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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM
8-K
CURRENT
REPORT
Pursuant
to Section 13 or 15(d) of the
Securities
Exchange Act of 1934.
Date
of Report: October 9, 2024
(Date
of earliest event reported)
Oragenics,
Inc.
(Exact
name of registrant as specified in its charter)
FL |
|
001-32188 |
|
59-3410522 |
(State
or other jurisdiction
of
incorporation) |
|
(Commission
File
Number) |
|
(IRS
Employer
Identification
Number) |
1990
Main Street
Suite
750
Sarasota,
FL |
|
34236 |
(Address
of principal executive offices) |
|
(Zip
Code) |
813-286-7900
(Registrant’s
telephone number, including area code)
(Former
Name or Former Address, if changed since last report)
Check
the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under
any of the following provisions:
☐ |
Written
communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
|
|
☐ |
Soliciting
material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
|
|
☐ |
Pre-commencement
communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
|
|
☐ |
Pre-commencement
communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities
registered pursuant to Section 12(b) of the Act:
Title
of each class |
|
Trading
Symbol(s) |
|
Name
of each exchange on which registered |
Common
Stock |
|
OGEN |
|
NYSE
American |
Indicate
by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405
of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging
growth company ☐
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
ITEM
8.01. OTHER INFORMATION.
On
October 9, 2024, Oragenics, Inc. (the “Company”) issued a press release updating the Company’s shareholders on recent
milestones related to ONP-002 the Company’s new concussion drug, an innovative neurosteroid designed to treat mild Traumatic Brain
Injury (mTBI), commonly referred to as concussion. The Company also updated the shareholders on the recently completed public offering.
A copy of the Press Release is attached hereto as Exhibit 99.1 and is incorporated by reference herein.
ITEM
9.01. FINANCIAL STATEMENTS AND EXHIBITS.
(d)
Exhibits
SIGNATURES
In
accordance with the requirements of the Exchange Act, the registrant caused this report to be signed on its behalf by the undersigned,
thereunto duly authorized on this 9th day of October, 2024.
|
ORAGENICS,
INC. |
|
(Registrant) |
|
|
|
BY: |
/s/
Janet Huffman |
|
|
Janet
Huffman |
|
|
Chief
Financial Officer |
Exhibit 99.1
Oragenics,
Inc. Updates Shareholders on Concussion Drug Progress and Phase II Trial Preparation
Sarasota,
FL – October 9, 2024
Oragenics,
Inc. (NYSE American: OGEN), a biopharmaceutical company committed to developing novel therapies for neurological disorders, today provided
a corporate update reflecting on the company’s progress throughout 2024, including key milestones in the development of ONP-002,
its lead candidate for the treatment of concussions.
Company
Overview: A Vision for Innovation in Neurology
Oragenics
is focused on revolutionizing drug delivery for neurological disorders using innovative intranasal technology. The company’s lead
program, ONP-002, is a first-in-class neurosteroid being developed to treat moderate to severe concussions. Intranasal delivery provides
numerous advantages over traditional systemic methods, including faster brain delivery, reduced systemic exposure, and a non-invasive
approach.
“Our
mission is to address significant unmet medical needs by developing cutting-edge therapies,” stated Michael Redmond, President
of Oragenics. “There are over 3 million annual concussion occurrences in the U.S. and an estimated 69 million globally, however
it is believed that a substantial number, up to 50%, of cases go unreported. Given that there is still no FDA approval, and patients
in need continue to face limited treatment options, the urgency to advance our efforts is greater than ever.
Key
Milestones in Concussion Drug Development
Oragenics
has made significant advancements in the development of ONP-002 during 2024, including:
Strengthened
Clinical Leadership: In 2024, the company appointed two renowned experts—Dr. James “Jim” Kelly as Chief Medical
Officer and Dr. William “Frank” Peacock as Chief Clinical Officer—bringing deep expertise in brain health and emergency
medicine to oversee the clinical development of ONP-002.
Phase
II Clinical Trial Preparation: Building on successful Phase I trials, which demonstrated the safety and tolerability of ONP-002,
the company is preparing to initiate Phase II clinical trials, which will evaluate the drug’s efficacy based on patient outcomes.
Successful
Cardiotoxicity Testing: In July 2024, ONP-002 demonstrated a strong cardiac safety margin, clearing FDA-required cardiotoxicity tests.
These results suggest that the treatment is unlikely to cause cardiac arrhythmias, a crucial milestone that derisks the program as it
moves forward into the Phase II clinical trial.
FDA-Required
Genotoxicity Studies: In August 2024, ONP-002 successfully completed the necessary studies regarding FDA-required genotoxicity testing,
confirming that the drug does not cause DNA damage, further strengthening its safety profile as it advances towards Phase II.
