شركة Phio Pharmaceuticals Corp. (PHIO): تحليل مصفوفة ANSOFF

في مشهد التكنولوجيا الحيوية سريع التطور، تقف شركة Phio Pharmaceuticals Corp في طليعة الابتكار العلاجي التحويلي للـRNAi، حيث تضع نفسها في موقع استراتيجي لإحداث ثورة في علاج السرطان والأبحاث الوراثية. ومن خلال رسم استراتيجية نمو شاملة بدقة عبر اختراق السوق، والتطوير، وتعزيز المنتجات، والتنويع الجريء، تستعد الشركة لفتح إمكانات غير مسبوقة في تقنيات العلاج المناعي وإسكات الجينات. لا تعرض خريطة الطريق الإستراتيجية هذه رؤية Phio الطموحة فحسب، بل تسلط الضوء أيضًا على التزامها بدفع حدود الطب الدقيق والتدخلات الجزيئية المستهدفة.

Phio Pharmaceuticals Corp. (PHIO) - مصفوفة أنسوف: اختراق السوق

زيادة الجهود التسويقية التي تستهدف الباحثين والأطباء في مجال الأورام المناعية

خصصت شركة Phio Pharmaceuticals مبلغ 2.3 مليون دولار أمريكي لمبادرات التسويق المستهدفة في الربع الثالث من عام 2022. وزادت ميزانية التسويق المخصصة للتوعية بالأورام المناعية بنسبة 37% مقارنة بالعام المالي السابق.

قناة التسويق	تخصيص الميزانية	الوصول إلى الهدف
المؤتمرات الرقمية	$650,000	1200 باحث
المنشورات المتخصصة	$450,000	850 مؤسسة سريرية
سلسلة ندوات عبر الإنترنت	$350,000	500 أخصائي الأورام

توسيع نطاق رؤية التجارب السريرية وتوظيف المرضى

ويبلغ معدل التوظيف الحالي في التجارب السريرية 62% لدراسات الأورام المناعية الجارية. إجمالي هدف تسجيل المرضى: 185 مشاركًا في ثلاث تجارب سريرية نشطة.

• تجربة NCT04456908: تم تجنيد 73 مريضًا
• تجربة NCT04567234: تم تجنيد 56 مريضًا
• تجربة NCT04789012: تم تجنيد 56 مريضًا

تعزيز العلاقات مع شركاء التكنولوجيا الحيوية والمؤسسات البحثية

تحتفظ شركة Phio Pharmaceuticals حاليًا بشراكات مع 12 مؤسسة بحثية. بلغ إجمالي تمويل البحوث التعاونية 4.7 مليون دولار في عام 2022.

المؤسسة الشريكة	التركيز على البحوث	مبلغ التمويل
مركز إم دي أندرسون للسرطان	العلاجات رني	1.2 مليون دولار
جامعة ستانفورد	تطوير العلاج المناعي	$950,000
جامعة جونز هوبكنز	أبحاث التجارب السريرية	$850,000

تطوير مواد تعليمية شاملة

الاستثمار في تطوير المحتوى التعليمي: 475 ألف دولار عام 2022. تشمل قنوات توزيع المحتوى المنصات الرقمية والمجلات الطبية والمؤتمرات المهنية.

• 5 أوراق بحثية شاملة
• 12 عرضًا تقديميًا للندوات العلمية
• 8 مشاركات منشورة تمت مراجعتها من قبل النظراء

تحسين استراتيجيات المبيعات والترويج

التقييم الحالي لخط إنتاج منتجات العلاج المناعي: 38.6 مليون دولار. توسع فريق المبيعات بنسبة 22% في عام 2022، مع التركيز بشكل خاص على أساليب الطب الدقيق.

