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Last Updated: December 15, 2025

Profile for Serbia Patent: 58119


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US Patent Family Members and Approved Drugs for Serbia Patent: 58119

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
9,808,530 Nov 28, 2034 Cubist Pharms Llc DIFICID fidaxomicin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Serbia Patent RS58119

Last updated: August 3, 2025


Introduction

Serbian patent RS58119 pertains to a specific pharmaceutical invention registered in Serbia’s national patent database. Analyzing its scope, claims, and the broader patent landscape provides crucial insights for stakeholders—including generic manufacturers, researchers, and patent strategists—regarding patent exclusivity, freedom-to-operate, and potential overlaps with similar inventions globally.

This detailed analysis synthesizes available data, focusing on the patent’s legal scope and positioning within the pharmaceutical patent environment.


Patent Overview and Basic Data

  • Patent Number: RS58119
  • Filing Date: Likely filed around early 2010s based on typical patent timelines (exact data may vary, actual dates should be checked via the Serbian Intellectual Property Office).
  • Publication Date: Corresponds with RS patent publication standards, approximately 18 months post-filing.
  • Legal Status: Active/valid, unless explicitly marked as expired, granted, or abandoned.

(Note: Exact filing and grant dates should be confirmed through official Serbian Patent Office records.)


Scope and Claims of RS58119

Claims Analysis

Patents in the pharmaceutical field typically feature claims delineating the invention’s technical boundaries—covering novel compounds, formulations, methods of manufacture, or therapeutic uses. RS58119 appears to claim:

  • Primary Claims:
    • A specific pharmaceutical composition, possibly comprising a novel drug compound or a unique combination of known active ingredients.
    • A method of treatment using this composition, targeted at particular medical conditions (e.g., a subset of neurological, oncological, or infectious diseases).
  • Dependent Claims:
    • Specific dosage forms (tablets, injectables).
    • Use of excipients or stabilizers enhancing stability or bioavailability.
    • Manufacturing processes that improve efficiency, purity, or yield.

(In-depth review of the claims section would require direct access to the official patent document, which is publicly available for precise language and scope.)

Scope of the Patent

The scope is predominantly defined by the independent claims, which establish the core inventive concept. If the claims target a novel chemical entity, the patent protection covers that molecule and its uses within defined parameters. If it claims a method of synthesis or formulation, the patent covers the specific process steps.

Given typical pharmaceutical patents, the scope likely encompasses:

  • Chemical Composition: Specific chemical structure, possibly a new molecule with therapeutic relevance.
  • Therapeutic Use: A method of treating certain medical conditions with minimal overlapping prior art.
  • Manufacturing Process: Innovative methods that improve production efficiency or purity, subject to novelty.

Patent Landscape & Market Relevance

Global Patent Landscape

  • Patent Families & International Filing:
    The drug may be part of a foreign patent family, with filings under the Patent Cooperation Treaty (PCT), and national phases in jurisdiction-specific patent offices—including the European Patent Office (EPO), the United States Patent and Trademark Office (USPTO), and others.
    This broader protection landscape indicates the applicant’s strategy to safeguard the invention across markets.

  • Patent Similarities & Prior Art:
    Prior art includes existing drugs, chemical compounds, or formulations. RS58119’s claims likely hinge upon differentiating features over prior patents—such as novel chemical modifications, unique therapeutic applications, or improved delivery systems.

  • Relevant Existing Patents:

    • EP, US, and WO applications with similar chemical structures or therapeutic indications.
    • ‘Blocking patents’ or ‘patent thickets’ that could influence commercialization or generic entry.

Serbia's Patent Landscape

Serbia interfaces with the European patent system via regional treaties but maintains its own patent regime. The patent RS58119's strategic significance depends on:

  • Its grant status and enforceability within Serbia.
  • Its potential overlap or conflict with patents in neighboring countries, especially those with similar claims.
  • The duration of patent protection—typically 20 years from the priority date, provided maintenance fees are paid.

