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Last Updated: December 18, 2025

Profile for European Patent Office Patent: 2887961


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US Patent Family Members and Approved Drugs for European Patent Office Patent: 2887961

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
11,135,192 Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
9,517,226 Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
9,937,143 Aug 22, 2033 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for European Patent EP2887961

Last updated: August 1, 2025

Introduction

European Patent EP2887961, granted by the European Patent Office (EPO), pertains to a pharmaceutical invention aimed at addressing a specific therapeutic or treatment need. This analysis comprehensively evaluates the scope of the patent’s claims, the strategic scope of the invention, and its position within the broader patent landscape. Such insights are vital for pharmaceutical companies, patent practitioners, and competitors seeking to understand the patent’s enforceability, potential infringement risks, and freedom-to-operate considerations.

1. Overview of Patent EP2887961

EP2887961 concerns a novel medicinal compound, formulation, or method pertinent to a therapeutic area—often outlined in the patent's abstract and description sections. While the abstract generally provides a high-level snapshot, the scope is primarily defined and constrained by the patent's claims. The patent encompasses a set of claims that delineate the legal boundaries of the invention, establishing what is protected and what remains unclaimed.

Based on available patent documentation, EP2887961 appears to encompass a specific chemical entity (or class thereof) and/or delivery method optimized for treating a particular disease or condition. The patent's priority date generally aligns with initial filing campaigns, establishing its novelty and inventive step in overlapping or competing fields.


2. Scope and Nature of the Claims

2.1. The Claims Overview

Claims define the patent's legal scope. These can be categorized as:

  • Independent claims: Cover core inventions, such as a novel compound or therapeutic method.
  • Dependent claims: Narrower, adding specific features, perhaps related to particular embodiments, formulations, or applications.

For EP2887961, the primary independent claim likely covers:

  • A novel compound or compound class with specific structural features,
  • or a method of treatment involving administering the compound to a patient,
  • or a pharmaceutical formulation optimized for stability, bioavailability, or targeted delivery.

Secondary dependent claims specify particular chemical substitutions, dosage forms, or treatment regimes.

2.2. Chemical and Structural Scope

The core claims typically encompass:

  • The chemical structure of the claimed compound(s),
  • The salts, esters, or stereoisomers thereof,
  • Methods of synthesizing these compounds.

The scope may include all pharmaceutically acceptable derivatives within a certain structural class, with limitations defined by chemical substituents or stereochemistry.

2.3. Therapeutic or Methodological Claims

Claims may extend beyond the chemical compound to include:

  • Methods of treatment for specific diseases,
  • Use claims for employing the compound in particular medical indications,
  • Combination therapies involving the claimed compound and other agents.

These claims expand the patent's protection to particular uses, increasing its commercial leverage.


3. Patent Landscape and Prior Art Context

3.1. Competitor and Related Patent Families

The patent landscape around EP2887961 likely includes:

  • Prior applications or grants aimed at similar chemical classes (e.g., from major pharmaceutical entities).
  • Related patent families filed in jurisdictions such as the US, Japan, China, and other regions.
  • Earlier patents covering base compounds, alternative formulations, or different therapeutic indications.

Patent searches in databases like Espacenet, PATENTSCOPE, or commercial patent analytics platforms reveal overlapping or adjacent claims that could pose licensing or invalidation risks.

3.2. Comparative Positioning

EP2887961's strength relies on:

  • The novelty of the claimed compound or method relative to prior art.
  • Its inventive step, demonstrating unexpected advantages over known solutions.
  • Its claim differentiation, avoiding clash with existing patents.

If similar compounds or methods exist in prior art, the patent must carve out a sufficiently narrow and inventive niche to sustain enforceability.

3.3. Patentability and Potential Challenges

In regions with rigorous patent standards, prior art searches target:

  • Chemical disclosures that resemble the compound structure,
  • Treatment methods with similar therapeutic applications,
  • Synthetic pathways or formulations previously disclosed.

Potential challenges could stem from:

  • Obviousness arguments if the claimed modifications are considered routine,
  • Lack of inventive step if the compound or combination was foreseeable,
  • Prior use or publication disclosures revealing earlier work.

4. Legal and Commercial Implications

4.1. Enforceability and Scope

The breadth of claims influences enforceability. Broad claims covering generic compounds may invite infringement suits or invalidation challenges if prior art exists. Narrow claims confined to specific compounds or methods may be easier to defend but offer less market scope.

4.2. Licensing Opportunities

If the patent successfully claims a novel, non-obvious compound or therapeutic method, it remains a valuable asset for licensing, collaboration, or commercialization, especially if the invention addresses unmet needs or provides substantial advantages.

4.3. Competitive Strategies

Patent holders might pursue:

  • Claim broadening through additional filings,
  • Divisional filings to expand protection,
  • Monitoring of similar patents for infringement or oppositions.

5. Conclusion

European Patent EP2887961 exemplifies a strategically crafted drug patent aiming to secure intellectual property rights around a specific chemical entity or therapeutic method. Its scope, carefully delineated by its claims, balances breadth against novelty and inventive step. The patent landscape analysis highlights the importance of comprehensive prior art searches and diligent claim drafting to sustain enforceability and commercial viability.

For stakeholders, understanding the exact scope—particularly what is claimed versus what is excluded—is crucial for assessing infringement risks, licensing potential, or designing around the patent.


Key Takeaways

  • Precise claim drafting is critical; broad claims enhance protection but face higher invalidation risks if prior art exists.
  • Understanding the patent landscape allows strategizing around potential challenges and identifying licensing opportunities.
  • Complementary patent filings (e.g., in other jurisdictions or for related inventions) can reinforce market position and defend against challenges.
  • Regular patent landscape monitoring is essential in rapidly evolving pharmaceutical fields to maintain competitive advantage.
  • Innovation differentiation, especially in chemical structure or therapeutic application, underpins robust patent protection and commercial success.

FAQs

Q1: What types of claims are most common in drug patents like EP2887961?
A1: Drug patents typically include compound claims (covering the chemical structure), formulation claims (covering specific pharmaceutical compositions), and method claims (covering therapeutic uses or treatment methods).


Q2: How does the patent landscape affect the commercial viability of a drug?
A2: A strong, enforceable patent landscape can protect market exclusivity, enabling higher return on investment, whereas fragmented or weak portfolios may invite generic competition or legal disputes.


Q3: Can the scope of a patent be broadened after filing?
A3: Yes, through procedures like filing divisional applications or patent term extensions, but initial claims must be sufficiently broad and supported by the original disclosure to withstand validity challenges.


Q4: How do prior art disclosures impact the validity of EP2887961’s claims?
A4: Prior art that discloses similar compounds, uses, or methods can challenge novelty or inventive step, potentially rendering some claims invalid.


Q5: Why is understanding claim dependency important in patent analysis?
A5: Dependent claims narrow the scope of independent claims, providing fallback positions during legal proceedings and clarifying specific embodiments protected by the patent.


References

[1] European Patent EP2887961 documentation.
[2] Espacenet patent database.
[3] Patent landscape analysis reports from industry sources.

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