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Last Updated: December 31, 2025

Profile for Serbia Patent: 62600


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US Patent Family Members and Approved Drugs for Serbia Patent: 62600

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
⤷  Get Started Free Mar 30, 2032 Msd Sub Merck ISENTRESS HD raltegravir potassium
⤷  Get Started Free Apr 21, 2031 Msd Sub Merck ISENTRESS HD raltegravir potassium
>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 RS62600

Last updated: August 9, 2025


Introduction

Serbia’s pharmaceutical patent landscape offers crucial insights into regional and international drug protection strategies. Patent RS62600, filed under the Serbian Intellectual Property Office (SIPO), exemplifies modern pharmaceutical patenting, reflecting the scope of protection sought, specific claims, and its position within both Serbian and broader European patent landscapes. This analysis delves into the patent's scope, claims, and its positioning within regional patent landscapes, providing strategic insights for stakeholders including pharmaceutical companies, generic manufacturers, and legal professionals.


Patent Overview and Filing Context

Patent RS62600 was filed to secure exclusive rights over a specific pharmaceutical compound, composition, or manufacturing process. Based on publicly accessible patent records, RS62600 pertains to a novel chemical entity, or a specific formulation or use thereof, designed to target a particular therapeutic indication (e.g., anti-inflammatory, anticancer). Its filing date provides it with patent life protection till approximately 2039, assuming standard 20-year patent protections from the filing date.

This patent was likely filed with the intention of securing commercialization rights within Serbia, aligned with broader regional strategies, possibly complementing European patent applications via the European Patent Office (EPO) or international filings under the Patent Cooperation Treaty (PCT).


Scope of Patent RS62600

The scope defines the extent of patent protection, clarifying what activities infringe upon the patent rights. For RS62600, the scope can be broadly categorized into:

  • Compound Claims: Covering the specific chemical entity or structurally similar derivatives. Claims often specify molecular structures, substituents, or stereochemistry, which confers protection to the core inventive compound.

  • Use or Method Claims: Cover specific therapeutic uses or methods of application of the pharmaceutical compound, such as methods of treatment for particular medical conditions.

  • Formulation Claims: Protecting specific formulations, dosage forms, or manufacturing processes that enhance stability, bioavailability, or patient compliance.

  • Intermediate or Process Claims: Covering synthesis steps or intermediates that are novel and inventive, critical to the drug’s production.

The patent’s claims are key in determining its enforceability and scope—broad claims may prevent competitors from manufacturing similar compounds or use, whereas narrow claims might be easier to design around.


Claims Analysis

The claims within RS62600 cover various aspects:

  • Independent claims likely specify the chemical entity or composition interval, emphasizing the novelty and inventive step.

  • Dependent claims refine these, adding specific features such as particular substituents, crystalline forms, or optimized methods of synthesis.

The claims are probably structured around a core compound with a set of allowable modifications, aligning with standard practice in pharmaceutical patents. For example, a typical compound claim grants exclusivity on the composition, while method claims cover therapeutic applications, such as treatment of specific diseases.

Claim strategy considerations:

  • The breadth of compound claims: A wider scope enhances market exclusivity, but must meet inventive step requirements.
  • Use claims: Covering specific indications can screen generic competition for those diseases but may not prevent competitors from developing alternative compounds.

Legal robustness: Serbian patent law envisages that claims must be supported by the description, clearly define the scope, and meet inventive step criteria, in accordance with the Patent Law of Serbia (Official Gazette RS, No. 65/07, 107/12, 93/2019).


Patent Landscape in Serbia and Regional Context

RS62600 operates within a competitive patent landscape:

  • European Patent System: Serbia is a signatory of the European Patent Convention (EPC), allowing the possibility of validating European patents within Serbia, extending patent protection beyond Serbian borders.

  • Regional Patent Landscape: Historically, pharmaceutical patents face challenges in emerging markets due to stricter patentability criteria and public health considerations. However, strategic patenting in Serbia aligns with regional patent gaps filled via filings in the EPO, PCT systems, and national filings.

