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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
DC 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): November 14, 2024
ABEONA
THERAPEUTICS INC.
(Exact
name of registrant as specified in its charter)
Delaware |
|
001-15771 |
|
83-0221517 |
(State
or other jurisdiction
of
incorporation) |
|
(Commission
File
Number) |
|
(I.R.S.
Employer
Identification
No.) |
6555
Carnegie Ave, 4th Floor
Cleveland,
OH 44103
(Address
of principal executive offices) (Zip Code)
(646)
813-4701
(Registrant’s telephone number, including area code)
N/A
(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 (see General Instruction A.2. below):
☐ |
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 |
|
Name
of each exchange on which registered |
Common
Stock, $0.01 par value |
|
ABEO |
|
The
Nasdaq Capital Market |
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 2.02. Results of Operations and Financial Condition.
On
November 14, 2024, Abeona Therapeutics Inc. (the “Company”) issued a press release entitled “Abeona Therapeutics Reports
Third Quarter 2024 Financial Results and Recent Corporate Updates” regarding its financial results for the quarter ended September
30, 2024. The full text of the press release is filed as. Exhibit 99.1 to this Current Report on Form 8-K and is incorporated herein.
The
information in Item 2.02 of this Current Report on Form 8-K and Exhibit 99.1 attached hereto shall not be deemed “filed”
for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject
to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933,
as amended, or the Exchange Act, except as expressly set forth by specific reference in such a filing.
Item 9.01 Financial Statements and Exhibits.
(d)
Exhibits.
SIGNATURE
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.
|
Abeona Therapeutics Inc. |
|
(Registrant) |
|
|
|
|
By: |
/s/ Joseph
Vazzano |
|
Name: |
Joseph Vazzano |
|
Title: |
Chief Financial Officer |
|
|
|
Date:
November 14, 2024 |
|
|
Exhibit 99.1
Abeona
Therapeutics® Reports Third Quarter 2024 Financial Results and Recent Corporate Updates
FDA
accepts BLA resubmission of pz-cel in recessive dystrophic epidermolysis bullosa and sets PDUFA target action date of April 29, 2025
Company
makes significant progress toward potential commercialization of pz-cel in 2025; Builds momentum with payor discussions and target treatment
centers
CLEVELAND,
November 14, 2024 – Abeona Therapeutics Inc. (Nasdaq: ABEO) today reported financial results for the third quarter ended September
30, 2024, and recent corporate updates.
“With
the acceptance of our Biologics License Application (BLA) resubmission for pz-cel, we are ramping up our commercial readiness efforts,
especially with respect to onboarding potential pz-cel treatment sites and continuing discussions with payors,” said Vish Seshadri,
Chief Executive Officer of Abeona.
Third
Quarter and Recent Progress
Pz-cel
for RDEB
● | Abeona
completed a Type A meeting in August 2024 where it aligned with the FDA on the content for
the resubmission of the Company’s BLA for pz-cel, its investigational first-in-class,
autologous cell-based gene therapy currently in development for RDEB, including additional
information to satisfy all Chemistry Manufacturing and Controls (CMC) requirements noted
in the Complete Response Letter (CRL) issued in April 2024. The CRL required that certain
CMC issues be addressed in the BLA resubmission, and did not identify any deficiencies related
to the clinical efficacy or clinical safety data in the BLA. The FDA did not request any
new clinical trials or clinical data to support the approval of pz-cel. |
● | Also
in August 2024, the Centers for Medicare and Medicaid Services (CMS) granted a product-specific
procedure code ICD-10-PCS (International Classification of Diseases, 10th Revision, Procedure
Coding System) for pz-cel. Also, as part of the Inpatient Prospective Payment System (IPPS)
Final Rule for fiscal year 2025, CMS assigned Medicare reimbursement of pz-cel to Pre-Major
Diagnostic Category, Medicare Severity Diagnosis Related Group 018 (Pre-MDC MS-DRG 018),
which is among the highest available inpatient hospital reimbursement levels for cell and
gene therapies. The favorable Medicare decisions support efficient hospital billing, reimbursement
and patient access. |
● | In
October 2024, Abeona
resubmitted its BLA for pz-cel to the FDA, seeking approval
of pz-cel as a potential new treatment for patients with RDEB. |
● | Also
in October 2024, Abeona entered into a lease agreement for additional facility space in Cleveland,
Ohio to enable manufacturing capacity expansion beyond the current planned manufacturing
footprint. |
● | Also
in October 2024, the United States Patent and Trademark Office issued a new patent (U.S.
