, as compared to $34.7 million, or $0.65 per diluted share, in the same period last year.
As of June 30, 2021, the Company had $855.3 million in cash, cash equivalents, current and long-term 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 including an increase to the lower end of its operating earnings guidance as set forth below:
Full Year 2021 Guidance
($ in millions)
Total revenues (1)
$550 - $580
Combined R&D and SG&A expenses (2)
$380 - $410
Operating earnings (3)
$70 - $90
Amortization of intangible assets$24
Effective tax rate (4)
28% - 31%
___________________________________________
(1) Total revenues include 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 (gain). Reflects an increase from the
original guidance of $65 - $90 million.
(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.
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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, August 4, 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) 288-1043
International dial-in:(970) 315-0267
Conference ID:1687420
Conference Call Name:Supernus Pharmaceuticals Second 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 expenditures; the Company’s ability to increase the number of prescriptions written for each of its products; the Company’s ability to increase its net revenue; 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, and projected expenditures; the Company’s ability to receive, and the timing of any receipt of, regulatory approvals to develop and commercialize the Company’s product candidates; 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.
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Supernus Pharmaceuticals, Inc.
Condensed Consolidated Balance Sheets
(in thousands, except share data)
June 30,
2021
December 31, 2020
(unaudited)
Assets
Current assets
Cash and cash equivalents$223,771 $288,640 
Marketable securities186,070 133,893 
Accounts receivable, net137,275 140,877 
Inventories, net58,391 48,325 
Prepaid expenses and other current assets33,737 18,682 
Total current assets639,244 630,417 
Long term marketable securities445,473 350,359 
Property and equipment, net17,065 37,824 
Intangible assets, net352,628 364,342 
Goodwill77,963 77,911 
Other assets40,687 43,249 
Total assets$1,573,060 $1,504,102 
Liabilities and stockholders’ equity
Current liabilities
Accounts payable and accrued liabilities$79,993 $78,934 
Accrued product returns and rebates173,598 126,192 
Contingent consideration, current portion23,540 30,900 
Other current liabilities6,316 9,082 
Total current liabilities283,447 245,108 
Convertible notes, net370,383 361,751 
Contingent consideration, long term45,430 45,800 
Operating lease liabilities, long term36,143 28,579 
Deferred income tax liabilities32,986 35,215 
Other liabilities19,092 42,791 
Total liabilities787,481 759,244 
Stockholders’ equity
Common stock, $0.001 par value; 130,000,000 shares authorized; 53,144,759 and 52,868,482 shares issued and outstanding as of June 30, 2021 and December 31, 2020, respectively
53 53 
Additional paid-in capital424,175 409,332 
Accumulated other comprehensive earnings, net of tax5,433 8,975 
Retained earnings355,918 326,498 
Total stockholders’ equity785,579 744,858 
Total liabilities and stockholders’ equity$1,573,060 $1,504,102 


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Supernus Pharmaceuticals, Inc.
Condensed Consolidated Statements of Earnings
(in thousands, except share and per share data)

Three Months ended
June 30,
Six Months ended
June 30,
2021202020212020
(unaudited)(unaudited)
Revenues
Net product sales$138,628 $123,984 $267,009 $216,474 
Royalty revenues2,701 2,745 5,252 5,231 
Total revenues141,329 126,729 272,261 221,705 
Costs and expenses
Cost of goods sold (a)
25,028 8,386 39,982 12,538 
Research and development15,455 22,247 49,735 41,184 
Selling, general and administrative69,535 48,103 130,992 89,717 
Amortization of intangible assets5,948 2,445 11,955 3,706 
Contingent consideration gain(8,750)— (7,730)— 
Total costs and expenses107,216 81,181 224,934 147,145 
Operating earnings34,113 45,548 47,327 74,560 
Other income (expense)
Interest expense(5,467)(5,815)(11,564)(11,570)
Interest and other income, net2,589 7,477 6,401 13,254 
Total other income (expense)(2,878)1,662 (5,163)1,684 
Earnings before income taxes31,235 47,210 42,164 76,244 
Income tax expense7,509 12,543 12,744 20,059 
Net earnings$23,726 $34,667 $29,420 $56,185 
Earnings per share
Basic$0.45 $0.66 $0.56 $1.07 
Diluted$0.43 $0.65 $0.54 $1.05 
Weighted-average shares outstanding
Basic53,005,344 52,557,035 52,985,472 52,545,910 
Diluted54,724,146 53,645,828 54,601,533 53,611,418 
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(a) Excludes amortization of acquired intangible assets

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CONTACTS:

Jack A. Khattar, President and CEO
Jim Kelly, Executive Vice President and CFO
Supernus Pharmaceuticals, Inc.
Tel: (301) 838-2591

or

INVESTOR CONTACT:
Peter Vozzo
Westwicke/ICR
Office: (443) 213-0505
Mobile: (443) 377-4767
Email: peter.vozzo@westwicke.com

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