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Heron Therapeutics Announces Financial Results for the Three Months Ended

Key Takeaway: Heron Therapeutics Announces Financial Results for the Three Months Ended March 31, 2020 and Highlights Recent Corporate Updates SAN DIEGO, May 6, 2020 /PRNewswire/ -- Heron Therapeutics, Inc. (Nasdaq: HRTX), a commercial-stage biotechnology company focused on improving the live

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Heron Therapeutics Announces Financial Results for the Three Months Ended March 31, 2020 and Highlights Recent Corporate Updates
SAN DIEGO, May 6, 2020 /PRNewswire/ -- Heron Therapeutics, Inc. (Nasdaq: HRTX), a commercial-stage biotechnology company focused on improving the lives of patients by developing best-in-class treatments to address some of the most important unmet patient needs, today announced financial results for the three months ended March 31, 2020 and highlighted recent corporate updates.
Recent Corporate Updates
Pain Management Franchise
"We are encouraged by a recent communication with the FDA where they indicated that they continue on schedule with their review of the NDA for HTX-011, with a PDUFA date of June 26, 2020," said Barry Quart, Pharm.D., President and Chief Executive Officer of Heron. "For the CINV franchise, our customers are benefiting from the administration of CINVANTI by 2-minute IV push, an important product advantage compared to competitive products, which has led to strong first-quarter net product sales of $25.4 million."
Net product sales for the three months ended March 31, 2020 were $25.4 million, compared to $31.6 million for the same period in 2019.
Heron's net loss for the three months ended March 31, 2020 was $51.6 million, or $0.57 per share, compared to $63.0 million, or $0.80 per share, for the same period in 2019. Net loss for the three months ended March 31, 2020 included non-cash, stock-based compensation expense of $12.0 million, compared to $17.9 million for the same period in 2019.
As of March 31, 2020, Heron had cash, cash equivalents and short-term investments of $356.3 million, compared to $391.0 million as of December 31, 2019. Net cash used for operating activities for the three months ended March 31, 2020 was $32.9 million, compared to $49.0 million for the same period in 2019. Heron expects that its current cash, cash equivalents and short-term investments will be sufficient to fund its operations into 2022.
About HTX-011 for Postoperative Pain
HTX-011, an investigational non-opioid, is a dual-acting, fixed-dose combination of the local anesthetic bupivacaine with a low dose of the nonsteroidal anti-inflammatory drug meloxicam. It is the first and only extended-release local anesthetic to demonstrate in Phase 3 studies significantly reduced pain and opioid use through 72 hours compared to bupivacaine solution, the current standard-of-care local anesthetic for postoperative pain control. HTX-011 was granted Fast Track designation from the U.S. Food and Drug Administration (FDA) in the fourth quarter of 2017 and Breakthrough Therapy designation in the second quarter of 2018. Heron submitted a New Drug Application (NDA) to the FDA for HTX-011 in October of 2018 and received Priority Review designation in December of 2018. A Complete Response Letter (CRL) was received from the FDA regarding the NDA for HTX-011 on April 30, 2019 relating to chemistry, manufacturing and controls and non-clinical information. No issues related to clinical efficacy or safety were noted. Heron resubmitted an NDA to the FDA for HTX-011 in September 2019. The Prescription Drug User Fee Act (PDUFA) goal date is June 26, 2020. A Marketing Authorisation Application (MAA) for HTX-011 was validated by the European Medicines Agency (EMA) in March 2019 for review under the Centralised Procedure. Heron's New Drug Submission (NDS) for HTX-011 for the management of postoperative pain was granted Priority Review status by Health Canada in October 2019 and accepted by Health Canada in November 2019.
About CINVANTI (Aprepitant) Injectable Emulsion
CINVANTI, in combination with other antiemetic agents, is indicated in adults for the prevention of acute and delayed nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy (HEC) including high-dose cisplatin as a single-dose regimen, delayed nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy (MEC) as a single-dose regimen, and nausea and vomiting associated with initial and repeat courses of MEC as a 3-day regimen. CINVANTI is an IV formulation of aprepitant, a substance P/neurokinin-1 (NK1) receptor antagonist (RA). CINVANTI is the first IV formulation to directly deliver aprepitant, the active ingredient in EMEND capsules. Aprepitant (including its prodrug, fosaprepitant) is the only single-agent NK1 RA to significantly reduce nausea and vomiting in both the acute phase (0-24 hours after chemotherapy) and the delayed phase (24-120 hours after chemotherapy). The FDA-approved dosing administration included in the United States prescribing information for CINVANTI is a 30-minute IV infusion or a 2-minute IV injection.
Please see full prescribing information at www.CINVANTI.com.
About SUSTOL (Granisetron) Extended-Release Injection
SUSTOL is indicated in combination with other antiemetics in adults for the prevention of acute and delayed nausea and vomiting associated with initial and repeat courses of moderately emetogenic chemotherapy (MEC) or anthracycline and cyclophosphamide (AC) combination chemotherapy regimens. SUSTOL is an extended-release, injectable 5-HT3 receptor antagonist that utilizes Heron's Biochronomer drug delivery technology to maintain therapeutic levels of granisetron for 5 days. The SUSTOL global Phase 3 development program was comprised of two, large, guideline-based clinical studies that evaluated SUSTOL's efficacy and safety in more than 2,000 patients with cancer. SUSTOL's efficacy in preventing nausea and vomiting was evaluated in both the acute phase (0-24 hours after chemotherapy) and delayed phase (24-120 hours after chemotherapy).
