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Entera Bio to Participate in Upcoming Investor Conferences

Key Takeaway: Entera Bio Ltd. will participate in the H.C. Wainwright 25th Annual Global Investment Conference and the BIO Investor Forum, presenting key strategies and updates on their product candidates. The company is focusing on innovative peptide therapies, including EB613, which has shown promising results for osteoporosis. Entera plans to initiate a Phase 3 study for EB613, amidst various risk factors like regulatory hurdles and clinical uncertainties.

Market Sentiment Analysis

POSITIVE FACTORS

  • Entera is participating in two notable investor conferences, which can enhance visibility.
  • The company is advancing its most promising product candidate, EB613, towards a Phase 3 study.
  • EB613 shows positive results in earlier clinical trials, indicating potential market viability.

CONCERNS & RISKS

  • Forward-looking statements highlight uncertainties in clinical trial outcomes and regulatory approval.
  • The company faces risks related to supply chain disruptions and workforce availability.

Full Press Release Details

JERUSALEM, Sept. 05, 2023 (GLOBE NEWSWIRE) -- Entera Bio Ltd. (NASDAQ: ENTX), (“Entera” or the “Company”) a leader in the development of orally delivered peptides and therapeutic proteins, today announced that it will participate in the upcoming investor conferences:
H.C. Wainwright 25th Annual Global Investment Conference September 11-13th
Presentation:  Monday September 11th, 7:00am ET
Presenter: Miranda Toledano, CEO
Location: New York, NY
BIO Investor Forum October 17-18th
Panel Session: Exploring Funding Opportunities for Diverse Founders and Executives
Time:  Wednesday October 18, 2023, 11:00-11:50am PT
Presenter: Miranda Toledano, CEO
Location: San Francisco, CA
Entera focuses on significant unmet medical needs where a daily mini tablet form of a peptide treatment or replacement therapy holds the potential to transform the standard of care. The Company’s most advanced product candidate, EB613 (oral synthetic hPTH (1-34)), is being developed as the first oral, osteoanabolic (bone building) once a day 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. EB612 is being developed as the first tablet peptide replacement therapy for the treatment of hypoparathyroidism. The Company expects to report results from a phase 1B PK study of novel PTH formulations using its proprietary, next generation oral delivery platform in the second half of 2023. In May 2023, Entera announced pre-clinical results from its oral GLP-2 program which is being developed as an injection-free alternative for patients suffering from short bowel syndrome and other severe intestinal and malabsorption metabolic conditions. For more information on Entera Bio, visit www.enterabio.com.
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 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 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 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 Statements 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 the company’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.

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Frequently Asked Questions

When will Entera Bio present at the H.C. Wainwright conference?

Entera Bio will present on September 11, 2023, at 7:00am ET.

What is the focus of Entera Bio's product EB613?

EB613 is aimed at treating post-menopausal women with low bone mineral density.

What is the purpose of the Phase 3 study for EB613?

The Phase 3 study will register EB613 as an oral treatment for osteoporosis.

Where is the BIO Investor Forum location?

The BIO Investor Forum will be held in San Francisco, CA.

What is Entera's approach to peptide therapies?

Entera develops orally delivered peptides for unmet medical needs.

Last updated: Sep 5, 2023