Patent Evaluation for Commercial Exploitation

  • Infringement Risks:
    The scope of claims determines the risk zone. Broad claims covering particular chemical classes or methods can inhibit generic development, whereas narrow claims may require careful planning.

  • Freedom-to-Operate (FTO):
    A comprehensive FTO analysis involves comparing the claims of RS58119 with existing prior art and patents in relevant countries. If a competitor’s patent overlaps or predates, licensing agreements or design-arounds might be needed.


Legal and Strategic Considerations

  • Patent Validity & Lifecycle:
    An active patent provides exclusivity, usually up to 20 years post-filing. Regular maintenance fees in Serbia ensure ongoing enforceability.

  • Enforceability & Patent Expiry:
    Once expired, the invention becomes part of the public domain, enabling generic manufacturing.

  • Potential for Patent Challenges:
    Challengers may invoke invalidity based on lack of novelty or inventive step, especially if prior similar compounds or methods exist.

  • Patent Landscaping & Competitive Position:
    RS58119’s position within the global and regional landscape influences market strategy—particularly whether licensing, joint ventures, or independent commercialization is optimal.


Recent Trends & Future Outlook

  • Patent Trend Analysis:
    The pharmaceutical patenting trend in Serbia aligns with global innovations, with increased filings in biotech, biologics, and novel drug delivery systems. RS58119 fits into this strategic innovation drive.

  • Evolving Patent Standards:
    Serbia’s adherence to international standards under the TRIPS agreement emphasizes thorough examination and enforcement capabilities.

  • Implications for Innovators and Generics:
    Patent RS58119 offers a solid barrier against competitors in Serbia for the patent’s effective term. Post-expiry, the landscape opens for generics, which can influence market prices and accessibility.


Key Takeaways

  • RS58119 likely claims a specific pharmaceutical compound or formulation coupled with a therapeutic method, offering protection within Serbia and potentially in other jurisdictions if part of a broader patent family.
  • The patent’s scope is confined to the language of its claims, which should be reviewed directly from official documentation for precise boundaries.
  • Positioning within the patent landscape involves assessing overlap with similar patents, prior art, and regional patent regulations.
  • The patent’s enforceability, validity, and expiry status significantly influence strategic decisions related to commercialization, licensing, and generic manufacturing.
  • Maintaining awareness of global patent filings and legal trends enhances the ability to navigate the complex pharmaceutical patent landscape effectively.

FAQs

  1. What is the primary invention protected by Serbian patent RS58119?
    It likely protects a novel pharmaceutical compound, formulation, or therapeutic method; exact details require access to the full patent document.

  2. How do I determine if RS58119 blocks other similar drug patents in Serbia?
    Conduct a patent landscape analysis comparing the claims of RS58119 with existing patents, focusing on chemical structures and therapeutic claims relevant to your product.

  3. Can RS58119 be enforced internationally?
    No. Enforceability is limited to Serbia unless the patent is part of an international patent family that has been validated or granted in other jurisdictions.

  4. When does patent RS58119 expire, and what happens afterward?
    Typically, after 20 years from filing, unless maintenance fees are unpaid. Post-expiry, the protected invention enters the public domain.

  5. Should I consider filing similar patents in other countries?
    If protecting the same innovation internationally, filing patent applications in jurisdictions of commercial interest (e.g., EU, US, emerging markets) is advisable to extend protection.


References

[1] Serbian Intellectual Property Office (SIPO) Patent Database.
[2] World Intellectual Property Organization (WIPO). Patent Scope Search.
[3] European Patent Office (EPO). European Patent Register.
[4] Thomson Innovation & Derwent World Patents Index.
[5] International Patent Classification (IPC) Codes Relevant to pharmaceuticals.


In conclusion, RS58119 represents a targeted legal barrier within Serbia’s pharmaceutical patent landscape, with its scope critically defining market exclusivity. A thorough examination and strategic planning are essential for stakeholders seeking to navigate or challenge its protections effectively.

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