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Phio Pharmaceuticals Announces "A Groundbreaking Approach to Treating Skin Cancer" in a Fireside Chat with Force Family Office

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Phio Pharmaceuticals (NASDAQ: PHIO) will participate in a virtual fireside chat with Force Family Office on March 18, 2026 at 4 PM EDT to discuss its INTASYL gene‑silencing approach to immuno‑oncology.

Key clinical updates: lead candidate PH‑762 is in a Phase 1b intratumoral program (22 patients treated), with no dose‑limiting toxicities or serious adverse events, an overall pathological response in cSCC of ~65% and an 85% pathological response (6 of 7) in the highest dose cohort. The company targets FDA engagement in Q2 2026 and reports cash to sustain operations into H1 2027.

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Positive

  • No dose‑limiting toxicities or serious adverse events across 22 treated patients
  • Pathological response ~65% in cSCC across all dosing cohorts
  • Highest‑dose cohort pathological response 85% (6 of 7 patients)
  • Targeted FDA engagement for next‑stage development in Q2 2026
  • Cash runway projected into H1 2027

Negative

  • Small Phase 1b sample size: only 22 patients total
  • Highest‑dose efficacy figure based on just 7 patients
  • Program remains early‑stage (Phase 1b) with uncertain next‑stage outcomes

Market Reaction – PHIO

-3.17% $1.22
15m delay 13 alerts
-3.17% Since News
$1.22 Last Price
$1.19 $1.29 Day Range
-$479K Valuation Impact
$15M Market Cap
0.7x Rel. Volume

Following this news, PHIO has declined 3.17%, reflecting a moderate negative market reaction. Our momentum scanner has triggered 13 alerts so far, indicating notable trading interest and price volatility. The stock is currently trading at $1.22. This price movement has removed approximately $479K from the company's valuation.

Data tracked by StockTitan Argus (15 min delayed). Upgrade to Silver for real-time data.

Key Figures

Patients treated: 22 patients Dose cohorts: 5 cohorts Overall cSCC response: 65% pathological response +5 more
8 metrics
Patients treated 22 patients Phase 1b PH-762 intratumoral trial
Dose cohorts 5 cohorts Phase 1b dose-escalation design
Overall cSCC response 65% pathological response cSCC across all PH-762 dosing cohorts
High-dose cSCC response 85% pathological response (6 of 7) Highest-dose cohort in cSCC patients
FDA engagement timing Q2 2026 Targeted next-stage PH-762 development discussions
Cash runway Into first half of 2027 Projected cash and cash equivalents coverage
Event date March 18, 2026, 4 PM EDT Force Family Office fireside chat
52-week high vs price $4.1899 vs $1.17 Pre-news price relative to 52-week high

Market Reality Check

Price: $1.26 Vol: Volume 81,679 vs 20-day a...
low vol
$1.26 Last Close
Volume Volume 81,679 vs 20-day average 1,981,850 (relative volume 0.04) shows subdued trading ahead of this event-focused news. low
Technical Shares at $1.17 are trading below the 200-day MA of $1.78 and sit about 72% under the 52-week high of $4.1899.

Peers on Argus

The stock was down 6.4% while momentum peers like PHGE and SNSE also showed decl...
2 Down

The stock was down 6.4% while momentum peers like PHGE and SNSE also showed declines (scanner median about -8.0%), indicating broader biotech pressure rather than company-specific trading around this fireside chat announcement.

Historical Context

5 past events · Latest: Mar 10 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Mar 10 Investor presentation Positive +1.6% Life Sciences Investor Forum presentation reviewing INTASYL platform and PH-762 data.
Mar 05 Earnings update Positive -0.8% 2025 results with PH-762 progress and cash of about $21M reported.
Mar 05 Roadshow participation Positive +1.7% Renmark virtual roadshow to discuss INTASYL platform and PH-762 progress.
Feb 19 Leadership changes Positive -1.7% Leadership alignment to support next-stage PH-762 and PH-894 development.
Feb 10 Clinical safety update Positive +24.4% SMC review of PH-762 Phase 1b showing strong responses and no DLTs.
Pattern Detected

Stock often reacts positively to clinical and investor-relations updates, but responses to corporate/earnings news have been mixed with some divergences.