Patent No. 12,110,504) (“the ‘504 Patent”) and allowed the claims of a
second patent (based on U.S. Patent Application No. 16/066,253) that is expected to issue
in the coming weeks. Both patents are entitled “Gene Therapy for Recessive Dystrophic
Epidermolysis Bullosa Using Genetically Corrected Autologous Keratinocytes,” and include
claims that cover the use of pz-cel for the treatment of RDEB. The ‘504 Patent has
an expiration date of January 3, 2037, subject to any applicable patent term extension. |
● | In
November 2024, the FDA accepted for review the resubmission of Abeona’s pz-cel BLA
and set a PDUFA target action date of April 29, 2025. |
● | In
preparation for potential commercialization, Abeona continues to make progress on several
key initiatives, including onboarding high-volume epidermolysis bullosa treatment centers
in the U.S. for pz-cel treatment, engaging payers to ensure patient access, and educating
key stakeholders. |
● | In
preparation for potential pz-cel launch, Abeona has hired and trained personnel to support
commercialization, manufacturing, supply chain and quality. |
Pipeline
and partnered programs
● | In
July 2024, Abeona announced a non-exclusive agreement with Beacon Therapeutics, under which
Beacon Therapeutics will evaluate Abeona’s patented AAV204 capsid for its potential
use in AAV gene therapies for select ophthalmology indications. |
● | In
October 2024, Ultragenyx participated in a successful pre-BLA meeting with the FDA during
which Ultragenyx aligned on the details of its BLA for partnered program UX111 AAV gene therapy
for Sanfilippo syndrome type A (MPS IIIA) that is expected to be filed around the end of
2024. |
Third
Quarter Financial Results and Cash Runway Guidance
Cash,
cash equivalents, short-term investments and restricted cash totaled $110.0 million as of September 30, 2024. As of June 30, 2024, cash,
cash equivalents, short-term investments and restricted cash totaled $123.0 million.
Abeona
estimates that its current cash and cash equivalents, short-term investments and restricted cash, as well as its credit facility, are
sufficient resources to fund operations into 2026, before accounting for any potential revenue from commercial sales of pz-cel, if approved,
or proceeds from the sale of a Priority Review Voucher (PRV), if awarded by the FDA.
Research
and development expenses for the three months ended September 30, 2024 were $8.9 million, compared to $7.1 million for the same period
of 2023. General and administrative expenses were $6.4 million for the three months ended September 30, 2024, compared to $4.2 million
for the same period of 2023. The increase in general and administrative expenses is primarily due to commercial and launch preparation
costs. Net loss for the third quarter of 2024 was $30.3 million, including a $15.2 million loss resulting from the quarterly remeasurement
of the fair value of warrant and derivative liabilities. In the third quarter of 2023, net loss was $11.8 million, including a $1.1 million
loss resulting from the quarterly remeasurement of the fair value of warrant liabilities.
Conference
Call Details
The
Company will host a conference call and webcast on Thursday, November 14, 2024, at 8:30 a.m. ET, to discuss the quarter results. To access
the call, dial 877-545-0320 (U.S. toll-free) or 973-528-0002 (international) and Entry Code: 500590 five minutes prior to the start of
the call. A live, listen-only webcast and archived replay of the call can be accessed on the Investors & Media section of Abeona’s
website at https://investors.abeonatherapeutics.com/events. The archived webcast replay will be available for 30 days following
the call.