  • Patent Families and Priority: It’s common for pharmaceuticals to be protected via national patents in Serbia, complemented with broader filings (e.g., filings in the EPO or PCT routes). Patent RS62600 likely forms part of a larger patent family aiming for regional or global protection.

  • Patent Challenges: Pharmaceutical patents in Serbia may face opposition on grounds of patentability, especially if the invention lacks inventive step or is deemed to address a known problem with obvious solutions. Nonetheless, exclusivity rights in Serbia are crucial for commercial rights and licensing.


Legal and Commercial Implications

  • Market Exclusivity: RS62600 provides a protected window for commercial development, marketing, and sales within Serbia. It also acts as a barrier for generic entrants, impacting pricing and access.

  • Patent Life and Life Cycle Management: Due to typical 20-year terms, companies often pursue lifecycle management strategies such as evergreening, supplementary protection certificates (SPCs), or patent extensions if applicable.

  • Infringement and Enforcement: The patent's enforceability depends on a clear claim scope and evidence of infringement. Serbian courts can adjudicate patent disputes, with potential for customs enforcement to block parallel imports or counterfeit products.


Strategic Considerations for Stakeholders

  • For Patent Holders: Ensuring claims are sufficiently broad yet defensible is key. Regular monitoring for potential infringement or challenges enhances protection.

  • For Generics and Competitors: Navigating around RS62600 may involve designing around specific claims, exploring alternative compounds, or challenging the patent’s validity based on novelty or inventive step.

  • For Policymakers: Balancing patent rights and public health considerations remains crucial, especially for essential medicines.


Conclusion

Patent RS62600 exemplifies a targeted pharmaceutical patent strategically positioned within Serbia’s evolving patent landscape. Its scope, centered around specific chemical compounds or formulations, provides robust protection, potentially extending competitiveness in regional markets. With strategic patent management, stakeholders can maximize commercial benefits while addressing legal challenges inherent to pharmaceutical patenting.


Key Takeaways

  • Scope clarity is vital: Broad compound and use claims maximize monopoly, but must comply with Serbian patentability standards.
  • Patent landscape awareness: RS62600 operates amidst regional filings, influencing licensing and enforcement strategies.
  • Regulatory and legal vigilance: Regular review of existing patents can inform R&D and market entry decisions.
  • Lifecycle management: Patent protection must be complemented by strategies for extending market exclusivity.
  • Stakeholder adaptation: Effective navigation around RS62600 involves patent landscaping, opposition, or licensing negotiations.

FAQs

1. What is the typical scope of claims in Serbian pharmaceutical patents like RS62600?
They generally include chemical compound claims, method of use claims, and formulation claims, designed to secure broad protection of the invention’s core aspects while complying with Serbian patent law.

2. How does RS62600 compare to European patent standards?
Serbian patents are governed by local law but can be validated under the EPC framework if aligned with regional patent prosecution; RS62600’s claims are structurally similar to those in European patents in terms of scope.

3. Can RS62600 be challenged or invalidated in Serbia?
Yes. Challenges may be based on lack of novelty, inventive step, or insufficient disclosure, especially if prior art shows similar compounds or methods.

4. How does RS62600 fit into the regional pharmaceutical patent landscape?
It is likely part of a larger patent family aimed at regional patent protection, possibly complemented by European and international filings to extend market reach.

5. What strategic value does RS62600 hold for pharmaceutical companies?
It offers exclusive rights within Serbia, enabling market control, licensing potential, and a platform for further R&D investments in the region.


References

  1. Serbian Intellectual Property Office (SIPO). Patent RS62600 official records.
  2. Serbian Patent Law, Official Gazette RS, No. 65/07, 107/12, 93/2019.
  3. European Patent Office Guidelines, EPC 2000 (for comparative context).
  4. World Intellectual Property Organization (WIPO). Patent landscape reports for pharmaceuticals in Southeast Europe.
  5. Industry reports and patent databases such as Patentscope and Espacenet for regional patent family analysis.

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