Recent Company History

Over recent months, the company has repeatedly highlighted progress for PH-762, including Phase 1b data with strong pathological responses and no dose-limiting toxicities, along with multiple investor-facing presentations. Earnings and SEC filings on March 5, 2026 emphasized a strengthened balance sheet and cash runway into H1 2027. Today’s event-focused news continues that communication pattern, reinforcing the same PH-762 data and development timeline rather than introducing new clinical inflection points.

Regulatory & Risk Context

Active S-3 Shelf · $24.5 million
Shelf Active
Active S-3 Shelf Registration 2025-11-20
$24.5 million registered capacity

An effective resale shelf filed on November 20, 2025 covers up to 11,763,800 warrant shares held by existing stockholders. The company is not selling shares under this prospectus but could receive up to $24.5 million in cash upon full warrant exercise, which has been earmarked to support PH-762 development and working capital.

Market Pulse Summary

This announcement highlights continued outreach to investors via a fireside chat focused on PH-762, ...
Analysis

This announcement highlights continued outreach to investors via a fireside chat focused on PH-762, which has shown a 65% overall pathological response in cSCC and 85% in the highest-dose cohort, with no dose-limiting toxicities in 22 patients. The company is targeting FDA engagement in Q2 2026 and projects cash runway into the first half of 2027. Investors may watch for regulatory feedback, any trial design updates, and how communication efforts translate into future financings and clinical milestones.

Key Terms

sirna, intratumoral, cutaneous squamous cell carcinoma, merkel cell carcinoma, +3 more
7 terms
sirna medical
"clinical-stage siRNA biopharmaceutical company developing therapeutics using its proprietary"
Small interfering RNA (siRNA) is a short strand of genetic material that binds to and destroys the messenger RNA that carries instructions for making a specific protein, effectively switching that gene off. Investors care because siRNA is a platform for precise medicines: successful trials or approvals can create high-value drugs, while delivery challenges, manufacturing complexity, patent positions and regulatory risk can sharply affect a biotech company's prospects.
intratumoral medical
"PH-762, is being evaluated as an intratumoral therapy in cutaneous squamous"
"Intratumoral" describes something that occurs or exists within a tumor, which is an abnormal growth of tissue. For investors, understanding intratumoral is important because it relates to medical treatments or research aimed at targeting the tumor directly, potentially leading to more effective therapies. Think of it as focusing treatment straight into the problem area, much like fixing a leak by working directly on the pipe itself.
cutaneous squamous cell carcinoma medical
"therapy in cutaneous squamous cell carcinoma (cSCC), melanoma and Merkel cell"
A common form of skin cancer that starts in the thin, outer layer of the skin and can grow or, in some cases, spread to nearby tissue or organs. For investors, it matters because diagnosis rates, available treatments, and regulatory approvals shape demand for therapies, influence clinical trial results, and affect potential revenue for companies developing drugs, devices, or diagnostics — like spotting a stubborn weed that may require different tools to remove.
merkel cell carcinoma medical
"carcinoma (cSCC), melanoma and Merkel cell carcinoma. In its Phase 1b"
Merkel cell carcinoma is a rare, fast-growing form of skin cancer that starts in cells near the base of the skin and often spreads quickly to nearby tissues and organs. For investors, it matters because treatments for this aggressive disease can create high-value opportunities or risks: successful drugs or tests can unlock significant revenue and partnerships, while failed trials or regulatory setbacks can sharply affect a biotech company’s prospects — like a single critical test determining whether a new product succeeds or stalls.
pathological response rate medical
"reported a pathological response rate in cSCC across all dosing cohorts"
Pathological response rate is the proportion of treated patients whose tissue samples, examined by a pathologist after therapy, show a meaningful reduction or complete disappearance of disease. For investors, it is an early measurable sign of a treatment’s effectiveness—like checking how many houses are truly fixed after a renovation—and can influence expectations for regulatory approval, future sales, and a company’s valuation.
immuno-oncology medical
"why we believe INTASYL represents a differentiated approach to immuno-oncology," said"
Immuno-oncology is a field of medicine focused on using the body's immune system to fight cancer. It involves developing treatments that help the immune system recognize and attack cancer cells more effectively. For investors, advancements in immuno-oncology can signal promising new therapies that may lead to improved patient outcomes and potentially significant commercial opportunities.
fda regulatory
"Phio has indicated that FDA engagement regarding next-stage clinical development"
The FDA is the U.S. federal agency that evaluates and approves medical drugs, devices, biological therapies and certain foods; think of it as the gatekeeper that decides whether a medical product is safe and effective for patients. For investors, FDA decisions determine whether a company can sell a product, affect expected revenue and introduce regulatory risk, so approvals, rejections or safety warnings can quickly move a company's valuation and stock price.

