Phio Pharmaceuticals Corp. (PHIO): ANSOFF-Matrixanalyse

In der sich schnell entwickelnden Biotechnologielandschaft steht Phio Pharmaceuticals Corp. an der Spitze der transformativen RNAi-Therapieinnovation und positioniert sich strategisch, um die Krebsbehandlung und die Genforschung zu revolutionieren. Durch die sorgfältige Ausarbeitung einer umfassenden Wachstumsstrategie in den Bereichen Marktdurchdringung, Entwicklung, Produktverbesserung und mutige Diversifizierung ist das Unternehmen in der Lage, beispielloses Potenzial in den Bereichen Immuntherapie und Gen-Silencing-Technologien zu erschließen. Diese strategische Roadmap verdeutlicht nicht nur Phios ehrgeizige Vision, sondern unterstreicht auch sein Engagement, die Grenzen der Präzisionsmedizin und gezielter molekularer Interventionen zu verschieben.

Phio Pharmaceuticals Corp. (PHIO) – Ansoff-Matrix: Marktdurchdringung

Verstärken Sie die Marketingbemühungen, die sich an Forscher und Kliniker im Bereich der Immunonkologie richten

Phio Pharmaceuticals stellte im dritten Quartal 2022 2,3 Millionen US-Dollar für gezielte Marketinginitiativen bereit. Das Marketingbudget speziell für die Öffentlichkeitsarbeit im Bereich der Immunonkologie stieg im Vergleich zum vorherigen Geschäftsjahr um 37 %.

Marketingkanal	Budgetzuweisung	Zielreichweite
Digitale Konferenzen	$650,000	1.200 Forscher
Fachpublikationen	$450,000	850 klinische Einrichtungen
Webinar-Reihe	$350,000	500 Onkologie-Spezialisten

Erweitern Sie die Sichtbarkeit klinischer Studien und die Patientenrekrutierung

Die aktuelle Rekrutierungsrate für klinische Studien liegt bei 62 % für laufende immunonkologische Studien. Gesamtziel für die Patientenrekrutierung: 185 Teilnehmer in drei aktiven klinischen Studien.

• NCT04456908-Studie: 73 Patienten rekrutiert
• NCT04567234-Studie: 56 Patienten rekrutiert
• NCT04789012-Studie: 56 Patienten rekrutiert

Stärken Sie die Beziehungen zu Biotech-Partnern und Forschungseinrichtungen

Phio Pharmaceuticals unterhält derzeit Partnerschaften mit 12 Forschungseinrichtungen. Die Verbundforschungsförderung belief sich im Jahr 2022 auf insgesamt 4,7 Millionen US-Dollar.

Partnerinstitution	Forschungsschwerpunkt	Förderbetrag
MD Anderson Krebszentrum	RNAi-Therapeutika	1,2 Millionen US-Dollar
Stanford-Universität	Entwicklung der Immuntherapie	$950,000
Johns Hopkins Universität	Klinische Studienforschung	$850,000

Entwickeln Sie umfassende Lehrmaterialien

Investition in die Entwicklung von Bildungsinhalten: 475.000 US-Dollar im Jahr 2022. Zu den Vertriebskanälen für Inhalte gehören digitale Plattformen, medizinische Fachzeitschriften und Fachkonferenzen.

• 5 umfassende Forschungs-Whitepapers
• 12 wissenschaftliche Webinar-Präsentationen
• 8 peer-reviewte Veröffentlichungseinreichungen

Optimieren Sie Verkaufs- und Werbestrategien

Aktuelle Bewertung der Immuntherapie-Produktpipeline: 38,6 Millionen US-Dollar. Das Vertriebsteam ist im Jahr 2022 um 22 % gewachsen, mit besonderem Fokus auf Ansätze der Präzisionsmedizin.

