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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):
May 9, 2024
PHIO
PHARMACEUTICALS CORP.
(Exact name of registrant as specified in its
charter)
Delaware |
|
001-36304 |
|
45-3215903 |
(State or other jurisdiction of incorporation)
|
|
(Commission File Number) |
|
(I.R.S. Employer Identification No.) |
11 Apex Drive, Suite 300A, PMB 2006
|
|
Marlborough, Massachusetts |
01752 |
(Address of principal executive offices) |
(Zip Code) |
Registrant’s telephone number, including
area code: (508) 767-3861
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(s): |
|
Name
of each exchange on which registered: |
Common
Stock, par value $0.0001 per share |
|
PHIO |
|
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 May 9, 2024, Phio Pharmaceuticals Corp. (the
“Company”) reported its financial results for the period ended March 31, 2024. A copy of the press release is furnished herewith
as Exhibit 99.1 to this Current Report on Form 8-K (the “Report”).
The information in this Item 2.02 and attached
as Exhibit 99.1 to this Report will not be treated as “filed” for the 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. This information will not
be incorporated by reference into any filing under the Securities Act of 1933, as amended, or into another filing under the Exchange Act,
unless that filing expressly incorporates this information by reference.
Item 9.01. Financial Statements and Exhibits.
(d) 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.
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PHIO PHARMACEUTICALS CORP. |
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Date: May 9, 2024 |
|
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By: |
/s/
Robert Bitterman |
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Robert Bitterman
President & Chief Executive Officer |
Exhibit 99.1
Phio Pharmaceuticals Reports Q1 2024 Results
and Provides Business Update
–Four sites across the country participating
in Phase 1b clinical trial for lead product candidate PH-762
–Three patients have been enrolled
MARLBOROUGH, Mass., May 9, 2024 (GLOBE NEWSWIRE)—Phio Pharmaceuticals
Corp. (Nasdaq: PHIO), a clinical stage biotechnology company whose proprietary INTASYL™ siRNA gene silencing technology is designed
to make immune cells more effective in killing tumor cells, today reported its Q1 2024 financial results and provided a business update.
Recent Corporate Updates
| · | Phio’s
INTASYL compound PH-762 is currently being investigated in an open-label Phase 1b clinical study (NCT 06014086) to evaluate the safety
and tolerability of intratumoral PH-762 in cutaneous squamous cell (cSCC), melanoma, or Merkel cell carcinoma. Two patients have
already completed treatment. Four sites across the US are now engaged in the Phase 1b study. The sites are: |
| o | George Washington University in Washington DC |
| o | Banner MD Anderson in Arizona |
| o | Centricity Research in Ohio |
| o | Integrity Research in Florida. |
| · | Presented
new data on the immunotherapeutic activity of INTASYL at: |
| o | 10th Annual Immunotherapy of Cancer Conference (ITOC10):
this preclinical data demonstrates the potential of the INTASYL compound PH-905 targeting Cbl-b to improve the function of natural killer
(NK) cells. |
| o | 27th Annual American Society of Gene and Cell Therapy
(ASGCT): this preclinical data demonstrates that intratumoral injection of PH-762 significantly inhibits tumor growth in murine cells
and may generate memory-specific T cells. |
| · | The
INTASYL siRNA platform is the focus of a National Spotlight on PBS Viewpoint, a national program hosted by Dennis Quaid, and on Fox Business
Network; both are airing through May. |
| · | Patent
granted by USPTO for two of its INTASYL Compounds, RXI-185 and RXI-231 that treat age-related skin disorders including photo-aging and
dermal hyperpigmentation targeting down-regulation of the Matrix metalloproteinase-1(MMP-1) and Tyrosinase (TYR) proteins. |
Financial Results
Cash Position
At March 31, 2024, we had cash of $6.5 million as compared with $8.5
million at December 31, 2023.
Research and Development Expenses
Research and development expenses were $1.1 million for the three months
ended March 31, 2024 as compared with $2.1 million for the three months ended March 31, 2023, a decrease of 46%. The decrease was primarily
driven by the Company’s cost rationalization measures in transitioning from a discovery research company to a product development
company resulting in decreased costs for the wind-down of preclinical studies, salary-related costs and lab supplies. Additional decreases
in research and development expenses were due to clinical consulting fees incurred in connection with the Company’s IND filing and
manufacturing fees for PH-762 in the prior year period.
General and Administrative Expenses
General and administrative expenses were $1.1 million for the three
months ended March 31, 2024 as compared with $1.5 million for the three months ended March 31, 2023, a decrease of 28%. The decrease was
primarily due to decreases in consulting expenses and legal expenses as compared to the prior year period.
Net Loss
Net loss was $2.2 million for the three months ended March 31, 2024
as compared with $3.6 million for the three months ended March 31, 2023. The decrease in net loss was primarily due to the changes in
research and development expenses, as described above.