About
Abeona Therapeutics
Abeona Therapeutics Inc. is a clinical-stage biopharmaceutical company developing cell and gene therapies for serious diseases. Prademagene
zamikeracel (pz-cel) is Abeona’s investigational autologous, COL7A1 gene-corrected epidermal sheets currently in development for
recessive dystrophic epidermolysis bullosa. The Company’s fully integrated cell and gene therapy cGMP manufacturing facility served
as the manufacturing site for pz-cel used in its Phase 3 VIITAL™ trial, and is capable of supporting commercial production of pz-cel
upon FDA approval. The Company’s development portfolio also features AAV-based gene therapies for ophthalmic diseases with high
unmet medical need. Abeona’s novel, next-generation AAV capsids are being evaluated to improve tropism profiles for a variety of
devastating diseases. For more information, visit www.abeonatherapeutics.com.
Forward-Looking
Statements
This press release contains
certain statements that are forward-looking within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section
21E of the Securities Exchange Act of 1934, as amended, and that involve risks and uncertainties. We have attempted to identify forward-looking
statements by such terminology as “may,” “will,” “believe,”
“anticipate,” “expect,” “intend,” “potential,” and similar words and expressions (as
well as other words or expressions referencing future events, conditions or circumstances), which constitute and are intended to identify
forward-looking statements. Actual results may differ materially from those indicated by such forward-looking statements as a result
of various important factors, numerous risks and uncertainties, including but not limited to, the timing and outcome of the FDA’s
review of our BLA resubmission for pz-cel; the FDA’s grant of a Priority Review Voucher upon pz-cel approval; continued interest
in our rare disease portfolio; our ability to enroll patients in clinical trials; the outcome of future meetings with the FDA or other
regulatory agencies, including those relating to preclinical programs; the ability to achieve or obtain necessary regulatory approvals;
the impact of any changes in the financial markets and global economic conditions; risks associated with data analysis and reporting;
and other risks disclosed in the Company’s most recent Annual Report on Form 10-K and subsequent periodic reports filed with the
Securities and Exchange Commission. The Company undertakes no obligation to revise the forward-looking statements or to update them to
reflect events or circumstances occurring after the date of this press release, whether as a result of new information, future developments
or otherwise, except as required by the federal securities laws.
Investor
and Media Contact:
Greg
Gin
VP, Investor Relations and Corporate Communications
Abeona Therapeutics
ir@abeonatherapeutics.com
ABEONA
THERAPEUTICS INC. AND SUBSIDIARIES
Condensed Consolidated Statements of Operations and Comprehensive Loss
($
in thousands, except share and per share amounts)
(Unaudited)
| |
For the three months
ended September 30, | | |
For the nine months
ended September 30, | |
| |
2024 | | |
2023 | | |
2024 | | |
2023 | |
| |
| | |
| | |
| | |
| |
Revenues: | |
| | | |
| | | |
| | | |
| | |
License and other revenues | |
$ | — | | |
$ | — | | |
$ | — | | |
$ | 3,500 | |
| |
| | | |
| | | |
| | | |
| | |
Expenses: | |
| | | |
| | | |
| | | |
| | |
Royalties | |
| — | | |
| 30 | | |
| — | | |
| 1,605 | |
Research and development | |
| 8,941 | | |
| 7,148 | | |
| 25,366 | | |
| 23,712 | |
General and administrative | |
| 6,404 | | |
| 4,156 | | |
| 22,173 | | |
| 13,174 | |
Gain on operating lease right-of-use assets | |
| — | | |
| — | | |
| — | | |
| (1,065 | ) |
Total expenses | |
| 15,345 | | |
| 11,334 | | |
