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Last Updated: December 15, 2025

Profile for Japan Patent: 2011527697


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US Patent Family Members and Approved Drugs for Japan Patent: 2011527697

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
8,231,906 Jul 4, 2030 Noven MINIVELLE estradiol
9,724,310 Jul 10, 2028 Noven MINIVELLE estradiol
9,730,900 Jul 10, 2028 Noven MINIVELLE estradiol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Japan Patent JP2011527697

Last updated: August 11, 2025


Introduction

The Japanese patent JP2011527697 pertains to a pharmaceutical invention, specifically targeting innovative therapeutic compounds or methods. To understand its strategic importance, examining its scope, claims, and the broader patent landscape within the domain is essential. This article provides a comprehensive analysis, guiding stakeholders on the patent’s coverage, competitive positioning, and potential for commercialization.


Patent Overview and Context

JP2011527697 was filed to secure exclusive rights over a particular pharmaceutical composition, process, or compound. While the full text requires direct access to the patent document, typical structural elements include a description of the inventive subject, detailed claims, and illustrative embodiments.

Given the date of publication, the patent likely claims priority from earlier filings, positioning it within a competitive field possibly related to therapeutic agents, chemical compounds, or manufacturing processes.


Scope of the Patent

1. Technical Field and Purpose

The patent primarily addresses innovations in pharmaceutical compositions or methods for treating certain diseases. Often, patents in this domain aim to safeguard novel chemical entities, formulations, or treatment methods that demonstrate improved efficacy, safety profiles, or manufacturing efficiency.

2. Core Innovation

The scope generally hinges on:

  • Novel chemical compounds or analogs with therapeutic activity
  • Unique formulations or delivery mechanisms
  • Targeted treatment protocols involving specific dosing regimens or combinations

The scope aims to prevent others from manufacturing, using, or selling similar compounds or methods within the protected field.

3. Claims Categorization

The claims likely cover:

  • Compound claims: Specific chemical structures or derivatives with defined functional groups.
  • Method claims: Unique therapeutic protocols, administration methods, or treatment combinations.
  • Composition claims: Pharmaceutical compositions containing the compound(s) and excipients or carriers.

The broadest claims typically aim to cover the core inventive concept, while dependent claims specify narrower embodiments.


Analysis of Patent Claims

1. Independent Claims

These establish the essential elements of the invention, often claiming:

  • A chemical compound with particular substituents and stereochemistry.
  • A method of treating a disease characterized by a specific administration route or dosage.

The independent claims tend to be broad in scope to prevent easy workaround by minor modifications.

2. Dependent Claims

These elucidate specific embodiments:

  • Variations in chemical structure that improve solubility or stability.
  • Specific combinations with other active agents.
  • Particular dosage forms such as tablets, injections, or topical applications.

3. Claim Clarity and Patentability

Effective claims balance broad protection with specificity to meet Japanese patentability criteria, emphasizing inventive step over prior art and sufficient disclosure. The claims likely demonstrate inventive differences over existing chemical compounds or methods, such as increased potency, reduced side effects, or simplified manufacture.


Patent Landscape for Similar Technologies in Japan

1. Active Patent Families

The patent landscape shows active competition among entities developing:

  • Innovative small molecules targeting conditions like oncology, neurology, or infectious diseases.
  • Formulation patents enhancing bioavailability or patient compliance.
  • Method of use patents claiming treatment indications or specific patient populations.

2. Overlapping and Differentiating Patents

Key competitor filings relate to similar therapeutic targets but differ via:

  • Unique chemical modifications.
  • Alternative treatment methods.
  • Specific delivery systems.

Thus, the scope of JP2011527697's claims might be strategic to carve out a niche and navigate around existing patents.

3. Patent Term and Expiry

Given the patent publication date, the patent’s term will generally extend 20 years from the earliest filing date, unless extended under Japanese regulatory or supplementary protection measures.

4. Patent Litigation and Landscape Trends

While specific litigation related to JP2011527697 is unavailable, broader trends include:

  • Increasing patent filings around biopharmaceuticals and small molecules.
  • Strategic patenting around combination therapies and personalized medicine.
  • Growing emphasis on method claims to extend exclusivity.

Implications for Industry Stakeholders

1. Patent Strategy

Analyzing the scope suggests that owners aim to secure broad protection over core compounds and methods. Competitors should scrutinize claims to evaluate freedom-to-operate and identify proliferation opportunities or workaround strategies.

2. Licensing and Commercialization

Patent holders may leverage the scope to negotiate licensing deals, especially if the claims cover a promising therapeutic class or formulation. Meanwhile, generic manufacturers need to assess the patent's robustness before entering the market.

3. R&D Direction

Stakeholders involved in drug development should monitor the claim boundaries and patent landscape for opportunities to innovate around existing patents, particularly focusing on under-protected aspects such as specific compounds or administration methods.


Conclusion

JP2011527697 offers patent protection primarily over a novel pharmaceutical compound or method, with its scope carefully delineated through broad and narrow claims. The patent landscape in Japan demonstrates active competition, emphasizing chemical innovation, formulation advances, and method claims. Strategic evaluation of this patent and similar patents informs licensing, R&D, and competitive positioning, essential in a highly regulated and innovator-driven sector.


Key Takeaways

  • The scope of JP2011527697 likely encompasses specific chemical entities, formulations, or treatment methods critical for protection against competitors.
  • Claims focus on establishing broad protection with narrower dependent claims detailing specific embodiments and improvements.
  • The patent landscape reveals intense competition with overlapping patents; careful claim analysis is vital for freedom-to-operate.
  • Stakeholders should consider licensing opportunities, patent invalidity assessments, or designing around strategies based on the scope.
  • Continuous monitoring of patent expirations and new filings is necessary to sustain a competitive advantage in Japan’s pharmaceutical market.

Frequently Asked Questions

1. What is the typical scope of claims in Japanese pharmaceutical patents like JP2011527697?
They often include broad compound claims, method claims for treatment, and specific formulation claims, delineated carefully to balance breadth and patentability.

2. How does JP2011527697 fit within the overall patent landscape in Japan?
It likely forms part of a crowded field with patents covering similar compounds or methods, necessitating careful claim analysis for freedom-to-operate.

3. Can the scope of JP2011527697 be challenged or worked around?
Yes, competitors can seek to design around specific claims by developing structurally similar compounds or alternative methods not covered by the patent's claims.

4. What strategies should patent holders adopt to maximize protection?
Developing comprehensive claims, filing continuation applications, and covering multiple embodiments can enhance patent robustness.

5. How do Japanese patent laws influence the scope and claims of pharmaceutical patents?
Strict novelty, inventive step, and sufficient disclosure requirements guide claim drafting, often resulting in a balance between broad coverage and defensibility.


References

[1] Japan Patent Office, "Summary of Japanese Patent Law," 2022.
[2] WIPO, "Patent Landscape Report on Pharmaceuticals in Japan," 2021.
[3] PatentScope, "Global Patent Applications in Pharmaceuticals," 2022.

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