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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 (Date of earliest event reported): December 28, 2023
HARROW,
INC.
(Exact
name of registrant as specified in its charter)
Delaware |
|
001-35814 |
|
45-0567010 |
(State
or other jurisdiction
of
incorporation) |
|
(Commission
File
Number) |
|
(IRS
Employer
Identification
No.) |
102
Woodmont Blvd., Suite 610 |
|
|
Nashville,
Tennessee |
|
37205 |
(Address
of principal executive offices) |
|
(Zip
Code) |
Registrant’s
telephone number, including area code: (615) 733-4730
Not
Applicable
(Former
Name or Former Address, if Changed Since Last Report)
Securities
registered pursuant to Section 12(b) of the Act:
Title
of each class |
|
Trading
Symbol(s) |
|
Name
of exchange on which registered |
Common
Stock, $0.001 par value per share |
|
HROW |
|
The
Nasdaq Stock Market LLC |
8.625%
Senior Notes due 2026 |
|
HROWL |
|
The
Nasdaq Stock Market LLC |
11.875%
Senior Notes due 2027 |
|
HROWM |
|
The
Nasdaq Stock Market LLC |
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)) |
Indicate
by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 or Rule 12b-2
of the Securities Act of 1934: 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
1.02. Termination of a Material Definitive Agreement.
To
the extent required, the information contained in Item 8.01 hereof is incorporated herein by reference.
Item
5.02 Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers; Compensatory Arrangements of
Certain Officers.
Effective
January 2, 2024, Harrow, Inc. (the “Company”) appointed John P. Saharek as the President and Chief Executive Officer of the
Company’s ImprimisRx division, in addition to his current role as Chief Commercial Officer of the Company. Mr.
Saharek’s annual base salary was adjusted to $450,000 and his target bonus will remain at 50% of his annual base salary. Mr. Saharek
will continue to report to Mark L. Baum, Chief Executive Officer and Chairman of the Company.
Item
5.05. Amendments to the Registrant’s Code of Ethics, or Waiver of a Provision of the Code of Ethics.
Effective
December 28, 2023, the Board of Directors of the Company approved certain amendments to the Company’s Code of Business Conduct
and Ethics (the “Code”) upon the recommendation of the Nomination and Corporate Governance Committee of the Board. The amendments
to the Code update the Company’s corporate name and revise and clarify the Company’s obligations with respect to political
activities. The amendments to the Code do not relate to or result in any waiver, explicit or implicit, of any provision of the Code in
effect prior to the amendments. Each of the Company’s directors, employees and officers, including the Company’s Chief Executive
Officer, Chief Financial Officer, and all of its other principal executive officers, are required to comply with the Code.
The
Code is available for review on the Investors section of the Company’s website, www.harrow.com, under Corporate Governance, and
is also available in print, without charge, to any stockholder who requests a copy by writing to Harrow, Inc., 102 Woodmont Blvd., Suite
610, Nashville, TN 37205, Attention: Investor Relations.
Item
8.01. Other Events.
On
December 28, 2023, the Company terminated the Loan and Security Agreement (the “Loan Agreement”), dated as of September 1,
2021, as amended, by and between the Company, as lender, and Melt Pharmaceuticals, Inc. (“Melt”), as borrower, which provided
for a senior secured term loan with an initial aggregate principal amount of $13.5 million bearing interest at 12.50% per annum. As of
the date of termination, approximately $18.4 million remained outstanding under the Loan Agreement. Pursuant to the terms of a Settlement
and Payoff Agreement, dated as of December 28, 2023, by and between the Company and Melt (the “Settlement Agreement”), the
Company received 2,260,000 shares of Melt’s Series B-1 Preferred Stock and 74,256 shares of Melt’s Series B Preferred Stock
in consideration for the full payment of all amounts outstanding under the Loan Agreement (other than contingent indemnification obligations
for which no claim has been made). The Settlement Agreement contains customary representations, warranties and releases of the parties
and requires the parties to enter into a registration rights agreement providing the Company with rights consistent with other holders
of preferred stock of Melt.