| 47,539 | | |
| 37,426 | |
| |
| | | |
| | | |
| | | |
| | |
Loss from operations | |
| (15,345 | ) | |
| (11,334 | ) | |
| (47,539 | ) | |
| (33,926 | ) |
| |
| | | |
| | | |
| | | |
| | |
Interest income | |
| 1,189 | | |
| 593 | | |
| 3,223 | | |
| 1,374 | |
Interest expense | |
| (1,102 | ) | |
| (105 | ) | |
| (3,126 | ) | |
| (309 | ) |
Change in fair value of warrant and derivative liabilities | |
| (15,156 | ) | |
| (1,101 | ) | |
| (7,530 | ) | |
| (7,465 | ) |
Other income | |
| 145 | | |
| 111 | | |
| 531 | | |
| 2,729 | |
Net Loss | |
$ | (30,269 | ) | |
$ | (11,836 | ) | |
$ | (54,441 | ) | |
$ | (37,597 | ) |
Basic and diluted loss per common share | |
$ | (0.63 | ) | |
$ | (0.48 | ) | |
$ | (1.41 | ) | |
$ | (1.89 | ) |
| |
| | | |
| | | |
| | | |
| | |
Weighted average number of common shares outstanding - basic and diluted | |
| 48,081,758 | | |
| 24,797,564 | | |
| 38,504,273 | | |
| 19,942,613 | |
| |
| | | |
| | | |
| | | |
| | |
Other comprehensive income (loss): | |
| | | |
| | | |
| | | |
| | |
Change in unrealized gains (losses) related to available-for-sale debt securities | |
| 50 | | |
| (33 | ) | |
| (18 | ) | |
| 1 | |
Foreign currency translation adjustments | |
| — | | |
| 29 | | |
| — | | |
| 29 | |
Comprehensive loss | |
$ | (30,219 | ) | |
$ | (11,840 | ) | |
$ | (54,459 | ) | |
$ | (37,567 | ) |
ABEONA
THERAPEUTICS INC. AND SUBSIDIARIES
Condensed
Consolidated Balance Sheets
($
in thousands, except share and per share amounts)
(Unaudited)
| |
September 30, 2024 | | |
December 31, 2023 | |
| |
| | |
| |
ASSETS | |
| | | |
| | |
Current assets: | |
| | | |
| | |
Cash and cash equivalents | |
$ | 15,726 | | |
$ | 14,473 | |
Short-term investments | |
| 93,975 | | |
| 37,753 | |
Restricted cash | |
| 338 | | |
| 338 | |
Other receivables | |
| 1,613 | | |
| 2,444 | |
Prepaid expenses and other current assets | |
| 1,005 | | |
| 729 | |
Total current assets | |
| 112,657 | | |
| 55,737 | |
Property and equipment, net | |
| 4,058 | | |
| 3,533 | |
Operating lease right-of-use assets | |
| 3,789 | | |
| 4,455 | |
Other assets | |
| 88 | | |
| 277 | |
Total assets | |
$ | 120,592 | | |
$ | 64,002 | |
LIABILITIES AND STOCKHOLDERS’ EQUITY | |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable | |
$ | 2,789 | | |
$ | 1,858 | |
Accrued expenses | |
| 5,210 | | |
| 5,985 | |
Current portion of long-term debt | |
| 4,444 | | |
| — | |
Current portion of operating lease liability | |
| 1,057 | | |
| 998 | |
Current portion payable to licensor | |
| 4,921 | | |
| 4,580 | |
Other current liabilities | |
| 1 | | |
| 1 | |
Total current liabilities | |
| 18,422 | | |
| 13,422 | |
Long-term operating lease liabilities | |
| 3,402 | | |
| 4,402 | |
Long-term debt | |
| 14,206 | | |
| — | |
Warrant liabilities | |
| 38,789 | | |
| 31,352 | |
Total liabilities | |
| 74,819 | | |
| 49,176 | |
Commitments and contingencies | |
| | | |
| | |
Stockholders’ equity: | |
| | | |
| | |
Preferred stock - $0.01 par value; authorized 2,000,000 shares; No shares issued and outstanding as of September 30, 2024 and December 31, 2023, respectively | |
| — | | |
| — | |
Common stock - $0.01 par value; authorized 200,000,000 shares; 43,404,706 and 26,523,878 shares issued and outstanding as of September 30, 2024 and December 31, 2023, respectively | |
| 434 | | |
| 265 | |
Additional paid-in capital | |
| 849,388 | | |
| 764,151 | |
Accumulated deficit | |
| (803,965 | ) | |
| (749,524 | ) |
Accumulated other comprehensive loss | |
| (84 | ) | |
| (66 | ) |
Total stockholders’ equity | |
| 45,773 | | |
| 14,826 | |
Total liabilities and stockholders’ equity | |
$ | 120,592 | | |
$ | 64,002 | |
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Abeona Therapeutics (NASDAQ:ABEO)
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