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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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Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
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Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a -12)
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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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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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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: May 10, 2024
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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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• |
In March 2024, Entera echoed the American Society for Bone and Mineral Research (ASBMR) announcement that U.S. Food and Drug Administration (FDA) expects to provide a
ruling qualifying bone mineral density (BMD) as a surrogate endpoint for fractures within 10 months. FDA’s expected ruling is a key catalyst to the potential initiation of EB613’s pivotal phase 3 study. 200 million women globally are
estimated to be afflicted with osteoporosis. No new drugs have been approved for osteoporosis since 2019. Fracture rates, morbidity and mortality rates are rising despite effective injectable treatments. EB613 is the first and only
PTH(1-34) bone building peptide in tablet format.
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• |
In April 2024, Entera announced that the Journal of Bone and Mineral Research (JBMR) published EB613 placebo controlled Phase 2 Trial results, highlighting its dual
mechanism of action, differentiated BMD profile versus injectable PTH(1-34) treatment and its potential to address the treatment chasm in this serious disease.
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• |
In April 2024, Entera submitted to the Endocrine Society Annual Meeting (ENDO 2024) pharmacokinetic (PK) and early PD data from a Phase 1 study evaluating an
unmodified PTH(1-34) peptide and a new generation of Entera’s N-Tab™ platform.
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• |
In March 2024, Entera announced positive in vivo PK results
from its program combining OPKO Health, Inc.’s (Nasdaq: “OPK”) long acting GLP-2 analogue with N-Tab™ technology. Oral GLP-2 tablets exhibited significant
systemic exposure with plasma levels that were approximately 10-fold higher than therapeutic plasma concentrations reported for teduglutide (Gattex®). Pharmacology data is expected early in the second half of 2024
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• |
Collaborative work is ongoing combining N-Tab™ with OPKO’s long-acting Oxyntomodulin (OXM) analogues for potential treatment for obesity and other metabolic diseases.
We expect to report PK data for the oral OXM tablet in mid-2024, pursuant to which a pharmacology study would be initiated.
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Entera is collaborating with leading researchers in orthopedics and sports medicine to contribute its proprietary oral PTH(1-34) tablets for an investigator sponsored
Phase 2 Study seeking to treat young women athletes who experience stress fractures as a result of intense sports training. Enter expects to provide more details on this study in the second half of 2024.
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ENTERA BIO LTD.
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CONSOLIDATED BALANCE SHEETS
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(U.S. dollars in thousands)
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March 31,
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December 31,
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|||||||
2024
|
2023
|
|||||||
(Unaudited)
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(Audited)
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|||||||
Cash and cash equivalents
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9,189
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11,019
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||||||
Accounts receivable and other current assets
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562
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238
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||||||
Property and equipment, net
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87
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100
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||||||
Other assets, net
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401
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408
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Total assets
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10,239
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11,765
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||||||
Accounts payable and other current liabilities
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1,121
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1,091
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Total non-current liabilities
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255
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288
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Total liabilities
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1,376
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1,379
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Total shareholders' equity
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8,863
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10,386
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Total liabilities and shareholders' equity
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10,239
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11,765
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Three Months Ended
March 31,
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||||||||
2024
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2023
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|||||||
OPERATING EXPENSES:
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||||||||
Research and development
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735
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931
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||||||
General and administrative
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1,327
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1,294
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||||||
Other income
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-
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(13
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)
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|||||
TOTAL OPERATING EXPENSES
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2,062
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2,212
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||||||
OPERATING LOSS
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2,062
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2,212
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||||||
FINANCIAL EXPENSES (INCOME), NET
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(45
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)
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(22
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)
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||||
NET LOSS
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2,017
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2,190
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||||||
BASIC AND DILUTED LOSS PER SHARE
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0.05
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0.08
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||||||
WEIGHTED AVERAGE NUMBER OF SHARES OUTSTANDING USED IN COMPUTATION OF BASIC AND DILUTED LOSS PER SHARE
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36,735,429
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28,809,922
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