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Phio Pharmaceuticals Reports Second Quarter 2023 Financial Results and Provides Business Update

Key Takeaway: Phio Pharmaceuticals Corp. has reported its financial results for the second quarter of 2023, revealing a net loss of $2.5 million. The company has received FDA clearance for an Investigational New Drug application for PH-762 and is initiating a Phase 1b clinical trial to evaluate its safety and tumor response in skin cancers. Despite a decrease in cash reserves, the company's ongoing research highlights its commitment to developing effective cancer therapies using their INTASYL RNAi platform.
Price reaction · baseline $21.06 (2023-08-09 close) · hit after-hours · clean, no other PHIO news in the window
day 0 close · peak
-2.6%

Market Sentiment Analysis

POSITIVE FACTORS

  • FDA clearance for IND related to new clinical trial for PH-762.
  • Plans to evaluate PH-762's safety and efficacy in various skin cancers.
  • Ongoing development and research support for innovative cancer treatments.

CONCERNS & RISKS

  • Net loss remains significant at $2.5 million, consistent with prior year.
  • Cash reserves decreased slightly from $11.8 million to $11.3 million.
  • Overall operating loss and expenses continue to rise.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Cash runway
~9 mo
Medium dilution risk
Lead asset
DP CD8 TIL
Phase 1 · HNSCC

Full Press Release Details

Phio Pharmaceuticals
Reports Second Quarter 2023 Financial Results and Provides Business Update
MARLBOROUGH, Mass., August 10, 2023-Phio Pharmaceuticals Corp.
(Nasdaq: PHIO), a clinical stage biotechnology company whose proprietary INTASYL RNAi platform technology is designed to make immune
cells more effective in killing tumor cells, today reported its financial results for the quarter ended June 30, 2023 and provided a business
"Following FDA clearance of our IND for PH-762, we are moving
forward with plans for a clinical trial for stages one, two and four of cutaneous squamous cell (cSCC), stage four melanoma and Merkel
cell," said Robert Bitterman, President and CEO.
The initial multi-center, dose-escalating, Phase 1b clinical trial
is designed to evaluate the safety and tolerability of neoadjuvant use of intratumorally injected PH-762, assess the tumor response, and
determine the dose or dose range for continued study of PH-762.
Recent Corporate Updates
At June 30, 2023, the Company had cash of $11.3 million as compared
with $11.8 million at December 31, 2022.
Research and Development Expenses
Research and development expenses were $1.4 million for the quarter
ended June 30, 2023 compared with $1.3 million for the quarter ended June 30, 2022, an increase of 6%. The increase was primarily due
to increased clinical-related costs to support the two PH-762 Phase 1 clinical trials in the U.S., partially offset by decreased costs
related to the completion of the Company's IND-enabling preclinical studies for PH-894 as compared to the prior year period.
General and Administrative Expenses
General and administrative expenses were $1.2 million for the quarter
ended June 30, 2023 compared with $1.2 million for the quarter ended June 30, 2022. General and administrative expenses were primarily
consistent with the prior year period.
Net loss was $2.5 million, or $1.47 per share, for the quarter ended
June 30, 2023, compared with $2.5 million, or $2.22 per share, for the quarter ended June 30, 2022. Overall, net loss was primarily consistent
with the prior year period with changes in research and development expense as described above.
INTASYL compounds are chemically modified siRNAs that provide efficient,
spontaneous cellular uptake and potent, long lasting intracellular activity, targeting a broad range of cell types and tissues. INTASYL
drugs are designed to precisely target specific proteins that reduce the body's ability to fight cancer, without the need for specialized
formulations or drug delivery systems. INTASYL has demonstrated preclinical efficacy in both Direct-to-Tumor and Adoptive Cell Therapy
In comparison to biologics and cell and gene therapies, INTASYL has
a favorable preclinical toxicity and safety profile, and a streamlined chemical synthesis that reduces costs and offers substantial dosing
convenience to the prescriber and patient.
About Phio Pharmaceuticals Corp.
Phio Pharmaceuticals Corp. (Nasdaq: PHIO) is a clinical stage biotechnology
company whose proprietary INTASYL RNAi 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 are designed to 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 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 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.
PHIO PHARMACEUTICALS CORP.
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS
(Amounts in thousands, except share and per
Three Months Ended June 30, Six Months Ended June 30,
2023 2022 2023 2022
Operating expenses:
Research and development $ 1,383 $ 1,304 $ 3,517 $ 2,890
General and administrative 1,164 1,217 2,632 2,271
Total operating expenses 2,547 2,521 6,149 5,161
Operating loss (2,547 ) (2,521 ) (6,149 ) (5,161 )
Total other expense, net (2 ) (10 ) (2 ) (12 )
Net loss $ (2,549 ) $ (2,531 ) $ (6,151 ) $ (5,173 )
Net loss per common share: Basic and diluted $ (1.47 ) $ (2.22 ) $ (4.28 ) $ (4.56 )
Weighted average number of common shares outstanding: Basic and diluted 1,728,490 1,138,227 1,436,971 1,134,307
PHIO PHARMACEUTICALS CORP.
CONDENSED CONSOLIDATED BALANCE SHEETS
(Amounts in thousands, except share data)
June 30, 2023 December 31, 2022
ASSETS
Cash $ 11,307 $ 11,781
Restricted cash 50 50
Prepaid expenses and other current assets 678 615
Right of use asset 98 161
Property and equipment, net 157 183
Other assets 6 24
Total assets $ 12,296 $ 12,814
LIABILITIES, PREFERRED STOCK AND STOCKHOLDERS' EQUITY
Accounts payable $ 641 $ 779
Accrued expenses 1,647 1,025
Lease liability 104 170
Total preferred stock - 2
Total stockholders' equity 9,904 10,838
Total liabilities, preferred stock and stockholders' equity $ 12,296 $ 12,814

Frequently Asked Questions

What is INTASYL technology used for?

INTASYL technology enhances immune cells' effectiveness in targeting tumor cells.

What trials is Phio Pharmaceuticals initiating?

Phio plans a Phase 1b trial for PH-762 addressing cutaneous squamous cell carcinoma.

What were the R&D expenses for Q2 2023?

Research and development expenses were $1.4 million in Q2 2023.

What was Phio's net loss for Q2 2023?

The net loss for Q2 2023 was $2.5 million, or $1.47 per share.

How much cash did Phio have on June 30, 2023?

Phio Pharmaceuticals had $11.3 million in cash on June 30, 2023.

Last updated: Aug 10, 2023