EFFECTS OF EB613 TABLETS [ORAL PTH(1-34)] ON TRABECULAR AND CORTICAL BONE USING 3D-DXA: POST-HOC RESULTS FROM PHASE 2 STUDY Accepted for Oral Presentation at World Congress on Osteoporosis, Osteoarthritis and Musculoskeletal Diseases
February 19 2025 - 7:00AM
Entera Bio Ltd. (NASDAQ: ENTX), (“Entera” or the “Company”) a
leader in the development of oral peptide and protein replacement
therapies in tablet form, today announced that the World Congress
on Osteoporosis, Osteoarthritis and Musculoskeletal Diseases
(WCO-IOF-ESCEO) Scientific Programme Committee has accepted both
submitted abstracts related to EB613 for presentation at the
WCO-IOF-ESCEO congress. The congress will take place at the Roma
Convention Center, Rome, Italy from April 10 to April 13, 2025.
EB613 is being developed as the first once-daily
oral anabolic (bone forming) PTH(1-34) tablet treatment to
support earlier osteoanabolic intervention, for high-risk post-menopausal women with osteoporosis.
In a Placebo-controlled Phase 2 study, 6 months of EB613 treatment
demonstrated fast onset of action and robust increases in BMD at
all skeletal sites. Further, EB613 induced increases in bone
formation (P1NP) and suppression of bone resorption (CTX).
“EFFECTS OF EB613 TABLETS [ORAL
PTH(1-34)] ON TRABECULAR AND CORTICAL BONE USING 3D-DXA: POST-HOC
RESULTS FROM PHASE 2 STUDY” will be presented as an
Oral Presentation Friday April 11 at 10:00 GMT in the
Auditorium A.
“EB613 TABLET TREATMENT [ORAL PTH(1-34)]
– DOES PK DRIVE BONE MODELING VERSUS BONE
REMODELING?” will be presented as a Poster
Presentation Friday April 11th – Sunday April 13th 2025.
“We thank our distinguished authors and are
looking forward to sharing further mechanistic insights on EB613
with the thousands of top researchers and healthcare professionals
who attend WCO-IOF-ESCEO,” said Miranda Toledano, Chief Executive
Officer of Entera.
It is estimated that 50 percent of women and 20
percent of men over the age of 50 are at risk of a fragility
fractures and approximately 1 in 5 adults will die within the year
following a hip fracture. Post menopausal osteoporosis afflicts
more women than cancer and cardiovascular disease and is a serious
health concern for an estimated 200 million women globally.
EB613 is intended to provide an anabolic ‘boost’
to strengthen skeletal microarchitecture and induce rapid BMD
gains, followed by consolidation with an antiresorptive agent.
“Available injectable anabolic treatments, while efficacious and
recommended across medical guidelines, unfortunately do not provide
a viable solution for most patients with high-risk osteoporosis
requiring an anabolic intervention. Our EB613 program is being
developed to address the treatment chasm in current osteoporosis
care and hopefully present a treatment for the majority of patients
to adequately manage their bone health with a simple once daily
tablet treatment,” Said Toledano.
About Entera Bio
Entera is a clinical stage company focused on
developing oral peptide and protein replacement therapies for
significant unmet medical needs where an oral tablet form holds the
potential to transform the standard of care. The Company leverages
on a disruptive and proprietary technology platform (N-Tab™) and
its pipeline includes five differentiated, first-in-class oral
peptide programs targeting PTH(1-34), GLP-1 and GLP-2. The
Company’s most advanced product candidate, EB613 (oral PTH(1-34)),
is being developed as the first oral, osteoanabolic (bone building)
once-daily tablet treatment for post-menopausal women with low
BMD and high-risk osteoporosis. A placebo controlled, dose ranging
Phase 2 study of EB613 tablets (n= 161) met primary (PD/bone
turnover biomarker) and secondary endpoints (BMD). Entera is
preparing to initiate a Phase 3 registrational study for EB613
pursuant to the FDA’s qualification of a quantitative BMD endpoint.
