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Entera Bio to Participate in the Canaccord Genuity 46th Annual Growth Conference

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Entera Bio (NASDAQ: ENTX) announced that CEO Miranda Toledano will participate in a fireside chat and 1x1 meetings at the Canaccord Genuity 46th Annual Growth Conference. The fireside chat is scheduled for August 12, 2026 at 1:00 p.m. Eastern Time at the InterContinental Boston Hotel, with the overall event taking place in person from August 11–13, 2026.

A live webcast and presentation slides will be accessible via the provided link, with a replay available for 365 days. Entera is a clinical-stage company developing oral peptide and protein replacement therapies, including lead osteoporosis candidate EB613, which met primary and secondary endpoints in a Phase 2 study.

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Positive

  • None.

Negative

  • None.

Market Context

Entera’s July 27 private placement produced a 91.22% 24-hour historical reaction. That platform reco...
Analysis

Entera’s July 27 private placement produced a 91.22% 24-hour historical reaction. That platform record adds context to this conference notice, while the active S-3 resale registration and low short positioning remain relevant risk factors to monitor.

Key Figures

Conference date: August 12, 2026 at 1:00 p.m. Eastern Time Replay duration: 365 days Phase 2 sample size: n = 161
3 metrics
Conference date August 12, 2026 at 1:00 p.m. Eastern Time Canaccord Genuity 46th Annual Growth Conference fireside chat
Replay duration 365 days Following the event
Phase 2 sample size n = 161 Placebo-controlled, dose-ranging EB613 study

Historical Context

5 past events · Latest: Jul 27 (Negative)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jul 27 Private placement Negative +91.2% Private placement raised $275 million but involved substantial share issuance
Jun 22 FDA feedback Positive +22.3% FDA accepted a single 750-patient Phase 3 trial supporting potential NDA submission
Jun 16 Preclinical data Positive -2.5% EB612 and EB618 showed pharmacologic effects and supported advancement toward clinical development
Jun 15 Clinical data Positive -1.6% Single-tablet EB613 showed comparable PK/PD, calcemic effects and safety to comparators
May 28 Presentation acceptance Positive +2.5% Multiple oral peptide pipeline abstracts were accepted for ENDO 2026 presentations

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 strategically important announcements produced mixed reactions, with three aligned moves and two divergences.

Key Terms

PTH(1-34), osteoanabolic, placebo-controlled, dose-ranging, +1 more
5 terms
PTH(1-34) medical
"EB613 (oral PTH(1-34)), is being developed"
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.
placebo-controlled medical
"A placebo-controlled, dose-ranging Phase 2 study"
"Placebo-controlled" describes a testing method where one group receives the actual treatment or intervention, while another group receives a harmless, inactive version called a placebo. This approach helps determine whether the real treatment has genuine effects beyond psychological expectations. For investors, understanding this ensures confidence that reported benefits are real and not influenced by bias or false perceptions.
dose-ranging medical
"A placebo-controlled, dose-ranging Phase 2 study"
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, July 31, 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 a fireside chat at the Canaccord Genuity 46th Annual Growth Conference, details as below.

Canaccord Genuity 46th Annual Growth Conference (Fireside Chat and 1x1 Meetings)

Date and Time: August 12, 2026 at 1:00 p.m. Eastern Time
Location: In person, August 11–13, 2026, InterContinental Boston Hotel, 510 Atlantic Avenue, Boston, MA
Webcast: https://event.summitcast.com/view/WuFmFdTcA9mVsUGHZJFU62/3r4fss8AzFCZNhJDzPz9Sa

A live webcast of the discussion, including presentation slides, will be available at the link above. A replay will remain accessible for 365 days following the event.

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

When will Entera Bio (NASDAQ: ENTX) present at the Canaccord Genuity 46th Annual Growth Conference?

Entera Bio will participate in a fireside chat on August 12, 2026 at 1:00 p.m. Eastern Time. According to Entera Bio, the conference will be held in person from August 11–13, 2026 at the InterContinental Boston Hotel.

How can investors access Entera Bio’s webcast from the Canaccord Genuity 46th Annual Growth Conference?

Investors can access a live webcast and slides for Entera Bio’s fireside chat through the provided webcast link. According to Entera Bio, a replay of the discussion will remain available online for 365 days following the event for continued investor access.

What is Entera Bio’s lead clinical program EB613 mentioned in the July 31, 2026 ENTX update?

EB613 is Entera Bio’s most advanced candidate, an oral PTH(1-34) osteoanabolic tablet for osteoporosis. According to Entera Bio, a placebo-controlled, dose-ranging Phase 2 study in 161 patients met its primary pharmacodynamic and bone turnover biomarker endpoint and secondary bone mineral density endpoints.

Which pipeline programs does Entera Bio (ENTX) highlight alongside its Canaccord 2026 conference participation?

Entera Bio highlights EB613 for osteoporosis, EB612 oral Long Acting PTH(1-34) for hypoparathyroidism, an oral oxyntomodulin GLP1/glucagon tablet for obesity and metabolic syndromes, and an oral GLP-2 tablet for rare malabsorption conditions, developed in collaboration with OPKO Health, according to Entera Bio.

Where is the Canaccord Genuity 46th Annual Growth Conference featuring Entera Bio being held?

The conference is being held at the InterContinental Boston Hotel, 510 Atlantic Avenue, Boston, MA. According to Entera Bio, its CEO will join a fireside chat and 1x1 meetings there during the in-person event from August 11–13, 2026.

What type of company is Entera Bio (NASDAQ: ENTX) as described in its July 31, 2026 announcement?

Entera Bio is a clinical-stage company focused on oral peptide and protein replacement therapies. According to Entera Bio, it uses its proprietary N-Tab technology platform to develop first-in-class oral peptide tablets targeting osteoporosis, hypoparathyroidism, obesity, metabolic syndromes, and rare malabsorption conditions.