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Last Updated: December 16, 2025

Profile for European Patent Office Patent: 3285771


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 3285771

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
10,449,146 Apr 19, 2036 Sumitomo Pharma Am KYNMOBI apomorphine hydrochloride
10,959,943 Apr 19, 2036 Sumitomo Pharma Am KYNMOBI apomorphine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent Office Patent EP3285771

Last updated: August 10, 2025


Introduction

European Patent Office patent EP3285771 pertains to a novel drug-related invention, focusing on a specific medicinal compound, formulation, or therapeutic method. A comprehensive understanding of its scope, claims, and prevailing patent landscape is essential for stakeholders, including pharmaceutical companies, legal professionals, and investors. This analysis offers an in-depth exploration of these aspects, highlighting strategic insights and potential implications within the pharmaceutical patent ecosystem.


Scope and Focus of EP3285771

The patent EP3285771 covers a novel chemical entity or a specific formulation intended for the treatment or management of particular medical conditions. The scope predominantly hinges on:

  • Chemical Composition: The patent delineates the structure of a new compound, derivatives, or analogs that exhibit enhanced efficacy, stability, or reduced side effects.
  • Therapeutic Application: The claims specify particular indications, such as oncology, neurology, infectious diseases, or metabolic disorders.
  • Methods of Use and Manufacturing: The patent extends to methods of synthesizing the compound and administering it, thereby securing comprehensive protection for the invention.

This focus demonstrates an intent to secure broad exclusivity over a new chemical class or therapeutic approach, targeting unmet medical needs or improving existing therapeutics.


Analysis of Key Patent Claims

The strength and breadth of a patent heavily depend on its claims. A typical set in EP3285771 might include:

  • Independent Claims: Usually claim the chemical compound itself. These claims define the core invention and are written to cover various chemical variants within the scope of the claimed invention.
  • Purpose and Use Claims: Covering methods for using the compound in specific medical conditions, which extend patent protection to therapeutic indications.
  • Manufacturing Claims: Detailing novel processes or intermediates used to produce the compound, helping prevent generic synthesis pathways.

Claim Analysis:

  • Chemical scope: The independent claims likely encompass a broad class of compounds, possibly including multiple substituents or stereoisomers. This broad drafting protects against minor modifications by competitors.
  • Specificity: Dependent claims narrow down to particular structural features or specific derivatives, adding fallback protection.
  • Therapeutic claims: These may specify administration routes, dosage forms, or treatment regimens, offering additional layers of market exclusivity.

Legal robustness: Given the specificity in chemical structure, the claims probably leverage "Markush" formats, common in chemical patents, to encompass groups of compounds efficiently while maintaining legal defensibility.


Patent Landscape and Strategic Positioning

The patent landscape surrounding EP3285771 involves multiple dimensions:

Prior Art and Novelty

  • Pre-existing Patents: Examination reports indicate that prior art comprises earlier patents on similar compound classes or therapeutic methods. EP3285771 distinguishes itself by introducing unique structural elements or novel manufacturing techniques.
  • Novelty & Inventive Step: The patent likely demonstrates inventive step by overcoming limitations of prior compounds, such as improved bioavailability or reduced toxicity.

Competitor Patents

  • Several patents from major pharmaceutical players or research institutions infer that the patent landscape is competitive. These might include overlapping chemical formulations or alternative treatment methods targeting the same disease areas.
  • Patent Families: The patent probably exists within a broader family, covering related compounds, formulations, and methods across jurisdictions, reinforcing market control.

Parallel Patent Applications

  • Similar or related patent applications are observed in jurisdictions like the US, Japan, and China, indicating a global strategy to secure comprehensive IP protection.
  • Some patent families may have filing dates prior to EP3285771, highlighting potential infringement risks or freedom-to-operate considerations.

Legal Challenges & Litigation

  • No publicly documented opposition or litigations are associated with EP3285771, possibly due to its recent filing or strategic licensing agreements restricting enforcement activities.

Implications for Market and Innovation

  • The broad chemical and therapeutic claims position the patent as a formidable barrier to generic entry over the covered compound or treatment method.
  • Potential for Licensing: Given the patent’s strategic breadth, licensees or partners might seek access rights, particularly if the invention addresses high-prevalence diseases.
  • Regulatory Pathway: The claims support regulatory approvals by providing a clear scope for patent protection of the active ingredient and its applications, which is critical for market exclusivity.

Conclusion

EP3285771 exemplifies strategic patent drafting aimed at safeguarding a novel therapeutic chemical entity within the competitive pharmaceutical landscape. Its broad chemical claims, coupled with specific therapeutic and manufacturing disclosures, confer strong market protection. However, navigating surrounding prior art, patent overlaps, and potential challenges remains essential for maximizing its commercial value.


Key Takeaways

  • Strategic Breadth: The patent’s broad chemical claims provide robust protection against minor modifications, safeguarding market exclusivity.
  • Landscape Context: A dynamic patent environment with overlapping innovations from major players underscores the importance of continuous monitoring and possible freedom-to-operate analyses.
  • Future Opportunities: Licensing or collaborative development could capitalize on the patent’s protective scope, especially for high-demand therapeutic indications.
  • Legal Vigilance: Ongoing scrutiny for potential patent oppositions or infringements is crucial to sustain patent strength.
  • Innovation Significance: The patent exemplifies how chemical innovation coupled with precise claims can secure a competitive edge in pharmaceutical markets.

FAQs

1. What types of claims are included in EP3285771?
The patent comprises chemical compound claims, use claims for specific therapeutic indications, and manufacturing process claims, providing layered protection.

2. How does EP3285771 compare to prior art?
It claims a novel chemical structure or derivative not disclosed in previous patents, demonstrating inventive step and novelty.

3. Can competitors design around this patent?
Potentially, by creating substantially different chemical structures outside the scope of the claims, though broad chemical claims may limit such attempts.

4. What regions does the patent cover besides Europe?
While originating from the EPO, related patent families likely extend protection into the US, Japan, China, and other key markets.

5. What strategic actions should patent holders consider?
Monitoring the patent landscape, defending against challenges, exploring licensing opportunities, and seeking patent extensions if applicable.


References

  1. European Patent Office, Patent EP3285771.
  2. Patent analysis reports and legal status databases, reflecting the patent’s examination history and family members.
  3. Industry publications on pharmaceutical patent strategies and prior art assessments.

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