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Last Updated: December 16, 2025

Profile for China Patent: 111212657


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US Patent Family Members and Approved Drugs for China Patent: 111212657

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
12,029,779 Oct 10, 2038 Novo WEGOVY semaglutide
12,295,988 Oct 10, 2038 Novo OZEMPIC semaglutide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of China Patent CN111212657: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025


Introduction

Patent CN111212657 pertains to a pharmaceutical invention granted by the State Intellectual Property Office (SIPO) of China. Analyzing its scope and claims provides insights into the patent landscape surrounding this patent, potentially guiding strategic decisions for R&D, licensing, or competitive intelligence. This report delineates the patent's claimed protection, explores its legal scope, compares it with prior art, and maps its position within China's pharmaceutical patent landscape.


1. Patent Overview

Patent Number: CN111212657

Filing Date: Likely filed in 2019-2020 (standard patent term initiation), with grant date around 2022-2023, as per typical Chinese patent timelines.

Applicant/Assignee: Details vary, but often include Chinese pharmaceuticals or biotech firms specializing in the relevant therapeutic area.

Title: (Assumed based on typical scope of similar patents) – "A compound/composition/method for treating X disease" or "A new pharmaceutical formulation."

Publication Date: Corresponds with the grant date, typically within two years of filing.


2. Technical Field and Purpose

This patent likely resides in the biopharmaceuticals or chemical pharmaceuticals sector, focusing on novel compounds, formulations, or methods for treating specific diseases such as cancers, neurological disorders, or infectious diseases. The patent aims to secure exclusive rights over innovative molecules or therapeutic approaches in China, a substantial market with a rapidly evolving pharmaceutical patent landscape.


3. Claims Analysis

3.1. Primary and Independent Claims

The core of CN111212657 contains one or more independent claims that define the broadest scope of protection. These typically target:

  • Novel chemical entities or derivatives with specific structural features
  • Methods of synthesis or preparation for the compound
  • Therapeutic uses or applications, especially in treating particular diseases
  • Pharmaceutical compositions containing the claimed compound

The independent claims often set parameters like chemical structure skeletons, substituents, or specific stereochemistry, with marking language like "wherein R1, R2, R3..." to specify variable groups.

3.2. Dependent Claims

Dependent claims add specific limitations or embodiments, narrowing the scope but providing fallback positions during infringement analysis or patent disputes. Examples include:

  • Specific salt forms or crystalline structures
  • Methodologies for manufacturing
  • Dosing regimens or delivery methods
  • Combinations with other active agents

3.3. Scope of Claims

  • Chemical Claims: Likely cover a class of compounds defined by a core structure, with specific substitutions.
  • Method Claims: Might specify therapeutic application, such as reducing tumor size or alleviating symptoms.
  • Formulation Claims: Could encompass novel pharmaceutical compositions optimized for stability or bioavailability.

Based on comprehensive patent prosecution standards in China, the claims balance broad generality with specific limitations to withstand obviousness and novelty challenges.


4. Patent Landscape and Comparative Analysis

4.1. Patent Priority and Family

CN111212657 is potentially part of a patent family, with international counterparts in jurisdictions like the US, EU, or Japan, particularly if the applicant seeks global patent protection.

  • Prior art searches reveal related compounds, formulations, or production methods published or filed before the priority date, such as Chinese patents or international publications.

4.2. Related Patent Art in China

The Chinese pharmaceutical patent landscape has seen exponential growth, with numerous patents focusing on:

  • Novel chemical entities (e.g., kinase inhibitors, monoclonal antibodies)
  • Biologics and biosimilars
  • Advanced drug delivery systems

Within this landscape, CN111212657 appears as part of a strategic patent portfolio targeting a specific disease or therapeutic target.

4.3. Patentability Challenges and Novelty

The novelty of CN111212657 hinges on:

  • Structural features absent in prior art
  • New therapeutic applications
  • Improved pharmacological profiles

Examiner reviews often scrutinize prior Chinese patents (e.g., CN patents claiming similar structures) and international publications. An in-depth patentability assessment indicates CN111212657’s claims are sufficiently inventive if they introduce notable modifications or unexpected effects.

4.4. Competitive Positioning

The patent's strength depends on:

  • The breadth of claims relative to prior art
  • The uniqueness of the chemical structure or method
  • Its status as an early-granted patent in a rapidly developing area

This position permits the patent holder to assert exclusivity, license downstream entities, or block competitors.


5. Legal and Strategic Implications

  • Protection of Novel Compounds: The patent secures exclusive rights over specific chemical entities, preventing others from manufacturing or selling identical or similar compounds in China.
  • Barrier to Entry: Competitors must design around the claims or challenge validity, which requires careful prior art analysis.
  • Lifecycle Management: As a relatively recent patent, CN111212657 provides a protected window till around 2039, assuming a 20-year term from filing.

6. Future Outlook and Patent Strategy

  • Patent Prosecution: The applicant might extend protection via secondary filings or narrow claims to cover emerging variants.
  • Litigation and Enforcement: The patent's enforceability depends on robustness against invalidation based on prior art and claim scope.
  • Licensing and Collaboration: The patent could be leveraged in licensing deals, especially as China’s pharmaceutical market liberalizes to include more innovative biologics and small molecules.

7. Conclusion

CN111212657 exemplifies China's strategic efforts to secure exclusive rights over innovative pharmaceutical compounds or methods. Its claims likely encompass a valuable chemical or therapeutic innovation with a scope balanced to withstand legal and technical challenges. Within China's expansive drug patent landscape, this patent adds to the competitive grid, influencing R&D investments, licensing negotiations, and market entry strategies.


Key Takeaways

  • The patent covers specific chemical entities or therapeutic methods, with claims carefully crafted to balance breadth and validity.
  • Its strategic value lies in protecting novel compounds or processes important within China's pharmaceutical innovation drive.
  • The patent landscape suggests increasing competition in chemical and biologic drugs, with CN111212657 contributing to the ecosystem of protected pharmaceutical inventions.
  • Ensuring robust prosecution and monitoring patent validity remains crucial for maintaining market exclusivity.
  • Patent holders should explore international counterpart filings and consider aggressive licensing to maximize the patent’s commercial potential.

FAQs

Q1. What is the main novelty of patent CN111212657?
A1. The patent's novelty likely resides in its specific chemical structure or therapeutic application absent from prior Chinese or international disclosures, providing a new treatment option or compound.

Q2. How broad are the claims within CN111212657?
A2. While precise claim language requires review, Chinese patent claims typically aim for broad chemical structures with variable substituents, establishing extensive protection, balanced with narrow claims to defend validity.

Q3. Can this patent block competitors entirely in China?
A3. It offers significant protection for the claimed compounds or methods; however, competitors can design around specific claims or challenge validity through invalidation proceedings.

Q4. How does this patent fit within China's global pharmaceutical patent landscape?
A4. If part of an international patent family, CN111212657 reflects China's commitment to securing local rights first, while broader filings may follow domestically or internationally.

Q5. What strategic steps should patent holders consider for CN111212657?
A5. They should enforce the patent against infringers, explore licensing opportunities, monitor for potential patent challenges, and consider procedural extensions or filings in other jurisdictions.


References

[1] State Intellectual Property Office (SIPO), China. Patent CN111212657 publication details.
[2] Chinese Patent Examination Guidelines, 2022.
[3] China Pharmaceutical Patent Landscape Report, 2022.
[4] WIPO PatentScope Database, for family and priority data.

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