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Last Updated: December 12, 2025

Profile for Serbia Patent: 64845


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US Patent Family Members and Approved Drugs for Serbia Patent: 64845

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
7,635,704 Apr 26, 2027 Gilead Sciences Inc GENVOYA cobicistat; elvitegravir; emtricitabine; tenofovir alafenamide fumarate
7,635,704 Apr 26, 2027 Gilead Sciences Inc STRIBILD cobicistat; elvitegravir; emtricitabine; tenofovir disoproxil fumarate
7,635,704 Apr 26, 2027 Gilead Sciences Inc VITEKTA elvitegravir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Serbia Patent RS64845

Last updated: July 27, 2025


Introduction

Patent RS64845, granted in Serbia, represents a significant intellectual property asset within the pharmaceutical sector. Its scope and claims delineate the legal boundaries of the invention, influencing market exclusivity, licensing opportunities, and potential infringements. Analyzing these aspects in the context of Serbia’s patent landscape provides insights essential for stakeholders—including pharmaceutical companies, generic manufacturers, and legal professionals—to strategize effectively.


Overview of Patent RS64845

Patent Title and Filing Details:

While specific details such as the patent's title are not provided here, RS64845 pertains to a pharmaceutical invention registered in Serbia. It is essential to contextualize the patent within Serbia’s patent framework, governed by the Law on Patents (Official Gazette of the Republic of Serbia, No. 62/2004, and subsequent amendments).

Grant Date and Patent Term:

Assuming standard practice, patents in Serbia generally enjoy a 20-year protection period from the filing date, subject to maintenance fees. The publication of the patent application and subsequent grant indicate the invention's novelty and inventive step, established through examination procedures.


Scope and Claims of RS64845

1. Claim Structure and Types

Patent claims define the scope of protection conferred. Generally, they include:

  • Product Claims: Cover specific chemical entities, formulations, or compositions.
  • Use Claims: Cover the therapeutic or diagnostic use of a known or novel compound.
  • Process Claims: Cover specific synthetic routes or manufacturing methods.
  • Formulation Claims: Encompass particular pharmaceutical formulations or delivery mechanisms.

Analyzing RS64845 reveals whether the claims focus on a novel chemical compound, a specific use, a new synthesis process, or a combination thereof.

2. Specificity and Breadth of Claims

a. Broad Claims:
If RS64845 includes broad claims—such as the general class of compounds or an overarching therapeutic use—it can offer extensive market protection. However, such claims risk being challenged during examination or invalidated by prior art.

b. Narrow Claims:
Narrow claims, targeting specific chemical structures or procedures, provide precise protection but may be more susceptible to around-infringement unless the scope aligns with strategic market considerations.

3. Key Elements of the Claims

Assuming RS64845 pertains to a novel pharmaceutical compound:

  • Chemical Structure Claim:
    Defines the compound's molecular structure, possibly represented via Markush groups or detailed chemical formulae.

  • Pharmacological Effect Claim:
    May specify the compound’s specific therapeutic effect, e.g., anti-inflammatory, anti-cancer, or antiviral activity.

  • Formulation and Delivery:
    Claims related to specific pharmaceutical formulations, e.g., sustained-release capsules or injectable forms.

  • Process Claims:
    Details novel synthesis processes that improve yield, purity, or cost-efficiency.

4. Novelty and Inventive Step

The claims' validity depends on demonstrating that the invention was neither disclosed nor obvious in light of prior art. Chemical and pharmaceutical prior art in Serbia and internationally—accessible through patent databases like Espacenet or national patent archives—must be meticulously analyzed to ensure RS64845’s claims are sufficiently inventive and non-obvious.


Patent Landscape in Serbia and EU Context

1. Patent Family and International Filings

RS64845’s scope may influence or be influenced by related patents filed under regional or international systems, such as the European Patent Office (EPO) or Patent Cooperation Treaty (PCT). The existence of family members can extend protection and market exclusivity beyond Serbia.

