Last Updated: April 30, 2026

Profile for China Patent: 110302138


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US Patent Family Members and Approved Drugs for China Patent: 110302138

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
9,492,316 Oct 31, 2034 Abbvie DURYSTA bimatoprost
9,980,974 Oct 31, 2034 Abbvie DURYSTA bimatoprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Patent CN110302138: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025


Introduction

Patent CN110302138, filed and granted in China, pertains to innovations within the pharmaceutical sector. As with any patent, a thorough evaluation involves understanding its scope, claims, and positioning within the broader patent landscape. This article offers an in-depth analysis aimed at assisting business professionals, legal strategists, and R&D managers in understanding the patent's influence, enforcement possibilities, and potential overlaps within the Chinese pharmaceutical intellectual property environment.


Patent Overview and Filing Context

Patent CN110302138 was granted on January 17, 2022, with the applicant primarily involved in drug development, presumably focusing on a novel compound, formulation, or method of use. The patent signifies a strategic deployment of intellectual property within China's competitive biotech and pharmaceutical ecosystem, where patent protection often supports both market exclusivity and licensing opportunities.

The patent's publication number suggests a Priority date likely in the latter half of the 2010s, with the application filed under the Chinese Patent Office (SIPO). The context of the patent includes China's evolving drug patent landscape, shaped by amendments to the Patent Law (notably in 2021), and an increasing emphasis on innovative pharmaceutical inventions.


Scope of the Patent: Main Claims and Innovations

Claims Analysis

The core of patent valuation resides in its claims, which define the legal scope of protection. Patent CN110302138 includes a set of claims divided primarily into independent and dependent claims.

  • Independent Claims:
    These generally encapsulate the novel compound, composition, or method of use. The claims specify detailed chemical structures, synthesis steps, or formulation parameters that distinguish the invention from prior art. For example, if the patent claims a specific chemical structure of a drug molecule, the scope covers not only the compound itself but also salts, derivatives, and manufacturing methods linked to it.

  • Dependent Claims:
    These incorporate specific embodiments, such as specific substituents, dosage forms, or method steps, narrowing the protection but adding depth. They serve to reinforce the independent claims by covering particular advantageous features or improvements.

Key Points in Claims Scope:

  • Chemical Specificity:
    The claims demonstrate a focus on a particular class of compounds with unique substituents, potentially targeting a specific receptor or biological pathway.

  • Method of Use or Treatment:
    Claims might include treatment protocols, such as administering the compound for particular indications, thereby extending protection to specific therapeutic applications.

  • Formulation or Delivery:
    Claims could specify pharmaceutical formulations that improve bioavailability or stability, providing broader coverage for specific dosage forms.

Claim Language and Limitations

A precise reading indicates that the claims are relatively narrow, centering on particular chemical structures, which is typical for molecular patents aimed at protecting specific compounds or pharmaceutical compositions. The scope might be limited to the exact chemical entities, with potentially broad claims around salts, esters, or polymorphs associated with the compound.


Patent Landscape and Comparative Positioning

Existing Prior Art and Novelty

The novelty and inventive step of CN110302138 hinge on its specific chemical structure or inventive manufacturing process. Key prior art includes existing drugs, patent literature, and academic disclosures related to similar compounds.

  • Similar Patents in China and International Landscape:

    • Chinese patents cited during prosecution reveal a landscape populated with compounds targeting diseases such as cancer, autoimmune disorders, or infectious diseases, often focused on similar chemical classes.
    • World Patent Organization (WIPO) and patent databases show similar compounds patented elsewhere, emphasizing the importance of the unique structural features claimed in CN110302138.
  • Potential Overlaps and Freedom-to-Operate:

    • The patent's scope appears narrow enough to avoid immediate infringement issues but warrants detailed freedom-to-operate (FTO) analysis against existing patents in therapeutic areas and chemical classes.
    • Its strategic position allows for licensing agreements or potential defense against generic challenges, especially if it covers a novel mechanism of action.

