Arcellx Provides First Quarter Financial Results
- Arcellx has a strong financial position with $533.6 million in cash, cash equivalents, and marketable securities. Collaboration revenue increased to $17.9 million. The company is focused on key drivers of its business, including completing enrollment of iMMagine-1 and initiating iMMagine-2.
- The net loss for Q1 2023 was $27.3 million.
"Delivering our novel CAR-T therapy to multiple myeloma patients is at the heart of our mission," said Rami Elghandour, Arcellx's Chairman and Chief Executive Officer. "With the closing of our Kite partnership in the first quarter, we believe we are well capitalized to fund our operations through the first half of 2025. We remain laser-focused on key drivers of our business which include completing enrollment of iMMagine-1, initiating iMMagine-2 in earlier multiple myeloma lines, and presenting longer-term data from our Phase 1 expansion study of CART-ddBCMA. This is a pivotal and exciting time for our organization, and we are excited about our progress made to date and look forward to continuing our momentum."
First Quarter 2023 Financial Highlights
Cash, cash equivalents, and marketable securities:
As of March 31, 2023, Arcellx had cash, cash equivalents, and marketable securities of
Collaboration revenue:
Collaboration revenue was
R&D expenses:
Research and development expenses were
G&A expenses:
General and administrative expenses were
Net loss:
Net loss was
About Arcellx, Inc.
Arcellx, Inc. is a clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. Arcellx believes that cell therapies are one of the forward pillars of medicine and Arcellx's mission is to advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Arcellx's lead product candidate, CART-ddBCMA, is being developed for the treatment of relapsed or refractory multiple myeloma (rrMM) in a Phase 2 pivotal trial. CART-ddBCMA has been granted Fast Track, Orphan Drug, and Regenerative Medicine Advanced Therapy designations by the
Arcellx is also advancing its dosable and controllable CAR-T therapy, ARC-SparX, through two clinical-stage programs: a Phase 1 study of ACLX-001 for rrMM, initiated in the second quarter of 2022; and ACLX-002 in relapsed or refractory acute myeloid leukemia and high-risk myelodysplastic syndrome, initiated in the fourth quarter of 2022. For more information on Arcellx, please visit www.arcellx.com. Follow Arcellx on Twitter (@arcellx) and LinkedIn.
Forward-looking Statements
This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. All statements in this press release that are not purely historical are forward-looking statements, including Arcellx's plans for the clinical development of its product candidates, including anticipated announcements of additional data; and the sufficiency of cash, cash equivalents and marketable securities and its ability to fund operations. The forward-looking statements contained herein are based upon Arcellx's current expectations and involve assumptions that may never materialize or may prove to be incorrect. These forward-looking statements are neither promises nor guarantees and are subject to a variety of risks and uncertainties, including risks that may be found in the section entitled Part II, Item 1A (Risk Factors) in the Quarterly Report on Form 10-Q for the quarter ended March 31, 2023, filed with the Securities and Exchange Commission (SEC) on or about the date hereof, and the other documents that Arcellx may file from time to time with the SEC. These forward-looking statements are made as of the date of this press release, and Arcellx assumes no obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.
ARCELLX, INC. | ||
SELECTED CONSOLIDATED BALANCE SHEET DATA | ||
(in thousands) | ||
March 31, | December 31, | |
2023 | 2022 | |
Cash, cash equivalents, and marketable securities | $ 254,835 | |
Total assets | 622,943 | 313,817 |
Total liabilities | 319,226 | 108,863 |
Total stockholders' equity | 303,717 | 204,954 |
ARCELLX, INC. | ||
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS | ||
(in thousands, except share and per share amounts) | ||
Three Months Ended March 31, | ||
2023 | 2022 | |
Revenue | $ 17,912 | $ — |
Operating expenses: | ||
Research and development | 32,932 | 18,057 |
General and administrative | 15,437 | 8,034 |
Total operating expenses | 48,369 | 26,091 |
Loss from operations | (30,457) | (26,091) |
Other income, net | 3,442 | 50 |
Loss before income taxes | (27,015) | (26,041) |
Income tax expense | 329 | - |
Net loss | (27,344) | (26,041) |
Other comprehensive loss: | ||
Unrealized gain (loss) on marketable securities | 307 | (24) |
Comprehensive loss | $ (27,037) | $ (26,065) |
Net loss per share attributable to common stockholders—basic and diluted | (0.58) | (1.25) |
Weighted-average common shares outstanding—basic and diluted | 46,769,380 | 20,760,722 |
Investor Contact:
Myesha Lacy
Arcellx, Inc.
ir@arcellx.com
510-691-6361
Media Contact
Andrea Cohen
Sam Brown Inc.
andreacohen@sambrown.com
917-209-7163
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SOURCE Arcellx, Inc.
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