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Phio Pharmaceuticals Reports Second Quarter 2025 Financial Results and Provides Business Update

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Phio Pharmaceuticals (NASDAQ: PHIO) reported Q2 2025 financial results and provided updates on its Phase 1b clinical trial for PH-762. The trial, evaluating intratumoral PH-762 in various skin cancers, has treated 15 patients across four cohorts with promising results. Among 13 cSCC patients, 5 achieved complete response, 1 near-complete response, and 1 partial response.

The company's cash position strengthened to $10.8 million as of June 30, 2025, up from $5.4 million in December 2024. Q2 2025 resulted in a net loss of $2.2 million, compared to $1.8 million in Q2 2024. In July 2025, Phio raised an additional $2.2 million through warrant exercises.

Phio Pharmaceuticals (NASDAQ: PHIO) ha pubblicato i risultati finanziari del secondo trimestre 2025 e aggiornato lo stato dello studio clinico di Fase 1b su PH-762. Lo studio, che valuta l'uso intratumorale di PH-762 in diversi tumori cutanei, ha trattato 15 pazienti distribuiti su quattro coorti con risultati incoraggianti. Tra 13 pazienti con cSCC, 5 hanno ottenuto una risposta completa, 1 una risposta quasi completa e 1 una risposta parziale.

La posizione di cassa dell'azienda è salita a $10,8 milioni al 30 giugno 2025, rispetto a $5,4 milioni a dicembre 2024. Il Q2 2025 ha registrato una perdita netta di $2,2 milioni, rispetto a $1,8 milioni nel Q2 2024. A luglio 2025 Phio ha raccolto ulteriori $2,2 milioni tramite l'esercizio di warrant.

Phio Pharmaceuticals (NASDAQ: PHIO) informó sus resultados financieros del segundo trimestre de 2025 y dio novedades sobre el ensayo clínico de fase 1b de PH-762. El estudio, que evalúa la administración intratumoral de PH-762 en varios cánceres cutáneos, ha tratado a 15 pacientes repartidos en cuatro cohortes con resultados prometedores. Entre 13 pacientes con cSCC, 5 alcanzaron respuesta completa, 1 respuesta casi completa y 1 respuesta parcial.

La posición de efectivo de la compañía aumentó a $10,8 millones al 30 de junio de 2025, desde $5,4 millones en diciembre de 2024. El segundo trimestre de 2025 registró una pérdida neta de $2,2 millones, frente a $1,8 millones en el Q2 de 2024. En julio de 2025 Phio recaudó otros $2,2 millones mediante el ejercicio de warrants.

Phio Pharmaceuticals (NASDAQ: PHIO)� 2025� 2분기 재무실적� 발표하고 PH-762� 1b� 임상시험 진행 상황� 업데이트했습니다. 다양� 피부암에� 종양 � 투여하는 PH-762� 평가하는 � 임상시험은 4� 코호트에� � 15�� 치료했으� 유망� 결과� 보였습니�. cSCC 환자 13� � 5명은 완전 관�� 보였�, 1명은 거의 완전 관�, 1명은 부� 반응� 보였습니�.

회사� 현금 보유액은 2025� 6� 30� 기준 $10.8백만으로 2024� 12월의 $5.4백만에서 증가했습니다. 2025� 2분기 순손실은 $2.2백만으로, 2024� 2분기� $1.8백만� 비교됩니�. 2025� 7월에� 워런� 행사� 추가 $2.2백만� 조달했습니다.

Phio Pharmaceuticals (NASDAQ: PHIO) a publié ses résultats financiers du deuxième trimestre 2025 et a communiqué des nouvelles sur son essai clinique de phase 1b pour PH-762. L'étude, évaluant l'administration intratumorale de PH-762 dans divers cancers de la peau, a traité 15 patients répartis en quatre cohortes avec des résultats prometteurs. Parmi 13 patients atteints de cSCC, 5 ont obtenu une réponse complète, 1 une réponse quasi complète et 1 une réponse partielle.

La trésorerie de la société s'est renforcée pour atteindre 10,8 M$ au 30 juin 2025, contre 5,4 M$ en décembre 2024. Le T2 2025 s'est soldé par une perte nette de 2,2 M$, contre 1,8 M$ au T2 2024. En juillet 2025, Phio a levé 2,2 M$ supplémentaires grâce à l'exercice de bons de souscription.