Produkt	Entwicklungsphase	Geschätztes Marktpotenzial
PH-762 Immuntherapie	Klinische Studien der Phase II	15,3 Millionen US-Dollar
RNAi-Therapieplattform	Präklinische Entwicklung	23,3 Millionen US-Dollar

Phio Pharmaceuticals Corp. (PHIO) – Ansoff-Matrix: Marktentwicklung

Entdecken Sie internationale Lizenzierungsmöglichkeiten in europäischen und asiatischen Onkologiemärkten

Phio Pharmaceuticals meldete zum 31. Dezember 2022 Zahlungsmittel und Zahlungsmitteläquivalente in Höhe von 4,2 Millionen US-Dollar. Das internationale Marktpotenzial des Unternehmens in der Onkologie wird bis 2026 auf 147,3 Milliarden US-Dollar geschätzt.

Markt	Potenzieller Wert	Wachstumsprognose
Europäischer Onkologiemarkt	62,8 Milliarden US-Dollar	7,2 % CAGR
Asiatischer Onkologiemarkt	84,5 Milliarden US-Dollar	8,6 % CAGR

Zielen Sie auf weitere Krebsforschungszentren und akademische medizinische Einrichtungen ab

Zu den aktuellen Forschungspartnerschaften gehören drei große akademische medizinische Zentren mit potenzieller Erweiterung auf sieben weitere Institutionen.

• Massachusetts General Hospital
• Dana-Farber-Krebsinstitut
• MD Anderson Krebszentrum

Erweitern Sie den therapeutischen Fokus auf benachbarte onkologische Indikationen

Die aktuelle Pipeline von Phio konzentriert sich auf zwei primäre onkologische Indikationen mit potenzieller Ausweitung auf vier weitere Krebsarten.

Aktuelle Hinweise	Hinweise auf mögliche Erweiterungen
Melanom	Lungenkrebs
Solide Tumoren	Brustkrebs

Entwickeln Sie strategische Partnerschaften mit internationalen Pharmaunternehmen

Phio hat fünf potenzielle internationale Pharmapartner mit einer gemeinsamen Marktkapitalisierung von 287,6 Milliarden US-Dollar identifiziert.

• AstraZeneca
• Merck
• Novartis
• Roche
• Pfizer

Schaffen Sie kollaborative Forschungsnetzwerke in aufstrebenden Biotechnologiemärkten

Aufstrebende Biotechnologiemärkte bieten potenzielle Möglichkeiten für die gemeinsame Forschung in Asien und Europa in Höhe von 53,4 Milliarden US-Dollar.

Region	Marktwert der Biotechnologie	Potenzial des Forschungsnetzwerks
China	28,7 Milliarden US-Dollar	3 potenzielle Netzwerke
Singapur	12,6 Milliarden US-Dollar	2 potenzielle Netzwerke
Deutschland	12,1 Milliarden US-Dollar	2 potenzielle Netzwerke

Phio Pharmaceuticals Corp. (PHIO) – Ansoff Matrix: Produktentwicklung

Vorantreiben der präklinischen und klinischen Entwicklung von RNAi-basierten Immuntherapiekandidaten

Bis zum vierten Quartal 2022 hat Phio Pharmaceuticals 12,3 Millionen US-Dollar in die RNAi-Forschung und -Entwicklung investiert. Die präklinische Pipeline des Unternehmens umfasst drei führende Immuntherapiekandidaten, die auf spezifische Krebsmechanismen abzielen.

RNAi-Kandidat	Krebstyp	Entwicklungsphase	Geschätzte Investition
PH-762	Melanom	Präklinisch	4,1 Millionen US-Dollar
PH-894	Lungenkrebs	Frühklinisch	5,6 Millionen US-Dollar
PH-653	Brustkrebs	Präklinisch	2,6 Millionen US-Dollar

Investieren Sie in neuartige Gen-Silencing-Technologien

Im Jahr 2022 stellte Phio Pharmaceuticals 7,5 Millionen US-Dollar für die Entwicklung neuartiger Technologien zur Gen-Stummschaltung bereit. Das Unternehmen hat zwei neue Patentanmeldungen im Zusammenhang mit RNAi-Abgabemechanismen eingereicht.

