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Hoth Therapeutics Awarded U.S. Patent for Cancer-Fighting HT-KIT Oncology Platform

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Hoth Therapeutics (NASDAQ:HOTH)/b) received a U.S. Patent and Trademark Office Notice of Allowance for its HT-KIT antisense oncology platform, targeting MS4A6A pre-mRNA splicing to reduce surface expression of the high-affinity IgE receptor (FcεRI).Key highlights include composition-of-matter coverage for the lead antisense oligomer (SEQ ID NO: 22), mechanistic differentiation via exon-skipping upstream of histamine release, and method claims spanning asthma, atopic dermatitis, chronic rhinitis, allergic conjunctivitis, chronic sinusitis, anaphylaxis prevention, mastocytosis, and mast cell tumors. The patent strengthens the intellectual property basis for HT-KIT, an orphan drug–designated mast cell program, and supports future dual-target compositions combining MS4A6A and FcεRIβ (MS4A2) antisense oligomers.

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Positive

  • USPTO Notice of Allowance for HT-KIT antisense therapeutic
  • Composition-of-matter coverage for lead oligomer SEQ ID NO: 22
  • Patent supports broad allergic and mast cell–driven disease indications
  • Strengthens IP foundation for orphan drug–designated HT-KIT program
  • Claims enable potential dual-target MS4A6A and MS4A2 antisense strategies

Negative

  • None.

News Market Reaction – HOTH

+2.65% 99.2x vol
91 alerts
+2.65% Session close to close
+182.2% Peak Tracked
-2.9% Trough Tracked
$29.46M Market Cap
99.2x Rel. Volume

In the May 26 session, HOTH gained 2.65%, reflecting a moderate positive market reaction. Argus tracked a peak move of +182.2% during that session. Argus tracked a trough of -2.9% from its starting point during tracking. Our momentum scanner triggered 91 alerts that day, indicating high trading interest and price volatility. Trading volume was exceptionally heavy at 99.2x the daily average, suggesting very strong buying interest.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement details a U.S. patent Notice of Allowance for Hoth’s HT-KIT mast cell platform, se...
Analysis

This announcement details a U.S. patent Notice of Allowance for Hoth’s HT-KIT mast cell platform, securing composition-of-matter coverage for antisense oligomers (including SEQ ID NO: 22) and methods targeting MS4A6A pre-mRNA splicing to reduce FcεRI expression. The claims span multiple allergic and mast cell–driven indications and reinforce HT-KIT’s orphan drug–designated status. Investors may track how this strengthened IP interacts with the company’s capital-raising capacity under its $50 million shelf and ongoing strategic pivot.

Key Figures

Oligomer length range: 25–50 linked nucleosides Lead sequence ID: SEQ ID NO: 22
2 metrics
Oligomer length range 25–50 linked nucleosides Length of antisense oligomers covered by allowed patent claims
Lead sequence ID SEQ ID NO: 22 Lead antisense oligomer covered by composition-of-matter claims

Historical Context

5 past events · Latest: May 19 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 19 Strategic pivot / acquisition Positive -2.1% Announced AI semiconductor pivot and exclusive rights to acceleration technology.
May 05 Clinical trial update Positive +4.2% Spain Phase 2a authorization and positive interim HT-001 efficacy data.
Apr 14 Preclinical data release Positive +26.2% HT-VA preclinical data showing liver fat metabolism improvements vs semaglutide.
Apr 13 Preclinical data release Positive +26.2% Positive HT-VA CRADA data reprogramming liver fat metabolism pathways.
Apr 02 Equity offering Negative +3.0% Closed $2.0M registered direct offering with concurrent warrants.

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

Pattern Detected

Recent positive R&D updates often aligned with strong upside moves, while financing and pivot news showed mixed or divergent reactions.

Recent Company History

Over the last few months, HOTH has reported multiple pipeline and strategic developments. Positive preclinical HT-VA data on Apr 13–14, 2026 coincided with strong gains of 26.18%. A Phase 2a update for HT-001 on May 5, 2026 saw a more modest 4.15% rise. In contrast, an AI semiconductor pivot announcement on May 19, 2026 led to a -2.07% move, and an equity financing on Apr 2, 2026 rose 3.04% despite its dilutive nature. Today’s IP-focused mast-cell patent news fits the pattern of science-driven catalysts moving the stock independently of sector trends.

