Delivering Rapid Relief When Every Second Counts

Nasus Pharma Ltd. (NYSE American: NSRX) is a clinical-stage pharmaceutical company focused on the development of innovative intranasal products, utilizing its proprietary powder-based intranasal (PBI) platform to address acute medical conditions and public health threats.

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Nasus Pharma Advances NS002 Towards Pivotal Study Following Positive Phase 2; Reports Annual Results and Provides Business Update


5 Reasons Investors Are Watching Nasus Pharma Ltd.

Proprietary Powder-Based Intranasal (PBI) Platform – Nasus Pharma's PBI technology disperses uniform spherical powder particles broadly across the nasal cavity, enabling faster and higher drug absorption than liquid-based nasal solutions by leveraging the nasal mucosa's rich vascular network for near-immediate systemic delivery.

NS002 Phase 2 Clinical Validation vs. EpiPen – Nasus Pharma completed a Phase 2 study demonstrating statistically significant improvements in time to therapeutic threshold and a higher proportion of participants reaching therapeutic epinephrine levels within the first minutes of administration compared to EpiPen, with consistent absorption confirmed under simulated anaphylaxis conditions.

Expanding Multi-Asset Pipeline – Beyond its lead NS002 epinephrine program, Nasus Pharma is advancing NS003 (intranasal ondansetron for chemotherapy-induced nausea) and NS004 (targeting metabolic disorders) into first-in-human Phase 1 studies expected in the second half of 2026, with NS005 for cardiovascular diseases in preclinical development, and the PBI platform also tested with midazolam for seizures and atropine for organophosphate poisoning.

NYSE American IPO and $15 Million Private Placement – Nasus Pharma completed its firm commitment IPO on NYSE American in August 2025, followed by a $15 million private placement that closed in February 2026, extending the company's cash runway through the second quarter of 2027 and providing capital to advance NS002 through Phase 3 initiation and NS003/NS004 into first-in-human studies.

Experienced Leadership Team with Proven Biotech Track Record – Nasus Pharma is led by CEO Dan Teleman (MBA, M.Sc.) and Co-Founder and Executive Chairman Udi Gilboa, a serial life-science entrepreneur and co-founder of multiple NASDAQ- and TASE-listed companies including BioBlast Ltd. (NASDAQ: ORPN), Alcobra Ltd. (NASDAQ: ADHD), and Endospan. CFO Eyal Rubin brings over two decades of financial leadership including prior roles at Protalix BioTherapeutics, BrainStorm Cell Therapeutics, and Teva Pharmaceutical Industries.

Identifying The Opportunity

KEY LEVELS

Key Level #1 - $3.14

Key Level #2 - $3.48

Key Level #3 - $4.07

Support: $2.62

About Nasus Pharma Ltd.

Nasus Pharma Ltd. (NYSE American: NSRX) is a clinical-stage pharmaceutical company incorporated in 2019 and based in Tel Aviv-Yafo, Israel. The company is focused on the development of innovative intranasal products utilizing its proprietary powder-based intranasal (PBI) platform to address acute medical conditions and public health threats. Nasus Pharma's mission is to offer better protection to patients during severe, life-threatening conditions through effective, user-friendly, safe, and immediately active intranasal products, with a focus on rapid drug delivery, ease of use, non-invasiveness, and safety. The company completed its NYSE American IPO in August 2025 and its ordinary shares trade under the ticker symbol NSRX.


Nasus Pharma Ltd.


Proprietary PBI Platform Technology


  • Nasus Pharma's powder-based intranasal (PBI) platform disperses drug particles broadly across the nasal cavity, creating a larger absorption area than liquid-based nasal solutions, enabling rapid and high drug absorption.

  • Uniform spherical powder particles enhance dose consistency and reliability, leveraging the nasal cavity's rich vascular network for near-immediate systemic delivery.

  • The platform has been validated in clinical studies with NS002 (epinephrine) and in preclinical or in-vitro settings with NS001 (naloxone), midazolam, and atropine.