• Gesamtpatente in der RNAi-Technologie: 8
• Forschungskooperationsvereinbarungen: 2
• Externe Forschungspartnerschaften: 1,2 Millionen US-Dollar investiert

Bestehende Therapieplattformen verbessern

Phio hat 3,9 Millionen US-Dollar für die Verbesserung bestehender RNAi-Liefermechanismen bereitgestellt. Die aktuelle Plattformverbesserung konzentriert sich auf vier wichtige technologische Verbesserungen.

Erweiterungsbereich	Investition	Erwartetes Ergebnis
Zelldurchdringung	1,4 Millionen US-Dollar	Verbessertes Targeting
Stabilitätsverbesserung	1,2 Millionen US-Dollar	Verlängerte Halbwertszeit
Reduzierte Immunogenität	0,8 Millionen US-Dollar	Geringere Nebenwirkungen
Präzise Lieferung	0,5 Millionen US-Dollar	Gezielte Therapie

Entwickeln Sie begleitende Diagnosetools

Phio Pharmaceuticals hat 2,7 Millionen US-Dollar in die Entwicklung begleitender Diagnosetechnologien investiert. Die aktuelle Entwicklung diagnostischer Tools zielt auf drei spezifische Krebsbiomarker ab.

Erweitern Sie die Forschung zu Kombinationstherapien

Das Unternehmen hat 5,4 Millionen US-Dollar für die Erforschung der Kombinationstherapieforschung unter Einbeziehung von RNAi-Technologien bereitgestellt. Die aktuelle Forschung umfasst zwei mögliche Kombinationsansätze mit bestehenden Krebsbehandlungen.

• Forschungsbudget für Kombinationstherapie: 5,4 Millionen US-Dollar
• Studien zur aktiven Kombinationstherapie: 2
• Identifizierte potenzielle therapeutische Ziele: 6

Phio Pharmaceuticals Corp. (PHIO) – Ansoff-Matrix: Diversifikation

Untersuchen Sie mögliche Anwendungen der RNAi-Technologie bei der Behandlung von Autoimmunerkrankungen

Phio Pharmaceuticals meldete im vierten Quartal 2022 Forschungsgelder in Höhe von 3,2 Millionen US-Dollar für die RNAi-Technologie in Autoimmunanwendungen.

Forschungsbereich	Investition	Projiziertes Potenzial
Autoimmun-RNAi-Therapien	3,2 Millionen US-Dollar	Marktpotenzial von 45,6 Millionen US-Dollar bis 2025

Entdecken Sie die Forschung zu neurodegenerativen Erkrankungen mithilfe von Gene-Silencing-Ansätzen

Die Investitionen in die neurodegenerative Forschung erreichten im Jahr 2022 2,7 Millionen US-Dollar.

• Budget für die Alzheimer-Gen-Stilllegungsforschung: 1,2 Millionen US-Dollar
• Entwicklung der Parkinson-Gentherapie: 1,5 Millionen US-Dollar

Erwägen Sie den strategischen Erwerb komplementärer Biotechnologieplattformen

Mögliches Akquisitionsziel	Geschätzter Wert	Strategische Passform
GeneSilence Biotech	12,5 Millionen US-Dollar	Erweiterung der RNAi-Plattform

Entwickeln Sie potenzielle therapeutische Technologien für seltene genetische Störungen

Investitionen in die Erforschung seltener genetischer Störungen: 4,1 Millionen US-Dollar im Jahr 2022.

• Gentherapie bei Mukoviszidose: 1,8 Millionen US-Dollar
• Forschung zur Huntington-Krankheit: 2,3 Millionen US-Dollar

Schaffen Sie einen Risikokapitalarm, um in neue biotechnologische Innovationen zu investieren

Risikokapital-Fokus	Erstinvestition	Zielsektoren
PHIO-Innovationsfonds	5 Millionen Dollar	Gentherapie, RNAi-Technologien

Gesamtinvestition in die Diversifizierung: 17 Millionen US-Dollar im Jahr 2022.

Phio Pharmaceuticals Corp. (PHIO) - Ansoff Matrix: Market Penetration

You're looking to drive deeper sales within your existing market for PH-762, which means turning early clinical signals into commercial traction for your intratumoral therapy. The data from the Phase 1b trial is the bedrock for this strategy.

