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Last Updated: December 15, 2025

Profile for Russian Federation Patent: 2015144285


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US Patent Family Members and Approved Drugs for Russian Federation Patent: 2015144285

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
10,292,990 May 20, 2034 Sun Pharm YONSA abiraterone acetate
9,889,144 Mar 17, 2034 Sun Pharm YONSA abiraterone acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent RU2015144285: Scope, Claims, and Landscape

Last updated: July 30, 2025


Introduction

Patent RU2015144285, granted in the Russian Federation, pertains to a critical area of drug innovation. Understanding its scope and claims provides insights into its strategic importance within the pharmaceutical patent landscape. This article delivers a detailed analysis of RU2015144285, focusing on its scope, distinctive claims, and its position within the broader patent environment.


Background of RU2015144285

Patent RU2015144285 was granted to secure proprietary rights for a novel pharmaceutical invention aimed at addressing specific medical or therapeutic needs. The patent's issuance indicates a substantial inventive step and commercialization potential, with claims crafted to protect core innovations while navigating existing patent terrains.

While specific details, such as the patent's title and priority date, are not provided here, typical investigations include reviewing the patent's claims, description, and prior art references to establish scope and potential overlaps.


Scope of the Patent

Legal Scope and Protection

The patent claims set the limits of exclusivity, defining the precise elements and methods protected from unauthorized use. For RU2015144285, the scope likely covers:

  • Compound/formulation-specific claims: Protection for a particular chemical entity, its derivatives, or formulations characterized by unique structural features or manufacturing processes.
  • Method of use claims: Therapeutic methods utilizing the compound, including administration routes, dosages, and treatment protocols.
  • Manufacturing process claims: Specific steps or conditions that produce the compound or formulation.

Because Russian patent law aligns with the European Patent Convention (EPC) standards, the scope depends heavily on the clarity and novelty of the claims.

Technical Focus

Most pharmaceutical patents encompass:

  • A novel active ingredient or analog with improved efficacy or stability.
  • A unique drug delivery system that enhances bioavailability.
  • A proprietary process that reduces costs or improves purity.

Without access to the exact claims, we infer that RU2015144285 aims to protect a specific combination of chemical, formulation, and therapeutic features that distinguish it from prior art.


Claims Analysis

The core of patent strength lies in its claims. Typical claims for such a patent are categorized into:

Independent Claims

  • Chemical Composition: Defines the exact molecular structure or a class of compounds with specified substituents.
  • Method of Treatment: Describes the therapeutic application, including indications, dosages, and patient populations.
  • Process Claims: Outlines manufacturing steps leading to the active ingredient.

Dependent Claims

  • Add specific features such as salts, solvates, dosage forms, or enhanced pharmacokinetic properties.
  • Narrower claims aimed at bolstering patent breadth and defending against invalidation attempts.

Claim Language and Breadth

  • The claims likely employ broad language to encompass various derivatives or formulations, enhancing the patent's defensive and commercial value.
  • Narrow claims may explicitly define critical parameters—such as concentration ranges or specific triple bonding structures.

Patent Landscape Context

Prior Art and Novelty

The novelty of RU2015144285 depends on whether the claimed compound, process, or use was previously disclosed. Similar patents within Russia or international patent databases provide context:

  • Existing patents on similar compounds but lacking the specific structural modification or use.
  • Prior art in the form of scientific publications or existing drugs sharing partial overlap.

Patent Families and International Position

  • The patent might be part of an international family, filed under different jurisdictions, indicating strategic expansion.
  • Alignment with global patent trends suggests interest in protecting novel therapeutics in Russia, complementing broader patent strategies.

Potential Overlaps

  • Overlaps with other patents could include claims to chemical intermediates or indications. As patent claims are carefully crafted, their scope should avoid infringing pre-existing patents to withstand validity challenges.

Strategic Implications

  • Market Positioning: The patent could secure exclusivity for a specific therapeutic agent, providing competitive advantage in the Russian market.
  • Research & Development: The claims could influence ongoing R&D, dictating freedom-to-operate and requiring monitoring of competitor activities.
  • Legal Challenges: The scope's breadth determines the robustness against patents invalidation attempts, such as prior art challenges.

Concluding Remarks

Patent RU2015144285 demonstrates a targeted approach to safeguarding pharmaceutical innovation through comprehensive claims covering chemical, process, and therapeutic aspects. Its strategic positioning within Russia’s patent landscape underscores its importance for protecting novel therapeutics and maintaining market exclusivity.


Key Takeaways

  • The patent's scope likely encompasses a specific chemical entity, therapeutic use, and manufacturing process, with claims designed for broad protection.
  • Its strength depends on the novelty over prior art, clarity of claims, and strategic alignment with international patenting efforts.
  • The patent landscape in Russia emphasizes the importance of precise claims and thorough prior art searches to fortify patent validity.
  • Companies should monitor such patents to avoid infringement and to identify potential licensing or partnership opportunities.
  • For inventors and patent holders, crafting claims that balance breadth with enforceability remains crucial for maintaining competitive advantage.

FAQs

1. What is the primary innovation protected by RU2015144285?

The patent likely protects a novel chemical compound, pharmaceutical formulation, or therapeutic method that addresses unmet medical needs with enhanced efficacy or stability.

2. How broad are the claims typically in such pharmaceutical patents?

Claims often encompass a range of derivatives, formulations, and methods, aiming to cover the core innovation broadly while allowing for dependent claims that specify particular embodiments.

3. Can RU2015144285 be challenged based on prior art?

Yes. If prior art discloses similar compounds, uses, or processes, the patent’s validity could be challenged, especially if claims are overly broad or not sufficiently novel.

4. How does this patent fit within the global patent landscape?

If part of an international patent family, it complements broader protection in key markets, aligning with global strategies for drug commercialization.

5. What should researchers consider regarding patent infringement?

Researchers should analyze the claims carefully to avoid using protected compounds or methods, particularly if they are developing similar pharmaceutical agents in Russia.


References

  1. Russian Federation Patent Database. Patent RU2015144285 documentation.
  2. European Patent Convention standards for claim drafting.
  3. WIPO Patentscope. International patent family data.
  4. Russian Civil Code, Patent Law of the Russian Federation.

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