Partnership
with Avance Clinical: In May 2024, the company entered into a partnership with Avance Clinical, a leading CRO, strengthening the
company’s ability to execute its Phase II trial for ONP-002 and leveraging Avance’s expertise in clinical trial management
and regulatory pathways.
Temperature
Stability Achieved: ONP-002 demonstrated stability across a wide temperature range, eliminating the need for cold-chain storage.
This milestone is especially important for field delivery, where concussions frequently occur, such as in sports or military environments.
Spray-Dry
Manufacturing and Device Completion: The company completed the spray-dry formulation of ONP-002 and filled intranasal delivery devices
needed for upcoming Phase II trial. These ready-to-use devices should enable fast, targeted treatment to patients following a concussion.
Improved
Drug Percentage in Final Formulation: A novel nanoparticle spray dried powder formulation was created that should enhance intranasal
absorption and increase the amount of ONP-002 per dose by 4-fold. This new formulation is expected to allow for more drug to enter the
brain at each treatment increasing the chance for reaching therapeutic levels and patient improvement.
Completion
of FDA-Recognized Study for Concussion Drug, ONP-002: Intranasal casting studies are critical for FDA approval of pharmaceuticals
delivered via the nasal passage. The study results demonstrated the drug successfully targets the interior nose that is made from cast
metal (AINI), making it more likely to reach and treat the brain after a concussion. This model is standard for intranasal drug delivery
and is accepted by the FDA as a surrogate for the actual nasal.
Recent
Financing and Strategic Growth
In
September 2024, Oragenics closed a public offering, raising approximately $4.45 million, contributing to a total of over $6 million raised
throughout the year, including previous financing efforts. These funds will support the continued development of ONP-002, allowing the
company to advance toward Phase II clinical trials and further address the unmet medical need for concussion treatments.
“We
are grateful for the confidence that our investors have placed in our vision,” added Redmond. “This financing allows us to
continue advancing ONP-002, which we believe has the potential to be the first approved drug for concussion treatment.”
Looking
Ahead: Key Milestones
Oragenics
anticipates several key milestones in the coming months, including:
Initiation
of Phase II Clinical Trials: The company plans to begin Phase II trials later this year, initially in Australia, followed by U.S.
trials. These trials will evaluate safety and efficacy - evaluating the effects of ONP-002 on concussion patient symptom reduction and
functional recovery.
Clinical
Site Selection The company is currently working with Avance Clinical, a clinical CRO along with major neurotrauma centers in Australia
on Phase II clinical protocols. A key feature of the Phase II trial is to develop emergency department protocols for patient inclusion/exclusion
with the goal of having the first dose occur within 8 hours of the injury. Efficacy evaluations during this 10-day trial include testing
of visual-motor and neurocognitive functional performance while also assessing patient symptoms relative to drug treatment.
Australian
Regulatory Submission Brochure
In
preparation for its upcoming Phase II clinical trials, Oragenics plans to submit the Australian Regulatory Submission Brochure during
the fourth quarter of 2024. This submission is a critical component for the regulatory approval of the trial in Australia and outlines
the clinical trial safety and efficacy protocols, informed consent protocols, and data collection methods.
Continued
Development of Intranasal Delivery System: Oragenics’ intranasal system is a breakthrough in brain injury drug delivery, designed
to provide rapid, targeted brain delivery with minimal side effects. This system will continue to be a key focus as the company advances
ONP-002. This includes the breath-propelled and automated device technologies.
Commitment
to Shareholders
Oragenics
remains committed to maintaining transparency and open communication with its shareholders. The company will continue to provide updates
on its progress as it advances toward key milestones and works to commercialize ONP-002.
Forward-Looking
Statements
This
communication contains “forward-looking statements” within the meaning of the safe harbor provisions of the U.S. Private
Securities Litigation Reform Act of 1995. These forward-looking statements are based on management’s beliefs and assumptions and
information currently available. The words “believe,” “expect,” “anticipate,” “intend,”
“estimate,” “project” and similar expressions that do not relate solely to historical matters identify forward-looking
statements. Investors should be cautious in relying on forward-looking statements because they are subject to a variety of risks, uncertainties,
and other factors that could cause actual results to differ materially from those expressed in any such forward-looking statements. These
factors include, but are not limited to, those described in our Form 10-K and other filings with the U.S. Securities and Exchange Commission.
All information set forth in this press release is as of the date hereof. You should consider these factors in evaluating the forward-looking
statements included in this press release and not place undue reliance on such statements. We do not assume any obligation to publicly
provide revisions or updates to any forward-looking statements, whether as a result of new information, future developments or otherwise,
circumstances should change, except as otherwise required by law.
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