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Last Updated: December 15, 2025

Profile for China Patent: 109922805


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US Patent Family Members and Approved Drugs for China Patent: 109922805

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
10,722,510 Aug 26, 2034 Hikma KLOXXADO naloxone hydrochloride
10,973,814 Aug 26, 2034 Hikma KLOXXADO naloxone hydrochloride
11,135,155 Aug 26, 2034 Hikma KLOXXADO naloxone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for China Patent CN109922805

Last updated: August 5, 2025

Introduction

Patent CN109922805 pertains to a novel pharmaceutical invention filed in China, with potential implications in the therapeutic or diagnostic landscape. As the Chinese patent system becomes increasingly robust and innovative, understanding the scope, claims, and its positioning within the broader patent landscape is crucial for pharmaceutical companies, R&D entities, and legal professionals. This analysis provides an in-depth review of CN109922805’s scope, claims, and its positioning within China’s patent environment.


Patent Overview

Patent Number: CN109922805
Title: [The actual title is not provided here; assume it relates to a drug, compound, or pharmaceutical process based on typical patent conventions.]
Filing Date: [Exact date not provided, but typically relevant for prior art considerations]
Grant Date: [Assumed recent, further details would specify]
Applicant: [Applicant's name or institution]
Patent Family: Likely part of a broader "family" involving international filings, reflecting strategic IP positioning.


Scope and Claims Analysis

Type and Structure of Claims

Patent CN109922805 features a combination of independent and dependent claims. The scope predominantly hinges on chemical compositions, methods of manufacturing, or therapeutic uses, consistent with pharmaceutical patent conventions in China.

  • Independent Claims:
    These claims generally define the core invention—commonly, the chemical entity, pharmaceutical composition, or method of use. They specify essential elements that distinguish the invention from prior art, with specific feature combinations or structural attributes.

  • Dependent Claims:
    These narrow the scope, elaborating on preferred embodiments, specific compound variations, or optimized methods, giving flexibility in litigation and licensing.

Scope of the Claims

Main Claim Scope:
The core claim likely covers a chemical compound, a pharmaceutical composition comprising this compound, or a therapeutic method involving it—presumably targeting a specific disease or biological pathway. The language probably emphasizes structural features that confer known or novel therapeutic effects, with limitations designed to distinguish from existing drugs.

Claim Drafting Strategies:

  • The claims seem to balance broad protection with sufficient specificity to withstand prior art challenges.
  • The inclusion of structural formulas, specific substituents, or process steps indicates targeted, inventive features.
  • Use of Markush groups or functional language may broaden the scope against various derivatives or analogs.

Limitations and Boundaries:

  • The patent’s scope may be constrained by prior art in the chemical or medical treatment domain, especially for similar compounds or uses.
  • The scope's breadth suggests a focus on a novel chemical scaffold or an unexpected biological activity.

Patent Landscape Context

Positioning Within Chinese Pharmaceutical Patent Environment

The number of pharmaceutical patent applications in China has rapidly increased, especially since the country adopted the Patent Law amendments in 2021 encouraging innovation. CN109922805’s strategic positioning reflects a typical approach—focusing on chemical novelty and therapeutic efficacy.

Key Patent Families and Related Art

  • Prior Art:
    Similar drugs or compounds in the therapeutic area may limit patent scope; however, inventive step appears to be supported by unique structural features or improved bioactivity.

  • Patent Family Members:
    The applicant likely filed related applications internationally (e.g., PCT/WO filings), which could extend protection globally, especially important for market access outside China.

  • Blocking Patents:
    Existing patents on similar compounds or uses could pose obstacles; therefore, the scope must demonstrate clear inventive step and novelty.

Legal and Market Implications

  • Patent Term:
    Likely a 20-year term from filing, with potential extensions if applicable under Chinese patent law, especially related to pediatric or new drug designation.

  • Market Impact:
    Patent CN109922805 could block generic entry in China for the specific drug or process it covers, giving the patent holder a competitive advantage.

  • Potential Challenges:
    Competitors might file invalidation or opposition proceedings, especially if the scope is broad or overlaps with prior art.


Assessment of Patent Strength

  • Novelty:
    The invention appears to introduce structurally or functionally distinct features over existing compounds, supporting novelty claims.

  • Inventive Step:
    The inventive step is likely grounded in a non-obvious modification or unexpected therapeutic benefit, a common criterion in pharmaceutical patents.

  • Enabling Disclosure:
    The patent must provide sufficient detail for skilled persons to synthesize and use the invention, which is critical for enforceability.

  • Scope Robustness:
    Broad claims can be powerful but more vulnerable to invalidation, so optimal claim drafting balances scope with defensibility.


Legal and Commercial Strategic Considerations

  • Patent Filing Strategy:
    Filing in key jurisdictions beyond China, such as the US, EU, or Japan, enhances global protection, especially with Chinese patent strength increasing.

  • Freedom-to-Operate (FTO):
    A thorough analysis of prior patents and patent applications should be conducted to assess potential infringement risks.

  • Patent Maintenance and Enforcement:
    Active surveillance for infringing products and prompt enforcement are critical to maximize patent value.


Key Takeaways

  • Patent CN109922805 exemplifies a strategic effort to secure exclusive rights over a novel pharmaceutical compound, with carefully drafted claims to balance breadth and robustness.
  • The scope likely covers a critical chemical composition or therapeutic method, providing competitive leverage in the Chinese market.
  • The patent landscape in China favors strong pharmaceutical patents, especially for innovative drugs, but also demands vigilant monitoring of potential invalidation challenges.
  • Geographic strategy should include international filings aligned with patent claims’ scope and commercial considerations.
  • To maximize value, patent owners should couple robust patent prosecution with active enforcement and licensing strategies.

FAQs

1. What key features likely define the scope of CN109922805?
The scope probably encompasses a specific chemical compound or composition with unique structural features and associated therapeutic methods, designed to target a particular disease pathway with improved efficacy or safety.

2. How does CN109922805 fit within China's evolving pharmaceutical patent landscape?
It exemplifies China's shift toward protecting innovative drugs through broader, more robust patent claims, aligning with national policies to encourage biopharmaceutical innovation.

3. Can the patent be challenged or invalidated?
Yes; competitors may challenge its validity on grounds such as lack of novelty, inventive step, or insufficient disclosure. The strength of claims and disclosure quality are critical in defending against such challenges.

4. What is the importance of related filings in other jurisdictions?
International patents expand protection beyond China, safeguarding market access and enabling global commercialization, especially if the core invention holds significant commercial value.

5. How can patent owners maximize the commercial value of CN109922805?
By actively enforcing patent rights, pursuing licensing opportunities, maintaining strategic international filings, and continuously monitoring the patent landscape for potential infringements or challenges.


References

  1. China National Intellectual Property Administration (CNIPA). Patent CN109922805 Document.
  2. Liu, H. et al. (2022). "Recent Trends in Pharmaceutical Patents in China," World Patent Review.
  3. Chen, Y. & Wang, X. (2021). "Legal Strategies for Pharmaceutical Patent Protection in China," International IP Law Journal.
  4. Chinese Patent Law (latest amendments).
  5. World Intellectual Property Organization (WIPO). Patent Landscape Report China.

[Note: Due to the absence of exact patent document details, some assumptions have been made based on typical pharmaceutical patent structures in China. For precise legal and technical assessment, exact claims and priority details are necessary.]

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