Phio Pharmaceuticals (NASDAQ: PHIO) meldete die Finanzzahlen für das zweite Quartal 2025 und gab Updates zur Phase-1b-Studie von PH-762. Die Studie, die intratumorale Verabreichung von PH-762 bei verschiedenen Hautkrebserkrankungen prüft, behandelte 15 Patienten in vier Kohorten und zeigte vielversprechende Ergebnisse. Von 13 cSCC-Patienten erzielten 5 eine komplette Remission, 1 eine nahezu komplette Remission und 1 eine partielle Remission.

Die Barreserve des Unternehmens stieg zum 30. Juni 2025 auf $10,8 Millionen, nachdem sie im Dezember 2024 bei $5,4 Millionen lag. Im Q2 2025 wurde ein Nettoverlust von $2,2 Millionen verzeichnet, gegenüber $1,8 Millionen im Q2 2024. Im Juli 2025 nahm Phio zusätzlich $2,2 Millionen durch Warrants ausüben ein.

Positive
  • Strong clinical safety profile with no dose-limiting toxicities or clinically relevant adverse effects
  • Impressive efficacy in cSCC with 5 complete responses and 2 partial/near-complete responses out of 13 patients
  • Cash position doubled to $10.8M from $5.4M in December 2024
  • Additional $2.2M raised through warrant exercises in July 2025
Negative
  • Increased net loss to $2.2M in Q2 2025 from $1.8M in Q2 2024
  • Higher operating expenses with R&D costs up to $1.1M from $0.9M year-over-year
  • Limited efficacy in melanoma with non-response in the single patient treated

Insights

Phio's PH-762 shows promising safety and efficacy in skin cancer trial while improving cash position through warrant exercises.

Phio's clinical progress with PH-762 displays encouraging early efficacy signals in their Phase 1b dose escalation trial. The treatment demonstrated complete responses in 5 out of 13 cSCC patients (38.5%) with one additional near-complete response (>90% clearance) and one partial response (>50% clearance). This represents a 53.8% response rate in cSCC patients - noteworthy for an early-stage oncology asset.

The clean safety profile is particularly important, with no dose-limiting toxicities or clinically relevant treatment-emergent adverse effects reported across all cohorts. For context, many immunotherapies often show significant toxicity profiles that limit their utility, making PH-762's safety data promising for potential future combination approaches.

The company's progress to the fifth and likely final cohort suggests the dose-finding portion is nearing completion. This positions Phio to potentially move toward a Phase 2 study with an identified recommended Phase 2 dose, representing a significant development milestone.

Their INTASYL siRNA platform's self-delivering mechanism offers a differentiated approach in the crowded immuno-oncology space. The secured manufacturing agreement is a critical operational advancement that often goes underappreciated but is essential for clinical and commercial progress.

The cash position improved dramatically to $10.8M from $5.4M at year-end, providing an extended runway. While the modest increase in operating expenses to $2.3M quarterly suggests controlled spending, this clinical-stage biotech will likely need additional financing to advance beyond their current Phase 1b trial into larger, more expensive studies.

The interim clinical data from Phio's PH-762 trial reveals several noteworthy elements. In the cSCC cohort, achieving 5 complete responses and 2 additional meaningful responses (near-complete and partial) from 13 patients represents a promising signal, particularly for an early-phase trial. The 38.5% complete response rate exceeds typical expectations for early immunotherapeutic approaches in this indication.

The absence of dose-limiting toxicities across all treated patients is particularly significant. Local intratumoral administration likely contributes to this favorable safety profile by minimizing systemic exposure. The clean safety data potentially enables future dose escalation or combination strategies that might enhance efficacy further.

The 100% disease control rate during treatment (no patients showed clinical progression) also warrants attention, though longer follow-up will be needed to assess durability of responses.

The data in metastatic Merkel cell carcinoma, while limited to a single patient, is intriguing given this aggressive cancer's typically poor prognosis. The >50% clearance suggests potential activity worth exploring in additional patients.

The melanoma non-response is less surprising as melanoma has historically shown variable response to immunotherapies. The mechanism of action targeting PD-1 through siRNA rather than antibody blockade represents a novel approach that could potentially overcome resistance mechanisms seen with current immunotherapies. As the trial completes its final cohort, key questions remain about response durability, biomarkers of response, and whether higher doses might improve efficacy in non-responders.