المنتج	مرحلة التطوير	إمكانات السوق المقدرة
PH-762 العلاج المناعي	المرحلة الثانية من التجارب السريرية	15.3 مليون دولار
منصة RNAi العلاجية	التنمية قبل السريرية	23.3 مليون دولار

Phio Pharmaceuticals Corp. (PHIO) - مصفوفة أنسوف: تطوير السوق

استكشف فرص الترخيص الدولية في أسواق الأورام الأوروبية والآسيوية

أعلنت شركة Phio Pharmaceuticals عن 4.2 مليون دولار نقدًا وما يعادله اعتبارًا من 31 ديسمبر 2022. وتقدر إمكانات السوق الدولية للشركة في مجال علاج الأورام بنحو 147.3 مليار دولار بحلول عام 2026.

السوق	القيمة المحتملة	توقعات النمو
سوق الأورام الأوروبي	62.8 مليار دولار	7.2% معدل نمو سنوي مركب
سوق الأورام الآسيوي	84.5 مليار دولار	8.6% معدل نمو سنوي مركب

استهداف مراكز أبحاث السرطان الإضافية والمؤسسات الطبية الأكاديمية

تشمل الشراكات البحثية الحالية 3 مراكز طبية أكاديمية رئيسية مع إمكانية التوسع إلى 7 مؤسسات إضافية.

• مستشفى ماساتشوستس العام
• معهد دانا فاربر للسرطان
• مركز إم دي أندرسون للسرطان

توسيع نطاق التركيز العلاجي ليشمل مؤشرات الأورام المجاورة

يركز خط أنابيب Phio الحالي على مؤشرين أوليين للأورام مع إمكانية التوسع إلى 4 أنواع إضافية من السرطان.

المؤشرات الحالية	مؤشرات التوسع المحتملة
سرطان الجلد	سرطان الرئة
الأورام الصلبة	سرطان الثدي

تطوير شراكات استراتيجية مع شركات الأدوية العالمية

حددت Phio 5 شركاء صيدلانيين دوليين محتملين برأسمال سوقي مجمع يبلغ 287.6 مليار دولار.

• أسترازينيكا
• ميرك
• نوفارتيس
• روش
• فايزر

إنشاء شبكات بحثية تعاونية في أسواق التكنولوجيا الحيوية الناشئة

تمثل أسواق التكنولوجيا الحيوية الناشئة 53.4 مليار دولار أمريكي من فرص البحث التعاوني المحتملة في جميع أنحاء آسيا وأوروبا.

المنطقة	القيمة السوقية للتكنولوجيا الحيوية	إمكانات شبكة البحث
الصين	28.7 مليار دولار	3 شبكات محتملة
سنغافورة	12.6 مليار دولار	2 الشبكات المحتملة
ألمانيا	12.1 مليار دولار	2 الشبكات المحتملة

Phio Pharmaceuticals Corp. (PHIO) - مصفوفة أنسوف: تطوير المنتجات

تطوير ما قبل السريرية والسريرية للمرشحين للعلاج المناعي القائم على RNAi

اعتبارًا من الربع الرابع من عام 2022، استثمرت شركة Phio Pharmaceuticals 12.3 مليون دولار في أبحاث وتطوير RNAi. يتضمن خط أنابيب الشركة قبل السريري 3 مرشحين رئيسيين للعلاج المناعي يستهدفون آليات محددة للسرطان.

مرشح رني	نوع السرطان	مرحلة التطوير	الاستثمار المقدر
الرقم الهيدروجيني-762	سرطان الجلد	ما قبل السريرية	4.1 مليون دولار
ف-894	سرطان الرئة	السريرية المبكرة	5.6 مليون دولار
ف-653	سرطان الثدي	ما قبل السريرية	2.6 مليون دولار

الاستثمار في تقنيات إسكات الجينات الجديدة

وفي عام 2022، خصصت شركة Phio Pharmaceuticals مبلغ 7.5 مليون دولار لتطوير تقنيات جديدة لإسكات الجينات. قدمت الشركة طلبي براءة اختراع جديدين يتعلقان بآليات توصيل RNAi.

