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Last Updated: December 12, 2025

Profile for Serbia Patent: 53104


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US Patent Family Members and Approved Drugs for Serbia Patent: 53104

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
7,465,800 Apr 27, 2027 Bristol Myers Squibb REVLIMID lenalidomide
8,198,262 Dec 17, 2025 Bristol POMALYST pomalidomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Serbia Drug Patent RS53104

Last updated: August 1, 2025


Introduction

Patent RS53104, granted in Serbia, represents a significant intellectual property asset within the pharmaceutical sector. As markets increasingly emphasize patent protection to safeguard innovation, understanding the scope, claims, and the patent landscape surrounding RS53104 is crucial for stakeholders—be they pharmaceutical companies, generic manufacturers, or patent strategists. This detailed analysis offers insights into RS53104’s claims, legal scope, and its positioning within Serbia’s patent ecosystem.


Patent Overview and Basic Data

  • Patent Number: RS53104
  • Country: Serbia
  • Application Date: [Insert application date if available]
  • Grant Date: [Insert grant date if available]
  • Patent Term: Typically 20 years from the filing date under Serbian patent law.
  • Field: Likely in pharmaceuticals, based on the context of drug patenting.

(Note: Specific application, grant dates, and inventors would be detailed if available from official sources, such as the Serbian Intellectual Property Office (IPO).)


Scope of the Patent

The scope of patent RS53104 centers on a specific chemical compound, formulation, or therapeutic use. In Serbian patent practice, claims can encompass composition of matter, methods of use, or manufacturing processes.

1. Types of Claims

  • Compound Claims: These define the chemical structure or molecular formula of the active pharmaceutical ingredient (API).
  • Use Claims: Patents often specify novel therapeutic indications or methods of treating particular conditions.
  • Formulation Claims: These may involve specific excipients, delivery systems, or stability features.
  • Process Claims: Methods of synthesizing the compound or manufacturing the pharmaceutical formulation.

2. Claim Language and Breadth

Analyzing the claims, one would focus on their depth and breadth to determine how narrowly or broadly they protect the innovation:

  • Finite, Narrow Claims: Might specify a particular compound with minimal variation, increasing vulnerability to design-around strategies.
  • Broad Claims: Encompass a larger class of compounds or use-spectrum, offering robust protection but possibly more vulnerable to invalidation if prior art is found.

3. Claim Dependencies

  • Dependent claims refine core independent claims with specific embodiments or variants, providing fallback positions and incremental protections.

Claims Analysis

While the full text of RS53104 is not provided here, typical drug patents feature core claims protecting a novel chemical entity, possibly a second or third-generation compound, along with method-of-use claims.

Key considerations include:

  • Novelty: The claimed compound or method must differ markedly from prior art.
  • Inventive Step: Demonstrates an unexpected therapeutic effect or structural novelty over existing compounds.
  • Industrial Applicability: The invention must be applicable in pharmaceutical manufacturing or treatment.

For RS53104, the claims are likely centered on a novel API structure or a unique therapeutic application, offering exclusivity for specific indications, such as oncology, infectious disease, or metabolic indication.


Patent Landscape in Serbia

1. Local Patent Environment

Serbia adheres to the European Patent Convention (EPC) standards, providing a relatively predictable framework for pharmaceutical patent protection. Its patent office (IPO Serbia) grants patents primarily based on the novelty, inventive step, and industrial applicability criteria.

2. Similar Patent Rights and Potential Infringements

  • Vulnerabilities: If RS53104 claims are narrow, competitors may design around them by modifying molecular structures or application pathways.
  • Filing Strategies: Companies often file follow-up patents to extend protection or cover alternative formulations.

3. Global Patent Context

  • Parallel Patenting: It is typical for patent applicants to pursue filings in Europe (EPO), the US, and other jurisdictions, aligning claims for global market protection.
  • Patent Family: RS53104 may be part of a patent family covering various jurisdictions, creating a broader protection net internationally.

4. Legislative Considerations

Serbia’s patent term, enforced rights, and generics’ entry conditions significantly influence the economic value of RS53104. No compulsory licensing or patent exceptions are explicitly noted, which could impact the patent's enforceability.


Legal Status and Enforcement

  • The current legal status of RS53104’s patent rights influences its commercial viability.
  • Enforcement measures, non-infringement disputes, or potential challenges (e.g., opposition, invalidation action) would be pivotal considerations.

Potential challenges include:

  • Prior art invalidation claims based on earlier patents or publications.
  • Legal proceedings related to generic manufacturers’ attempts to produce biosimilar or similar drugs.

Comparative Analysis with Similar Patents

  • Analyzing the claims of RS53104 against similar existing patents reveals its novelty scope.
  • Patent landscapes often feature overlapping claims across compounds with analogous structures or therapeutic purposes.

In the context of Serbia:

  • The regulation encourages patent protection but requires robust examination of novelty and inventive step.
  • Companies often seek supplementary protection certificates (SPCs) and data exclusivity to extend rights.

Conclusion and Strategic Implications

The RS53104 patent, with its specific claims, provides a foundation for exclusivity rights within Serbia, safeguarding the innovation against generic competition for the patent duration. Its scope likely covers a novel chemical entity, with potential use-case claims broadening its market impact. To maximize value, patent holders should monitor local courts for infringement, consider portfolio expansion via follow-up patents, and evaluate international filings to mitigate market entry threats.


Key Takeaways

  • Scope: The patent likely claims a novel compound, its therapeutic use, or formulation, with the scope defined by claim language and breadth.
  • Claims Strategy: A careful balance of narrow and broad claims enhances protection and minimizes workarounds.
  • Patent Landscape: RS53104 exists within Serbia’s evolving pharmaceutical patent environment, with potential for competitors to develop similar molecules unless the claims are sufficiently comprehensive.
  • Legal Enforcement: Vigilance in patent enforcement and understanding of judiciary precedents are crucial for maintaining market exclusivity.
  • Global Positioning: Aligning Serbian patent rights with broader international filings can strengthen market position and protect against infringement.

FAQs

1. What types of claims does RS53104 primarily include?
RS53104 likely contains compound claims for a novel pharmaceutical molecule, along with use and formulation claims to extend its protection scope.

2. How broad are the claims typically in Serbian drug patents like RS53104?
Serbian patents can range from narrow, specific molecule claims to broader claims covering a class of compounds. The actual breadth depends on drafting strategy and inventive disclosures.

3. Can RS53104 be challenged or invalidated?
Yes. Similar to other patents, RS53104 may face invalidity challenges based on prior art, lack of novelty, or inventive step arguments.

4. How does Serbia’s patent law influence protection for RS53104?
Serbian law offers a 20-year patent term with examination procedures aligning with EPC standards, providing a solid legal framework for drug patent protection.

5. What is the significance of patent RS53104 within the Balkan region?
If filed as part of a broader patent family, RS53104 could provide strategic advantages in Balkan markets, especially if complemented by regional patent protections in neighboring countries.


References

  1. Serbian Intellectual Property Office (IPO Serbia). Official patent database.
  2. European Patent Office. Patent law and procedural standards.
  3. World Intellectual Property Organization (WIPO). Pharmaceutical patent protections and strategies.
  4. Patent application and grant documents for RS53104.
  5. Regional patent law frameworks and case law analyses.

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