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Coherus BioSciences Reports First Quarter 2020 Financial Results - First Quarter UDENYCA Net Sales of $116.2 Million - -Net Income of $35.6 Million - - Non-GAAP Net Income of $49.8 Million

Key Takeaway: Coherus BioSciences Reports First Quarter 2020 Financial Results - First Quarter UDENYCA Net Sales of $116.2 Million - -Net Income of $35.6 Million - - Non-GAAP Net Income of $49.8 Million - REDWOOD CITY, Calif., May 7, 2020 - Coherus BioSciences, Inc. ("Coherus" or the "Comp

Full Press Release Details

Coherus BioSciences Reports First Quarter 2020 Financial Results
- First Quarter UDENYCA Net Sales of $116.2 Million -
-Net Income of $35.6 Million -
- Non-GAAP Net Income of $49.8 Million -
REDWOOD CITY, Calif., May 7, 2020 - Coherus BioSciences, Inc. ("Coherus" or the "Company", Nasdaq: CHRS), today reviewed corporate events and reported financial results for the quarter ended March 31, 2020.
First Quarter 2020 and Recent Corporate Highlights
First Quarter 2020 Financial Results
Net product revenue for first quarter of 2020 was $116.2 million. Cost of goods sold for the same quarter was $6.9 million, resulting in a gross profit margin of 94%, a 213% increase compared to the net product revenue of $37.1 million for the same period in 2019. Net product revenue increased year-over-year markedly as a result of market penetration.
Research and development (R&D) expenses for the first quarter 2020 were $33.1 million, as compared to $18.8 million for the same period in 2019. The increase in R&D expenses was largely due to an upfront payment obligation of $5.0 million pursuant to the Innovent license agreement and increased expenses related to
preparations for the filing of the 351(k) BLA for CHS-1420 (Humira (adalimumab) biosimilar) and the development of other biosimilar product candidates.
Selling, general and administrative (SG&A) expenses for the first quarter of 2020 were $35.4 million, as compared to $32.7 million for the same period in 2019. The increases in SG&A expenses were mainly attributable to an increase in salesforce personnel, related commercial functions and marketing programs to support the continued growth in UDENYCA sales. The increases were partially offset by a decrease in legal costs attributable to the legal settlement that the Company entered into with Amgen in May 2019.
Cash, cash equivalents were $193.3 million as of March 31, 2020, as compared to $177.7 million as of December 31, 2019.
Net income (loss) for the first quarter of 2020 was $35.6 million, or $0.48 per share on a diluted basis, compared to a net loss of ($20.0) million, or ($0.29) per share on a basic and diluted basis for the same period in 2019.
Non-GAAP net income (loss) for the first quarter of 2020 was $49.8 million, or $0.67 per share on a diluted basis, compared to a non-GAAP net loss of ($10.5) million, or ($0.15) per share on a basic and diluted basis for the same period in 2019. See "Non-GAAP Financial Measures" below for a discussion on how we calculate non-GAAP net income (loss) and a reconciliation to the most directly comparable GAAP measure.
Guidance for the Next Nine Months from March 31, 2020
Coherus will continue delivering on the promise of biosimilars and laying the foundation for long-term growth across its three therapeutic areas:
Conference Call Information
When: Thursday, May 7, 2020 starting at 4:30 p.m. ET
Dial-in: (844) 452-6826 (Toll Free) or (765) 507-2587 (International)
Conference ID: 6167564
Please join the conference call at least 10 minutes early to register. The webcast will be archived on the Coherus website.
First quarter 2020 financial results, are posted on the Coherus website at https://investors.coherus.com/.
About Coherus BioSciences, Inc.
Coherus is a leading biosimilar company that develops and commercializes its own high-quality therapeutics as well as those of others seeking capable access to the United States market. Biosimilars are intended for use in place of existing, branded biologics to treat a range of chronic and often life-threatening diseases, with the potential to reduce costs and expand patient access. Composed of a team of proven industry veterans with world-class expertise in process science, analytical characterization, protein production, sales and marketing and clinical-regulatory development, Coherus is positioned as a leader in the global biosimilar marketplace. Coherus commercializes UDENYCA (pegfilgrastim-cbqv) in the United States and has received regulatory approval for UDENYCA in the European Union. Coherus is advancing late-stage clinical products CHS-1420, a Humira (adalimumab) biosimilar, Bioeq's Lucentis (ranibizumab) biosimilar and Innovent's Avastin (bevacizumab) biosimilar towards commercialization, and early-stage clinical products, CHS-2020, an Eylea (aflibercept) biosimilar, and CHS-131, a small molecule for nonalcoholic steatohepatitis (NASH) and multiple sclerosis. For additional information, please visit www.coherus.com.