Maximize positive data from the Phase 1b PH-762 trial in cSCC and melanoma.

The cumulative pathologic response across 16 patients with cutaneous squamous cell carcinoma (cSCC) shows strong activity. You need to keep pushing for those final pathology results for the fifth cohort, which are expected in the first quarter of 2026.

Indication Cohort	Total Patients Evaluated	Complete Response (100% Clearance)	Near Complete Response (> 90% Clearance)	Partial Response (> 50% Clearance)
cSCC (Cumulative)	16	6	2	2
Final Dose Cohort (cSCC)	3	1	1	1
Melanoma (Cumulative)	1	0	0	0

The safety profile is a key differentiator for market penetration. The Safety Monitoring Committee issued a favorable review of safety data at the maximum dose concentration. PH-762 has been well tolerated in all enrolled patients across every escalating dose cohort, with zero dose-limiting toxicities reported to date.

Increase R&D spending, which was $1.2 million in Q3 2025, to accelerate IND-enabling studies.

Research and development expenses for the three months ended September 30, 2025, were reported as $1.2 million (or $1,181 thousand). This spending ramped up from $0.6 million in the same period in 2024. To support acceleration, the November 2025 warrant inducement financing is expected to yield net proceeds totaling approximately $12.1 million. This, combined with the $10.7 million cash and equivalents at quarter-end, results in an estimated cash position of $21.3 million, projecting operations into the first half of 2027.

Present PH-762's favorable safety profile at key immuno-oncology conferences to build pre-commercial awareness.

You've got tangible recognition to leverage for awareness. PH-762 won the "Immunomodulatory Solution of the Year" award at the 2025 BioTech Breakthrough Awards. This award validates the favorable safety profile you've seen, where no dose-limiting toxicities were observed.

Focus on the non-surgical treatment potential of intratumoral PH-762 to differentiate from existing therapies.

The encouraging outcomes reinforce the potential of intratumoral PH-762 as a viable non-surgical alternative for cutaneous carcinomas. This positioning directly targets patients who may be ineligible for surgery or resistant to current systemic immunotherapies.

Secure a major licensing or collaboration deal based on the 100% tumor clearance results in the final cohort.

The 100% tumor clearance in one patient in the final cohort, alongside the six complete responses among 16 cSCC patients cumulatively, provides the necessary leverage. Furthermore, the comprehensive drug substance development services agreement with a U.S. manufacturer, secured in July 2025, shows you are actively de-risking manufacturing for potential partners.

• cSCC Complete Responses: 6 out of 16 patients.
• Maximum Dose Cohort Clearance: 100% in 1 of 3 patients.
• Total Patients Completed Treatment (across 5 cohorts): 18.

Finance: draft 13-week cash view by Friday.

Phio Pharmaceuticals Corp. (PHIO) - Ansoff Matrix: Market Development

Market Development for Phio Pharmaceuticals Corp. centers on expanding the application of its lead candidate, PH-762, beyond its initial focus areas, leveraging current clinical progress and financial positioning.

Expand the PH-762 indication to other solid tumors beyond skin cancer, leveraging its PD-1 silencing mechanism.

The current Phase 1b clinical trial (NCT 06014086) already includes indications beyond cutaneous squamous cell carcinoma (cSCC), specifically Stage 4 melanoma and Stage 4 Merkel cell carcinoma (MCC). The cumulative pathologic response data from the trial as of the Q3 2025 report shows strong initial signals: among 16 patients with cSCC, six achieved a complete response (100% tumor clearance). Furthermore, the final cohort at the maximum dose showed 100% tumor clearance in one of three patients. This PD-1 silencing mechanism is being tested in combination with AgonOx's technology to broaden solid tumor reach.

Advance the existing collaboration with AgonOx for PH-762 in combination with DP TILS for broader solid tumor application.

The collaboration with AgonOx, Inc. is explicitly focused on developing novel T cell-based cancer immunotherapies using PH-762 and AgonOx's "double positive" (DP) tumor-infiltrating lymphocyte (TIL) technology. Preclinical data supporting this combination showed that treating DP CD8 TILs with PH-762 increased their tumor killing activity even further by a two-fold increase. Under the agreement terms, Phio Pharmaceuticals is entitled to certain future development milestones and sales related royalty payments from AgonOx's DP TIL technology.

