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Entera to Participate in Upcoming Fall Investor Conferences

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Entera (NASDAQ: ENTX) announced that CEO Miranda Toledano will present at three fall 2026 investor conferences: the Cantor Global Healthcare Conference on September 10 in New York, the Guggenheim Securities 3rd Annual Healthcare Innovation Conference on November 9 in Boston, and the Evercore ISI 9th Annual Healthcare Conference from November 30–December 2 in Miami.

Entera is a clinical-stage company developing oral peptide and protein replacement therapies using its N-Tab® platform, with lead candidate EB613 for osteoporosis and additional programs in hypoparathyroidism, obesity, metabolic syndromes, and rare malabsorption conditions.

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Positive

  • None.

Negative

  • None.

Market Context

The active resale S-3, filed Aug. 21, 2026 and expiring Aug. 21, 2029, provides financing context fo...
Analysis

The active resale S-3, filed Aug. 21, 2026 and expiring Aug. 21, 2029, provides financing context for this conference schedule. It covers resale shares, with no proceeds going to Entera from selling shareholders.

Key Figures

Cantor conference date: September 10, 2026 Guggenheim conference date: November 9, 2026 Evercore conference dates: November 30–December 2, 2026 +3 more
6 metrics
Cantor conference date September 10, 2026 2026 Cantor Global Healthcare Conference
Guggenheim conference date November 9, 2026 3rd Annual Healthcare Innovation Conference
Evercore conference dates November 30–December 2, 2026 9th Annual Healthcare Conference
Study phase Phase 2 Placebo-controlled, dose-ranging EB613 study
Sample size n = 161 EB613 Phase 2 study
Dosing frequency Once-daily EB613 oral tablet development

Historical Context

5 past events · Latest: Aug 18 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Aug 18 Chief medical officer appointment Positive -0.5% Added pharmaceutical development leadership ahead of planned EB613 Phase 3 initiation.
Aug 07 Second-quarter earnings Positive +5.9% Reported FDA Phase 3 acceptance and $275 million private placement supporting pipeline development.
Aug 04 Phase 2 data presentation Positive -3.0% Phase 2 EB613 data received plenary poster and additional poster selections.
Jul 31 Investor conference participation Neutral -1.0% CEO scheduled a fireside chat and one-on-one meetings at Canaccord conference.
Jul 29 Private placement Positive -8.0% Completed oversubscribed $275 million PIPE to support Phase 3 studies and cash runway.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent positive or neutral announcements more often coincided with negative price reactions than positive reactions.

Key Terms

pTH(1-34), osteoanabolic, dose-ranging, bmd
4 terms
pTH(1-34) medical
"EB613 (oral PTH(1-34)), is being developed as the first oral"
pth(1-34) is the active 34-amino-acid fragment of human parathyroid hormone used as a prescription injectable that stimulates bone growth, commonly developed as an osteoporosis treatment. Investors watch it because clinical trial results, regulatory approvals, patent status and manufacturing scale determine how widely it can be prescribed and how much revenue it might generate—think of it like a new fertilizer that helps a garden regrow, where effectiveness, safety and supply shape market value.
osteoanabolic medical
"the first oral, osteoanabolic (bone building) once-daily tablet"
Osteoanabolic describes a drug, therapy, or biological process that stimulates new bone formation by increasing the activity or number of bone-forming cells (osteoblasts) and related signaling pathways. For investors, it identifies a treatment approach that rebuilds bone rather than just preventing breakdown—like renovating a damaged wall instead of merely patching cracks—which affects clinical development timelines, regulatory considerations, and potential market demand in bone-disease therapies.
dose-ranging medical
"A placebo-controlled, dose-ranging Phase 2 study of EB613 tablets"
A dose-ranging study is a clinical trial that tests multiple amounts of a drug to find what dose works best and is safest, much like trying different spice levels in a recipe to get the right balance. For investors, results clarify whether a medicine is effective at practical doses, how likely it is to win regulatory approval, what side effects to expect, and how the treatment might be priced and used in the market.
bmd medical
"secondary endpoints (BMD)."
Bone mineral density (BMD) is a medical measure of how much mineral — mainly calcium — is packed into a specific volume of bone, often reported as a number from a scan. Investors care because changes in BMD are common primary endpoints for drugs and devices treating osteoporosis and bone disorders; stronger effects on BMD can signal higher chances of regulatory approval, broader market use, and bigger revenue potential. Think of it as a method for checking how solid a building’s concrete is.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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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

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:
IR@enterabio.com


FAQ

What investor conferences will Entera (NASDAQ: ENTX) attend in fall 2026?

Entera will attend three conferences in fall 2026. According to Entera, these are the Cantor Global Healthcare Conference, Guggenheim Securities 3rd Annual Healthcare Innovation Conference, and Evercore ISI 9th Annual Healthcare Conference, across New York, Boston, and Miami.

When is Entera (ENTX) presenting at the 2026 Cantor Global Healthcare Conference?

Entera will present at the Cantor Global Healthcare Conference on September 10, 2026. According to Entera, the CEO’s fireside chat is scheduled for 1:00 p.m. Eastern Time at the Waldorf Astoria New York, 301 Park Avenue, New York.

What is Entera’s EB613 oral PTH(1-34) osteoporosis program mentioned by ENTX?

EB613 is Entera’s most advanced product candidate for osteoporosis. According to Entera, EB613 is a once-daily oral osteoanabolic tablet whose placebo-controlled Phase 2 trial (n = 161) met primary pharmacodynamic and secondary bone mineral density endpoints.

Which pipeline programs is Entera (NASDAQ: ENTX) developing beyond EB613?

Entera is developing several additional oral peptide therapies. According to Entera, these include EB612 for hypoparathyroidism, an oral oxyntomodulin GLP1/glucagon tablet for obesity and metabolic syndromes, and an oral GLP-2 tablet for rare malabsorption conditions such as short bowel syndrome.

What is Entera’s N-Tab platform and business focus as a clinical-stage company (ENTX)?

Entera focuses on oral peptide and protein replacement therapies. According to Entera, its proprietary N-Tab platform supports first-in-class oral peptide programs targeting significant unmet medical needs where an oral tablet could replace injectable treatments and change standard care.

How can investors contact Entera (ENTX) investor relations about these 2026 conferences?

Investors can contact Entera’s investor relations team by email. According to Entera, the company lists IR@enterabio.com as the primary contact address for inquiries related to its activities, including participation in upcoming investor conferences.