Key Terms

composition-of-matter, antisense oligomers, pre-mRNA splicing, IgE, +2 more
6 terms
composition-of-matter regulatory
"Allowed Claims Cover Composition-of-Matter and Methods Targeting MS4A6A..."
A composition-of-matter is a legal description of a specific chemical or biological substance or mixture—think of it as the exact recipe and ingredients that make up a drug, material, or chemical product. For investors, ownership of a composition-of-matter patent can act like a locked recipe that keeps competitors out, protecting future sales and profit margins and reducing the risk that a product will be easily copied.
antisense oligomers medical
"The allowed claims cover antisense oligomers of 25 to 50 linked nucleosides..."
Short, lab-made strands of genetic code designed to stick to a specific cellular instruction (messenger RNA) and block or alter the production of a target protein; think of them as a sticky note placed over a line in a recipe so that step can’t be followed. Investors watch antisense oligomers because they form a platform for drugs that can precisely target genetic causes of disease, so clinical trial results, manufacturing progress, or regulatory decisions can rapidly change a developer’s value.
pre-mRNA splicing medical
"...targeting MS4A6A pre-mRNA splicing to Reduce Surface Expression..."
Pre-mRNA splicing is the cellular process that edits a newly copied RNA message by cutting out non-coding bits and joining the remaining pieces so a correct blueprint for a protein is produced; think of it like film editing, where raw footage is cut and stitched into the final scene. For investors, splicing matters because errors or deliberate changes in this editing can cause disease or be targeted by drugs and diagnostics, influencing the commercial value and risk of biotech and pharmaceutical programs.
IgE medical
"...High-Affinity IgE Receptor (FcεRI); Strengthens Intellectual Property..."
IgE (immunoglobulin E) is a type of antibody the immune system makes in response to allergens and certain parasites; it acts like a sensor that triggers allergy reactions when it binds to a allergen. For investors, IgE levels matter because many allergy and asthma drugs, diagnostics, or tests are designed to reduce or measure IgE activity—so changes in IgE can indicate whether a treatment is likely to work or how a product might be used in the market.
FcεRI medical
"...Reduce Surface Expression of the High-Affinity IgE Receptor (FcεRI)..."
A high‑affinity IgE receptor found on certain immune cells that acts like an alarm sensor: when it binds the allergy antibody IgE it triggers release of chemicals that cause allergic reactions. Investors watch this protein because it is a common drug target and diagnostic marker—therapies that block or modulate it can prevent symptoms, affect clinical trial outcomes, regulatory approval prospects, and market potential for allergy and asthma treatments.
orphan drug–designated regulatory
"...HT-KIT, the Company's orphan drug–designated program for mast cell–driven disease."
A medicine that is "orphan drug–designated" has received a special regulatory status because it targets a rare disease or condition with very few treatment options. Regulators grant this to encourage development by offering incentives such as tax breaks, fee waivers, and a period of exclusive sales once approved; for investors, that can mean lower development risk, potential pricing power, and reduced competition in a small but often high-value market.

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

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Allowed Claims Cover Composition-of-Matter and Methods Targeting MS4A6A Pre-mRNA Splicing to Reduce Surface Expression of the High-Affinity IgE Receptor (FcεRI); Strengthens Intellectual Property Foundation Underlying the HT-KIT Mast Cell Program

HOBOKEN, N.J., May 26, 2026 /PRNewswire/ -- Hoth Therapeutics, Inc. (NASDAQ: HOTH) ("Hoth" or the "Company"), a clinical-stage biopharmaceutical company, today announced that the U.S. Patent and Trademark Office ("USPTO") has issued a Notice of Allowance for Hoth's HT-KIT therapeutic.

The allowed claims cover antisense oligomers of 25 to 50 linked nucleosides directed to splicing-relevant regions of the MS4A6A pre-mRNA, including intron 3, exon 4, and the intron 3/exon 4 junction, together with pharmaceutical compositions and methods for modulating MS4A6A mRNA splicing in cells or tissues. Hybridization of the disclosed oligomers is intended to reduce cell-surface expression of the high-affinity IgE receptor (FcεRI), a central driver of mast cell activation in allergic and inflammatory disease.

