Xencor Reports First Quarter 2023 Financial Results
-- Management to Host Conference Call at
“In the first quarter, we and our partners continued to enroll patients across multiple Phase 1 and Phase 2 clinical studies of XmAb drug candidates in oncology and autoimmune diseases. Two new programs are planned to advance into clinical development this year, XmAb662, our engineered IL12-Fc cytokine, on track to start a Phase 1 study mid-year, and XmAb541, our CLDN6 x CD3 bispecific antibody for ovarian cancer, for which we anticipate submitting the IND by year end,” said
Program and Corporate Updates
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XmAb564 (IL2-Fc): The Company will present updated results from the Phase 1a single-ascending dose study in healthy volunteers at
European Alliance of Associations for Rheumatology (EULAR) Congress , being held fromMay 31 to June 1 , inMilan, Italy . The update will include additional biomarker data. Data previously presented demonstrate a single dose, administered subcutaneously in healthy volunteers, was well tolerated and generated durable, dose-dependent and selective expansion of regulatory T cells.
- XmAb104 (PD-1 x ICOS): XmAb104 is a bispecific antibody that targets PD-1, an immune checkpoint receptor, and ICOS, an immune co-stimulatory receptor, to selectively activate the tumor microenvironment. Initial dose-escalation data from a Phase 1 study, presented at ASCO 2022, indicates that XmAb104 was well tolerated and exhibited a distinct safety profile compared to other clinical-stage ICOS programs. Anti-tumor activity was observed in patients, and biomarker activity was consistent with engagement with T cells. The Company has opened an expansion portion in the study (Part C) to evaluate XmAb104 in combination with ipilimumab in patients with microsatellite stable or proficient mismatch repair colorectal cancer.
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Preclinical Data Presentation: Preclinical data generated from engineered CD28 bispecific antibodies targeting the solid tumor antigens CEACAM5, ENPP3, mesothelin, STEAP1 and Trop-2 were presented at the
American Association for Cancer Research (AACR) Annual Meeting inApril 2023 .
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Corporate Update:
Nancy Valente , M.D., was appointed as Xencor’s Executive Vice President, Chief Development Officer, effectiveMay 1 , having previously served as an independent member of the Company’s Board of Directors fromSeptember 2022 throughApril 2023 .Dr. Valente brings with her more than 20 years of experience in late-stage biopharmaceutical product development. She most recently served as a senior vice president atGenentech , a member of the Roche Group, and as its global head and co-lead of global product development of its oncology and hematology therapeutic area.
Progress Across Partnered Programs
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Alexion Pharmaceuticals, Inc.: In
April 2023 , Ultomiris® (ravulizumab-cwvz), which incorporates Xencor’s Xtend™ Fc domain, was recommended for marketing authorization in the EU for the treatment of adult patients with neuromyelitis optica spectrum disorder (NMOSD) who are anti-aquaporin-4 antibody positive. In addition, AstraZeneca recently announced that a Phase 3 study of Ultomiris has been initiated in cardiac surgery-associated acute kidney injury. In the first quarter of 2023,Xencor earned$10.5 million of royalty revenue from Alexion on net sales of Ultomiris.
Ultomiris is a registered trademark of Alexion Pharmaceuticals, Inc.
Financial Results for the First Quarter Ended
Cash, cash equivalents, receivables and marketable debt securities totaled
Revenues for the first quarter ended
Research and development expenses for the first quarter ended
General and administrative expenses for the first quarter ended
Non-cash, stock-based compensation expense for the first quarter ended
Net loss for the first quarter ended
The total shares outstanding were 60,381,600 as of
Financial Guidance
Based on current operating plans,
Conference Call and Webcast
The live webcast will be available under “Events & Presentations” in the Investors section of the Company’s website located at investors.xencor.com and will be archived for at least 30 days. Active participants in the conference call may receive credentials for telephone access by registering at the following link: https://register.vevent.com/register/BI0da076297f5f4f3b920845d8b0e7f2d3.
