Artiva Biotherapeutics Reports Third Quarter 2024 Financial Results and Recent Business Highlights
13 November 2024 - 8:05AM
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.
AlloNK® Clinical Updates
- 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.
Third Quarter 2024 Financial Results
- 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.
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 StatementsThis 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 |
) |
|
|
|
|
|
|
|
|
ContactsInvestors: Neha
Krishnamohan, Artiva
Biotherapeutics, ir@artivabio.comMedia:
Jessica Yingling, Ph.D., Little Dog Communications
Inc., jessica@litldog.com,
+1.858.344.8091
Source: Artiva Biotherapeutics, Inc.
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