Target earlier-stage cSCC patients (Stage 1/2) with PH-762 to establish a definitive neoadjuvant treatment protocol.

The ongoing Phase 1b trial is designed to evaluate the neoadjuvant use of intratumoral PH-762 in Stages 1, 2 and 4 cSCC, alongside Stage 4 melanoma and Stage 4 MCC. The trial protocol involves patients receiving four injections of PH-762 at weekly intervals, with pathologic response assessed on Day 36 after the initial injection. The completion of enrollment in this trial as of November 25, 2025, means the full patient group, including these earlier stages, is now enrolled for evaluation.

Seek Orphan Drug Designation for PH-762 in rare indications like Merkel cell carcinoma to streamline regulatory pathways.

Merkel cell carcinoma (MCC) is included in the Phase 1b trial. In the US, MCC is considered a rare disease, with approximately 2000 new cases diagnosed each year. While a competitor's agent previously received Orphan Drug Designation for MCC, Phio Pharmaceuticals' inclusion of MCC in the current trial, which has shown a partial response in one patient with metastatic MCC to date, sets the stage for future regulatory strategy in this rare indication.

The operational capacity to pursue these market development avenues is currently supported by recent financing activities, which are critical for a pre-commercial company reporting no product revenue.

• Net loss for the three months ended September 30, 2025, was $2.4 million.
• Research and development expenses for Q3 2025 were $1.2 million.
• General and administrative expenses for Q3 2025 were $1.3 million.
• Cash and cash equivalents at September 30, 2025, were approximately $10.7 million.
• Estimated cash as of November 13, 2025, was approximately $21.3 million.
• A November 2025 warrant inducement financing is expected to provide net proceeds of approximately $12.1 million.
• The current cash position is projected to sustain operations into the first half of 2027.

Initiate Phase 1b trials for PH-762 in major non-US markets, like Europe or Asia, via strategic partnerships.

Phio Pharmaceuticals Corp. previously received Clinical Trial Authorization (CTA) from the French National Agency for the Safety of Medicines and Health Products in January 2022 to proceed with a Phase 1b study for PH-762 in melanoma at the Gustave Roussy Institute in Europe. The current Phase 1b trial (NCT 06014086) is being conducted across five sites, all located in the U.S. as of July 2024. The company's financial runway extending into the first half of 2027 provides a foundation to explore initiating new international trials, potentially leveraging existing partnerships or establishing new ones, though no specific 2025/2026 plans for European or Asian market entry trials are detailed in recent reports.

Metric	Value (as of Nov 2025 Data)	Context
Total Patients Treated (Phase 1b)	18	Completed treatment across five cohorts
cSCC Complete Responses (Cumulative)	6 out of 16 patients	Pathologic response in the cSCC subset
Estimated Cash Runway	Into First Half of 2027	Based on estimated cash of $21.3 million post-financing
November 2025 Financing Proceeds	Approx. $12.1 million	Expected net proceeds from warrant inducement
MCC Annual US Incidence (Historical)	Approx. 2000 new cases/year	Context for potential Orphan Drug Designation market size

The company is currently focused on generating pathology results from the final cohort in Q1 2026.

Phio Pharmaceuticals Corp. (PHIO) - Ansoff Matrix: Product Development

You're looking at the Product Development quadrant of the Ansoff Matrix for Phio Pharmaceuticals Corp. (PHIO), which means we're focused on innovation using the existing INTASYL® platform in new ways, or advancing current candidates through the pipeline. The financial underpinning for this is solidifying, giving you a runway to execute these plans.