Please see full prescribing information at www.SUSTOL.com.
About Heron Therapeutics, Inc.
Heron Therapeutics, Inc. is a commercial-stage biotechnology company focused on improving the lives of patients by developing best-in-class treatments to address some of the most important unmet patient needs. Heron is developing novel, patient-focused solutions that apply its innovative science and technologies to already-approved pharmacological agents for patients suffering from pain or cancer.
For more information, visit www.herontx.com.
Forward-looking Statements
This news release contains "forward-looking statements" as defined by the Private Securities Litigation Reform Act of 1995. Heron cautions readers that forward-looking statements are based on management's expectations and assumptions as of the date of this news release and are subject to certain risks and uncertainties that could cause actual results to differ materially, including, but not limited to, those associated with: whether the U.S. Food and Drug Administration (FDA) approves the New Drug Application (NDA) for HTX-011; the timing of the commercial launch of HTX-011; the timing of the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) review process for HTX-011; whether the European Commission (EC) authorizes the Marketing Authorisation Application (MAA) for HTX-011; the timing of Health Canada's New Drug Submission (NDS) review process for HTX-011; whether Health Canada issues a Notice of Compliance for the NDS for HTX-011; the full-year 2020 net product sales guidance for the CINV franchise; the expected future balances of Heron's cash, cash equivalents and short-term investments; the expected duration over which Heron's cash, cash equivalents and short-term investments balances will fund its operations; and other risks and uncertainties identified in the Company's filings with the U.S. Securities and Exchange Commission. Forward-looking statements reflect our analysis only on their stated date, and Heron takes no obligation to update or revise these statements except as may be required by law.
HERON THERAPEUTICS, INC.
Consolidated Balance Sheets
March 31, 2020 December 31, 2019
(Unaudited)
ASSETS
Current assets:
Cash and cash equivalents $ 103,285 $ 71,898
Short-term investments 253,061 319,074
Accounts receivable, net 34,811 39,879
Inventory 34,849 24,968
Prepaid expenses and other current assets 12,442 23,245
Total current assets 438,448 479,064
Property and equipment, net 21,908 19,618
Right-of-use lease assets 18,239 13,754
Other assets 346 346
Total assets $ 478,941 $ 512,782
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable $ 11,562 $ 2,758
Accrued clinical and manufacturing liabilities 35,321 34,614
Accrued payroll and employee liabilities 8,770 15,248
Other accrued liabilities 32,423 36,535
Current lease liabilities 2,755 1,926
Convertible notes payable to related parties, net of discount 5,934 5,624
Total current liabilities 96,765 96,705
Non-current lease liabilities 16,708 12,242
Total liabilities 113,473 108,947
Stockholders' equity:
Common stock 906 903
Additional paid-in capital 1,580,903 1,568,317
Accumulated other comprehensive income 708 85
Accumulated deficit (1,217,049 ) (1,165,470 )
Total stockholders' equity 365,468 403,835
Total liabilities and stockholders' equity $ 478,941 $ 512,782
HERON THERAPEUTICS, INC.
Condensed Consolidated Statements of Operations
(In thousands, except per share amounts)
Three Months Ended
March 31,
2020 2019
(Unaudited)
Revenues:
Net product sales $ 25,400 $ 31,602
Operating expenses:
Cost of product sales 10,622 14,962
Research and development 36,894 42,972
General and administrative 10,422 9,648
Sales and marketing 20,196 28,720
Total operating expenses 78,134 96,302
Loss from operations (52,734 ) (64,700 )
Other income, net 1,155 1,688
Net loss $ (51,579 ) $ (63,012 )
Basic and diluted net loss per share $ (0.57 ) $ (0.80 )
Shares used in computing basic and diluted net loss per share 90,409 78,419
HERON THERAPEUTICS, INC.
Consolidated Statements of Cash Flows
Three Months Ended March 31,
2020 2019
(Unaudited)
Operating activities:
Net loss $ (51,579 ) $ (63,012 )
Adjustments to reconcile net loss to net cash used for operating activities:
Stock-based compensation expense 11,974 17,902
Depreciation and amortization 621 467
Amortization of debt discount 310 247
Realized gain on available-for-sale securities - (8 )
Accretion of discount on short-term investments (117 ) (1,357 )
Impairment of property and equipment 27 27
Loss on disposal of property and equipment - 52
Change in operating assets and liabilities:
Accounts receivable 5,068 (9,355 )
Prepaid expenses and other assets 10,803 (346 )
Inventory (9,881 ) 7,611
Accounts payable 8,804 (6,052 )
Accrued clinical and manufacturing liabilities 707 (868 )
Accrued payroll and employee liabilities (6,478 ) (6,757 )
Other accrued liabilities (3,194 ) 12,425
Net cash used for operating activities (32,935 ) (49,024 )
Investing activities:
Purchases of short-term investments (28,922 ) (127,763 )
Maturities and sales of short-term investments 95,675 164,009
Purchases of property and equipment (2,938 ) (2,136 )
Net cash provided by investing activities 63,815 34,110
Financing activities:
Proceeds from stock option exercises 504 6,539
Proceeds from warrant exercises 3 -
Net cash provided by financing activities 507 6,539
Net increase (decrease) in cash and cash equivalents 31,387 (8,375 )
Cash and cash equivalents at beginning of year 71,898 31,836
Cash and cash equivalents at end of period $ 103,285 $ 23,461
Investor Relations and Media Contact:
Chief Legal, Business and Administrative Officer
Heron Therapeutics, Inc.
Last updated: May 6, 2020