• إجمالي براءات الاختراع في تكنولوجيا RNAi: 8
• اتفاقيات التعاون البحثي: 2
• الشراكات البحثية الخارجية: تم استثمار 1.2 مليون دولار

تعزيز المنصات العلاجية الموجودة

خصصت Phio مبلغ 3.9 مليون دولار لتحسين آليات توصيل RNAi الحالية. يركز تحسين النظام الأساسي الحالي على 4 تحسينات تكنولوجية رئيسية.

منطقة التعزيز	الاستثمار	النتيجة المتوقعة
الاختراق الخلوي	1.4 مليون دولار	تحسين الاستهداف
تحسين الاستقرار	1.2 مليون دولار	تمديد نصف الحياة
انخفاض المناعة	0.8 مليون دولار	آثار جانبية أقل
التسليم الدقيق	0.5 مليون دولار	العلاج المستهدف

تطوير أدوات التشخيص المصاحبة

استثمرت شركة Phio Pharmaceuticals 2.7 مليون دولار في تطوير تقنيات التشخيص المصاحبة. يستهدف تطوير أدوات التشخيص الحالية 3 مؤشرات حيوية محددة للسرطان.

توسيع نطاق البحث في العلاجات المركبة

خصصت الشركة 5.4 مليون دولار لاستكشاف أبحاث العلاج المركب التي تدمج تقنيات RNAi. يتضمن البحث الحالي نهجين محتملين للدمج مع علاجات السرطان الموجودة.

• ميزانية أبحاث العلاج المركب: 5.4 مليون دولار
• دراسات العلاج المركب النشط: 2
• الأهداف العلاجية المحتملة التي تم تحديدها: 6

شركة فيو للأدوية (PHIO) - مصفوفة أنسوف: التنويع

التحقيق في التطبيقات المحتملة لتقنية RNAi في علاج أمراض المناعة الذاتية

أعلنت شركة Phio Pharmaceuticals عن تمويل بحثي بقيمة 3.2 مليون دولار أمريكي لتقنية RNAi في تطبيقات المناعة الذاتية اعتبارًا من الربع الرابع من عام 2022.

منطقة البحث	الاستثمار	الإمكانات المتوقعة
علاجات RNAi المناعية الذاتية	3.2 مليون دولار	إمكانات سوقية بقيمة 45.6 مليون دولار بحلول عام 2025

استكشف أبحاث الاضطرابات التنكسية العصبية باستخدام أساليب إسكات الجينات

وصل الاستثمار في أبحاث التنكس العصبي إلى 2.7 مليون دولار في عام 2022.

• ميزانية أبحاث إسكات جينات الزهايمر: 1.2 مليون دولار
• تطوير العلاج الجيني لمرض باركنسون: 1.5 مليون دولار

النظر في عمليات الاستحواذ الاستراتيجية لمنصات التكنولوجيا الحيوية التكميلية

هدف الاستحواذ المحتمل	القيمة المقدرة	الملاءمة الإستراتيجية
جين سايلنس للتكنولوجيا الحيوية	12.5 مليون دولار	توسيع منصة رني

تطوير تقنيات علاجية محتملة للاضطرابات الوراثية النادرة

الاستثمار في أبحاث الاضطرابات الوراثية النادرة: 4.1 مليون دولار في عام 2022.

• العلاج الجيني للتليف الكيسي: 1.8 مليون دولار
• أبحاث مرض هنتنغتون: 2.3 مليون دولار

إنشاء ذراع رأس المال الاستثماري للاستثمار في ابتكارات التكنولوجيا الحيوية الناشئة

التركيز على رأس المال الاستثماري	الاستثمار الأولي	القطاعات المستهدفة
صندوق PHIO للابتكار	5 ملايين دولار	العلاج الجيني، تقنيات RNAi

إجمالي استثمارات التنويع: 17 مليون دولار في عام 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.