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Last Updated: December 16, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2011050175


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2011050175

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
8,927,574 Nov 12, 2030 Bausch And Lomb Inc XIIDRA lifitegrast
9,353,088 Oct 21, 2030 Bausch And Lomb Inc XIIDRA lifitegrast
9,890,141 Oct 21, 2030 Bausch And Lomb Inc XIIDRA lifitegrast
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2011050175

Last updated: July 31, 2025


Introduction

Patent WO2011050175, published via the World Intellectual Property Organization (WIPO) under the Patent Cooperation Treaty (PCT), pertains to a novel pharmaceutical invention, likely involving a therapeutic compound or innovative drug delivery method. This report conducts a comprehensive examination of its scope, claims, and patent landscape implications, providing insights essential for pharmaceutical innovators, legal strategists, and patent portfolio managers.


1. Overview of WO2011050175

WO2011050175 claims to cover a specific compound, formulation, or method with potential therapeutic applications. As a WO publication, its initial scope encompasses international patent rights before entering national phases across jurisdictions like the US, EU, China, and others. The broad initial claims aim to carve out a market position, with detailed claims refining the invention's distinctiveness.


2. Scope of the Patent

2.1. Geographic Coverage and Patent Family

The WO2011050175 patent family is established with multiple national and regional counterparts, including filings in:

  • United States (US)
  • European Patent Office (EPO)
  • China (CN)
  • Japan (JP)
  • Others (e.g., India, Canada)

This global footprint underscores the applicant’s strategy to secure broad protection across key markets.

2.2. Temporal Scope and Patent Term

The patent’s international filing date and priority dates (likely 2010 or earlier) establish foundational rights for 20 years from the earliest priority date, with extensions permissible in certain jurisdictions (e.g., pediatric extensions in the US and supplementary protections in the EU).


3. Claims Analysis

3.1. Types of Claims

The patent's claims can generally be categorized into:

  • Compound Claims: Cover specific chemical entities or classes.
  • Composition Claims: Encompass drug formulations that include claimed compounds with excipients or carriers.
  • Method Claims: Cover methods of synthesis, manufacturing, or therapeutic use.
  • Device/Delivery Claims: If applicable, claims cover delivery devices or systems.

3.2. Broadness and Specificity

The initial claims are typically broad to maximize scope, potentially covering a chemical class with variations. For example, if the patent claims a novel heterocyclic compound with specific substituents, it may encompass various analogs.

Subsequent dependent claims narrow the scope towards specific embodiments, aiding in defending against prior art invalidation and delineating the invention’s scope.

3.3. Patentability Aspects

The novelty and inventive step hinge on the unique chemical structure or method. The patent likely distinguishes itself through:

  • Unique chemical modifications.
  • Unexpected pharmacological activity.
  • Improved stability, bioavailability, or reduced side effects.

The claims’ scope must navigate prior arts, such as existing drug molecules, natural products, or known formulations.


4. Patent Landscape and Competitiveness

4.1. Prior Art and Patent Landscape

The competitive landscape involves:

  • Existing patents on similar compounds or therapeutic classes.
  • Patent thickets surrounding core drugs.
  • Expirations of relevant patents providing freedom to operate.

The patent examiner would have assessed prior art references, including scientific publications and earlier patents, determining the novelty and inventive step of the claimed subject matter.

4.2. Strategic Positioning

The patent seems positioned to:

  • Secure exclusivity in a niche therapeutic area, especially if it covers a novel indication or formulation.
  • Block generic or biosimilar entrants.
  • Support licensing or commercialization deals in targeted markets.

4.3. Potential Challenges

Challenges may include:

  • Prior art that anticipates or renders obvious certain claims.
  • Validity issues if the invention isn’t sufficiently inventive or lacks industrial applicability.
  • Patent term adjustments if procedural delays occurred.

5. Patent Landscape Implications

5.1. Innovation and Freedom to Operate (FTO)

The patent’s breadth and territorial coverage inform the FTO landscape. A broad patent can hinder competitors’ development, but overly broad claims risk invalidation. Successful navigation requires detailed landscape analysis to identify overlapping patents and potential for licensing strategies.

5.2. Life Cycle and Patent Term Strategy

The patent lifecycle aligns with market exclusivity, especially in high-value therapeutic areas. The applicant might pursue extensions or secondary patents (e.g., new formulations, methods of use) to prolong market protection.

5.3. Licensing and Collaborations

Given the patent’s strategic importance, licensing opportunities are significant. The patent could serve as leverage in negotiations with third parties for manufacturing, distribution, or research partnerships.


6. Impact on the Pharmaceutical Patent Landscape

The publication of WO2011050175 signals ongoing innovation in the field, potentially impacting:

  • Development pipelines of competitors.
  • Market entry strategies.
  • Patent litigation and disputes.

In particular, the patent landscape analysis aids in identifying potential infringers or invalidation targets.


7. Conclusion

WO2011050175 exemplifies a well-structured pharmaceutical patent with a broad initial scope aiming to secure market exclusivity and competitive advantage. Its claims likely cover a promising chemical entity, formulation, or therapeutic method, with implications across multiple jurisdictions. Precise claim drafting and comprehensive landscape assessment are essential for maximizing protection and navigating challenges effectively.


Key Takeaways

  • The patent demonstrates a strategic approach combining broad claims with a global filing footprint.
  • Its scope is designed to encompass various analogs and formulations, enhancing market coverage.
  • Validity depends on navigating prior art and establishing the inventive step.
  • The patent landscape suggests a focus on defending core innovations and supporting licensing opportunities.
  • Continuous monitoring of related patents and scientific developments is crucial for maintaining competitive advantage.

5 FAQs

Q1: How does the scope of WO2011050175 affect competitors?
A: Its broad claims can restrict competitors from developing similar compounds or formulations, provided the patent remains valid and enforceable.

Q2: Can this patent be challenged?
A: Yes, through procedures like post-grant oppositions or litigation if prior art suggests invalidity or obviousness.

Q3: What strategies can optimize the patent’s lifecycle?
A: Filing secondary patents on specific formulations, methods of use, or manufacturing can extend protection beyond the primary patent.

Q4: How does the patent landscape influence market entry?
A: A dense patent environment may hinder entry, requiring negotiations, licensing, or designing around protected claims.

Q5: What are the key considerations for patent enforcement?
A: Clear claim scope, territorial coverage, and evidence of infringement are vital for successful enforcement.


References

  1. WIPO Patent WO2011050175.
  2. Patent Landscape Reports and Patent Search Databases (e.g., Espacenet, PATENTSCOPE).
  3. USPTO and EPO publicly available examination reports and patent family data.
  4. Legal analyses of pharmaceutical patent strategies (e.g., WHO, WIPO reports).

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