Forward-Looking Statements
Except for the historical information contained herein, the matters set forth in this press release are forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995, including, but not limited to, Coherus' ability to continue delivering on the promise of biosimilars and laying the foundation for long-term growth across its three therapeutic areas; Coherus' ability to continue to maintain market position as the leading pegfilgrastim biosimilar of choice leveraging the validated branded-biosimilar strategy of offering a robust value proposition across all key customer segments; Coherus' ability to continue to increase penetration in market share from both Neulasta Onpro and Neulasta prefilled syringe; Coherus' ability to maintain ASP discipline for UDENYCA ; Coherus' ability to advance its Avastin (bevacizumab) oncology biosimilar candidate in-licensed from Innovent by completing a three-way PK study, as well as completing additional analytical similarity exercises; Coherus' ability to submit a 351(k) BLA with the FDA in 2021, for the Innovent biosimilar candidate to Avastin ; Coherus' ability to launch Innovent's biosimilar candidate to Avastin in the United States; Coherus' ability to facilitate Bioeq's resubmission of a 351(k) BLA with the U.S. FDA for the biosimilar candidate to Lucentis (ranibizumab) in the second half of 2020 and Coherus' ability to launch the product, if approved; Coherus' ability to advance CHS-2020 Eylea (aflibercept) ophthalmology biosimilar currently in preclinical development by initiating an expected Phase 3 clinical trial in 2021, with launch projected in 2025, if approved; Coherus' ability to complete certain manufacturing, regulatory and development activities for CHS-1420 with an anticipated filing of a 351(k) BLA in the second half of 2020; Coherus' ability to have a competitive market entry in the United States on or after July 1, 2023 for CHS-1420; Coherus' plans to pursue strategic alternatives for its program in CHS-131; and Coherus' ability to meet its R&D and SG&A expenses guidance for the full fiscal year 2020. Such forward-looking statements involve substantial risks and uncertainties that could cause Coherus' actual results, performance or achievements to differ significantly from any future results, performance or achievements expressed or implied by the forward-looking statements. Such risks and uncertainties include, among others, the risks and uncertainties inherent in the clinical drug development process; the risks and uncertainties of the regulatory approval process, including the timing of Coherus' regulatory filings; the risk that Coherus is unable to complete commercial transactions and other matters that could affect the availability or commercial potential of Coherus' biosimilar drug candidates; and the risks and uncertainties of possible patent litigation. All forward-looking statements contained in this press release speak only as of the date on which they were made. Coherus undertakes no obligation to update or revise any forward-looking statements. For a further description of the risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to Coherus' business in general, see Coherus' Quarterly Report on Form 10-Q for the three months ended March 31, 2020, to be filed with the Securities and Exchange Commission on May 7, 2020 and its future periodic reports to be filed with the Securities and Exchange Commission. Our results for the quarter ended March 31, 2020 are not necessarily indicative of our operating results for any future periods.
UDENYCA is a trademark of Coherus BioSciences, Inc.
Neulasta and Onpro are registered trademarks of Amgen Inc.
Avastin , Rituxan and Lucentis are registered trademarks of Genentech, Inc.
Humira is a registered trademark of AbbVie Inc.
Eylea is a registered trademark of Regeneron Pharmaceuticals, Inc.
Coherus BioSciences, Inc.
Condensed Consolidated Statements of Operations
(in thousands, except share and per share data)
Three Months Ended
March 31,
2020 2019
(unaudited)
Revenue:
Net product revenue $ 116,180 $ 37,098
Operating expenses:
Cost of goods sold 6,855 2,225
Research and development 33,107 18,789
Selling, general and administrative 35,350 32,683
Total operating expenses 75,312 53,697
Income (loss) from operations 40,868 (16,599)
Interest expense (4,431) (4,216)
Other income, net 68 811
Net income (loss) before income taxes 36,505 (20,004)
Income tax provision 933
Net income (loss) $ 35,572 $ (20,004)
Net income (loss) per share:
Basic $ 0.50 $ (0.29)
Diluted $ 0.48 $ (0.29)
Weighted-average number of shares used in computing net income (loss) per share:
Basic 70,662,185 69,140,697
Diluted 74,416,554 69,140,697
Coherus BioSciences, Inc.