Strategic Importance

  • Foundational IP Position. Allowance establishes composition-of-matter coverage for the Company's lead antisense oligomer (SEQ ID NO: 22), including modified, morpholino, and pharmaceutical composition embodiments, providing a defensible basis for the underlying chemistry of the platform.
  • Mechanistic Differentiation. By reducing surface expression of FcεRI via exon-skipping of MS4A6A pre-mRNA, the approach addresses a node upstream of histamine release and IgE-mediated degranulation, distinct from antihistamine, anti-IgE antibody, and small-molecule mast cell inhibitor approaches.
  • Broad Indication Coverage. Allowed method claims and related disclosures span asthma, atopic dermatitis, chronic rhinitis, allergic conjunctivitis, chronic sinusitis, anaphylaxis prevention, and mast cell–driven diseases including mastocytosis and mast cell tumors.
  • Reinforces HT-KIT. The allowed claims strengthen the intellectual property foundation underlying HT-KIT, the Company's orphan drug–designated program for mast cell–driven disease.
  • Combination Optionality. The application as filed also describes combination approaches with antisense oligomers targeting FcεRIβ (MS4A2) pre-mRNA splicing, supporting future development of dual-target compositions.

Management Commentary

"This Notice of Allowance is a meaningful validation of the science underlying our mast cell platform and an important addition to the intellectual property foundation supporting HT-KIT," said Robb Knie, Chief Executive Officer of Hoth Therapeutics.

About HT-KIT

HT-KIT is Hoth Therapeutics' orphan drug–designated program directed at mastocytosis and other mast cell–driven diseases. The program is built around antisense oligomer–mediated modulation of pre-mRNA splicing to reduce pathological mast cell signaling. Hoth expects to finalize its IND submission in 2026, followed by first-in-human studies.

Biotechnology Operations Continue Under Subsidiary Structure
The Company 's is exploring placing its biotechnology pipeline and therapeutic development programs under a separate, wholly owned subsidiary with dedicated management and operational resources. The restructuring is intended to preserve the value of the biotechnology portfolio for shareholders while enabling the parent company to pursue emerging opportunities in AI semiconductor infrastructure and advanced computing technologies.

About Rocket One, Inc.
Rocket One Inc. is focused on the development and commercialization of spintronic computing technologies for artificial intelligence hardware acceleration and radiation-tolerant computing applications. The Company holds exclusive rights to technologies licensed for nanomagnetic matrix multiplier architecture designed as a hardware accelerator for machine learning and artificial intelligence workloads, and a skyrmion-based spintronic memory technology with potential applications in radiation-tolerant computing for defense and space systems.

About Hoth Therapeutics, Inc.

Hoth Therapeutics is a clinical-stage biopharmaceutical company dedicated to developing innovative, impactful, and ground-breaking treatments with a goal to improve patient quality of life. We are a catalyst in early-stage pharmaceutical research and development, elevating drugs from the bench to pre-clinical and clinical testing. Utilizing a patient-centric approach, we collaborate and partner with a team of scientists, clinicians, and key opinion leaders to seek out and investigate therapeutics that hold immense potential to create breakthroughs and diversify treatment options. To learn more, please visit https://ir.hoththerapeutics.com/.