In
addition to the preferred stock acquired by the Company upon settlement of all amounts outstanding under the Loan Agreement, the Company
owns 3,500,000 shares of common stock of Melt. The equity of Melt held by the Company following the settlement represents an aggregate
of approximately 47% of the outstanding equity interests of Melt. The Company also owns royalty rights in certain drug candidates being
developed by Melt following the termination date of the Loan Agreement.
The
press release announcing the transactions described herein is filed as Exhibit 99 to this Current Report on Form 8-K.
Item
9.01 Financial Statements and Exhibits.
SIGNATURES
Pursuant
to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by
the undersigned hereunto duly authorized.
|
HARROW,
INC. |
|
|
|
Dated:
January 3, 2024 |
By:
|
/s/
Andrew R. Boll |
|
|
Andrew
R. Boll |
|
|
Chief
Financial Officer |
Exhibit
99
Melt
Pharmaceuticals Provides Corporate Update
NASHVILLE,
Tenn. (January 3, 2024) – Melt Pharmaceuticals, Inc. (“Melt”), a clinical-stage pharmaceutical company developing
novel approaches for procedural sedation, today provided a corporate update. The Company previously announced that MELT-300 achieved
the primary sedation endpoint in its Phase 2 Pivotal Efficacy and Safety Study in subjects undergoing cataract surgery. MELT-300, a non-IV,
non-opioid tablet that combines fixed doses of midazolam (3mg) and ketamine (50mg), is administered sublingually using Catalent Inc.’s
proprietary fast-dissolving Zydis® delivery technology to rapidly dissolve the tablet for absorption across the
very thin sublingual mucosa.
Melt
Pharmaceuticals recently received a written response from the U.S. Food and Drug Administration (FDA) regarding its planned MELT-300
Phase 3 program. Based on the FDA’s response, Melt Pharmaceuticals expects to begin Phase 3 program activities, which will consist
of a single pivotal study comparing MELT-300 to sublingual midazolam and placebo in subjects undergoing cataract surgery, in the first
quarter of 2024.
Additionally,
Melt has now reached an agreement with and paid in full all the outstanding principal and accrued and unpaid interest under its loan
facility with Harrow, Inc. (Nasdaq: HROW), Melt’s largest shareholder, through the issuance of shares of Melt’s Series
B and Series B-1 Preferred Stock. Following this transaction, in addition to certain royalty rights, Harrow’s equity ownership
percentage of Melt is approximately 47%.
“We
are very pleased to have received a response from the FDA that supports the investment we are making in our proposed MELT-300 Phase 3
program,” said Dr. Dillaha. “This was the last step needed to finalize our program design, paving the way for the commencement
of Phase 3 program activities in early 2024. Following the debt settlement with Harrow and our successful efforts to date to secure sufficient
funding to commence the Phase 3 program, we can now focus on the advancement of our non-IV, non-opioid MELT-300 product candidate, which
we believe has the potential to revolutionize short-duration procedural sedation for more than 100 million U.S. medical procedures, enhancing
the surgical patient experience by providing greater comfort and reducing reliance on opioids.”
About
Melt Pharmaceuticals
Melt
Pharmaceuticals, Inc. is a clinical-stage pharmaceutical company focused on developing proprietary non-opioid, non-IV, sedation, and
analgesia therapeutics for human medical procedures in the hospital, outpatient, and in-office settings. Melt intends to seek regulatory
approval through the FDA’s 505(b)(2) regulatory pathway for its proprietary, patented small-molecule product candidates, where
possible. Melt’s core intellectual property is the subject of multiple granted patents in North America, Europe, Asia, and the
Middle East. Melt Pharmaceuticals, Inc. is a former subsidiary of Harrow, Inc. (Nasdaq: HROW) and was carved out as a separately managed
business in 2019. To learn more about Melt, please visit their website, www.meltpharma.com.
Investor
Contact: |
Media
Contact: |
|
|
Larry
Dillaha, M.D. |
Deb
Holliday |
Chief
Executive Officer |
Holliday
Communications, Inc. |
ldillaha@meltpharma.com |
deb@hollidaycommunications.net |
|
412-877-4519 |
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