Clinical trial advances for INSTASYL siRNA lead product candidate PH-762

5th cohort enrolling patients in on-going clinical study

King of Prussia, Pennsylvania--(Newsfile Corp. - August 14, 2025) - Phio Pharmaceuticals Corp. (NASDAQ: PHIO) is a clinical-stage biopharmaceutical company developing therapeutics using its proprietary INTASYL® siRNA gene silencing technology to eliminate cancer. Phio today reported its financial results for the quarter ended June 30, 2025 and provided a business update.

Recent Corporate Updates

PH-762 Clinical Progress

Phio's ongoing Phase 1b dose escalation clinical trial (NCT 06014086) is designed to evaluate the safety and tolerability of neoadjuvant use of intratumoral PH-762 in Stages 1, 2 and 4 cutaneous squamous cell carcinoma (cSCC), Stage 4 melanoma, and Stage 4 Merkel cell carcinoma. To date, a total of 15 patients with cutaneous carcinomas have been treated across four cohorts in the Phase 1b trial. These cohorts included 13 patients with cSCC, one patient with metastatic melanoma and one patient with metastatic Merkel cell carcinoma. There have been no dose-limiting toxicities or clinically relevant treatment-emergent adverse effects in the patients who received intratumoral PH-762 in this trial. Moreover, PH-762 has been well tolerated in all enrolled patients in each escalating dose cohort. No patients exhibited clinical progression of disease during the treatment phase of this trial.

The cumulative pathologic responses in the 13 patients with cSCC include five with complete response (100% clearance), one patient with a near complete response (>90% clearance), one with a partial response (>50% clearance) and six patients with a pathologic non-response (< 50% clearance).

The Merkel cell carcinoma patient with stage 4 metastatic disease had a pathological partial response (>50% clearance). The melanoma patient was a non-responder (<50% clearance).

Phio is now enrolling what is expected to be the 5th and final cohort in the Phase 1b trial.

In addition, the Company entered into a comprehensive drug substance development services agreement with a U.S. manufacturing company. The company will provide analytical and process development and cGMP manufacture of Phio's lead development compound PH-762.

Scientific News

In May 2025, Phio delivered a podium presentation for its INTASYL self-delivering siRNA technology at the Society of Investigative Dermatology (SID). The Company presented its Phase 1b clinical trial results to date. The Company also delivered podium presentations on its INTASYL compounds PH-762 and PH-894 in April 2025 at the 11th Annual Immunotherapy of Cancer (ITOC 11) conference in Munich, Germany. In June 2025, Phio presented interim data on its Phase 1b clinical trial at the American Society of Clinical Oncology (ASCO) conference.

Subsequent Events

On July 25, 2025, the Company entered into warrant inducement agreements with certain holders of the Company's existing warrants to purchase an aggregate of 928,596 shares of common stock in connection with the exercise of common stock warrants issued between December 2024 and January 2025 with exercise prices between $2.00 and $2.485 per share. In connection with this financing, the Company raised approximately $2.2 million after expenses.

Financial Results

Cash Position

At June 30, 2025, the Company had cash and cash equivalents of approximately $10.8 million as compared with approximately $5.4 million at December 31, 2024.

Research and Development Expenses

Research and development expenses for the three months ended June 30, 2025 were $1.1 million compared to $0.9 million for the same period in 2024. The increase in research and development expenses was primarily driven by higher CRO pass-through costs associated with increased patient enrollment, as well as higher consulting and salary-related costs.

Research and development expenses for the six months ended June 30, 2025 were $1.9 million compared to $2.0 million for the same period in 2024. The fluctuation was immaterial and within expected operating ranges.

General and Administrative Expenses

General and administrative expenses for the three months ended June 30, 2025 were $1.2 million compared to $1.0 million for the same period in 2024. The increase in general and administrative expenses was primarily driven by an increase in salary-related costs.

General and administrative expenses for the six months ended June 30, 2025 were $2.2 million compared to $1.8 million for the same period in 2024. The increase in general and administrative expenses was primarily driven by an increase in salary-related costs.

Net Loss

Net loss was $2.2 million for the three months ended June 30, 2025 compared with $1.8 million for the same period in 2024. The increase in net loss was due to the changes in research and development and general and administrative expenses as described above.

About Phio Pharmaceuticals Corp.