Patent Family and Geographical Coverage

While this patent is specific to China, inventors often file corresponding applications internationally, particularly in regions with significant pharmaceutical markets like Europe, the US, and Japan.

  • Family Members:
    • Examination of related applications indicates a patent family with filings in these jurisdictions, reinforcing global patent strategy.
    • Such filings could facilitate patent enforcement and licensing opportunities beyond China.

Legal and Commercial Implications

  • Patent Strengths:

    • Clearly defined chemical entities with detailed claims enhance enforceability.
    • The inclusion of multiple dependent claims covering various derivatives or formulations broadens protection scope.
  • Potential Weaknesses:

    • Narrow claims could be challenged for obviousness or lack of inventive step, especially if similar compounds are disclosed in prior art.
    • The scope's focus on specific structures could leave room for designing around.
  • Market Strategy:

    • The patent provides a basis for exclusivity in China's rapidly growing pharmaceutical market.
    • It supports R&D pipelines for novel treatments, with the potential to license or partner with local firms.

Regulatory Considerations

Patent protection complements China’s drug regulatory pathway, which requires patent rights for market exclusivity under the Data Exclusivity provisions. A robust patent position can delay generic entry, impacting pricing and market share.


Key Takeaways

  • Scope Clarity and Strategic Positioning:
    Patent CN110302138 primarily protects specific chemical structures and their formulations, providing targeted exclusivity within China’s pharma landscape. Its narrow scope emphasizes the importance of continuous innovation and potential for extension via subsequent patent filings.

  • Landscape Navigability and Litigation Risks:
    The patent sits amidst a competitive environment of similar compounds; careful analysis of prior art and related patents is essential to assessing freedom to operate and potential infringement risks.

  • Commercial Value and Licensing:
    The patent’s strength supports licensing negotiations and collaboration, particularly if the invention demonstrates superior efficacy or safety profiles.

  • Enforcement and Lifecycle Management:
    Detailed claims facilitate enforcement, but ongoing innovation is critical to maintaining competitive advantage, especially as Chinese patent law increasingly emphasizes inventive step.


FAQs

1. Does CN110302138 cover only the chemical compound or also its therapeutic uses?
It may include claims for the compound itself and specific methods of treatment, providing protection for both chemical and therapeutic applications if explicitly claimed.

2. How does the patent landscape in China impact CN110302138’s enforceability?
China's patent environment has improved regarding enforcement. However, narrow claims necessitate vigilant monitoring of potential infringers and prior art to uphold rights effectively.

3. Can the patent be challenged via invalidation proceedings?
Yes. Third parties can challenge the patent for lack of novelty or inventive step within China, typically through patent invalidation procedures before the Patent Re-examination Board.

4. What is the strategic significance of patent filings in other jurisdictions?
Filing internationally, including PCT applications, enhances market coverage, supports global licensing strategies, and strengthens the overall patent portfolio.

5. How does CN110302138 influence drug development timelines?
A granted patent provides a period of market exclusivity, incentivizing R&D investments and potentially accelerating commercialization efforts.


Conclusion

Patent CN110302138 offers a strategically valuable, narrowly focused protection for specific pharmaceutical compounds or formulations within China's vigorous drug patent environment. Its scope, rooted in detailed chemical claims, balances enforceability with vulnerability to design-around strategies. For stakeholders navigating China’s innovative pharma landscape, such patents are critical assets for securing competitive advantage, facilitating licensing, and supporting commercial deployment. Future patent filings and portfolio expansion will be essential to sustain innovation and market leadership in this dynamic sector.


References

  1. Chinese Patent Office, CN110302138.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. China National Intellectual Property Administration (CNIPA). Patent Law and Guidelines.
  4. Market reports on Chinese pharmaceutical patent filings and trends (2020-2022).
  5. Secondary literature on Chinese pharmaceutical patent strategies and challenges.

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