Condensed Consolidated Balance Sheets
March 31, December 31,
2020 2019
(unaudited)
Assets
Cash and cash equivalents $ 193,252 $ 177,668
Trade receivables, net 167,450 141,992
Inventory 65,068 55,071
Other assets 40,769 34,196
Total assets $ 466,539 $ 408,927
Liabilities and Stockholders' Equity
Accrued rebate, fees and reserve $ 66,157 $ 51,120
Convertible notes 78,866 78,542
Convertible notes - related parties 26,289 26,181
Term loan 73,858 73,663
Other liabilities 64,094 74,207
Total stockholders' equity 157,275 105,214
Total liabilities and stockholders' equity $ 466,539 $ 408,927
Coherus BioSciences, Inc.
Condensed Consolidated Cash Flow
Three Months Ended
March 31,
2020 2019
(unaudited)
Cash, cash equivalents and restricted cash at beginning of the period $ 177,908 $ 73,191
Net cash provided by (used in) operating activities $ 13,477 $ (56,983)
Purchases of investments in marketable securities (14,864)
Purchases of property and equipment and cash used in other investing activities (1,616) (335)
Net cash used in investing activities $ (1,616) $ (15,199)
Proceeds from term loan, net of issuance costs 72,876
Proceeds from common stock offering, net of underwriters discounts, commissions and offering costs 8,153
Proceeds from issuance of common stock upon exercise of stock options 4,803 448
Cash used in other financing activities (880)
Net cash provided by financing activities $ 3,923 $ 81,477
Effect of exchange rate changes on cash (136)
Net increase in cash, cash equivalents and restricted cash $ 15,784 $ 9,159
Cash, cash equivalents and restricted cash at end of the period $ 193,692 $ 82,350
Reconciliation of cash, cash equivalents, and restricted cash
Cash and cash equivalents 193,252 81,515
Restricted cash balance 440 835
Cash, cash equivalents and restricted cash $ 193,692 $ 82,350
Non-GAAP Financial Measures
To supplement the financial results presented in accordance with GAAP, Coherus has also included in this press release non-GAAP net income (loss), and the related per share measures, which exclude from net income (loss), and the related per share measures, stock-based compensation expense, upfront and milestone payments under the license agreements and the related income tax effect of those non-GAAP adjustments. These non-GAAP financial measures are not prepared in accordance with GAAP, do not serve as an alternative to GAAP and may be calculated differently than similar non-GAAP financial information disclosed by other companies. Coherus encourages investors to carefully consider its results under GAAP, as well as its supplemental non-GAAP financial information and the reconciliation between these presentations set forth below, to more fully understand Coherus' business.
Coherus believes that the presentation of these non-GAAP financial measures provides useful supplementary information to, and facilitates additional analysis by, investors. In particular, Coherus believes that these non-GAAP financial measures, when considered together with its financial information prepared in accordance with GAAP, can enhance investors' and analysts' ability to meaningfully compare Coherus' results from period to period, and to identify operating trends in Coherus' business. Coherus also regularly uses these non-GAAP financial measures internally to understand, manage and evaluate its business and to make operating decisions.
Coherus BioSciences, Inc.
Reconciliation of GAAP Net Income (Loss) to Non-GAAP Net Income (Loss)
(in thousands, except share and per share data)
Three Months Ended
March 31,
2020 2019
(unaudited)
GAAP net income (loss) $ 35,572 $ (20,004)
Adjustments:
Stock based compensation expense 9,555 9,494
Upfront payment under the license agreement with Innovent 5,000
Income tax effect of the above adjustments (362)
Non-GAAP net income (loss) $ 49,765 $ (10,510)
GAAP net income (loss) per share, basic $ 0.50 $ (0.29)
GAAP net income (loss) per share, diluted $ 0.48 $ (0.29)
Non-GAAP net income (loss) per share, basic $ 0.70 $ (0.15)
Non-GAAP net income (loss) per share, diluted $ 0.67 $ (0.15)
Shares used in computing basic net income (loss) per share 70,662,185 69,140,697
Shares used in computing diluted net income (loss) per share 74,416,554 69,140,697
Investor Relations & Corporate Affairs
Coherus BioSciences, Inc.
Last updated: May 7, 2020