About Phio Pharmaceuticals Corp.
Phio Pharmaceuticals Corp. (Nasdaq: PHIO) is a clinical stage biotechnology
company whose proprietary INTASYL™ siRNA gene silencing technology is designed to make immune cells more effective in killing tumor
cells. INTASYL is the only self-delivering RNAi technology focused on immuno-oncology therapeutics. INTASYL drugs precisely target specific
proteins that reduce the body's ability to fight cancer, without the need for specialized formulations or drug delivery systems.
For additional information, visit the Company's website, www.phiopharma.com.
Forward Looking Statements
This press release contains forward-looking statements within the
meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements can be identified by words such as "intends,"
"believes," "anticipates," "indicates," "plans," "expects," "suggests," "may,"
"would," "should," "potential," "designed to," "will," "ongoing," "estimate,"
"forecast," "target," "predict," "could" and similar references, although not all forward-looking
statements contain these words. These statements, which include statements regarding the anticipated benefits of our INTASYL™ RNAi
platform and the results from our ongoing clinical trials, are based only on our current beliefs, expectations and assumptions and are
subject to inherent uncertainties, risks and changes in circumstances that are difficult to predict and many of which are outside of our
control. Our actual results may differ materially from those indicated in the forward-looking statements as a result of a number of important
factors, including, but not limited to, the impact to our business and operations by inflationary pressures, rising interest rates, recession
fears, the development of our product candidates, results from our preclinical and clinical activities, our ability to execute on business
strategies, our ability to develop our product candidates with collaboration partners, and the success of any such collaborations, the
timeline and duration for advancing our product candidates into clinical development, the timing or likelihood of regulatory filings and
approvals, the success of our efforts to commercialize our product candidates if approved, our ability to manufacture and supply our product
candidates for clinical activities, and for commercial use if approved, the scope of protection we are able to establish and maintain
for intellectual property rights covering our technology platform, our ability to obtain future financing, market and other conditions
and those risks identified in our Annual Report on Form 10-K and subsequent Quarterly Reports on Form 10-Q under the caption "Risk
Factors" and in other filings the Company periodically makes with the SEC. Readers are urged to review these risk factors and to
not act in reliance on any forward-looking statements, as actual results may differ from those contemplated by our forward-looking statements.
Phio does not undertake to update forward-looking statements to reflect a change in its views, events or circumstances that occur after
the date of this release, except as required by law.
Contact:
Phio Pharmaceuticals Corp.
ir@phiopharma.com
PR Contact
Michael Adams
Bridge View Media
adams@bridgeviewmedia.com
PHIO PHARMACEUTICALS CORP.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Amounts in thousands, except share and per
share data)
(Unaudited)
| |
Three Months Ended March 31, | |
| |
2024 | | |
2023 | |
Operating expenses: | |
| | | |
| | |
Research and development | |
$ | 1,148 | | |
$ | 2,134 | |
General and administrative | |
| 1,061 | | |
| 1,468 | |
Total operating expenses | |
| 2,209 | | |
| 3,602 | |
Operating loss | |
| (2,209 | ) | |
| (3,602 | ) |
Total other income, net | |
| 55 | | |
| – | |
Net loss | |
$ | (2,154 | ) | |
$ | (3,602 | ) |
| |
| | | |
| | |
Net loss per common share: Basic and diluted | |
$ | (0.47 | ) | |
$ | (3.15 | ) |
Weighted average number of common shares outstanding: Basic and diluted | |
| 4,580,072 | | |
| 1,142,213 | |
PHIO PHARMACEUTICALS CORP.
CONDENSED CONSOLIDATED BALANCE SHEETS
(Amounts in thousands, except share data)
(Unaudited)
| |
March 31,
2024 | | |
December 31, 2023 | |
ASSETS | |
| | | |
| | |
Cash and cash equivalents | |
$ | 6,475 | | |
$ | 8,490 | |
Prepaid expenses and other current assets | |
| 373 | | |
| 832 | |
Right of use asset | |
| – | | |
| 33 | |
Property and equipment, net | |
| 2 | | |
| 6 | |
Other assets | |
| 3 | | |
| 3 | |
Total assets | |
$ | 6,853 | | |
$ | 9,364 | |
LIABILITIES AND STOCKHOLDERS’ EQUITY | |
| | | |
| | |
Accounts payable | |
$ | 320 | | |
$ | 657 | |
Accrued expenses | |
| 929 | | |
| 942 | |
Lease liability | |
| – | | |
| 35 | |
Total liabilities | |
| 1,249 | | |
| 1,634 | |
Total stockholders’ equity | |
| 5,604 | | |
| 7,730 | |
Total liabilities and stockholders’ equity | |
$ | 6,853 | | |
$ | 9,364 | |
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