AI-generated analysis. Not financial advice.

Registration link below for Wednesday March 18, 2026 at 4 PM EDT

Phio invites individual and institutional investors, as well as advisors and analysts with an interest in the life sciences sector, to attend this virtual event

King of Prussia, Pennsylvania--(Newsfile Corp. - March 16, 2026) - Phio Pharmaceuticals Corp. (NASDAQ: PHIO) is a clinical-stage siRNA biopharmaceutical company developing therapeutics using its proprietary INTASYL® gene silencing technology to eliminate cancer. Phio announced today that Mr. Robert Bitterman, CEO and Chairman of the Board, Phio Pharmaceuticals will participate in a fireside chat with Steven Saltzstein, CEO, Force Family Office on Wednesday March 18, 2026.

"We are excited to participate in the fireside chat with Force Family Office and look forward to sharing the Phio story and why we believe INTASYL represents a differentiated approach to immuno-oncology," said Robert Bitterman, CEO and Chairman of Phio Pharmaceuticals.

DATE: Wednesday March 18, 2026

TIME: 4 PM EDT

REGISTRATION LINK: PHIO Pharma - Force Family Office

Recent Company Highlights
Phio's lead clinical candidate, PH-762, is being evaluated as an intratumoral therapy in cutaneous squamous cell carcinoma (cSCC), melanoma and Merkel cell carcinoma. In its Phase 1b trial, Phio has reported that 22 patients completed treatment across five dose-escalation cohorts, with no dose-limiting toxicities or serious adverse events. The Company has also reported a pathological response rate in cSCC across all dosing cohorts of approximately 65%, including an 85% pathological response (6 of 7 patients) in the highest-dose cohort.

Phio has indicated that FDA engagement regarding next-stage clinical development is targeted for the second quarter of 2026 and has reported cash and cash equivalents projected to sustain operations into the first half of 2027.

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 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, 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, the results from our ongoing clinical trials, our expectations that our cash runway will extend into the first half of 2027, our expectations regarding timing of FDA submissions intended to propose and seek guidance for next steps in clinical study design for PH-762, details regarding our planned non-clinical toxicology study, and our ability to support ongoing clinical development, operational requirements and strategic initiatives with the capital we currently have on hand, 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.

About FORCE Family Office
FORCE works with Family Offices, Ultra High Net Worth Individuals, their Foundations, and Endowments by introducing them to leaders of privately held businesses at the capital acquisition stage and public companies looking for open market buyers. FORCE is constantly bringing unique opportunities and information to their community of investors. In addition, their elite peer-to-peer community brings family offices, UHNW individuals, endowments and foundations together, facilitating co-investment opportunities, information sharing, philanthropy, and networking.

CONTACTS:

Phio Pharmaceuticals Corp.
Jennifer Phillips: jphillips@phiopharma.com
Corporate Affairs

Force Family Office
Harvey Briggs
608-361-8092
forcefamilyoffice.com

To view the source version of this press release, please visit https://www.newsfilecorp.com/release/288680

FAQ

When is Phio (PHIO) presenting with Force Family Office and how can I attend?

Phio will present on March 18, 2026 at 4 PM EDT. According to the company, individual and institutional investors can register via the provided virtual registration link to attend the fireside chat.

What are the Phase 1b results for PH‑762 reported by Phio (PHIO)?

PH‑762 showed no dose‑limiting toxicities or serious adverse events in the Phase 1b trial. According to the company, 22 patients completed treatment with an overall cSCC pathological response of ~65% and 85% in the highest‑dose cohort.

How large was the highest‑dose cohort for PH‑762 and what was the response rate?

The highest‑dose cohort included 7 patients with a pathological response in 6 of 7 patients (85%). According to the company, this figure reflects an early small‑cohort result from the Phase 1b study.

What is Phio's (PHIO) regulatory timeline for advancing PH‑762?

Phio targets engagement with the FDA in Q2 2026 to discuss next‑stage development. According to the company, discussions are planned to define the path forward following Phase 1b results.

How long does Phio (PHIO) say its cash will sustain operations?

Phio reports cash and cash equivalents projected to sustain operations into the first half of 2027. According to the company, this projection informs near‑term development planning and regulatory engagement timing.
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