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 second quarter ended June 30, 2024 and provided a
corporate update.
“Our focus and priority remain on the successful
execution of our Phase 2a biomarker study of GRI-0621 for the
treatment of IPF, with interim data by the end of the year and
topline data on track for Q1 2025. We are excited about this
product candidate and its potential to address a significant area
of unmet medical need,” commented Marc Hertz, PhD, Chief Executive
Officer of GRI Bio. “Additionally, we continue to generate
encouraging data in our GRI-0803 program for the treatment of
systemic lupus erythematosus. We currently estimate that we have
cash to support our planned operations into the first quarter of
2025 with plans to raise additional funds to support our planned
operations.”
Recent Highlights
- Expanded intellectual property
protection for proprietary NKT cell modulators with grant of Korea
patent title, “Prevention and Treatment of Inflammatory
Conditions;
- Closed a public offering with
aggregate gross proceeds of $4.0 million;
- Announced that the manuscript
titled, “Type 1 invariant natural killer T cells drive lung
fibrosis1,” has been published in the American Journal of
Respiratory and Critical Care Medicine;
- Presented positive preclinical data
demonstrating lead program GRI-0621 reduces the important
inflammatory and fibrotic drivers in IPF.
- Announced oral presentation at the
8th Annual Idiopathic Pulmonary Fibrosis Summit being held August
20-22, 2024; and
- Presented encouraging preclinical
data from the Company’s preclinical studies of type 2 NKT
activating molecules, GRI-0803 and GRI-0124 at the 14th
International Congress on Autoimmunity.
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 survival2
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 and has launched a Phase 2a biomarker study
evaluating GRI-0621 for the treatment of IPF. For more information
about the Phase 2a study, please visit clinicaltrials.gov and
reference identifier NCT06331624.
Expected GRI-0621 Upcoming
Milestones
- Q4 2024: Report interim data from
Phase 2a biomarker study
- Q1 2025: Report topline results
from Phase 2a biomarker study
GRI-0803: Novel
activator of human type 2 NKT cells in development for the
treatment of autoimmune disorders, with an initial focus on
systemic lupus erythematosus (SLE).
SLE is an autoimmune disease in which the immune
system attacks its own tissue and organs. SLE is the most common
form of lupus. Current treatments are limited, consisting primarily
of immunosuppressive therapies, with only two new therapies
approved in the past 50 years.
GRI Bio’s second asset in development, GRI-0803,
is a novel activator of human type 2 NKT cells. Activation of type
2 NKT leads to a dendritic cell-mediated inhibition of iNKT cells.
In the Company’s preclinical studies, type 2 NKT activating
molecules, GRI-0803 and GRI-0124, were observed to inhibit both
murine and human iNKT cells. Oral administration of these type 2
NKT activating molecules was observed to inhibit lupus nephritis
and to significantly improve overall survival. The Company is
currently focusing its available resources on GRI-0621, but,
pending additional funding, the GRI-0803 IND-enabling and Phase1
program will continue in 2025.
Summary of Financial Results for Second
Quarter 2024
Net loss was $2.4 million for the three months
ended June 30, 2024.
Research and development expenses were $0.9
million for each of the three-month periods ended June 30, 2024 and
2023, respectively.
General and administrative expenses were $1.4
million and $5.1 million for the three months ended June 30, 2024
and 2023, respectively.
As of June 30, 2024, the Company had cash and
cash equivalents of approximately $6.4 million. In June 2024, the
Company closed a public offering with aggregate gross proceeds of
$4.0 million. Based on the Company’s current operating plan, the
Company believes that its existing cash and cash equivalents will
be sufficient to fund its operating expenses and capital
expenditure requirements into the first quarter of 2025.
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 stakeholder 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 2024, and the Company’s beliefs and
expectations regarding the sufficiency of its existing cash and
cash equivalents to fund its planned operatings, its ability to
raise additional funds, which may not be available to the Company
on acceptable terms or at all, its ability to resume development of
GRI-0863 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(833) 475-8247GRI@jtcir.com
1 https://doi.org/10.1164/rccm.202402-0288LE
2 T. M. Maher et al., Global incidence and
prevalence of idiopathic pulmonary fibrosis. Respir Res
22, 197 (2021)
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