About
Forward-Looking Statements
Certain statements contained in this press release may constitute forward-looking statements within the meaning of applicable securities laws. Forward-looking statements include statements that are not purely statements of historical fact, and can generally be identified by the use of words such as “potential,” “can,” “will,” “plan,” “may,” “could,” “would,” “expect,” “anticipate,” “seek,” “look forward,” “believe,” “committed,” “investigational,” and similar terms, or by express or implied discussions relating to Xencor’s business, including, but not limited to, statements regarding planned additional clinical trials, the quotations from
Condensed Balance Sheets | ||||||||
(in thousands) | ||||||||
2023 |
2022 |
|||||||
(unaudited) | ||||||||
Assets | ||||||||
Current assets | ||||||||
Cash and cash equivalents |
$ |
72,394 |
$ |
53,942 |
||||
Marketable debt securities |
|
475,922 |
|
526,689 |
||||
Marketable equity securities |
|
39,706 |
|
42,431 |
||||
Accounts receivable |
|
19,861 |
|
28,997 |
||||
Prepaid expenses |
|
22,093 |
|
23,283 |
||||
Total current assets |
|
629,976 |
|
675,342 |
||||
Property and equipment, net |
|
66,685 |
|
59,183 |
||||
Intangible assets, net |
|
18,244 |
|
18,500 |
||||
Marketable debt securities - long term |
|
— |
|
3,826 |
||||
Marketable equity securities - long term |
|
54,210 |
|
54,383 |
||||
Right of use asset |
|
33,697 |
|
34,419 |
||||
Other assets |
|
599 |
|
613 |
||||
Total assets |
$ |
803,411 |
$ |
846,266 |
||||
Liabilities and stockholders’ equity | ||||||||
Current liabilities | ||||||||
Accounts payable and accrued liabilities |
$ |
30,481 |
$ |
28,816 |
||||
Deferred revenue |
|
30,104 |
|
30,320 |
||||
Lease liabilities |
|
4,471 |
|
4,708 |
||||
Total current liabilities |
|
65,056 |
|
63,844 |
||||
Lease liabilities, net of current portion |
|
54,772 |
|
54,926 |
||||
Total liabilities |
|
119,828 |
|
118,770 |
||||
Stockholders’ equity |
|
683,583 |
|
727,496 |
||||
Total liabilities and stockholders’ equity |
$ |
803,411 |
$ |
846,266 |
||||
The 2022 balance sheet was derived from the 2022 annual financial statements included in the Form 10-K that was filed on |
||||||||
Condensed Statements of Comprehensive Income (Loss) | ||||||||
(in thousands, except share and per share data) | ||||||||
Three months ended |
||||||||
2023 |
|
2022 |
|
|||||
(unaudited) | ||||||||
Revenues | $ |
18,962 |
|
$ |
85,495 |
|
||
Operating expenses: | ||||||||
Research and development |
64,379 |
|
47,756 |
|
||||
General and administrative |
13,948 |
|
11,273 |
|
||||
Total operating expenses |
78,327 |
|
59,029 |
|
||||
Income (loss) from operations |
(59,365 |
) |
26,466 |
|
||||
Other expense, net |
(1,398 |
) |
(2,872 |
) |
||||
Net income (loss) |
(60,763 |
) |
23,594 |
|
||||
Other comprehensive gain (loss) | ||||||||
Net unrealized gain (loss) on marketable debt securities |
3,327 |
|
(5,611 |
) |
||||
Comprehensive income (loss) | $ |
(57,436 |
) |
$ |
17,983 |
|
||
Net income (loss) per share: | ||||||||
Basic net income (loss) per share | $ |
(1.02 |
) |
$ |
0.40 |
|
||
Diluted net income (loss) per share | $ |
(1.02 |
) |
$ |
0.39 |
|
||
Weighted-average number of common shares used in net income (loss) per share applicable to common stockholders - basic |
59,771,674 |
|
59,407,829 |
|
||||
Weighted-average number of common shares used in net income (loss) per share applicable to common stockholders - diluted |
59,771,674 |
|
61,078,494 |
|
||||
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For Investors:
cliles@xencor.com
(626) 737-8118
For Media:
Evoke Canale
jason.spark@evokegroup.com
(619) 849-6005
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