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Phio Pharmaceuticals Announces "Nobel Prize Winning Science Takes on Skin Cancer" in a Fireside Chat with Force Family Office on Wednesday, April 15, 2026

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Phio Pharmaceuticals (NASDAQ: PHIO) announced a virtual fireside chat on April 15, 2026 with Force Family Office featuring CEO Robert Bitterman and Dr. R. Todd Plott to discuss INTASYL siRNA program and PH-762, an intratumoral PD-1–silencing candidate for skin cancers.

Phio reported that 22 patients completed Phase 1b treatment across five dose cohorts with no dose-limiting toxicities or serious adverse events, ~65% pathological response in cSCC overall and 85% response (6 of 7) at the highest dose. FDA engagement on next-stage development is targeted for Q2 2026. Cash is projected to sustain operations into H1 2027.

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Positive

  • 22 patients completed Phase 1b treatment
  • No dose-limiting toxicities or serious adverse events reported
  • Pathological response ~65% in cSCC across cohorts
  • Highest-dose cohort pathological response 85% (6 of 7)
  • FDA engagement targeted for Q2 2026

Negative

  • Only 22 patients completed treatment across five cohorts
  • Cash runway projected only into H1 2027

News Market Reaction – PHIO

+2.48%
1 alert
+2.48% Session close to close
$14.06M Market Cap
1.00K Volume

In the Apr 13 session, PHIO gained 2.48%, reflecting a moderate positive market reaction.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement reinforces Phio’s ongoing outreach around PH-762, spotlighting Phase 1b results wi...
Analysis

This announcement reinforces Phio’s ongoing outreach around PH-762, spotlighting Phase 1b results with a 65% pathological response rate in cSCC and 85% in the highest-dose cohort, alongside a cash runway into H1 2027. It follows a series of conference and fireside presentations emphasizing the same dataset. Investors evaluating this news may focus on upcoming FDA engagement targeted for Q2 2026, funding arrangements, and how future trials validate durability and safety across broader patient populations.

Key Figures

Patients treated: 22 patients Dose cohorts: 5 cohorts Pathological response rate: 65% +4 more
7 metrics
Patients treated 22 patients Phase 1b PH-762 trial across dose-escalation cohorts
Dose cohorts 5 cohorts Phase 1b PH-762 dose-escalation structure
Pathological response rate 65% cSCC pathological response across all dosing cohorts
High-dose response rate 85% (6 of 7 patients) cSCC pathological response in highest-dose cohort
Event date April 15, 2026 Scheduled fireside chat with Force Family Office
Event time 12 PM EDT Virtual fireside chat start time
Cash runway Into H1 2027 Projected cash and cash equivalents coverage

Historical Context

5 past events · Latest: Apr 09 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Apr 09 Investor presentation Positive -3.9% Announcement of Centri Capital Conference presentation on PH-762 progress.
Mar 30 Manufacturing agreement Positive -4.8% cGMP U.S. manufacturing deal plus Phase 1b PH-762 data and runway update.
Mar 23 Clinical results update Positive +2.5% AAD 2026 presentation featuring Phase 1b PH-762 skin cancer results.
Mar 16 Fireside chat Positive +7.3% Force Family Office chat on INTASYL approach and PH-762 Phase 1b data.
Mar 10 Investor forum Positive +1.6% Life Sciences Investor Forum presentation on INTASYL platform and PH-762.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Positive clinical and investor-relations news has more often led to gains, but there are notable instances of selloffs on seemingly constructive updates.

Recent Company History

Over the last month, Phio has repeatedly highlighted progress for PH-762 through investor forums, fireside chats, and conference presentations, emphasizing Phase 1b safety and response data and a cash runway into H1 2027. Manufacturing readiness and an upcoming FDA engagement targeted for Q2 2026 have also been featured. Today’s fireside chat announcement continues this pattern of outreach around the same core clinical story, extending the company’s ongoing visibility campaign to life sciences investors.

Key Terms

sirna, immuno-oncology, intratumoral, cutaneous squamous 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.
immuno-oncology medical
"INTASYL siRNA program represents a differentiated approach to immuno-oncology"
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.
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
"intratumoral therapy in cutaneous squamous cell carcinoma (cSCC), melanoma"
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
"melanoma and Merkel cell carcinoma. In its Phase 1b trial, Phio"
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.
pd-1 gene medical
"PH-762, an INTASYL compound, that silences the PD-1 gene implicated"
The PD‑1 gene encodes a protein that acts like a brake on certain immune cells, helping prevent an overactive immune response. For investors, it matters because drugs that block PD‑1 can release that brake to help the immune system attack cancer, making PD‑1 a major drug target and biomarker that drives clinical trial value, regulatory approvals, and commercial potential in oncology and immunotherapy.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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

R. Todd Plott, M.D., Chief Medical Officer, Epiphany Dermatology will join Robert Bitterman, Phio Pharmaceuticals and Steven Saltzstein, Force Family Office

King of Prussia, Pennsylvania--(Newsfile Corp. - April 13, 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. Joining them will be Dr. R. Todd Plott, Chief Medical Officer, Epiphany Dermatology and former consultant to the FDA who will provide additional insight on PH-762, an INTASYL compound, that silences the PD-1 gene implicated in various forms of skin cancer.

"We are excited to hold this fireside chat with Force Family Office. Dr. Plott will discuss why the INTASYL siRNA program represents a differentiated approach to immuno-oncology," said Robert Bitterman, CEO and Chairman of Phio Pharmaceuticals.

DATE: Wednesday April 15, 2026

TIME: 12 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/292112

FAQ

What will Phio (PHIO) discuss in the April 15, 2026 fireside chat?

They will discuss the INTASYL siRNA program and clinical candidate PH-762 for skin cancers. According to the company, speakers include CEO Robert Bitterman and Dr. R. Todd Plott, with commentary on PH-762 clinical findings and next-stage development timing.

What Phase 1b results did PHIO report for PH-762 in April 2026?

PHIO reported 22 patients completed Phase 1b with no dose-limiting toxicities or serious adverse events. According to the company, pathological response in cSCC was ~65% overall and 85% (6 of 7) at the highest dose cohort.

How does PH-762 work and which cancers is PHIO targeting with PH-762 (PHIO)?

PH-762 is an INTASYL siRNA compound that silences the PD-1 gene implicated in skin cancers. According to the company, it is being evaluated intratumorally in cSCC, melanoma and Merkel cell carcinoma.

When does PHIO expect FDA engagement for PH-762 development?

PHIO targets FDA engagement in the second quarter of 2026. According to the company, this interaction is aimed at discussing next-stage clinical development for PH-762.

Does the PHIO press release report safety concerns for PH-762?

No major safety concerns were reported in Phase 1b; no dose-limiting toxicities or serious adverse events were observed. According to the company, safety findings covered 22 patients across five dose-escalation cohorts.

How long is Phio's cash runway reported in April 2026 and what does it mean for investors?

Phio reported cash and equivalents projected to sustain operations into the first half of 2027. According to the company, this implies near-term funding needs for continued development beyond that period.