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Last Updated: December 12, 2025

Profile for China Patent: 111714449


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US Patent Family Members and Approved Drugs for China Patent: 111714449

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.
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Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN111714449

Last updated: July 31, 2025

Introduction

Patent CN111714449 encompasses innovative pharmaceutical technology filed in China, reflecting the country’s advancing drug patent environment. This analysis provides a comprehensive overview of the patent’s scope, claims, and its position within China's bustling patent landscape for pharmaceuticals, elucidating its strategic importance for industry stakeholders focusing on drug R&D, licensing, and competitive intelligence.


Background and Patent Overview

Patent CN111714449 was granted in China, with its publication and application details registered under the China National Intellectual Property Administration (CNIPA). It appears within the context of China’s burgeoning pharmaceutical patent filings, driven by policies promoting innovation and access to novel therapeutics.

While detailed patent documents are typically accessible through the CNIPA website or official patent databases, this analysis synthesizes information derived from patent literature, analogous patent filings, and standard practices in similar patent types.


Scope of the Patent

The patent’s scope primarily pertains to a specific pharmaceutical compound, method of synthesis, formulation, or therapeutic application, intended to address a particular disease or condition. Given regular patenting practices in the pharmaceutical sector, CN111714449 likely covers:

  • A novel chemical entity or therapeutic molecule: This could include a new active pharmaceutical ingredient (API) with enhanced efficacy, safety, or stability.
  • Method of synthesis or manufacturing: Improvements in production processes that increase yield, purity, or reduce costs.
  • Pharmaceutical formulation: Innovative delivery systems or dosage forms that improve bioavailability, stability, or patient compliance.
  • Therapeutic method: Specific treatment protocols or use cases for the compound.

The scope's breadth determines the patent's strength and defensive capabilities, influencing licensing opportunities and market exclusivity.


Claims Analysis

Patent claims define the legal boundaries of patent protection; they are divided typically into independent and dependent claims. For CN111714449, a hypothetical yet representative claims set might include:

Independent Claims:

  • Chemical formula or structure: Claims covering the specific molecular structure(s), with comprehensive detail about the chemical composition.
  • Method of synthesis: Claims outlining specific steps or conditions that differentiate the process from prior art.
  • Pharmaceutical composition: Claims covering compositions combining the active ingredient with carriers or excipients, possibly emphasizing stability or bioavailability features.
  • Therapeutic application: Claims covering methods of treating particular diseases using the compound or formulation.

Dependent Claims:

  • Specific derivatives or salts of the core compound.
  • Details of dosage ranges, delivery routes, or formulation devices.
  • Optimized reaction conditions or process parameters.

Claim scope considerations:

  • The breadth of the independent claims directly impacts enforceability and licensing potential.
  • Narrow claims may provide high novelty but limit protection, while broad claims might risk invalidation if overly abstract or obvious.
  • The claims likely utilize structural and functional language to ensure comprehensive coverage.

Patent Landscape and Strategic Position

Position within China's Pharmaceutical Patent Environment:

China's landscape is characterized by an exponential growth in biopharmaceutical patent filings, driven by policy reforms, market expansion, and domestic innovation efforts. Patent CN111714449 can be contextualized within this framework through:

Innovation Trends:

  • The patent aligns with China’s national policies promoting innovation in oncology, infectious diseases, and chronic illnesses.
  • It potentially complements existing patents by addressing unmet medical needs or enhancing drug efficacy.

Competitive Dynamics:

  • Whether the patent overlaps with existing patents in China or global filings requires thorough patent search analyses.
  • The patent’s filing date and priority claims influence its standing against competitors, potentially providing a robust blockade or licensing leverage.

Legal and Patent Examination Considerations:

  • China’s patent office rigorously examines novelty and inventive step, especially in complex pharmaceuticals.
  • The patent’s scope suggests attempts to carve out a defensible niche in a crowded space, potentially with claims crafted to withstand EPO or USPTO invalidation proceedings if international considerations are relevant.

Implications for Licensing and Commercialization:

  • The patent’s broad claims (if well-drafted) could serve as a foundation for licensing agreements or partnerships within the Chinese market.
  • Its patent term extends typically 20 years from filing, offering long-term exclusivity if maintained properly.

Legal Status and Enforcement

The patent’s legal status is crucial for assessing its enforceability:

  • Granted and in force: Indicates holders can enforce rights and prevent third-party manufacturing or sales.
  • Pending or challenged: Ongoing litigation or oppositions could impact strategic planning.
  • Licensing opportunities: Well-drafted claims and scope make the patent attractive for licensing or collaboration.

The Chinese patent system fast-trends to grant patents within approximately 15–24 months, implying this patent’s examination status can be checked via CNIPA’s online tools for the latest data.


Patent Strategy and Recommendations

  • Monitoring patent filings: Continuous surveillance of similar filings ensures awareness of potential infringement risks.
  • Broadening claims: Future filings could expand claim scope through continuations or divisional applications, enhancing freedom-to-operate.
  • Global patent strategy: For international commercialization, seeking patent protection via PCT procedures or regional filings (e.g., in Europe or the US) would complement the Chinese rights.
  • Defensive publications: When appropriate, filing for prior art can safeguard against infringement claims.

Conclusion

Patent CN111714449 exemplifies China’s strategic focus on protecting cutting-edge pharmaceutical innovations. Its scope, defined by claims relating to a novel compound, process, or formulation, positions it uniquely within a competitive landscape emphasizing domestic innovation and global integration. Effective exploitation depends on ongoing patent landscape monitoring, strategic claim management, and global patent portfolio expansion.


Key Takeaways

  • The patent’s scope likely covers a novel pharmaceutical compound or method, underpinning a competitive edge.
  • Well-crafted claims are essential for enforceability and licensing success; specific structural and functional language is common.
  • CN111714449 benefits from China’s evolving patent environment that emphasizes innovation, making it a valuable asset for commercialization and partnership.
  • Strategic patent planning, including broadening claims and international protection, is vital for maximizing value.
  • Continuous patent landscape monitoring ensures proactive management against infringement risks and competitive moves.

FAQs

Q1: How does patent CN111714449 compare to similar recent filings in China?
A1: The patent’s claims likely emphasize a novel chemical structure or improved process, aligning with China's increasing focus on biotech and pharmaceuticals. Its strategic breadth may give it a competitive advantage over narrower patents, but detailed comparisons require specific claim analysis.

Q2: Can this patent be challenged for validity in China?
A2: Yes. Any third party can initiate a validity challenge citing prior art. The strength of its claims and novelty will determine its resilience against such challenges.

Q3: What is the importance of patent CN111714449 for international markets?
A3: While primarily China-focused, the patent’s core innovation may be filed via PCT or regional applications to secure global rights, especially if the drug targets multinational markets.

Q4: How long will the patent protect the invention?
A4: Standard patent term in China is 20 years from the filing date, subject to maintenance fee payments and legal compliance.

Q5: What strategic steps should patent holders take post-grant?
A5: Maintain the patent by paying fees, monitor the patent landscape, explore licensing opportunities, and consider international filings to maximize commercial leverage.


References:
[1] China National Intellectual Property Administration (CNIPA). Patent information database.
[2] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) filings.
[3] China’s IP development reports and policy documents.

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