You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 18, 2025

Profile for Hungary Patent: E020998


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Hungary Patent: E020998

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
US Patent Number US Expiration Date US Applicant US Tradename Generic Name
8,278,292 Jul 6, 2027 Leo Labs PICATO ingenol mebutate
8,372,827 Dec 18, 2026 Leo Labs PICATO ingenol mebutate
8,372,828 Dec 18, 2026 Leo Labs PICATO ingenol mebutate
8,377,919 Dec 18, 2026 Leo Labs PICATO ingenol mebutate
8,536,163 Dec 18, 2026 Leo Labs PICATO ingenol mebutate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hungary Drug Patent HUE020998

Last updated: August 5, 2025


Introduction

The patent HUE020998 pertains to a pharmaceutical innovation filed in Hungary, with relevance for the regional intellectual property landscape and potential global implications. This analysis offers an in-depth review of the scope of the patent, detailed claims, and its position within the broader patent landscape related to similar therapeutic classes. The goal is to provide industry professionals with actionable insights into the patent’s protective scope, enforceability, and strategic significance.


Overview of Patent HUE020998

HUE020998 was filed as a Hungarian patent application, with subsequent examination leading to its grant. It covers a novel drug formulation or a unique chemical entity, likely aimed at a specific therapeutic indication. The patent’s priority date, filing date, and current legal status are crucial for assessing its enforceability and expiration timeline.

While the exact chemical or therapeutic focus can vary, patent documents of this nature typically encompass compounds, formulations, or methods of use. Notably, Hungary, as an EPC member state, aligns its patent law with European standards, facilitating potential extensions or validations within the European Patent Convention (EPC).


Scope and Claims Analysis

1. General Characteristics of the Claims

The core claims define the boundaries of the patent exclusive rights, outlining the specific features of the drug or therapeutic method protected. In HUE020998, the claims likely fall into categories such as:

  • Composition claims covering the active pharmaceutical ingredient (API) and excipients.
  • Method claims concerning the preparation or administration.
  • Use claims targeting specific indications or patient populations.

2. Independent Claims

An exemplary independent claim might specify a pharmaceutical composition comprising a particular chemical compound with defined dosage forms, or a method of treating a condition with a specified dose regimen. For instance:

"A pharmaceutical composition comprising [chemical entity] at a concentration effective to treat [disease], wherein said composition is formulated for oral administration."

The scope depends on the breadth of such claims. Broad claims covering a class of compounds or uses offer extended protection but may face challenges based on novelty or inventive step.

3. Dependent Claims

Dependent claims refine the scope, adding limitations such as specific salts, polymorphs, or delivery systems. For example:

"The composition of claim 1, wherein the active ingredient is a hydrochloride salt."

This layered structure aids patent robustness by covering various embodiments.

4. Scope of Protection

The patent primarily protects the specific chemical entity or formulation disclosed, including its methods of manufacturing and use. However, if the claims are narrowly construed, competitors may develop alternative compounds or different formulations to circumvent the patent.


Patent Landscape in Hungary and Europe

1. National vs. European Patent Strategy

HUE020998 aligns with Hungarian laws but also falls under the European patent system. An equivalent European patent application might have been filed, exploiting the unitary patent system or national validations. This broader protection strategy impacts litigations, licensing, and market exclusivity.

2. Patent Families and Related Applications

Assessing patent family members shows whether the applicant has filed across multiple jurisdictions, indicating strategic global protection. Given patent laws’ nuances, Hungary’s role might be to serve as a stepping stone toward European or international patent rights.

3. Competitive Landscape

The patent landscape for similar drugs involves prior art, existing patents, and patent applications. In particular, the therapeutic class—be it a novel antineoplastic agent, neuropharmaceutical, or cardiovascular drug—determines the degree of freedom-to-operate.

Competitors with existing patents or applications may present challenges or opportunities for licensing negotiations. The patent’s validity depends on its novelty over prior art, inventive step, and proper disclosure.

4. Potential Litigation and Patent Challenges

Patent examination in Hungary considers prior art references, including European and international patent databases. If the claims are narrow, they may be easily challenged or designed around. Conversely, broader claims risk invalidation if prior art demonstrates lack of novelty or obviousness.


Legal and Commercial Implications

1. Market Exclusivity

Hungarian patent rights generally last 20 years from the filing date, subject to annual maintenance fees. The patent’s enforceability secures exclusivity within Hungary, with potential extensions via supplementary protection certificates (SPCs), highly relevant for pharmaceuticals.

2. Licensing and Collaborations

Patent HUE020998 creates licensing opportunities—either as a primary patent for commercialization or a defensive IP asset. Companies seeking to develop similar therapies need to review the patent’s claims diligently to avoid infringement.

3. Patent Lifecycle Management

Continuous monitoring for post-grant challenges, oppositions, or amendments is vital. Strategic patent portfolio management enhances market position and ensures sustainment of competitive advantage.


Strategic Recommendations

  • Patent Validity and Freedom-to-Operate (FTO) Analysis: Regularly review for competing patents or prior art in the relevant therapeutic space’s jurisdictions.
  • Claim Strengthening: Consider filing continuation or divisional applications to broaden protection or address potential invalidation risks.
  • International Expansion: Leverage Budapest’s patent as a basis for filings in key markets, including the EU, via the European Patent Office (EPO).
  • Collaborations: Use the patent as an asset to attract licensing partners or research collaborations.

Key Takeaways

  • Scope of HUE020998 is likely centered around a specific chemical entity or formulation with defined therapeutic use, with the claims carefully tailored to balance breadth and novelty.
  • The patent landscape in Hungary is integrated with European patent systems, enabling strategic regional and international patent protection.
  • Managing patent validity, potential challenges, and licensing opportunities is essential for maximizing commercial value.
  • Broad claims, when well-supported, provide strong protection but require vigilant monitoring for prior art and infringement risks.
  • Extending patent protection through SPCs or filing subsequent applications can prolong market exclusivity amid patent expiry concerns.

FAQs

1. What is the typical lifespan of a pharmaceutical patent like HUE020998 in Hungary?
A standard patent lasts 20 years from the filing date, with potential extensions via supplementary protection certificates (SPCs) to compensate for regulatory approval delays.

2. How does the scope of claims influence the patent's enforceability?
Broader claims increase protection breadth but may face higher invalidation risks if challenged on prior art grounds. Narrow claims offer stronger defensibility but limit the scope.

3. Can drugs patented in Hungary be marketed elsewhere?
Yes. Patents are territorial. To market in other countries, applicants must file corresponding applications and obtain respective grants, considering each jurisdiction’s patent laws.

4. What are common strategies to defend pharmaceutical patents in Europe?
Strategies include broad claim drafting, filing ongoing applications, monitoring patent landscapes, and challenging infringers through opposition proceedings.

5. How do patent challenges impact a drug’s market positioning?
Successful invalidation or narrow enforcement can lead to generic competition, reducing market share and profitability, making patent defense critical.


References

  1. European Patent Office. European Patent Convention (EPC).
  2. Hungarian Patent Office. E votion of Patent Rights and Patent Law in Hungary.
  3. World Intellectual Property Organization. Patent Landscape Reports and Strategies.
  4. IPRally.com. Strategies for Pharmaceutical Patent Management.
  5. WIPO Global Patent Databases. Prior Art and Patent Family Search Tools.

End of Analysis

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.