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Israel
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001-38556
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Not Applicable
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(State or other jurisdiction
of incorporation) |
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(Commission File Number)
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(I.R.S. Employer
Identification) |
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☐
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Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
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☐
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Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a -12)
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☐
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Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d -2(b))
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☐
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Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e -4(c))
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Title of each class
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Trading Symbol(s)
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Name of each exchange on which registered
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Ordinary Shares, par value of NIS 0.0000769
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ENTX
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Nasdaq Capital Market
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Exhibit
Number
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Description
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104
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Cover Page Interactive Data File (embedded within the Inline XBRL document).
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ENTERA BIO LTD.
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Date: November 14, 2025
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By:
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/s/ Miranda Toledano
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Name: Miranda Toledano
Title: Chief Executive Officer
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• |
FDA Agreement on BMD as Primary Endpoint: In a written response
to a Type A meeting, the FDA agreed with Entera’s proposal that a single multinational, randomized, double-blind, placebo-controlled, 24-month Phase 3 study where change in total hip BMD is evaluated as the primary endpoint, and incidence
of new or worsening vertebral fractures as the key secondary endpoint, would support an NDA marketing application for EB613.
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|
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• |
Strong Phase 2 Data Reinforce Early Onset of EB613 Anabolism:
At the ASBMR 2025 Annual Meeting, Entera presented post-hoc 3D-DXA results showing significant increases in both trabecular and cortical bone indices after just six months of EB613 treatment, comparable to injectable teriparatide and
abaloparatide. Mechanistically, the findings suggest that bone strengthening and fracture resistance may occur rapidly with EB613.
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• |
Expanded Evidence in Early Postmenopausal Women: At the NAMS
2025 Meeting, new Phase 2 analysis demonstrated EB613 ability to drive significant and consistent gains in BMD at the spine, femoral neck and hip in younger women within 10 years of menopause, with improvements comparable to those observed
in women more than 10 years post-menopause. For younger high-risk women without a prior fracture, BMD is the single most important predictor of osteoporotic fractures. Today, it is estimated that less than 15% of women are willing to take
or have access to currently approved anabolics, which require daily or monthly injections.
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|
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• |
Next-Gen EB613: Preclinical PK data presented at ASBMR showed
comparable pharmacokinetic exposure to the current formulation using a single fixed dose regimen, validating the N-Tab™ platform and potential franchise expansion. A Phase 1 trial of Next-Gen EB613 currently remains on track to initiate in late 2025.
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• |
Positive PK data presented at ESPEN 2025: The joint Entera-OPKO
abstract highlighted a plasma half-life of approximately 15 hours, representing an 18-fold improvement over teduglutide (Gattex®), the only approved GLP-2 therapy, which requires a daily injection. The daily GLP-2 tablet candidate could fundamentally change how SBS
patients are treated, offering a less-invasive administration that can be titrated to enable personalized dosing in this rare and heterogeneous condition.
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• |
Encouraging preclinical data presented at the Endocrine Society (ENDO)
2025 annual meeting: In the abstract titled “First-in-Class Oral Dual GLP-1/Glucagon Agonist for Patients with Obesity and Metabolic Disorders” PK data reported from a minipig study show plasma levels of OPK-88006 consistent with
those reported in humans for the highest, 2.4 mg subcutaneous dose of Wegovy (semaglutide) weekly injection, a standard of care for the treatment of obesity. An IND for oral OXM is planned for H1 2026.
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• |
Collaborative studies evaluating a novel, long-acting PTH analog remain on track to deliver first PK/PD pre-clinical data for a single tablet candidate by year-end
2025.
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September 30,
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December 31,
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|||||||
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2025
|
2024
|
|||||||
|
(Unaudited)
|
(Audited)
|
|||||||
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Cash and cash equivalents
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8,574
|
8,660
|
||||||
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Accounts receivable and other current assets
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405
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312
|
||||||
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Restricted cash and deposit
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8,114
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80
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||||||
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Property and equipment, net
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114
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57
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||||||
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Other assets
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200
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281
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||||||
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Total assets
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17,407
|
9,390
|
||||||
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Accounts payable and other current liabilities
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1,571
|
1,176
|
||||||
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Total non-current liabilities
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602
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134
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||||||
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Total liabilities
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2,173
|
1,310
|
||||||
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Total shareholders' equity
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15,234
|
8,080
|
||||||
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Total liabilities and shareholders' equity
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17,407
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9,390
|
||||||
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Three Months Ended
September 30,
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||||||||
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2025
|
2024
|
|||||||
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REVENUES
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-
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42
|
||||||
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COST OF REVENUES
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-
|
42
|
||||||
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GROSS PROFIT
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-
|
-
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||||||
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OPERATING EXPENSES:
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||||||||
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Research and
development
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1,643
|
1,477
|
||||||
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General and administrative
|
1,613
|
1,544
|
||||||
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TOTAL OPERATING EXPENSES
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3,256
|
3,021
|
||||||
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OPERATING LOSS
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3,256
|
3,021
|
||||||
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FINANCIAL INCOME, NET
|
(56
|
)
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-
|
|||||
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NET LOSS
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3,200
|
3,021
|
||||||
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LOSS PER SHARE BASIC AND DILUTED
|
0.07
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0.08
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||||||
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WEIGHTED AVERAGE NUMBER OF SHARES OUTSTANDING USED IN COMPUTATION OF BASIC AND DILUTED LOSS PER SHARE
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47,085,722
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37,644,612
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||||||