Expanded Board of Directors with appointment of Dr. Alison Moore bringing cell therapy and manufacturing expertise to advance AlloNK® in autoimmune diseases
Initial data for AlloNK® in autoimmune indications expected H1 2025
Robust balance sheet with cash, cash equivalents and investments of $199.6 million as of September 30, 2024, is expected to fund operations at least through end of 2026
SAN DIEGO, Nov. 12, 2024 (GLOBE NEWSWIRE) -- Artiva Biotherapeutics, Inc. (Nasdaq: ARTV) (Artiva), a clinical-stage biotechnology company whose mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases and cancers, today announced financial results for the third quarter ended September 30, 2024, and highlighted recent progress.
"As AlloNK® advances in the clinic, we were pleased to expand our Board of Directors with the appointment of Dr. Alison Moore, an experienced executive in manufacturing and technical operations in allogenic cell therapies,” said Fred Aslan, M.D., CEO of Artiva. "We remain focused on generating clinical data and strengthening Artiva's talent in autoimmune disease and cell therapy across the organization as we prepare for this next stage of growth.”
Recent Business Highlights
Corporate and Financial Updates
- Expanded Board of Directors: In October 2024, Artiva appointed Alison Moore, Ph.D., as an independent member of its Board of Directors. Dr. Moore brings over 25 years of executive experience in the biotechnology and pharmaceutical industry, including an extensive background in cell therapy manufacturing. She currently serves as Chief Technical Officer (CTO) of Codexis Inc., a leading enzyme engineering company, and was the former CTO of Allogene Therapeutics, a pioneering clinical-stage company advancing CAR T-cell therapies.
- Completed upsized $179.0 Million initial public offering: In July 2024, Artiva sold 14,920,000 shares of its common stock, including partial exercise of the overallotment option, at a public offering price of $12.00 per share, for gross proceeds of $179.0 million.
- In August 2024, Artiva announced the treatment of its first patient was initiated in an investigator-initiated basket trial (IIT) assessing the safety, tolerability, and clinical activity of AlloNK® (AB-101) in combination with rituximab in patients with rheumatoid arthritis, pemphigus vulgaris, granulomatosis with polyangiitis/microscopic polyangiitis, and systemic lupus erythematosus (SLE). The trial is being conducted by Integral Rheumatology & Immunology Specialists, a community rheumatology clinic, demonstrating the potential to bring AlloNK® to patients in a community setting in addition to academic and transplant centers.
- AlloNK® is also in clinical evaluation in combination with rituximab or obinutuzumab in an Artiva sponsored Phase 1/1b trial for treatment of SLE, for patients with or without lupus nephritis.
- Initial data for AlloNK® in autoimmune indications from the Phase 1/1b trial or the basket IIT expected in the first half of 2025.
- Cash, Cash Equivalents and Investments. As of September 30, 2024, Artiva had cash, cash equivalents, and investments of $199.6 million. This includes $179.0 million in gross proceeds from Artiva's completed initial public offering in July 2024 in which it sold 14,920,000 shares of its common stock, including partial exercise of the overallotment option. Existing cash, cash equivalents, and investments as of September 30, 2024, are expected to fund operations at least through the end of 2026 and through key clinical data milestones.
- Collaboration Revenue. Collaboration revenue was $0 for the three months ended September 30, 2024, compared to $26.7 million for the three months ended September 30, 2023. Revenues in 2023 were related to the Merck Sharpe & Dohme Corp. collaboration which was terminated in October 2023.
- Research and Development Expenses. Research and development expenses were $13.5 million for the three months ended September 30, 2024, compared to $13.1 million for the three months ended September 30, 2023.
- General and Administrative Expenses. General and administrative expenses were $4.8 million for the three months ended September 30, 2024, compared to $2.8 million for the three months ended September 30, 2023.
- Other Income (Expense), net. Other income (expense), net, was $0.9 million for the three months ended September 30, 2024, compared to other income (expense), net, of $0.5 million for the three months ended September 30, 2023.
- Net Income (Loss). Net loss totaled $17.5 million for the three months ending September 30, 2024, as compared to net income of $11.3 million for the three months ending September 30, 2023, with non-cash stock-based compensation expense of $1.9 million and $1.4 million for the three months ended September 30, 2024 and 2023, respectively.
Artiva is a clinical-stage biotechnology company whose mission is to develop effective, safe and accessible cell therapies for patients with devastating autoimmune diseases and cancers. Artiva's lead program, AlloNK®, is an allogeneic, off-the-shelf, non-genetically modified, cryopreserved NK cell therapy candidate designed to enhance the antibody-dependent cellular cytotoxicity effect of monoclonal antibodies to drive B-cell depletion. AlloNK® is currently in clinical trials for treatment of systemic lupus erythematosus, for patients with or without lupus nephritis, and in an investigator-initiated basket trial in multiple autoimmune indications. Artiva's pipeline also includes CAR-NK candidates targeting both solid and hematologic cancers. Artiva was founded in 2019 as a spin out of GC Cell, formerly GC Lab Cell Corporation, a leading healthcare company in the Republic of Korea, pursuant to a strategic partnership granting Artiva exclusive worldwide rights (excluding Asia, Australia and New Zealand) to GC Cell's NK cell manufacturing technology and programs.
Artiva is headquartered in San Diego, California. For more information, please visit www.artivabio.com.
