GRI Bio, Inc. (NASDAQ: GRI) (“GRI Bio” or the “Company”), a
biotechnology company advancing an innovative pipeline of Natural
Killer T (“NKT”) cell modulators for the treatment of inflammatory,
fibrotic and autoimmune diseases, today reported its financial
results for the third quarter ended September 30, 2024 and provided
a corporate update.
“We continue to make fundamental progress on the
development and regulatory fronts of our lead program GRI-0621 for
the treatment of IPF. As we drive towards our interim data readout
early next year, we are generating a robust and growing body of
encouraging preclinical data with an innovative approach that we
believe continues to validate and derisk our clinical approach,”
commented Marc Hertz, PhD, Chief Executive Officer of GRI Bio.
“With our strengthened cash position and Phase 2a study execution,
we believe we are poised to drive value for shareholders in both
the near and long term.”
Recent Highlights
- Presented positive preclinical data
demonstrating GRI-0621’s ability to inhibit invariant Natural
Killer T (iNKT) cell activity and reduce important inflammatory and
fibrotic drivers in idiopathic pulmonary fibrosis (IPF) at the 22nd
International Colloquium on Lung and Airway Fibrosis in Athens,
Greece;
- Expanded intellectual property
protection for proprietary NKT cell modulators with granting of
Japan patent titled, “Prevention and Treatment of Inflammatory
Conditions;
- Received authorization to conduct
Phase 2a biomarker study evaluating GRI-0621 for the treatment of
IPF in Australia; and
- Participated in a Virtual Investor
KOL Connect segment with prominent key opinion leader in IPF – Dr.
Helen Parfrey, Respiratory Consultant at the Royal Papworth
Hospital and Affiliated Assistant Professor at the University of
Cambridge.
GRI-0621: Type 1 Invariant NKT (iNKT)
Antagonist in Development for the Treatment of IPF.
IPF is a rare chronic progressive pulmonary disease with
abnormal scarring of the lung blocking the movement of oxygen into
the bloodstream. Currently available treatments for IPF are limited
with only two approved drugs that come with significant
side-effects, limited compliance and no impact on overall survival1
leaving significant opportunity to augment IPF treatment with a new
therapeutic.
GRI Bio’s lead program, GRI-0621, is a small
molecule RAR-βɣ dual agonist that inhibits the activity of human
iNKT cells. In preliminary trials to date and previous trials with
the oral formulation, GRI-0621 has been shown to improve fibrosis
in multiple disease models and improve liver function tests and
other markers of inflammation and injury in patients.
The Company plans to leverage the 505(b)(2)
regulatory pathway. For more information about the Phase 2a study,
please visit clinicaltrials.gov and reference identifier
NCT06331624.
Expected GRI-0621 Upcoming
Milestones
- Q1 2025: Report interim data from
Phase 2a biomarker study
- Q2 2025: Report topline results
from Phase 2a biomarker study
Summary of Financial Results for Third Quarter
2024
Net loss was $6.3 million for the nine months ended September
30, 2024.
Research and development expenses were $2.9
million and $2.2 million for the nine months ended September 30,
2024 and 2023, respectively.
General and administrative expenses were $3.3
million and $7.2 million for the nine months ended September 30,
2024 and 2023, respectively.
As of September 30, 2024, the Company had cash
and cash equivalents of approximately $4.7 million.
About GRI Bio, Inc.
GRI Bio is a clinical-stage biopharmaceutical
company focused on fundamentally changing the way inflammatory,
fibrotic and autoimmune diseases are treated. GRI Bio’s therapies
are designed to target the activity of NKT cells, which are key
regulators earlier in the inflammatory cascade, to interrupt
disease progression and restore the immune system to homeostasis.