  • The PBI platform supports a growing pipeline across acute and life-threatening conditions:
  • NS002→ intranasal epinephrine for anaphylaxis (Phase 2 complete)
  • NS003→ intranasal ondansetron for chemotherapy-induced nausea

  • Earlier-stage assets includeNS004, targeting metabolic disorders, and NS005 for cardiovascular diseases


Operational Momentum and Scaling


  • NS002 is advancing toward a pivotal Phase 3 study, with an IND submission planned for Q3 2026 and Phase 3 initiation targeted for Q4 2026, following statistically significant Phase 2 results demonstrating superiority to EpiPen on time to therapeutic threshold.


  • In November 2025, Nasus launched an additional Phase 2 study in Canada evaluating NS002's pharmacokinetic parameters and hemodynamic responses vs. EpiPen in 50 healthy adults with a history of allergic rhinitis, further building the clinical package ahead of regulatory submission under Section 505(b)(2).


  • NS003 (intranasal ondansetron) and NS004 (metabolic disorders) are advancing toward first-in-human Phase 1 studies expected in H2 2026, while NS001 (intranasal naloxone) development is paused as the company pursues partnering opportunities for its further advancement.



Positioning for Long-Term Value Creation


  • Nasus Pharma is building a diversified intranasal drug delivery business around its proprietary PBI platform, targeting high-urgency, life-threatening conditions where rapid, non-invasive administration offers a meaningful clinical advantage.


  • With NS002 addressing the large and established epinephrine autoinjector market and earlier-stage assets in oncology support and metabolic disease, the company offers a portfolio approach to value creation across multiple indication areas.


  • The February 2026 $15 million private placement extended the cash runway through mid-2027, providing the capital needed to advance NS002 through Phase 3 initiation while progressing NS003 and NS004 into first-in-human studies.


Financials


Nasus Pharma reported a net loss of $5.9 million for fiscal year 2025, with R&D and G&A expenses reflecting the company's transition to public company status and acceleration of the NS002 program.

Key Financial Highlights (FY2025):

• Cash, Cash Equivalents and Marketable Securities: $4.3M (December 31, 2025)

• Post-Period Private Placement (February 2026): $15.0M gross proceeds

• FY2025 Net Loss: $(5.9M) (vs. $(1.5M) in FY2024)

• R&D Expenses: $2.4M (FY2025, up from $0.3M in FY2024)

• G&A Expenses: $2.7M (FY2025, up from $0.7M in FY2024)

• Accumulated Deficit: approximately $18.5M as of December 31, 2025



Introducing the Leadership Team of Nasus Pharma Ltd. (NYSE American: NSRX)

Dan Teleman, MBA, M.Sc.

Chief Executive Officer

Dan Teleman, MBA, M.Sc., has served as Chief Executive Officer of Nasus Pharma since January 2025 and as a Director since September 2025. He leads the company's strategic direction, clinical development programs, and capital markets activities as Nasus advances its lead asset NS002 toward a pivotal Phase 3 study.

Eyal Rubin

Executive Vice President and Chief Financial Officer

Eyal Rubin was appointed Executive Vice President and Chief Financial Officer of Nasus Pharma, effective November 20, 2025, bringing more than two decades of financial leadership experience in global biotechnology and pharmaceutical industries. He previously served as CFO and Senior Vice President of Protalix BioTherapeutics, CFO of BrainStorm Cell Therapeutics, and Vice President and Head of Corporate Treasury at Teva Pharmaceutical Industries. Mr. Rubin holds a BA in Business Management and an MBA in Accounting and Finance from Bar-Ilan University, both summa cum laude.

Dr. Dalia Megiddo

Co-Founder, Board Member, and Chief Development Officer

Dr. Dalia Megiddo serves as Co-Founder, Board Member, and Chief Development Officer of Nasus Pharma. She is one of the founding members of the company and has played a central role in the development of the proprietary PBI platform technology and the advancement of the clinical pipeline, including overseeing the NS002 intranasal epinephrine program and the broader product portfolio across acute medical conditions. The company's additional leadership team includes Tair Lapidot, PhD (VP of Research and Development and Clinical Development), Carolina Abrutzky (VP of CMC), Galia Temtsin Krayz, PhD (Director of Product Development), and Yifat Bar (VP of Administration and Human Resources).

We get our information from SEC filings and verified public sources.

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Sources

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https://www.sec.gov/ (NSRX SEC Filings, Form 20-F)

https://www.globenewswire.com/ (Press Releases)

https://www.biospace.com/ (News Coverage)

https://www.tradingview.com/symbols/AMEX-NSRX/

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