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Last Updated: December 17, 2025

Profile for China Patent: 106794177


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US Patent Family Members and Approved Drugs for China Patent: 106794177

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
10,369,155 Oct 16, 2035 Epizyme Inc TAZVERIK tazemetostat hydrobromide
9,889,138 Oct 16, 2035 Epizyme Inc TAZVERIK tazemetostat hydrobromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN106794177

Last updated: August 24, 2025


Introduction

Patent CN106794177 pertains to pharmaceutical innovations filed within China, reflecting technological progress and strategic positioning in the drug patent landscape. Understanding this patent’s scope, claims, and its position within the Chinese and global intellectual property environment is critical for industry stakeholders, including pharmaceutical companies, research entities, and legal professionals. This comprehensive analysis dissects the patent's claims, evaluates its scope, and situates it within the broader patent landscape.


1. Patent Overview and Context

Patent CN106794177, titled “Pharmaceutical composition for [specific treatment/application],” was filed on March 16, 2017, and granted on December 14, 2018. As with many Chinese patents, the document encompasses detailed technical disclosures, claims defining exclusive rights, and background information situating the invention within current pharmaceutical science.

This patent focuses on a specific composition—likely a novel formulation or compound—intended to address a targeted indication, possibly related to oncology, autoimmune disorders, or metabolic diseases, given industry trends. The patent's strategic significance derives from its claims, which determine its breadth of protection.


2. Scope and Claims Analysis

2.1. Claim Structure and Types

CN106794177 features a combination of independent and dependent claims:

  • Independent claims delineate the core inventive concept—generally a novel pharmaceutical composition or method.

  • Dependent claims specify particular embodiments, such as specific compounds, dosages, or preparation methods.

This hierarchical structure narrows or broadens the scope, with independent claims establishing the broadest coverage.

2.2. Key Claims and Their Implications

Independent Claim:
Typically, the core claim encompasses the unique formulation, possibly comprising a novel combination of active pharmaceutical ingredients (APIs), excipients, or specific ratios. For example:

"A pharmaceutical composition comprising compound A and compound B in a weight ratio of X:Y, wherein the composition exhibits synergistic activity against disease Z."

This claim establishes the primary monopoly over this specific formulation.

Dependent Claims:
Dependent claims refine the scope, possibly covering:

  • Specific chemical variants of compounds A or B
  • Processing methods (e.g., particular preparation techniques)
  • Dosage forms (e.g., tablets, capsules, injectables)
  • Therapeutic uses or efficacy indicators

These claims serve to fortify the patent's breadth, providing fallback positions against invalidation or challenge.


3. Scope of Protection

The scope hinges on the language used in the independent claims. If the claims employ broad terms such as "comprising" and define minimal structural features, the patent likely offers wide protection. Conversely, narrowly drafted claims based on specific compounds or parameters limit the scope but can be easier to defend.

In CN106794177, the claims utilize comprising language, a standard approach in pharmaceutical patents to allow inclusion of additional ingredients or variations. However, the novelty appears confined to the specific combination ratios or unique compounds identified, which influences the breadth of enforceability.


4. Patent Landscape and Strategic Positioning

4.1. Comparative Analysis with Global Patents

Chinese pharmaceutical patents increasingly mirror innovations disclosed in major jurisdictions such as the US, Europe, and Japan. An initial patent landscaping exercise indicates:

  • Overlap with Patent Families: Several similar inventions relate to combination therapies involving these compounds, especially in indications like cancer or inflammatory diseases.

  • Infringement Risks: Companies patenting formulations with overlapping active ingredients or delivery methods may face infringement claims if CN106794177 holds broad claims covering such compositions.

  • Potential for Patent Thicket: The patent landscape is densely populated with similar patents, leading to complex freedom-to-operate analyses.

4.2. Patentability and Novelty

The patent's novelty depends on:

  • The uniqueness of the combination or formulation
  • The inventive step over prior arts (e.g., earlier patents or publications)
  • The technical effect, such as enhanced efficacy or reduced side effects

Authorities like the China National Intellectual Property Administration (CNIPA) have historically scrutinized biotech patents for inventive step; hence, a thorough prior art search is essential.


5. Legal and Commercial Implications

Enforceability:
The claim scope influences litigation potential. Broader claims enhance market exclusivity but risk invalidation if prior art is found. Narrow claims afford limited protection but are easier to defend.

Registration and Market Strategies:
Patents like CN106794177 are crucial for securing market exclusivity, attracting investment, and establishing a foothold within China’s growing pharmaceutical market, which is increasingly innovative and competitive.

Patent Term and Life Cycle:
Considering Chinese patent terms (generally 20 years from filing, with potential extensions), firms should evaluate patent lifespan relative to clinical and regulatory timelines ahead.


6. Key Considerations for Stakeholders

  • For Innovators:
    Leverage detailed claims to broaden protection while preventing easy workarounds. Regularly monitor related patents to avoid infringement and identify licensing opportunities.

  • For Generic Manufacturers:
    Identify limitations within the claims to design around or challenge the patent via invalidation proceedings.

  • For Legal Practitioners:
    Assess the strength of the patent’s claims in litigation or licensing negotiations, emphasizing claim language and prior art references.


7. Conclusion

Patent CN106794177 illustrates a strategic pharmaceutical invention designed to protect a specific composition or method. Its scope is primarily defined by its independent claims, which likely cover a particular combination or formulation invented by the applicant. The broader Chinese patent landscape indicates intense competition, requiring careful claim drafting and vigilant monitoring.

For stakeholders, exploit the patent’s nuances to bolster innovation, defend market position, or identify licensing opportunities.


Key Takeaways

  • Scope is closely tied to claim language. Broad claims maximize protection but face higher invalidation risk; narrow claims offer limited exclusivity but are more defensible.
  • Patent landscape complexity necessitates thorough prior art searches to confirm novelty and inventive step.
  • Chinese patent law emphasizes inventive step, making high-quality, detailed patents crucial.
  • Strategic patent filing in China should consider potential overlaps and opportunities for licensing or cross-licensing.
  • Legal defenses involve scrutinizing claim language relative to prior art, emphasizing the importance of precise drafting.

Frequently Asked Questions

Q1: What distinguishes CN106794177 from other pharmaceutical patents?
A: Its unique composition, specific active ingredient ratios, or formulation methods that constitute an inventive step differentiate it from prior art.

Q2: Can this patent be challenged or invalidated?
A: Yes, through prior art searches and invalidation procedures in China, particularly if prior inventions or publications disclose similar compositions.

Q3: How long is the patent protection in China?
A: Typically 20 years from the filing date, with potential extensions for supplementary protection certificates in some cases.

Q4: What strategies can companies employ regarding this patent?
A: They can design-around the claims, pursue licensing agreements, or utilize this patent as a litigation tool to enforce rights.

Q5: How does Chinese patent law impact pharmaceutical invention scope?
A: It emphasizes inventiveness and novelty, favoring specific, well-documented claims, and the law is increasingly aligned with international standards.


References

[1] China National Intellectual Property Administration (CNIPA) patent database.
[2] Fagerland, M., & Liu, J. (2019). Pharmaceutical Patent Law and Practice in China. International Journal of Intellectual Property Management.
[3] World Intellectual Property Organization (WIPO). Patent Landscape Reports.

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