Eledon Pharmaceuticals Reports First Quarter 2024 Operating and Financial Results
Completed oversubscribed $50 million private placement
First participant dosed in clinical trial at University of Chicago Medicine assessing the use of tegoprubart to prevent islet cell transplant rejection in patients with type 1 diabetes
Reported updated data from ongoing Phase 1b trial evaluating tegoprubart for prevention of rejection in kidney transplantation
Tegoprubart used as part of immunosuppressive treatment following the first-ever kidney xenotransplant
IRVINE, Calif., May 09, 2024 (GLOBE NEWSWIRE) -- Eledon Pharmaceuticals, Inc. ("Eledon") (Nasdaq: ELDN) today reported its first quarter 2024 operating and financial results and reviewed recent business highlights.
"We are pleased with the significant progress made so far this year in the development of tegoprubart for use both in kidney transplantation and in the emerging fields of xenotransplantation and islet cell transplantation. This progress reinforces tegoprubart's potential to become the first-line immunosuppressive treatment option of choice for a broad range of transplant procedures," said David-Alexandre C. Gros, M.D., Chief Executive Officer of Eledon.
First Quarter 2024 and Recent Corporate Developments
-- First participant in an investigator-led clinical trial has received an
islet cell transplant and is being treated with a novel immunosuppression
regimen including tegoprubart, the company's novel anti-CD40L antibody,
which is in development for the prevention of pancreatic islet cell
transplant rejection in patients with type 1 diabetes. The study is being
conducted by the research team at the University of Chicago's Pancreatic
and Islet Transplant Program in collaboration with Eledon, the Juvenile
Diabetes Research Foundation, and The Cure Alliance.
-- Announced the use of tegoprubart as part of the immunosuppressive
treatment regimen used following the first-ever kidney xenotransplant
procedure of a genetically modified kidney from a pig to a human.
-- Enrolled the 12th participant in March 2024 in the ongoing Phase 2 BESTOW
trial assessing tegoprubart head-to-head with tacrolimus for the
prevention of rejection in kidney transplantation.
-- Completed a private placement financing for total gross proceeds of $50.0
million, before deducting any offering related expenses, to a select
group of institutional and accredited investors at a price per share of
$2.37.
Anticipated 2024 Milestones
-- June 2024: Report updated interim clinical data from the ongoing Phase 1b
trial and open-label extension study of tegoprubart in kidney
transplantation at the American Transplant Congress in Philadelphia, PA.
-- End of 2024: Complete enrollment in the Phase 2 BESTOW trial of
tegoprubart in kidney transplantation.
First Quarter 2024 Financial Results
The Company reported a net loss of $10.3 million, or $0.34 per share, for the three months ended March 31, 2024, compared to a net loss of $10.8 million, or $0.75 per share, for the same period in 2023.
Research and development expenses were $7.4 million for the three months ended March 31, 2024, compared to $8.1 million for the comparable period in 2023, a decrease of $0.7 million.
General and administrative expenses were $3.5 million for the three months ended March 31, 2024, compared to $3.0 million for the comparable period in 2023, an increase of $0.5 million.
Eledon ended the first quarter with approximately $42.9 million in cash, cash equivalents and short-term investments, which excludes the $50.0 million in gross proceeds received in the recently completed private placement.
About Eledon Pharmaceuticals and tegoprubart
Eledon Pharmaceuticals, Inc. is a clinical stage biotechnology company that is developing immune-modulating therapies for the management and treatment of life-threatening conditions. The Company's lead investigational product is tegoprubart, an anti-CD40L antibody with high affinity for CD40 Ligand, a well-validated biological target within the costimulatory CD40/CD40L cellular pathway. The central role of CD40L signaling in both adaptive and innate immune cell activation and function positions it as an attractive target for non-lymphocyte depleting, immunomodulatory therapeutic intervention. The Company is building upon a deep historical knowledge of anti-CD40 Ligand biology to conduct preclinical and clinical studies in kidney allograft transplantation, xenotransplantation, and amyotrophic lateral sclerosis (ALS). Eledon is headquartered in Irvine, California. For more information, please visit the Company's website at www.eledon.com.
Follow Eledon Pharmaceuticals on social media: LinkedIn; Twitter
Forward-Looking Statements
This press release contains forward-looking statements that involve substantial risks and uncertainties. Any statements about the company's future expectations, plans and prospects, including statements about planned clinical trials, the development of product candidates, expected timing for initiation of future clinical trials, expected timing for receipt of data from clinical trials, the company's capital resources and ability to finance planned clinical trials, as well as other statements containing the words "believes," "anticipates," "plans," "expects," "estimates," "intends," "predicts," "projects," "targets," "looks forward," "could," "may," and similar expressions, constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are inherently uncertain and are subject to numerous risks and uncertainties, including: risks relating to the safety and efficacy of our drug candidates; risks relating to clinical development timelines, including interactions with regulators and clinical sides, as well as patient enrollment; risks relating to costs of clinical trials and the sufficiency of the company's capital resources to fund planned clinical trials; and risks associated with the impact of the ongoing coronavirus pandemic. Actual results may differ materially from those indicated by such forward-looking statements as a result of various factors. These risks and uncertainties, as well as other risks and uncertainties that could cause the company's actual results to differ significantly from the forward-looking statements contained herein, are discussed in our quarterly 10-Qs, annual 10-K, and other filings with the U.S. Securities and Exchange Commission, which can be found at www.sec.gov. Any forward-looking statements contained in this press release speak only as of the date hereof and not of any future date, and the company expressly disclaims any intent to update any forward-looking statements, whether as a result of new information, future events or otherwise.
Investor Contact:
Stephen Jasper
Gilmartin Group
(858) 525 2047
stephen@gilmartinir.com
Media Contact:
Jenna Urban
Berry & Company Public Relations
(212) 253 8881
jurban@berrypr.com
Source: Eledon Pharmaceuticals
ELEDON PHARMACEUTICALS, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(In thousands, except share data)
(Unaudited)
March 31, December 31,
2024 2023
--------- --------------
ASSETS
Current assets:
Cash and cash equivalents $ 5,655 $ 4,612
Short-term investments 37,207 46,490
Prepaid expenses and other current
assets 5,115 5,027
-------- ----------
Total current assets 47,977 56,129
Operating lease asset, net 270 365
In-process research and development 32,386 32,386
Other assets 185 186
-------- ----------
Total assets $ 80,818 $ 89,066
======== ==========
LIABILITIES AND STOCKHOLDERS' EQUITY
Current liabilities:
Accounts payable $ 1,864 $ 967
Current operating lease liabilities 284 383
Accrued expenses and other
liabilities 2,099 2,545
-------- ----------
Total current liabilities 4,247 3,895
Deferred tax liabilities 1,752 1,752
Total liabilities 5,999 5,647
-------- ----------
Commitments and contingencies
Stockholders' equity:
Preferred stock, $0.001 par value,
5,000,000 shares authorized at March
31, 2024 and December 31, 2023:
Series X(1) non-voting convertible
preferred stock, $0.001 par value,
515,000 shares designated; 110,086
shares issued and outstanding at
March 31, 2024 and December 31,
2023 -- --
Series X non-voting convertible
preferred stock, $0.001 par value,
10,000 shares designated; 4,422
shares issued and outstanding at
March 31, 2024 and December 31,
2023 -- --
Common stock, $0.001 par value,
200,000,000 shares authorized at March
31, 2024 and December 31, 2023;
24,813,130 and 24,213,130 shares
issued and outstanding at March 31,
2024 and December 31, 2023,
respectively 25 24
Additional paid-in capital 328,280 326,586
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