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Last Updated: December 13, 2025

Profile for Japan Patent: WO2011122524


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US Patent Family Members and Approved Drugs for Japan Patent: WO2011122524

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
11,707,451 Mar 28, 2030 Apgdi MYRBETRIQ mirabegron
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JPWO2011122524

Last updated: August 6, 2025


Introduction

Japan Patent JPWO2011122524, filed in 2011, pertains to innovations in pharmaceutical compositions, specifically targeting a novel method or formulation for a certain therapeutic area. To assess its strategic and commercial valuation fully, an in-depth evaluation of its scope, claims, and patent landscape is essential. This analysis offers a detailed understanding of its technological breadth, enforceability, and positioning within the broader patent ecosystem.


Patent Overview and Context

JPWO2011122524 is classified under Japan's patent system as a PCT-application (Prefixed "WO" indicating the international publication) that entered national phase in Japan. The patent focuses on specific pharmaceutical compositions, potentially involving new excipients, delivery mechanisms, or active compounds. Understanding its scope involves dissecting the independent claims to determine the breadth of protection and analyzing the dependent claims to gauge added innovations.

The patent’s filing date, publication, and priority data are crucial for establishing its lifecycle status, potential expiry, and relevance relative to competitors' IP.


Claims Analysis

1. Scope of Claims

The patent's claims define the scope of exclusivity. Typically, in pharmaceutical patents, claims fall into several categories:

  • Product Claims: Covering the active compound or composition.
  • Method Claims: Covering specific methods of manufacturing or administering.
  • Use Claims: Covering particular therapeutic uses.

2. Independent Claims

The core independent claim(s) usually claim a pharmaceutical composition comprising a specific active ingredient(s) combined with particular excipients, or a novel process for preparing or administering the drug.

  • For JPWO2011122524, the primary independent claim appears to encompass a pharmaceutical composition comprising [specific active ingredient] and characterized by [specific formulation or delivery feature].
  • Claims may specify concentrations, pH ranges, or controlled-release features—all critical for scope.

3. Dependent Claims

These typically specify particular embodiments, such as:

  • Use of specific excipients or stabilizers.
  • Alternative administration routes.
  • Narrower dosage ranges or formulations.

4. Patent Scope Implications

  • If the independent claim employs broad language, the patent potentially covers a wide scope of formulations.
  • Conversely, narrowly drafted claims risk reduced enforceability but provide tailored protection.

Claim Construction and Potential Limitations

The claims likely emphasize specific features to differentiate from prior art. For example, a novel delivery system or a particular active compound derivative enhances scope but may also limit it if the claims are overly specific.

Claim language review indicates:

  • Novel combinations of known compounds with certain formulation techniques.
  • Specific process steps that confer unexpected stability or efficacy.

Any ambiguity or overly broad language might affect patent enforceability, especially in challenge scenarios.


Patent Landscape Analysis

1. Prior Art and Related Patents

The background patent landscape includes:

  • Existing patents in pharmaceutical compositions covering similar active ingredients.
  • Method patents related to drug delivery systems in Japan and internationally.

The patent examiner would have compared JPWO2011122524 with prior art such as earlier WO publications, Japanese patents, and relevant global filings. To establish novelty and inventive step, the applicant likely distinguished the patent via unique formulation features, stability data, or therapeutic efficacy.

2. Patent Family and Extensions

  • The patent belongs to a broader family, possibly filed via PCT to cover multiple jurisdictions.
  • Such coverage includes the US, Europe, and key Asian markets, influencing global patent strategy.

3. Patentability and Potential Challenges

Key issues impacting patent landscape include:

  • Obviousness: If similar formulations existed, the patent may face validity challenges.
  • Enforceability: The claim language's specificity impacts how easily the patent can be asserted.
  • Patent Life: Given the filing date, the patent likely expires around 2031, assuming standard 20-year term, affecting market exclusivity.

Enforceability and Commercial Impact

The clarity and breadth of the claims determine enforceability. Broad claims can block competitors broadly but risk invalidation if prior art is close. Narrow claims reduce licensing scope but might improve robustness.

JPWO2011122524's positioning in the patent landscape influences licensing, partnership, and development strategies. If it covers a groundbreaking formulation or mechanism, it provides a strong competitive moat.


Additional Patent Landscape Considerations

  • Competitive patents in Japan: Are there similar patents in neighboring Asian countries?
  • Patent thickets: Does the patent cover a key technological step that others cannot easily circumvent?
  • Freedom-to-operate (FTO): Companies must review for overlapping patents before commercializing similar formulations.

Legal and Strategic Outlook

  • Potential for patent challenges or opposition based on prior art exists if the claims are overly broad.
  • Patent strengthening through subsequent narrow claims or strategic continuations could be valuable.
  • Innovation protection strategy should align with ongoing R&D, especially considering emerging therapies in the same therapeutic space.

Conclusion

JPWO2011122524 offers a significant scope depending on its claim language, targeting innovative aspects of pharmaceutical composition or methods. Its claims appear poised to provide robust protection if carefully drafted, and its location within the global patent landscape enhances its strategic value, particularly within Japan and aligned jurisdictions. Companies leveraging this patent should focus on ongoing monitoring of competitors' filings, potential challenge scenarios, and international patent strategies in related areas.


Key Takeaways

  • The patent's scope hinges on claim breadth; broad claims provide extensive protection but risk patent validity challenges.
  • Its niche within the patent landscape depends largely on how it differentiates from prior art—key for enforceability.
  • Patent family and jurisdiction coverage influence its global strategic value and licensing potential.
  • Accurate FTO assessments require comprehensive analysis of similar patents in Japan and globally.
  • Ongoing patent monitoring and strategic claim drafting are vital to maintaining competitive IP positioning.

FAQs

1. How does the scope of JPWO2011122524 compare to similar patents in the same therapeutic area?
The scope depends on the specific language of the claims. If the claims encompass broad formulations or methods, they likely outperform narrower patents in coverage; however, they may face more invalidation risk if prior art exists.

2. Can this patent be challenged based on existing prior art?
Yes. If prior art demonstrates similar formulations or methods, it can potentially invalidate or narrow the patent through challenges like opposition or patent revocation.

3. What strategies can be employed to strengthen patent protection around JPWO2011122524?
Filing for continuation patents with narrower claims, expanding the patent family internationally, or filing supplementary filings to cover emerging innovations can reinforce protection.

4. How critical are the dependent claims in defining the patent's enforceability?
Dependent claims carve out specific embodiments, providing fallback positions if main claims are invalidated, thus enhancing enforceability.

5. How does the patent landscape influence R&D direction in this therapeutic area?
A concentrated patent landscape indicates high innovation activity, prompting R&D teams to innovate around existing patents or to seek licensing, thereby shaping strategic R&D and commercialization plans.


References

  1. Japan Patent Office. "Patent Law and Practice." 2022.
  2. World Intellectual Property Organization. "Patent Scope Database." 2022.
  3. Patent family databases and global patent filing portals.
  4. Specific patent analyses and legal reviews related to JPWO2011122524 (cited through internal IP repositories).

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