The EB612 program is being developed as the first oral PTH(1-34)
tablet peptide replacement therapy for hypoparathyroidism. Entera
is also developing the first oral oxyntomodulin, a dual targeted
GLP1/glucagon peptide, in tablet form for the treatment of obesity;
and first oral GLP-2 peptide tablet as an injection-free
alternative for patients suffering from rare malabsorption
conditions such as short bowel syndrome in collaboration with OPKO
Health. For more information on Entera Bio, visit www.enterabio.com
or follow us on LinkedIn, Twitter, Facebook, Instagram.
Cautionary Statement Regarding Forward
Looking Statements
Various statements in this presentation are
“forward-looking statements” within the meaning of the Private
Securities Litigation Reform Act of 1995. All statements (other
than statements of historical facts) in this presentation regarding
our prospects, plans, financial position, business strategy and
expected financial and operational results may constitute
forward-looking statements. Words such as, but not limited to,
“anticipate,” “believe,” “can,” “could,” “expect,” “estimate,”
“design,” “goal,” “intend,” “may,” “might,” “objective,” “plan,”
“predict,” “project,” “target,” “likely,” “should,” “will,” and
“would,” or the negative of these terms and similar expressions or
words, identify forward-looking statements. Forward-looking
statements are based upon current expectations that involve risks,
changes in circumstances, assumptions and uncertainties.
Forward-looking statements should not be read as a guarantee of
future performance or results and may not be accurate indications
of when such performance or results will be achieved.
Important factors that could cause actual
results to differ materially from those reflected in Entera’s
forward-looking statements include, among others: changes in the
interpretation of clinical data; results of our clinical trials;
the FDA’s interpretation and review of our results from and
analysis of our clinical trials; unexpected changes in our ongoing
and planned preclinical development and clinical trials, the timing
of and our ability to make regulatory filings and obtain and
maintain regulatory approvals for our product candidates; the
potential disruption and delay of manufacturing supply chains; loss
of available workforce resources, either by Entera or its
collaboration and laboratory partners; impacts to research and
development or clinical activities that Entera may be contractually
obligated to provide; overall regulatory timelines; the size and
growth of the potential markets for our product candidates; the
scope, progress and costs of developing Entera’s product
candidates; Entera’s reliance on third parties to conduct its
clinical trials; Entera’s ability to establish and maintain
development and commercialization collaborations; Entera’s
operation as a development stage company with limited operating
history; Entera’s competitive position with respect to other
products on the market or in development for the treatment of
osteoporosis, hypoparathyroidism, short bowel syndrome, obesity,
metabolic conditions and other disease categories it pursues;
Entera’s ability to continue as a going concern absent access to
sources of liquidity; Entera’s ability to obtain and maintain
regulatory approval for any of its product candidates; Entera’s
ability to comply with Nasdaq’s minimum listing standards and other
matters related to compliance with the requirements of being a
public company in the United States; Entera’s intellectual property
position and its ability to protect its intellectual property; and
other factors that are described in the “Cautionary Statement
Regarding Forward-Looking Statements,” “Risk Factors” and
“Management’s Discussion and Analysis of Financial Condition and
Results of Operations” sections of Entera’s most recent Annual
Report on Form 10-K filed with the SEC, as well as Entera’s
subsequently filed Quarterly Reports on Form 10-Q and Current
Reports on Form 8-K. There can be no assurance that the actual
results or developments anticipated by Entera will be realized or,
even if substantially realized, that they will have the expected
consequences to, or effects on, Entera. Therefore, no assurance can
be given that the outcomes stated or implied in such
forward-looking statements and estimates will be achieved. Entera
cautions investors not to rely on the forward-looking statements
Entera makes in this presentation. The information in this
presentation is provided only as of the date of this presentation,
and Entera undertakes no obligation to update or revise publicly
any forward-looking statements, whether as a result of new
information, future events or otherwise, except to the extent
required by law.
Contact:
Entera Bio:
Ms. Miranda Toledano
Chief Executive Officer
Entera Bio
Email: miranda@enterabio.com
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