Entera Bio and OPKO Health Provide Update on PK/PD Results of Oral Oxyntomodulin (GLP-1/Glucagon) Peptide Tablet Candidate for Obesity and Metabolic Disorders
September 25 2024 - 8:30AM
Entera Bio Ltd. (NASDAQ: ENTX) (Entera), a leader in the
development of orally delivered peptides, and OPKO Health, Inc.
(NASDAQ: OPK) (OPKO) announced today topline
pharmacokinetic/pharmacodynamic (PK/PD) results from their ongoing
collaborative research combining a proprietary long-acting
oxyntomodulin (OXM) analog developed by OPKO and Entera’s
proprietary N-Tab™ technology. The program is focused on developing
the first oral dual agonist GLP-1/glucagon peptide as a potential
once-daily treatment for patients with obesity, metabolic and
fibrotic disorders. OXM is a naturally occurring peptide hormone
found in the small intestine that acts to suppress appetite and
induce weight loss.
Entera and OPKO have completed in vivo
proof-of-concept PK/PD studies in rodent and pig models. The
studies’ objectives were met with oral OXM exhibiting significant
systemic exposure following a single dose in both models.
Furthermore, a favorable PK profile and bioavailability were shown
with oral OXM. In the pig model, oral OXM achieved high plasma
concentrations with prolonged systemic exposure, which is
consistent with the reported half-life for semaglutide (Rybelsus®),
the only approved oral GLP-1 analog.
To assess the pharmacologic effect of oral OXM,
a glucose tolerance test was performed in rats. Oral OXM showed a
statistically significant reduction in plasma glucose levels
post-glucose administration compared with placebo. Entera and OPKO
plan to present these data at an upcoming clinical conference.
“We are very pleased with the progress we are
making in our collaboration with OPKO. These bioavailability and
pharmacological data support continuing toward IND-enabling efforts
for the program,” said Miranda Toledano, Entera Chief Executive
Officer.
OPKO previously reported that weekly injections
of pegylated OXM demonstrated significant weight loss and reduction
in HbA1, triglyceride and cholesterol levels in 113 obese and
diabetic patients in a Phase 2B study. The OXM agonist peptide has
since been modified to maintain its long-acting profile while
increasing its potential potency. Currently, there are no approved
OXM agonists available, and those in development by others are
small molecules or require subcutaneous injections.
About Entera Bio
Entera is a clinical-stage company focused on
developing oral peptide or 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
a disruptive and proprietary technology platform (N-Tab™) and its
pipeline includes five differentiated, first-in-class oral peptide
programs, expected to enter the clinic (Phase 1 to Phase 3) by
2025. 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
(BMD) endpoints. Entera is preparing to initiate a Phase 3
registrational study for EB613 pursuant to the FDA’s qualification
of a quantitative BMD endpoint, which is expected to occur by
January 2025. The EB612 program is being developed as the first
oral PTH (1-34) tablet peptide replacement therapy for
hypoparathyroidism. In collaboration with OPKO Health, Entera is
also developing the first oral oxyntomodulin, a dual targeted
GLP-1/glucagon peptide, in tablet form for the treatment of
obesity; and the first oral GLP-2 peptide tablet as an
injection-free alternative for patients suffering from rare
malabsorption conditions such as short bowel syndrome. For more
information, visit www.enterabio.com or follow us
on LinkedIn, X (formerly Twitter), Facebook
and Instagram.
About OPKO Health
OPKO Health is a multinational biopharmaceutical
and diagnostics company that seeks to establish industry-leading
positions in large, rapidly growing markets by leveraging its
discovery, development and commercialization expertise, and its
novel and proprietary technologies. For more information, visit
www.opko.com.
Cautionary Statement Regarding Forward
Looking StatementsVarious statements in this press release
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 press release
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 and
OPKO’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 or OPKO 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 our product
candidates; Entera’s reliance on third parties to conduct its
clinical trials; Entera and OPKO’s expectations regarding
licensing, business transactions and strategic collaborations;
Entera’s operation as a development stage company with limited
operating history; Entera’s ability to continue as a going concern
absent access to sources of liquidity; 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 and OPKO’s intellectual property
position and its ability to protect its intellectual property; and
other factors that are described in the “Cautionary Statements
Regarding Forward-Looking Statements,” “Risk Factors” and
“Management’s Discussion and Analysis of Financial Condition and
Results of Operations” sections of Entera’s and OPKO’s most recent
Annual Report on Form 10-K filed with the SEC, as well as the
companies’ 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 and OPKO will
be realized or, even if substantially realized, that they will have
the expected consequences to, or effects on, Entera or OPKO as
applicable. Therefore, no assurance can be given that the outcomes
stated or implied in such forward-looking statements and estimates
will be achieved. Entera and OPKO caution investors not to rely on
the forward-looking statements made in this press release. The
information in this press release is provided only as of the date
of this press release, and Entera and OPKO undertake 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.
Contacts:
Entera Bio
Miranda Toledano
Chief Executive Officer
miranda@enterabio.com
OPKO Health
LHA Investor Relations
Yvonne Briggs, 310-691-7100
ybriggs@lhai.com
or
Bruce Voss, 310-691-7100
bvoss@lhai.com
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