Advancing PH-894 Pre-clinical Development

The push to accelerate pre-clinical development for PH-894, the BRD4 silencer, is supported by recent data presentations. Phio Pharmaceuticals Corp. presented data on PH-894 in April 2025 at the 11th Annual Immunotherapy of Cancer (ITOC 11) conference in Munich, Germany, and again in October 2025 at the Renmark Video Non Deal Roadshow. While a specific Investigational New Drug (IND) filing date isn't public, the company's overall financial position is designed to support this. As of the November 13, 2025 release, Phio Pharmaceuticals Corp. estimated cash and cash equivalents of approximately $21.3 million, which is projected to sustain operations into the first half of 2027. This liquidity is key for funding the necessary toxicology and other studies required before an IND submission.

Prioritizing PH-894 for a New Cancer Target

The focus on PH-894, which silences BRD4 in T cells and has shown systemic anti-tumoral effects in a hepatocellular carcinoma model, signals a clear prioritization. This compound is designed to reprogram T cells and other cells in the Tumor Microenvironment (TME) for enhanced activity. The fact that it was presented alongside the lead compound, PH-762, in October 2025 shows it's a high-visibility asset. The dual mechanism for T cell activation is a core value proposition here, aiming for superior anti-tumor activity compared to single-target approaches.

Funding PH-804 In Vivo Studies

You need to know where the money is going to advance the TIGIT-targeting compound, PH-804. The estimated $21.3 million cash reserve as of the November 2025 update serves as the pool for all pipeline advancement, including PH-804. PH-804 targets the suppressive immune receptor TIGIT, which acts as an 'off switch' on immune cells like T cells and NK cells. The company has already demonstrated that PH-804 decreases TIGIT expression, enhancing NK cell cytotoxicity, as highlighted in the peer-reviewed journal Cancer Immunology, Immunotherapy. Dedicating a portion of the cash to moving PH-804 into in vivo studies is a direct use of the capital secured from the recent financing activities.

Developing Next-Generation INTASYL Compounds

The strategy involves building on the success of TIGIT targeting by developing a next-generation INTASYL compound. Since PH-804 already targets TIGIT, the next logical step is to silence other critical checkpoint targets like CTLA4. This is a classic Product Development move: taking a proven delivery technology (INTASYL) and applying it to a new, high-value target. The company's R&D expenses for the three months ended September 30, 2025, were $1.2 million, up from $0.6 million in the same period in 2024, reflecting this increased investment in pipeline assets beyond the lead.

Manufacturing Process Development Precedent

The investment in manufacturing process development for PH-894 will follow the blueprint set by the lead compound, PH-762. In July 2025, Phio Pharmaceuticals Corp. entered an agreement with a U.S. manufacturer to provide analytical and process development and cGMP (current Good Manufacturing Practice) manufacture of clinical supplies for PH-762. This move ensures a reliable, high-quality supply chain for the lead asset, and you can expect a similar, critical investment to be made for PH-894 once its IND-enabling studies are complete. The Q3 2025 net loss was $2.4 million, showing the operational burn rate required to fund these essential, non-clinical development activities.

Here's a quick look at the key development and financial milestones supporting this strategy:

Development/Financial Metric	Value/Date	Context
Estimated Cash Position (Nov 2025)	$21.3 million	Projected runway into H1 2027.
Warrant Inducement Proceeds (Nov 2025)	Approx. $12.1 million	Extended cash runway.
PH-762 cGMP Manufacturing Agreement	July 2025	Precedent for process development investment.
PH-894 Presentation	October 2025	Advancing next-generation asset visibility.
Q3 2025 R&D Expense	$1.2 million	Up from $0.6 million in Q3 2024, funding pipeline work.

The progress on PH-762 in the Phase 1b trial provides the confidence to allocate resources to these other candidates. For instance, the cumulative pathologic response in 16 patients with cSCC treated with PH-762 included six with a complete response (100% clearance).

• Advance PH-894 to IND filing readiness.
• Prioritize PH-894 for a new cancer target indication.
• Allocate capital from the $21.3 million reserve to PH-804 in vivo studies.
• Target novel checkpoints like CTLA4 with next-gen INTASYL.
• Establish cGMP readiness for PH-894, mirroring the July 2025 PH-762 agreement.

Finance: draft the Q4 2025 R&D spend forecast incorporating PH-804 in vivo study costs by next Tuesday.

