Xeris Biopharma Reports Third Quarter 2023 Financial Results
- Record revenue growth
- Tightened full-year revenue guidance
- Positive product revenue growth and net revenue increase
- Successful formulation of target product profile for XeriJect™
- None.
Achieved record revenue of
Tightens full-year 2023 revenue guidance from
Ended Q3 with
Extended maturity of approximately two-thirds of 2025 Convertible Senior Notes to 2028
Successfully formulated the prespecified target product profile of the XeriJect™ formulation of TEPEZZA®
Hosting conference call and webcast today at 8:30 a.m. ET
“We continue to demonstrate record revenue growth as we execute on our strategy. Because of this strong performance, we are further tightening our full year 2023 revenue guidance from
Third Quarter 2023 Highlights
|
Three months ended
|
|
Change |
|||||||
|
2023 |
|
2022 |
|
$ |
% |
||||
Product revenue (in thousands): |
|
|
|
|
|
|
||||
Gvoke |
$ |
17,735 |
|
$ |
13,663 |
|
$ |
4,072 |
29.8 |
|
Keveyis |
|
15,865 |
|
|
13,371 |
|
2,494 |
18.7 |
||
Recorlev |
|
8,097 |
|
|
2,520 |
|
5,577 |
nm |
||
Product revenue, net |
|
41,697 |
|
|
29,554 |
|
12,143 |
41.1 |
||
Royalty, contract and other revenue |
|
6,623 |
|
|
171 |
|
6,452 |
nm |
||
Total revenue |
$ |
48,320 |
|
$ |
29,725 |
|
$ |
18,595 |
62.6 |
|
nm - not meaningful |
Commercial Products
-
Gvoke®: Third quarter 2023 net revenue was
as compared to$17.7 million in the third quarter of 2022 – an increase of approximately$13.7 million 30% . Gvoke prescriptions topped 58,000 for the first time, growing52% compared to the same period in 2022. Gvoke’s market share of the retail TRx glucagon market grew to over31% through late October. -
Keveyis®: Third quarter net revenue was
– an increase of approximately$15.9 million 19% compared to the same period in 2022. The average number of patients on Keveyis increased approximately5% from the same period in 2022. -
Recorlev®: Third quarter net revenue was
– an increase of$8.1 million compared to the same period of 2022. The average number of patients on Recorlev increased over$5.6 million 203% from the same period in 2022.
Pipeline Program
-
XeriSol® levothyroxine (XP-8121): The Phase 2 clinical study is over
85% enrolled, and the study should be completed in the first half of 2024 based on the current enrollment rate.
Technology Partnerships
-
Horizon/Amgen: Xeris successfully formulated the prespecified target product profile of the XeriJect™ formulation of TEPEZZA® which triggered revenue of
in the third quarter from a milestone payment under the research collaboration and option agreement with Horizon (subsequently acquired by Amgen) that was signed in November 2022. The payment was subsequently received in the fourth quarter. Amgen has the option to license the XeriJect technology to further the development of an ultra-concentrated, ready-to-use, subcutaneous injection of TEPEZZA®.$6.0 million
Year-to-Date 2023 Financial Results
|
Nine Months Ended September 30, |
|
Change |
|||||||
|
2023 |
|
2022 |
|
$ |
% |
||||
Product revenue (in thousands): |
|
|
|
|
|
|
||||
Gvoke |
$ |
48,406 |
|
$ |
37,595 |
|
$ |
10,811 |
28.8 |
|
Keveyis |
|
42,708 |
|
|
35,506 |
|
|
7,202 |
20.3 |
|
Recorlev |
|
19,741 |
|
|
3,623 |
|
|
16,118 |
nm |
|
Product revenue, net |
|
110,855 |
|
|
76,724 |
|
|
34,131 |
44.5 |
|
Royalty, contract and other revenue |
|
8,669 |
|
|
380 |
|
|
8,289 |
nm |
|
Total revenue |
$ |
119,524 |
|
$ |
77,104 |
|
$ |
42,420 |
55.0 |
|
nm - not meaningful |
-
Gvoke®: Net revenue was
for the nine months ended September 30, 2023, a$48.4 million 29% increase compared to prior year. Gvoke prescriptions for the first three quarters of 2023 were over 156,000 TRx’s, growing51% compared to the same period in 2022. The growth in product demand was partially offset by a decrease in net pricing. -
Keveyis®: Net revenue was
for the nine months ended September 30, 2023, a$42.7 million 20% increase from last year. This increase was driven by higher patient demand and an increase in net pricing. -
Recorlev®: Net revenue was
for the nine months ended September 30,2023, a$19.7 million increase from last year, driven primarily by increases in the number of patients on therapy.$16.1 million
Cost of goods sold increased by
Research and development expenses decreased by
Selling, general and administrative expenses increased by
Net Loss was
Cash, cash equivalents, and short-term investments at September 30, 2023 was
Shares outstanding at October 31, 2023 was 138,124,595.
