Initial data for AlloNK® from autoimmune program expected H1 2025

Updated clinical data from Phase 1/2 trial exploring AlloNK + rituximab in NHL showing continued durability of response to be presented at a medical conference in 2025

Strengthened key leadership with cell therapy and autoimmune expertise across organization

Robust balance sheet with cash, cash equivalents and investments of $185.4 million as of December 31, 2024, is expected to fund operations at least through end of 2026

SAN DIEGO, March 24, 2025 (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 full year ended December 31, 2024, and highlighted recent progress.

"2024 was a transformational year for Artiva including initiating dosing of AlloNK® in patients with autoimmune disease across our trials, a successful initial public offering strengthening our balance sheet, and expanding key leadership across the organization with expertise in cell therapy and autoimmune disease," said Fred Aslan, M.D., CEO of Artiva. "We look forward to sharing initial data from our AlloNK® program in autoimmune disease this year. We also look forward to sharing updated clinical data from our non-Hodgkin's lymphoma (NHL) trial with AlloNK® which continues to mature as one of the strongest data sets for the allogeneic field, demonstrating deep B-cell depletion, continued durability of response, and the compatibility of our treatment regimen with outpatient administration."

Recent Business Highlights

Corporate and Financial Updates

Upcoming Milestones

Full Year 2024 Financial Results

About Artiva Biotherapeutics

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 Company's clinical trials or the IIT; the Company's future results of operations and financial position, including cash runway; and the Company's presentation plans. 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 Annual Report on Form 10-K for the year ended December 31, 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)
 
  December 31, 2024 December 31, 2023
Assets    
Cash, cash equivalents and investments $185,428 $76,971 
Property and equipment, net  6,370  8,096 
Operating and financing lease right-of-use assets  14,055  16,547 
Other assets  3,728  3,500 
Total assets $209,581 $105,114 
Liabilities, convertible preferred stock, and stockholders' equity (deficit)    
Accounts payable and accrued expenses $8,513 $8,631 
Operating and financing lease liabilities  14,354  16,912 
Simple agreements for future equity (SAFEs)  —  25,100 
Other liabilities  73  73 
Total liabilities  22,940  50,716 
Convertible preferred stock  —  216,413 
Stockholders' equity (deficit)  186,641  (162,015)
Total liabilities, convertible preferred stock, and stockholders' equity (deficit) $209,581 $105,114 
     
     



 
Artiva Biotherapeutics, Inc.

Condensed Statements of Operation and Comprehensive Loss

(unaudited)

(in thousands, except share and per share data)

 
  Year Ended December 31,
   2024   2023 
Revenue    
Collaboration revenue $—  $32,923 
License and development support revenue  251   569 
Total revenue  251   33,492 
Operating expenses:    
Research and development  50,328   50,251 
General and administrative  17,205   13,912 
Total operating expenses  67,533   64,163 
Loss from operations  (67,282)  (30,671)
Other income, net    
Interest income  5,349   2,535 
Change in fair value of SAFEs  (3,597)  (707)
Other income, net  157   195 
Total other income, net  1,909   2,023 
Loss before provision for income taxes  (65,373)  (28,648)
Provision for income taxes  —   (72)
Net loss $(65,373) $(28,720)
Net loss per share, basic and diluted $(5.81) $(35.78)
Weighted-average common shares outstanding, basic and diluted  11,258,851   802,747 
Comprehensive loss:    
Net loss $(65,373) $(28,720)
Other comprehensive income (loss)  (437)  308 
Comprehensive loss $(65,810) $(28,412)
     

Contacts

Investors: Neha Krishnamohan, Artiva Biotherapeutics, ir@artivabio.com

Media: Jessica Yingling, Ph.D., Little Dog Communications Inc., jessica@litldog.com, +1.858.344.8091

Source: Artiva Biotherapeutics, Inc.



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