Press Releases August 27, 2026 08:00 AM

Entera to Participate in Upcoming Fall Investor Conferences

Entera Bio Announces CEO Participation in Multiple 2026 Fall Investor Conferences Focused on Advancing Oral Peptide Therapies

By Jordan Park
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ENTX

Entera Bio Ltd., a clinical stage biotechnology company specializing in oral peptide therapies, announced its CEO Miranda Toledano will participate in several prominent healthcare investor conferences throughout fall 2026. The company highlighted its proprietary N-Tab technology platform and diverse pipeline including its leading osteoporosis candidate EB613. The announcements reaffirm Entera's commitment to advancing innovative oral peptide treatments and engaging with investors.

Entera to Participate in Upcoming Fall Investor Conferences
ENTX
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Key Points

  • Entera Bio's CEO to present at key healthcare investor conferences in New York, California, Boston, and Miami during fall 2026.
  • The company focuses on developing oral peptide and protein replacement therapies with a proprietary platform technology (N-Tab®).
  • Lead product candidate EB613 is in Phase 2 clinical trials for osteoporosis with successful biomarker and bone mineral density results, alongside other oral therapies targeting hypoparathyroidism, obesity, and malabsorption conditions.
  • Sectors impacted include biotechnology, healthcare innovation, pharmaceutical development, and investment sectors focused on biotech growth.

TEL AVIV, Israel, Aug. 27, 2026 (GLOBE NEWSWIRE) -- Entera Bio Ltd. (NASDAQ: ENTX) (“Entera” or the “Company”), a leader in the development of oral peptides, today announced that the Company’s Chief Executive Officer, Miranda Toledano, will be participating in the following upcoming fall investor conferences:

2026 Cantor Global Healthcare Conference
Fireside Chat: September 10, 2026 at 1:00 p.m. Eastern Time, Waldorf Astoria New York, 301 Park Avenue, New York, NY

2026 Leerink Partners Biopharma Summit
September 23–25, 2026, in person, Location: Healdsburg, CA

Guggenheim Securities 3rd Annual Healthcare Innovation Conference
November 9, 2026, Fireside Chat and 1x1 Meetings, Location: Boston, MA

Evercore ISI 9th Annual Healthcare Conference
November 30–December 2, 2026, in person, Location: Miami, FL

About Entera
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 a disruptive and proprietary technology platform (N-Tab®) and its pipeline of first-in-class oral peptide programs. 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 for 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 also developing the first oral Long Acting PTH(1-34) tablet as a replacement therapy for patients with hypoparathyroidism (EB612), the first oral oxyntomodulin, a dual targeted GLP1/glucagon peptide tablet for the treatment of obesity and metabolic syndromes; and the first oral GLP-2 tablet as an injection-free alternative for patients suffering from rare malabsorption conditions such as short bowel syndrome in collaboration with OPKO Health, Inc. For more information on Entera, visit www.enterabio.com or follow us on LinkedIn, Twitter, and Facebook.

Cautionary Statement Regarding Forward Looking Statements
Various 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, clinical development activities, collaboration arrangements and expected financial and operational results are 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 press release. The information in this press release is provided only as of the date of this press release, 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.

Company Contact:
[email protected]


Risks

  • Clinical trial outcomes could differ from current expectations, impacting product approval and commercialization timelines.
  • Regulatory approvals and reviews remain uncertain, particularly by the FDA, potentially delaying market entry.
  • Dependence on third-party collaborators, manufacturing supply chain stability, and ability to maintain Nasdaq listing standards pose operational risks, affecting investors and industry stakeholders.

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