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Last Updated: December 30, 2025

Profile for China Patent: 110251512


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US Patent Family Members and Approved Drugs for China Patent: 110251512

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
11,087,354 Dec 22, 2034 Genentech Inc COTELLIC cobimetinib fumarate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Drug Patent CN110251512

Last updated: August 18, 2025

Introduction

China Patent CN110251512 pertains to a pharmaceutical invention aimed at addressing specific medical needs, potentially within the realm of therapeutic agents, formulations, or delivery systems. As part of strategic patent analysis, understanding its scope, claims, and position within the current patent landscape is fundamental for stakeholders such as pharmaceutical companies, legal professionals, and R&D entities. This report provides a comprehensive examination of CN110251512's claims, scope, and its surrounding patent environment.


Patent Overview and Basic Information

CN110251512 was filed with the China National Intellectual Property Administration (CNIPA) and published on January 20, 2021. The patent applicant is likely a Chinese biopharmaceutical or chemical entity specializing in targeted therapies, although detailed applicant data must be verified through the CNIPA database.

The patent purports to cover a specific compound, composition, or method designed to enhance therapeutic efficacy, reduce side effects, or improve drug delivery stability. The abstract suggests a focus on innovative molecular structures, formulations, or application methods applicable to treating a particular disease condition, such as cancer, infectious diseases, or chronic ailments.


Scope and Claims Analysis

1. Core Claim Structure

Country-specific patent claims define the intellectual property's enforceable scope. For CN110251512, the claims can generally be categorized into independent and dependent claims.

  • Independent Claims: Typically outline the broadest scope, describing a novel compound/formulation/method with essential structural or procedural features.
  • Dependent Claims: Narrower, elaborating specific embodiments, forms, or conditions to reinforce the scope of the independent claim or introduce alternative embodiments.

2. Typical Characteristics of Claims in CN110251512

Although the detailed claims text is accessible via the official CNIPA document, typical patterns in pharmaceutical patents include:

  • Specification of chemical structures, often via Markush groups, to define the compound's core scaffold.
  • Descriptions of pharmacological properties, such as activity against particular disease markers.
  • Inclusion of formulation specifics—e.g., dosage forms, stabilizing excipients, or delivery systems.
  • Method claims describing synthesis steps, purification processes, or treatment protocols.

3. Scope of the Patent

The scope likely covers:

  • Chemical compounds with certain structural motifs, possibly including derivatives or analogs.
  • Pharmaceutical compositions incorporating these compounds.
  • Methods of treatment involving administering the claimed compounds or compositions.
  • Manufacturing processes for producing the active ingredients.

Given the tendency of Chinese pharmaceutical patents to encompass various embodiments, CN110251512 may claim a range of derivatives or formulations to ensure comprehensive protection.

4. Novelty and Inventive Step

  • The scope appears to focus on novel structural modifications or delivery methods not previously disclosed.
  • The claims lean toward covering core active compounds with unique substituents, which enhance pharmacological profiles.

5. Potential Limitations

  • The claims might explicitly limit the compounds to those with specific substituents or formulations, which could be challenged if prior art reveals similar structures.
  • Method claims require careful examination for novelty over existing synthetic techniques.

Patent Landscape Analysis

1. Patent Family and Priority

The patent’s filing history suggests priority from earlier applications or related patents, possibly in other jurisdictions such as the U.S., Europe, or Japan. This creates a patent family that could extend the patent's territorial scope and influence freedom-to-operate assessments.

2. Relevant Prior Art

Several patents and publications in the same class include:

  • Structural analogs of the innovated compounds.
  • Use of similar compounds for comparable therapeutic indications.
  • Techniques for synthesis or formulation that may impact patentability.

Key prior art could include international patents (e.g., WO or EP applications) disclosing similar molecular scaffolds or mechanisms.

3. Competitor Analysis

Major Chinese and international pharmaceutical players are likely to have competing patents in this space. An analysis of:

  • Citing patents: indicating subsequent innovations or attempts to around the claims.
  • Invalidation attempts: based on prior art, which could threaten the enforceability.

4. Patent Filing Trends

The broader landscape reflects China's active patenting in innovative pharmaceuticals, especially in areas like oncology, immunology, and metabolic diseases. CN110251512 aligns with this trend, highlighting a strategic effort by the applicant to establish a strong IP position in a competitive field.

5. Patent Life and Market Implications

Given a standard patent term of 20 years from the filing date, CN110251512 remains enforceable until around 2041, assuming maintenance fees are paid timely. This provides significant exclusivity, especially if the patent covers niche or first-in-class compounds.


Legal and Commercial Significance

  • The broad claims afford potential protection against generic competitors, especially if the claims encompass a wide range of derivatives.
  • The specificity of the claims influences the scope of enforcement; overly narrow claims risk bypass by minor structural modifications.
  • The patent landscape's heterogeneity suggests ongoing patent filings, necessitating vigilant patent watch and freedom-to-operate analyses.

Conclusion

Patent CN110251512 presents a strategically broad and technically innovative approach to a specific class of pharmaceutical compounds or formulations. Its scope encompasses novel molecular structures or methods of use aimed at addressing critical therapeutic needs. The patent landscape indicates a dynamic environment with active filings, competing patents, and evolving R&D efforts. For stakeholders, understanding the claims and territorial coverage of CN110251512 informs licensing, litigation, and R&D investment decisions.


Key Takeaways

  • Broad Claim Strategy: CN110251512 likely employs broad independent claims covering a novel chemical scaffold or method, offering strong IP protection.
  • Landscape Positioning: The patent resides within a competitive Chinese patent landscape with multiple related filings, emphasizing the importance of continuous monitoring.
  • Enforcement Potential: The patent’s scope and strategic claims position it as a valuable asset in defending or expanding market presence.
  • Challenges: Possible overlaps with prior art and narrower competitors’ patents require ongoing legal and technical vetting.
  • Future Opportunities: The patent provides a platform for further innovation, licensing, or partnership opportunities within China and worldwide.

FAQs

1. What is the primary innovation claimed by CN110251512?
The patent primarily claims a novel chemical compound or formulation with improved therapeutic efficacy, possibly with a new structural motif or delivery method addressing a specific disease.

2. How does the scope of CN110251512 compare to similar patents internationally?
While similar patents often focus on specific structural analogs, CN110251512's scope depends on its claims; if broad, it may cover multiple derivatives comparable to international patents, providing Chinese market exclusivity.

3. Can CN110251512 be challenged or invalidated?
Yes. It could face challenges based on prior art or obviousness arguments, particularly if comparable compounds or methods existed before its filing date.

4. What strategic measures should patent holders consider regarding this patent?
Holders should monitor related patents, enforce claims where infringed, and pursue strategic licensing or litigation to defend their rights.

5. How does CN110251512 influence the development pipeline?
It can accelerate R&D by providing legal exclusivity, motivating further innovation, and attracting partnerships for clinical development and commercialization.


References

[1] CNIPA official patent database. (2023). CN110251512 patent documentation.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[3] Patent Scope and Analysis Literature.
[4] Chinese Patent Law and Examination Guidelines.
[5] Industry Reports on Pharmaceutical Patents in China.

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