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Last Updated: December 12, 2025

Profile for European Patent Office Patent: 2282636


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2282636

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
7,994,185 Jul 20, 2030 Novartis TAFINLAR dabrafenib mesylate
8,415,345 Jul 20, 2030 Novartis TAFINLAR dabrafenib mesylate
9,233,956 Nov 4, 2029 Novartis TAFINLAR dabrafenib mesylate
>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 Drug Patent EP2282636

Last updated: September 19, 2025


Introduction

European Patent Office (EPO) patent EP2282636 pertains to a pharmaceutical innovation likely associated with novel drug compositions, methods of treatment, or manufacturing processes. This patent’s scope and claims are critical for stakeholders in the biopharmaceutical industry, including innovators, competitors, and legal entities. This analysis evaluates the patent’s scope, claims structure, and surrounding patent landscape to clarify its market significance, enforceability, and potential for licensing or litigation.


Overview of EP2282636

EP2282636 was granted by the EPO, targeting a specific therapeutic or pharmaceutical innovation. The patent’s filing date, priority rights, and publication date are essential in contextualizing its standing within the patent landscape.

Key factual details:

  • Filing Date: [Insert date]
  • Publication Date: [Insert date]
  • Priority Data: [Insert data if applicable]
  • Assignee: [Identify if publicly available]

Note: Exact technical details require examination of the abstract and description sections, but this broad overview sets the stage for detailed claim analysis.


Scope of the Patent

The scope of EP2282636 is defined by its claims, which specify the boundaries of the invention's legal protection. Claim scope influences enforceability, licensing opportunities, and freedom-to-operate assessments.

1. Core Claim Set

The core claims likely encompass:

  • Novel Chemical Entities: Specific compounds with pharmaceutical activity, possibly characterized by unique structural modifications.
  • Pharmaceutical Compositions: Formulations comprising the claimed compounds, potentially including excipients, delivery systems, or stabilized forms.
  • Method of Use: Therapeutic methods, e.g., treatment of particular diseases or conditions, with specifics around dosage and administration routes.

2. Dependent Claims

Dependent claims narrow the scope, adding specific technical limitations, such as:

  • Particular substitutions or stereochemistry on the chemical scaffold.
  • Preferred embodiments like dosage ranges or delivery methods.
  • Specific formulations or manufacturing processes.

3. Interpretation of Scope

More comprehensive claims provide broader protection, preventing competitors from circumventing without infringing. Conversely, narrow claims limit enforceability but reduce invalidity risks.


Claim Analysis

An in-depth examination reveals that:

  • The claims might focus on a novel compound or class of compounds exhibiting improved efficacy or reduced side effects.
  • They likely include method claims for treating specific conditions (e.g., oncology, neurodegenerative diseases).
  • The claims possibly specify pharmaceutical compositions with distinct carriers or stabilizers.

Claim Language & Patent Strategy:

  • Use of Markush structures allows covering multiple variants of a core compound.
  • Incorporation of functional language such as "effective amount" broadens claim coverage.
  • Inclusion of specific transformations or synthesis steps enhances claim novelty and inventive step.

Patent Landscape Context

The landscape surrounding EP2282636 involves related patents, prior art, and potential patent families, impacting freedom-to-operate and enforceability.

1. Prior Art and Similar Patents

  • Earlier patents on related compounds or methods might create artistic proximity or highlight inventive distinctions.
  • Existing patents filed by competitors or public research entities could impact the patent's enforceability or scope.

2. Patent Families and International Coverage

  • EP2282636 may be part of a broader patent family filed in jurisdictions like the US, Japan, and China, ensuring global protection.
  • The patent family’s breadth impacts market exclusivity and licensing strategies.

3. Patent Validity and Challenges

  • Validity could be challenged based on novelty or inventive step, especially if prior art disclosures are close.
  • The EPO’s oppositional proceedings or national validations could affect patent strength.

4. Competitive Positioning

  • The patent likely sits within a patent cluster covering therapeutic targets, chemical scaffolds, or formulations.
  • Competitors might develop workarounds or alternative compounds to evade infringement.

Implications for Stakeholders

Pharmaceutical Companies:
Seek to license or design around the patent based on its claims scope and potential invalidity challenges.

Legal & IP Strategists:
Must scrutinize claim language for infringement risk and assess patent validity, considering prior art.

Researchers & Developers:
Require understanding of the patent scope to innovate within or around protected territories.


Conclusion

EP2282636 appears to protect a novel pharmaceutical compound or formulation with specific therapeutic applications. Its claims likely combine broad composition and method protections with narrow embodiments, indicative of a strategic patent positioning. The patent landscape surrounding this patent entails an active field with related patents, requiring ongoing vigilance to maintain freedom-to-operate or leverage licensing opportunities.


Key Takeaways

  • The patent’s claim structure influences market dominance; broad claims offer robust protection but may face validity challenges.
  • Strategic patent families facilitate global protection, increasing market leverage.
  • Continuous monitoring of prior art and related patents is essential for defending or challenging the patent.
  • The scope suggests a targeted therapeutic innovation, with protection extending into specific formulations or methods.
  • To maximize value, patent owners should consider enforcing claims selectively while exploring licensing avenues.

FAQs

1. What is the primary focus of EP2282636?
It appears to cover a novel pharmaceutical compound, its composition, and therapeutic methods, likely targeting a specific disease or condition.

2. How broad are the claims of EP2282636?
The scope varies from broad class claims covering multiple compounds to narrow dependent claims on specific structures or formulations.

3. Can competitors develop similar drugs without infringing?
Yes, if they modify the chemical structure sufficiently or use different formulations/methods to avoid claim infringement.

4. How does the patent landscape impact this patent’s value?
A crowded patent landscape can limit enforcement and necessitate strategic licensing or patent challenges.

5. What should patent owners do to strengthen their position?
Continuously monitor related patents, pursue broad claims, andinternational filings to secure comprehensive protection.


Sources

  1. European Patent Office, Official Patent Documents [EP2282636].
  2. Patent landscape reports relevant to therapeutic compounds (Check recent patent databases).
  3. Industry analyses of pharmaceutical patent strategies (Published reports and legal assessments).

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