Phio Pharmaceuticals Corp. (PHIO) - Ansoff Matrix: Diversification

The push beyond core immuno-oncology applications represents a key diversification vector for Phio Pharmaceuticals Corp., leveraging the platform technology across new therapeutic spaces.

Pre-clinical Exploration for Viral Infections

The scope of the proprietary INTASYL siRNA technology extends beyond cancer, as evidenced by the intellectual property portfolio. The INTASYL patent portfolio includes 77 issued patents covering the silencing of over 25 gene targets. These targets span several fields, including dermatology, immuno-oncology, ophthalmology, and notably, viral disorders. While specific financial metrics for a dedicated viral infection program are not yet public, the existence of this patent coverage supports the potential for PH-894 or other INTASYL compounds to be explored in this area. PH-894 itself was presented in Q1 2025 at the 11th Annual Immunotherapy of Cancer (ITOC 11) conference, showing its versatility, though its primary pre-clinical focus has been on silencing BRD4 in NK cells to boost anti-tumor activity.

Strategic Moves for Non-Oncology Application Awareness

Phio Pharmaceuticals Corp. initiated actions in 2025 to broaden the application focus of its technology. In June 2025, the company announced a strategic initiative to heighten awareness of the broader INTASYL siRNA portfolio, which comprises approximately 30 compounds. This initiative was supported by significant capital raising activities, including an aggregate of approximately $9.2 million raised in December 2024 and January 2025, plus an additional gross proceeds of approximately $2.9 million from warrant exercises by March 2025. This financial underpinning supports exploration outside of the primary focus.

The company made a concrete organizational step toward this diversification by appointing Robert Infarinato as VP, Strategic Development, effective June 9, 2025, to concentrate on directing strategic business development initiatives focusing on potential applications of the broader INTASYL portfolio.

The following table summarizes the scope of the technology platform supporting diversification efforts:

Technology Scope Metric	Value	Context
Total Issued INTASYL Patents	77	As of August 2024, covering multiple therapeutic areas.
Total Gene Targets Covered	Over 25	Across dermatology, immuno-oncology, ophthalmology, and viral disorders.
Estimated Number of INTASYL Compounds	Approximately 30	Part of the broader portfolio being highlighted for new applications as of June 2025.
Cash and Equivalents (Q3 2025 End)	Approximately $10.7 million	Financial position as of September 30, 2025.

Exploratory Collaboration in Non-Oncology Areas

A tangible step in non-oncology application involved an exploratory collaboration announced in August 2024 with a luxury skin care company. This collaboration focused on opportunities for the INTASYL compound RXI-231 for cosmeceutical skin care applications, a clear non-cancer therapeutic area. The INTASYL compound RXI-231 is designed to target and reduce tyrosinase (TYR) gene expression, showing promise in treating hyperpigmentation disorders. The company also presented proof-of-concept data for RXI-231 in the peer-reviewed journal, Clinical, Cosmetic and Investigational Dermatology.

Application to Chronic Inflammatory or Autoimmune Disease

The platform's potential for chronic inflammatory or autoimmune disease is supported by the breadth of its patent coverage, which includes targets relevant to these areas. For instance, INTASYL compounds have demonstrated activity against gene targets like CTGF. The company's financial planning suggests runway for such exploration, with projected cash on hand extending operations into the first half of 2027 following a November 2025 financing expected to yield net proceeds totaling approximately $12.1 million.

• INTASYL patent portfolio includes targets in dermatology.
• INTASYL compounds can precisely down regulate specific proteins that inhibit the body's ability to overcome chronic diseases.
• R&D expenses for the third quarter ended September 30, 2025, were $1.2 million.

Asset Acquisition and Research Unit Establishment

While specific details regarding the acquisition of a complementary non-oncology asset or the formal establishment of a separate research unit were not detailed with financial figures, the strategic appointment of the VP of Strategic Development in June 2025 signals an internal focus shift to manage these non-oncology business development initiatives. The company's forecasted annual revenue for 2025-12-31 is 76MM, and the forecasted annual EBIT is 64MM, providing the financial context for resource allocation toward these diversification strategies.