Upcoming Events
Xeris will participate in the following investor conferences:
- Jefferies London Healthcare Conference, November 14-16, 2023
- 14th Annual Craig-Hallum Alpha Select Conference, November 16, 2023 (1x1s only)
- 35th Annual Piper Sandler Healthcare Conference, November 28-30, 2023
Details of each event will be available on Xeris’ website. Contact the respective sponsor to request a 1x1 meeting.
Third Quarter Conference Call and Webcast Details
Xeris will host a conference call and webcast on Thursday, November 9, 2023 at 8:30 a.m. Eastern Time. To pre-register for the conference call, please use the following link: https://www.netroadshow.com/events/login?show=59946218&confId=55658. After registering, a confirmation email will be sent, including dial-in details and a unique code for entry. The Company recommends registering a minimum of ten minutes prior to the start of the call. Following the conference call, a replay will be available until Thursday, November 23, 2023 at US: 1 929 458 6194, US Toll Free: 1 866 813 9403,
In addition, a live audio of the conference call will be available as a webcast. To join the webcast, please visit “Events” on the investor relations page of the Company’s website at www.xerispharma.com or use the following link: https://events.q4inc.com/attendee/482975153.
About Xeris
Xeris (Nasdaq: XERS) is a growth-oriented biopharmaceutical company committed to improving patient lives by developing and commercializing innovative products across a range of therapies. Xeris has three commercially available products; Gvoke®, a ready-to-use liquid glucagon for the treatment of severe hypoglycemia, Keveyis®, the first and only FDA-approved therapy for primary periodic paralysis, and Recorlev® for the treatment of endogenous Cushing’s syndrome. Xeris also has a robust pipeline of development programs to extend the current marketed products into important new indications and uses and bring new products forward using its proprietary formulation technology platforms, XeriSol™ and XeriJect™, supporting long-term product development and commercial success.
Xeris Biopharma Holdings is headquartered in
Forward-Looking Statements
Any statements in this press release other than statements of historical fact are forward-looking statements. Forward-looking statements include, but are not limited to, statements about future expectations, plans and prospects for Xeris Biopharma Holdings, Inc. including statements regarding the financial outlook for 2023, including projections that the company will achieve cash flow breakeven in the fourth quarter and revenue guidance, the market and therapeutic potential of its products and product candidates, the timing of clinical studies and trials, including advancement of its levothyroxine clinical program and expected Phase 2 study completion in the first half of 2024, the potential utility of its formulation platforms, cash management, and other statements containing the words “will,” “would,” “continue,” “expect,” “should,” “anticipate” and similar expressions, constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. These forward-looking statements are based on numerous assumptions and assessments made in light of Xeris’ experience and perception of historical trends, current conditions, business strategies, operating environment, future developments, geopolitical factors and other factors it believes appropriate. By their nature, forward-looking statements involve known and unknown risks and uncertainties because they relate to events and depend on circumstances that will occur in the future. The various factors that could cause Xeris’ actual results, performance or achievements, industry results and developments to differ materially from those expressed in or implied by such forward-looking statements, include, but are not limited to, its financial position and need for financing, including to fund its product development programs or commercialization efforts, whether its products will achieve and maintain market acceptance in a competitive business environment, its reliance on third-party suppliers, including single-source suppliers, its reliance on third parties to conduct clinical trials, the ability of its product candidates to compete successfully with existing and new drugs, and its and collaborators’ ability to protect its intellectual property and proprietary technology. No assurance can be given that such expectations will be realized and persons reading this communication are, therefore, cautioned not to place undue reliance on these forward-looking statements. Additional risks and information about potential impacts of financial, operational, economic, competitive, regulatory, governmental, technological, and other factors that may affect Xeris can be found in Xeris’ filings, including its most recently filed Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission, the contents of which are not incorporated by reference into, nor do they form part of, this communication. Forward-looking statements in this communication are based on information available to us, as of the date of this communication and, while we believe our assumptions are reasonable, actual results may differ materially. Subject to any obligations under applicable law, we do not undertake any obligation to update any forward-looking statement whether as a result of new information, future developments or otherwise, or to conform any forward-looking statement to actual results, future events, or to changes in expectations.