NKT cells are innate-like T cells that share properties of both NK
and T cells and are a functional link between the innate and
adaptive immune responses. Type 1 invariant (iNKT) cells play a
critical role in propagating the injury, inflammatory response, and
fibrosis observed in inflammatory and fibrotic indications. GRI
Bio’s lead program, GRI-0621, is an inhibitor of iNKT cell activity
and is being developed as a novel oral therapeutic for the
treatment of idiopathic pulmonary fibrosis, a serious disease with
significant unmet need. The Company is also developing a pipeline
of novel type 2 NKT agonists for the treatment of systemic lupus
erythematosus. Additionally, with a library of over 500 proprietary
compounds, GRI Bio has the ability to fuel a growing pipeline.
Forward-Looking Statements
This press release contains “forward-looking
statements” within the meaning of the “safe harbor” provisions of
the Private Securities Litigation Reform Act of 1995.
Forward-looking statements may be identified by the use of words
such as “anticipate,” “believe,” “contemplate,” “could,”
“estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,”
“potential,” “predict,” “project,” “target,” “aim,” “should,”
“will,” “would,” or the negative of these words or other similar
expressions. These forward-looking statements are based on the
Company’s current beliefs and expectations. Forward-looking
statements include, but are not limited to, statements regarding:
the Company’s expectations with respect to development and
commercialization of the Company’s product candidates, the timing
of initiation or completion of clinical trials and availability of
resulting data, the potential benefits and impact of the Company’s
clinical trials and product candidates and any implication that the
data or results observed in preclinical trials or earlier studies
or trials will be indicative of results of later studies or
clinical trials, the Company’s beliefs and expectations regarding
potential shareholder value and future financial performance, the
Company’s beliefs about the timing and outcome of regulatory
approvals and potential regulatory approval pathways, the Company’s
expected milestones for the first half of 2025 and the Company’s
beliefs and expectations regarding the sufficiency of its existing
cash and cash equivalents to fund its planned operations, its
ability to raise additional funds, which may not be available to
the Company on acceptable terms or at all, and capital expenditure
requirements. Actual results may differ from the forward-looking
statements expressed by the Company in this press release and
consequently, you should not rely on these forward-looking
statements as predictions of future events. These forward-looking
statements are subject to inherent uncertainties, risks and
assumptions that are difficult to predict, including, without
limitation: (1) the inability to maintain the listing of the
Company’s common stock on Nasdaq and to comply with applicable
listing requirements; (2) changes in applicable laws or
regulations; (3) the inability of the Company to raise financing in
the future; (4) the success, cost and timing of the Company’s
product development activities; (5) the inability of the Company to
obtain and maintain regulatory clearance or approval for its
respective products, and any related restrictions and limitations
of any cleared or approved product; (6) the inability of the
Company to identify, in-license or acquire additional technology;
(7) the inability of the Company to compete with other companies
currently marketing or engaged in the development of products and
services that the Company is currently developing; (8) the size and
growth potential of the markets for the Company’s products and
services, and their respective ability to serve those markets,
either alone or in partnership with others; (9) the failure to
achieve any milestones or receive any milestone payments under any
agreements; (10) inaccuracy in the Company’s estimates regarding
expenses, future revenue, capital requirements and needs for and
the ability to obtain additional financing; (11) the Company’s
ability to protect and enforce its intellectual property portfolio,
including any newly issued patents; and (12) other risks and
uncertainties indicated from time to time in the Company’s filings
with the U.S. Securities and Exchange Commission (the “SEC”),
including the risks and uncertainties described in the “Risk
Factors” section of the Company’s most recent Annual Report on Form
10-K filed with the SEC on March 28, 2024 and subsequently filed
reports. Forward-looking statements contained in this announcement
are made as of this date, and the Company undertakes no duty to
update such information except as required under applicable
law.
Investor Contact:JTC Team, LLCJenene
Thomas(908) 824-0775GRI@jtcir.com
1 T. M. Maher et al., Global incidence and
prevalence of idiopathic pulmonary fibrosis. Respir Res
22, 197 (2021)
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