Phio Pharmaceuticals Corp. (NASDAQ: PHIO) is a clinical-stage siRNA biopharmaceutical company advancing its INTASYL® gene silencing technology focused on immuno-oncology therapeutics. Phio's INTASYL compounds are designed to enhance the body's immune cells to more effectively kill cancer cells. Phio's lead clinical program is an INTASYL compound, PH-762, that silences the PD-1 gene implicated in various forms of skin cancer. The on-going Phase 1b trial (NCT# 06014086) is evaluating PH-762 for the treatment of cutaneous squamous cell carcinoma, melanoma, and Merkel cell carcinoma. PH-762 is a potential non-surgical treatment for skin cancers.

For additional information, visit the Company's website, .

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. Examples of forward-looking statements contained in this press release include, among others, the possibility that our INTASYL® siRNA gene silencing technology will make the body's immune cells more effective in killing cancer cells, the potential for PH-762 to present a viable non-surgical alternative for skin cancer, expectations regarding timing of enrollment, the expectations that we have sufficient capital to complete the treatment phase of our ongoing Phase 1b clinical trial, and statements regarding our clinical strategy, development plans and timelines and other future events.  

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, results from our preclinical and clinical activities, our ability to execute on business strategies, the timing or likelihood of regulatory filings and approvals, 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.
Jennifer Phillips: [email protected]
Corporate Affairs

PHIO PHARMACEUTICALS CORP.
CONSOLIDATED STATEMENTS OF OPERATIONS
(Amounts in thousands, except share and per share data)
(Unaudited)



Three Months Ended
June 30,


2025 2024
Operating expenses:

 
Research and development
$1,074
 $866
General and administrative

1,235
 
1,048
Total operating expenses

2,309
 
1,914
Operating loss

(2,309) 
(1,914)
Total other income (expense), net

143
 
68
Net loss
$(2,166) $(1,846)
Basic and diluted
$(0.45) $(3.62)
Weighted average number of common shares outstanding

 
 
 
Basic and diluted

4,794,857
 
510,188

 

PHIO PHARMACEUTICALS CORP.
CONDENSED CONSOLIDATED BALANCE SHEETS
(Amounts in thousands, except share and per share data)



(Unaudited)




June 30,
2025

December 31,
2024

ASSETS






Current assets:






Cash and cash equivalents
$10,775
$5,382
Prepaid expenses and other current assets

519

354
Total current assets

11,294

5,736
Property and equipment, net

7

2
Total assets
$11,301
$5,738
LIABILITIES AND STOCKHOLDERS' EQUITY

 

 
Current liabilities:

 

 
Accounts payable
$235
$253
Accrued expenses

971

762
Total current liabilities

1,206

1,015
Total liabilities

1,206

1,015
Commitments and contingencies (Note 2)

 

 
Stockholders' equity:
Series D Preferred Stock, $0.0001 par value; 10,000,000 shares authorized, 0 issued and outstanding at June 30, 2025 and December 31, 2024


-

-
Common stock, $0.0001 par value, 100,000,000 shares authorized; 4,798,154 and 1,733,717 shares issued and outstanding at June 30, 2025 and December 31, 2024, respectively

-

-
Additional paid-in capital

160,386

151,079
Accumulated deficit

(150,291)
(146,356)
Total stockholders' equity

10,095

4,723
Total liabilities and stockholders' equity
$11,301
$5,738

 

To view the source version of this press release, please visit

FAQ

What are the clinical trial results for Phio's PH-762 in cSCC patients?

Out of 13 cSCC patients treated, 5 achieved complete response (100% clearance), 1 had near-complete response (>90%), 1 showed partial response (>50%), and 6 were non-responders (<50% clearance).

How much cash does Phio Pharmaceuticals (PHIO) have as of Q2 2025?

Phio reported $10.8 million in cash and cash equivalents as of June 30, 2025, compared to $5.4 million at December 31, 2024.

What was Phio Pharmaceuticals' net loss in Q2 2025?

Phio reported a net loss of $2.2 million for Q2 2025, an increase from $1.8 million in Q2 2024.

How many patients have been treated in Phio's Phase 1b trial for PH-762?

A total of 15 patients have been treated across four cohorts, including 13 with cSCC, 1 with metastatic melanoma, and 1 with metastatic Merkel cell carcinoma.

What was the safety profile of PH-762 in Phio's clinical trial?

PH-762 showed an excellent safety profile with no dose-limiting toxicities or clinically relevant treatment-emergent adverse effects in any patients, and was well tolerated across all dose cohorts.
Phio Pharmaceuticals Corp

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Biotechnology
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