XERIS BIOPHARMA HOLDINGS, INC. CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS (in thousands, except share and per share data) (unaudited) |
|||||||||||
|
Three Months Ended
|
|
Nine Months Ended
|
||||||||
|
2023 |
|
2022 |
|
2023 |
|
2022 |
||||
Product revenue, net |
$ |
41,697 |
|
$ |
29,554 |
|
$ |
110,855 |
|
$ |
76,724 |
Royalty, contract and other revenue |
|
6,623 |
|
|
171 |
|
|
8,669 |
|
|
380 |
Total revenue |
|
48,320 |
|
|
29,725 |
|
|
119,524 |
|
|
77,104 |
Costs and expenses: |
|
|
|
|
|
|
|
||||
Cost of goods sold |
|
8,201 |
|
|
5,260 |
|
|
21,075 |
|
|
16,343 |
Research and development |
|
5,034 |
|
|
6,043 |
|
|
15,959 |
|
|
16,011 |
Selling, general and administrative |
|
37,287 |
|
|
34,491 |
|
|
108,527 |
|
|
103,388 |
Amortization of intangible assets |
|
2,711 |
|
|
2,711 |
|
|
8,132 |
|
|
8,132 |
Total costs and expenses |
|
53,233 |
|
|
48,505 |
|
|
153,693 |
|
|
143,874 |
Loss from operations |
|
(4,913) |
|
|
(18,780) |
|
|
(34,169) |
|
|
(66,770) |
Other expense |
|
(7,614) |
|
|
(3,390) |
|
|
(15,709) |
|
|
(16,046) |
Net loss before benefit from income taxes |
|
(12,527) |
|
|
(22,170) |
|
|
(49,878) |
|
|
(82,816) |
Benefit from income taxes |
|
338 |
|
|
339 |
|
|
1,013 |
|
|
1,086 |
Net loss |
$ |
(12,189) |
|
$ |
(21,831) |
|
$ |
(48,865) |
|
$ |
(81,730) |
|
|
|
|
|
|
|
|
||||
Net loss per common share - basic and diluted |
$ |
(0.09) |
|
$ |
(0.16) |
|
$ |
(0.36) |
|
$ |
(0.60) |
|
|
|
|
|
|
|
|
||||
Weighted average common shares outstanding - basic and diluted |
|
138,059,781 |
|
|
135,951,761 |
|
|
137,523,202 |
|
|
135,508,203 |
XERIS BIOPHARMA HOLDINGS, INC. CONDENSED CONSOLIDATED BALANCE SHEETS (in thousands) |
|||||||
|
September 30, 2023 |
|
December 31, 2022 |
||||
|
(unaudited) |
|
|
||||
Assets |
|
|
|
||||
Current assets: |
|
|
|
||||
Cash and cash equivalents |
$ |
46,143 |
|
$ |
121,966 |
||
Short-term investments |
|
19,832 |
|
|
— |
||
Trade accounts receivable, net |
|
45,966 |
|
|
30,830 |
||
Inventory |
|
38,143 |
|
|
24,735 |
||
Prepaid expenses and other current assets |
|
7,967 |
|
|
9,287 |
||
Total current assets |
|
158,051 |
|
|
186,818 |
||
Property and equipment, net |
|
6,185 |
|
|
5,516 |
||
Intangible assets, net |
|
112,475 |
|
|
120,607 |
||
Goodwill |
|
22,859 |
|
|
22,859 |
||
Operating lease right-of-use assets |
|
23,407 |
|
|
3,992 |
||
Other assets |
|
4,807 |
|
|
4,730 |
||
Total assets |
$ |
327,784 |
|
$ |
344,522 |
||
Liabilities and Stockholders’ Equity |
|
|
|
||||
Current liabilities: |
|
|
|
||||
Accounts payable |
$ |
12,078 |
|
$ |
4,606 |
||
Current operating lease liabilities |
|
2,366 |
|
|
1,580 |
||
Other accrued liabilities |
|
19,073 |
|
|
36,786 |
||
Accrued trade discounts and rebates |
|
21,554 |
|
|
16,818 |
||
Accrued returns reserve |
|
13,328 |
|
|
11,173 |
||
Current portion of contingent value rights |
|
17,517 |
|
|
— |
||
Other current liabilities |
|
1,123 |
|
|
2,658 |
||
Total current liabilities |
|
87,039 |
|
|
73,621 |
||
Long-term debt, net of unamortized debt issuance costs |
|
190,423 |
|
|
187,075 |
||
Non-current contingent value rights |
|
5,099 |
|
|
25,688 |
||
Non-current operating lease liabilities |
|
35,154 |
|
|
9,402 |
||
Deferred tax liabilities |
|
2,504 |
|
|
3,518 |
||
Other liabilities |
|
3,700 |
|
|
31 |
||
Total liabilities |
|
323,919 |
|
|
299,335 |
||
Total stockholders’ equity |
|
3,865 |
|
|
45,187 |
||
Total liabilities and stockholders’ equity |
$ |
327,784 |
|
$ |
344,522 |
View source version on businesswire.com: https://www.businesswire.com/news/home/20231109523978/en/
Allison Wey
Senior Vice President, Investor Relations and Corporate Communications
awey@xerispharma.com
312-736-1237
Source: Xeris Biopharma Holdings, Inc.
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