Forward-Looking Statement
This press release includes forward-looking statements based upon Hoth's current expectations, which may constitute forward-looking statements for the purposes of the safe harbor provisions under the Private Securities Litigation Reform Act of 1995 and other federal securities laws, and are subject to substantial risks, uncertainties, and assumptions. These statements concern Hoth's business strategies; the timing of regulatory submissions; the ability to obtain and maintain regulatory approval of existing product candidates and any other product candidates we may develop, and the labeling under any approval we may obtain; the timing and costs of clinical trials, and the timing and costs of other expenses; market acceptance of our products; the ultimate impact of the current coronavirus pandemic, or any other health epidemic, on our business, our clinical trials, our research programs, healthcare systems, or the global economy as a whole; our intellectual property; our reliance on third-party organizations; our competitive position; our industry environment; our anticipated financial and operating results, including anticipated sources of revenues; our assumptions regarding the size of the available market, benefits of our products, product pricing, and timing of product launches; management's expectation with respect to future acquisitions; statements regarding our goals, intentions, plans, and expectations, including the introduction of new products and markets; and our cash needs and financing plans. There are a number of factors that could cause actual events to differ materially from those indicated by such forward-looking statements. You should not place reliance on these forward-looking statements, which include words such as "could," "believe," "anticipate," "intend," "estimate," "expect," "may," "continue," "predict," "potential," "project" or similar terms, variations of such terms, or the negative of those terms. Although the Company believes that the expectations reflected in the forward-looking statements are reasonable, the Company cannot guarantee such outcomes. Hoth may not realize its expectations, and its beliefs may not prove correct. Actual results may differ materially from those indicated by these forward-looking statements as a result of various important factors, including, without limitation, market conditions and the factors described in the section titled "Risk Factors" in Hoth's most recent Annual Report on Form 10-K and Hoth's other filings made with the U. S. Securities and Exchange Commission. All such statements speak only as of the date made. Consequently, forward-looking statements should be regarded solely as Hoth's current plans, estimates, and beliefs. Investors should not place undue reliance on forward-looking statements. Hoth cannot guarantee future results, events, levels of activity, performance, or achievements. Hoth does not undertake and specifically declines any obligation to update, republish, or revise any forward-looking statements to reflect new information, future events, or circumstances or to reflect the occurrences of unanticipated events, except as may be required by applicable law.

Investor Contact:
LR Advisors LLC
Email: investorrelations@hoththerapeutics.com
www.hoththerapeutics.com
Phone: (678) 570-6791

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/hoth-therapeutics-awarded-us-patent-for-cancer-fighting-ht-kit-oncology-platform-302781296.html

SOURCE Hoth Therapeutics, Inc.

FAQ

What patent did Hoth Therapeutics (NASDAQ:HOTH) receive for its HT-KIT platform on May 26, 2026?

Hoth Therapeutics received a USPTO Notice of Allowance covering its HT-KIT antisense therapeutic platform. According to Hoth Therapeutics, the allowed claims span composition-of-matter for its lead oligomer, related pharmaceutical compositions, and methods for modulating MS4A6A pre-mRNA splicing to affect FcεRI expression.

How does Hoth Therapeutics' HT-KIT patent target MS4A6A pre-mRNA splicing for HOTH shareholders?

The HT-KIT patent covers antisense oligomers targeting MS4A6A pre-mRNA splicing to reduce FcεRI surface expression. According to Hoth Therapeutics, hybridization in splicing-relevant regions is intended to modulate mast cell activation, potentially supporting development across multiple allergic and mast cell–driven indications.

Which diseases are included in the allowed method claims for Hoth Therapeutics' HT-KIT patent (HOTH)?

The allowed method claims span several allergic and mast cell–driven diseases. According to Hoth Therapeutics, these include asthma, atopic dermatitis, chronic rhinitis, allergic conjunctivitis, chronic sinusitis, anaphylaxis prevention, and mast cell–driven conditions such as mastocytosis and mast cell tumors.

What is the strategic importance of the HT-KIT composition-of-matter coverage for Hoth Therapeutics stock (HOTH)?

The composition-of-matter coverage establishes IP around Hoth's lead antisense oligomer SEQ ID NO: 22. According to Hoth Therapeutics, this includes modified, morpholino, and pharmaceutical composition embodiments, providing a defensible basis for the underlying chemistry of the HT-KIT mast cell platform.

How is Hoth Therapeutics' HT-KIT mechanism differentiated from antihistamines and anti-IgE antibodies for investors?

HT-KIT aims to reduce FcεRI surface expression via exon-skipping of MS4A6A pre-mRNA, acting upstream of histamine release. According to Hoth Therapeutics, this differs from antihistamines, anti-IgE antibodies, and small-molecule mast cell inhibitors that target downstream pathways or different molecular nodes.

Does the HT-KIT patent allow combination antisense approaches for Hoth Therapeutics (HOTH)?

The patent application describes potential combination approaches with antisense oligomers targeting FcεRIβ (MS4A2) pre-mRNA. According to Hoth Therapeutics, this supports future development of dual-target compositions that could modulate multiple components of the high-affinity IgE receptor complex in mast cell disease.