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Statements in this press release that are not statements of historical fact are forward-looking statements. Such forward-looking statements include, without limitation, statements regarding: expectations of Artiva Biotherapeutics, Inc. (the "Company”) regarding the potential benefits, accessibility, effectiveness and safety of AlloNK®; the Company's ability to advance AlloNK® in autoimmune disease; the Company's expectations regarding timing and availability of data from the Phase 1/1b trial or the IIT; and the Company's future results of operations and financial position, including cash runway. These forward-looking statements are based on the beliefs of the management of the Company as well as assumptions made by and information currently available to the Company. Such statements reflect the current views of the Company with respect to future events and are subject to known and unknown risks and uncertainties. In light of these risks and uncertainties, the events or circumstances referred to in the forward-looking statements may not occur. These and other factors that may cause the Company's actual results to differ from current expectations are discussed in the Company's filings with the Securities and Exchange Commission (the "SEC”), including the section titled "Risk Factors” in the Company's Quarterly Report on Form 10-Q for the quarter ended September 30, 2024. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date this press release is given. Except as required by law, the Company undertakes no obligation to publicly update any forward-looking statements, whether as a result of new information, future events or otherwise.
| Artiva Biotherapeutics, Inc. Condensed Balance Sheets (unaudited) (in thousands) | ||||||
| September 30,
2024 | December 31, 2023 | |||||
| Assets | ||||||
| Cash, cash equivalents and investments | $ | 199,597 | $ | 76,971 | ||
| Property and equipment, net | 6,857 | 8,096 | ||||
| Operating and financing lease right-of-use assets | 14,652 | 16,547 | ||||
| Other assets | 4,490 | 3,500 | ||||
| Total assets | $ | 225,596 | $ | 105,114 | ||
| Liabilities, convertible preferred stock, and stockholders' equity (deficit) | ||||||
| Accounts payable and accrued expenses | $ | 9,559 | $ | 8,631 | ||
| Operating and financing lease liabilities | 14,968 | 16,912 | ||||
| Simple agreements for future equity (SAFEs) | - | 25,100 | ||||
| Other liabilities | 73 | 73 | ||||
| Total liabilities | 24,600 | 50,716 | ||||
| Convertible preferred stock | - | 216,413 | ||||
| Stockholders' equity (deficit) | 200,996 | (162,015 | ) | |||
| Total liabilities, convertible preferred stock, and stockholders' equity (deficit) | $ | 225,596 | $ | 105,114 | ||
| Artiva Biotherapeutics, Inc.
Condensed Statements of Operation and Comprehensive Income (Loss) (unaudited) (in thousands, except share and per share data) | ||||||||||||||
| Three Months Ended September 30, | Nine Months Ended September 30, | |||||||||||||
| 2024 | 2023 | 2024 | 2023 | |||||||||||
| Revenue | ||||||||||||||
| Collaboration revenue | $ | - | $ | 26,656 | $ | - | $ | 31,142 | ||||||
| License and development support revenue | - | - | 251 | - | ||||||||||
| Total revenue | - | 26,656 | 251 | 31,142 | ||||||||||
| Operating expenses: | ||||||||||||||
| Research and development | 13,524 | 13,065 | 37,011 | 39,098 | ||||||||||
| General and administrative | 4,811 | 2,780 | 12,255 | 10,745 | ||||||||||
| Total operating expenses | 18,335 | 15,845 | 49,266 | 49,843 | ||||||||||
| Income (loss) from operations | (18,335 | ) | 10,811 | (49,015 | ) | (18,701 | ) | |||||||
| Other income (expense) | ||||||||||||||
| Interest income | 1,846 | 418 | 3,172 | 1,952 | ||||||||||
| Change in fair value of SAFEs | (977 | ) | - | (3,597 | ) | - | ||||||||
| Other income (expense), net | (6 | ) | 50 | 162 | 27 | |||||||||
| Total other income (expense) | 863 | 468 | (263 | ) | 1,979 | |||||||||
| Net income (loss) | $ | (17,472 | ) | $ | 11,279 | $ | (49,278 | ) | $ | (16,722 | ) | |||
| Net income (loss) per share, basic | $ | (0.92 | ) | $ | 13.98 | $ | (7.16 | ) | $ | (20.89 | ) | |||
| Net income (loss) per share, diluted | $ | (0.92 | ) | $ | 1.62 | $ | (7.16 | ) | $ | (20.89 | ) | |||
| Weighted-average common shares outstanding, basic | 18,896,829 | 806,714 | 6,883,271 | 800,541 | ||||||||||
| Weighted-average common shares outstanding, diluted | 18,896,829 | 6,967,099 | 6,883,271 | 800,541 | ||||||||||
| Comprehensive income (loss): | ||||||||||||||
| Net income (loss) | $ | (17,472 | ) | $ | 11,279 | $ | (49,278 | ) | $ | (16,722 | ) | |||
| Other comprehensive income | 217 | 144 | 30 | 271 | ||||||||||
| Comprehensive income (loss) | $ | (17,255 | ) | $ | 11,423 | $ | (49,248 | ) | $ | (16,451 | ) | |||
Investors: Neha Krishnamohan, Artiva Biotherapeutics, [email protected]
Media: Jessica Yingling, Ph.D., Little Dog Communications Inc., [email protected], +1.858.344.8091
Source: Artiva Biotherapeutics, Inc.