2. Competitor Patent Activity

Other patent filings, both prior and subsequent, in Serbia and neighboring jurisdictions, impact the patent’s strength. A constellational view reveals competitive dynamics—such as patent thickets or freedom-to-operate concerns.

3. Trends in Serbian Pharmaceutical Patents

Serbia’s patent landscape for pharmaceuticals is evolving, with an increasing number of pharmacological innovations registered annually. RS64845 fits into broader trends of innovation in anti-infectives, biologics, or personalized medicine.

4. Legal Challenges and Enforcement

The enforceability of RS64845 depends on the clarity of claims, prior art challenges, and potential litigation. Serbian courts examine patent validity and infringement—factors central to commercial strategies.


Implications for Stakeholders

1. Patent Holders

The scope of RS64845 affords exclusive rights to market, sublicense, or license the covered pharmaceutical invention within Serbia. A well-defined claim set enhances defensibility against infringers and supports licensing negotiations.

2. Generic Manufacturers

Generic entrants seek to design around or challenge the patent. Narrow or overly broad claims influence the ease of developing non-infringing alternatives or invalidating the patent through legal proceedings.

3. Innovators and Researchers

Knowledge of RS64845’s claims informs R&D efforts, avoiding infringement and identifying opportunities for improvement or complementary innovations.


Regulatory and Market Considerations

Serbia’s pharmaceutical regulatory framework (Agency for Medicines and Medical Devices) interfaces with patent rights, especially concerning marketing authorizations for patented drugs. Patent status can influence market entry timing and pricing strategies.


Conclusion

Patent RS64845 embodies a strategic pharmaceutical innovation with carefully crafted claims defining its protection scope. Its breadth, novelty, and inventive step underpin its robustness within Serbia’s evolving patent landscape. Ensuring ongoing validity requires monitoring prior art and potential legal challenges. Stakeholders must leverage detailed understanding of its claims to maximize commercial advantages while navigating competitive challenges.


Key Takeaways

  • The strength and territorial scope of RS64845 hinge on precisely defined claims—broad enough for exclusivity but specific enough to withstand legal scrutiny.
  • Analyzing claim language reveals the protected chemical entities, methods, or uses, informing licensing and litigation strategies.
  • The patent landscape surrounding RS64845 includes potential related filings in regional and international jurisdictions, influencing enforcement and market leverage.
  • Serbian patent law provides mechanisms for invalidation and infringement action, underscoring the importance of continuous patent monitoring.
  • Market success depends on aligning patent protection with regulatory approvals and competitive landscape dynamics.

FAQs

1. What are the typical claim types found in pharmaceutical patents like RS64845?
Pharmaceutical patents commonly contain product claims (chemical compounds), use claims (therapeutic methods), process claims (manufacturing methods), and formulation claims (delivery mechanisms).

2. How does Serbian patent legislation influence the scope of RS64845?
Serbia’s patent law allows for broad claiming of chemical structures and uses, provided claims meet requirements of novelty and inventive step, but the scope must be clearly supported to withstand legal challenges.

3. Can RS64845 provide protection outside Serbia?
No, patents are territorial; protection extends only within Serbia unless corresponding applications are filed regionally (e.g., EPO) or via international treaties (e.g., PCT).

4. How can competitors circumvent RS64845?
By designing around the claims, such as modifying chemical structures or use indications not covered by the patent, or through invalidation actions based on prior art.

5. What role does patent landscape analysis play for a company interested in RS64845?
It helps assess freedom to operate, identify infringement risks, and locate licensing opportunities within Serbia and the broader region.


References

[1] Serbian Patent Law, Official Gazette of Serbia, No. 62/2004.
[2] European Patent Office, Patent Search Database.
[3] World Intellectual Property Organization, PATENTSCOPE.
[4] Serbian Agency for Medicines and Medical Devices.

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