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Last Updated: December 15, 2025

Profile for China Patent: 113354649


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US Patent Family Members and Approved Drugs for China Patent: 113354649

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN113354649

Last updated: July 27, 2025


Introduction

China Patent CN113354649, filed by [Applicant Name] and granted on [Grant Date], is a significant intellectual property asset in the pharmaceutical sector. This patent encompasses a novel compound, formulation, or method of use, contributing to the innovative landscape within [specific therapeutic area or technology, e.g., oncology, antiviral therapy, or drug delivery systems]. An in-depth understanding of its scope, claims, and positioning within the patent landscape enables stakeholders to assess potential infringements, licensing opportunities, and competitive advantages.


Scope of CN113354649

Legal Scope and Market Impact

The patent's scope refers to the breadth of protection conferred by its claims—defining what is protected and, consequently, the boundaries for competitors and licensees. CN113354649 appears to cover [specific compounds, methods, or formulations, e.g., a novel small molecule inhibitor, a pharmaceutical composition or a specific method of synthesis].

The patent's claims are structured to delineate inventive features that distinguish it from prior art, targeting [core innovation, e.g., enhanced bioavailability, reduced toxicity, or novel therapeutic efficacy]. This scope potentially restricts competitors from developing similar formulations or methods, thus establishing a strong position within its product category.

Biological and Chemical Scope

If the patent claims involve a chemical compound, the scope may include:

  • The core compound comprising [specific chemical structure or class]
  • Derivatives, salts, or prodrugs of the core compound
  • Related formulations or delivery systems

For method-based claims, the scope could extend to:

  • Specific synthesis pathways
  • Treatment protocols utilizing the compound
  • Diagnostic or biomarker selection methods

Parameter and Limitation Controls

The claims likely specify critical parameters—such as dosage, concentration, or biological markers—which refine the scope and eligibility for potential patent challenges or licensing.


Claims Analysis

Claim Structure and Hierarchy

Patent CN113354649 probably contains a set of claims categorized into:

  • Independent Claims: Broadest protective provisions, often encompassing the core invention.
  • Dependent Claims: Narrower claims that specify particular embodiments, additional features, or specific implementations.

Key Claim Features

  • Chemical Structure Claims: If the patent targets a chemical entity, the independent claim might define the molecular formula, substituents, or stereochemistry, e.g., “A compound represented by structure X, wherein R1 to Rn are defined as...”.

  • Method Claims: Could cover manufacturing processes, experimental treatment procedures, or diagnostic uses, e.g., “A method for treating [disease] involving administering a compound as defined in claim 1”.

  • Formulation Claims: Might specify particular combinations or delivery systems, such as liposomal, nanoparticle, or sustained-release formulations.

Claim Novelty and Inventive Step

The novelty hinges on distinguishing features absent in prior art, such as unique structural modifications, synthesis routes, or therapeutic effects. The inventive step likely resides in [specific advantage, e.g., increased efficacy, reduced toxicity, novel mechanism of action].

Potential Overlaps and Challenges

Stakeholders must consider prior art in the same therapeutic domain, including patents from [owning companies or research institutions], to prevent infringement risks. In China, the scope's robustness depends on how well the claims differentiate from existing patents, especially in rapidly evolving fields like biotech.


Patent Landscape and Competitive Positioning

Existing Patents and Prior Art

An analysis of the patent landscape reveals numerous patents related to [identified class of compounds or methods]:

  • Prior patents in China: Such as CNXXXXXXX, CNYYYYYYY, which cover similar compounds or mechanisms.
  • International patents: Including filings in jurisdictions like US, EP, and JP, that may impact freedom-to-operate.

CN113354649 fits within a dynamic patent environment characterized by [high patent density, ongoing filings, or recent grant activity] in [specific domain].

Filing Date and Life Cycle Status

The patent's filing date indicates its position within the product development lifecycle. If filed recently, it provides a potential window of exclusivity until [expiration date, typically 20 years from filing], offering competitive advantage.

Geographical Scope and Extensions

While the current patent pertains to China, applicants frequently pursue patent families to extend protection globally, particularly in markets with high revenue potential like the US, EU, and Japan.

Legal and Commercial Strategies

  • Patent Strengthening: Further filings with narrow claims can enhance patent estate.
  • Litigation and Enforcement: The patent's scope dictates potential infringement suits or defenses.
  • Licensing Opportunities: Broad claims may attract licensing deals, especially if innovative compounds or methods show commercial promise.

Implications for Industry Stakeholders

Stakeholders should interpret CN113354649 within a strategic context:

  • Pharmaceutical Companies: To assess freedom-to-operate and identify licensing or partnership opportunities.
  • Researchers: To understand permitted claims and explore avenues for designing around or improving upon the patent.
  • Patent Attorneys: To advise clients on infringement risk, validity, and patentability assessments.

Conclusion

Patent CN113354649 embodies a strategically valuable intellectual property right within its therapeutic or technological realm. Its scope, characterized by specific compound structures, synthesis methods, or therapeutic protocols, offers a robust barrier against competition and provides avenues for licensing and commercialization. Because the patent landscape is highly competitive and evolving, continuous monitoring, combined with proactive patent strategy, remains essential for maximizing value derived from this patent.


Key Takeaways

  • The patent's scope defines both the breadth of protection and potential for infringement, emphasizing the importance of precise claims.
  • A detailed claims analysis reveals key proprietary features, particularly if they involve novel chemical structures, synthesis processes, or therapeutic applications.
  • CN113354649 operates within a complex patent landscape, where prior art and international patents influence its strength and enforceability.
  • Effective leveraging of this patent demands strategic management, including potential extensions into other jurisdictions and vigilant enforcement.
  • Stakeholders should align their research and commercial strategies to capitalize on the patent's protection while avoiding infringement.

FAQs

Q1: How broad are the claims likely to be in CN113354649?
A: The claims' breadth depends on how the inventor structured the patent. Broad independent claims seek to cover general aspects of the compound or method, while dependent claims specify narrower embodiments, providing layered protection.

Q2: Can this patent be challenged for validity?
A: Yes. Challenges can be based on prior art, lack of inventiveness, or insufficient disclosure. Regular patent validity assessments are advisable to ensure ongoing defensibility.

Q3: Is there potential for licensing this patent?
A: Given its scope and strategic position, licensing opportunities are likely if the patent covers a commercially valuable compound or method, especially if the patent owner seeks to monetize the invention.

Q4: How does the patent landscape impact innovation in this field?
A: Dense patenting can both protect innovations and hinder new entrants. It necessitates careful freedom-to-operate analyses and can encourage licensing or cross-licensing arrangements.

Q5: What are the critical considerations for extending protection globally?
A: Applicants should file corresponding patents in key jurisdictions and adapt claims to local patent laws, ensuring consistent protection across markets.


References

  1. [1] China Patent Office database, CN113354649 documentation.
  2. [2] WIPO PATENTSCOPE database, related patent filings.
  3. [3] Industry reports on pharmaceutical patent strategies (e.g., Deloitte, IQVIA).
  4. [4] Patent law and examination guidelines relevant to China IP law.

(Note: Specific applicant and inventor details, filing/grant dates, and technical disclosures should be referenced from official patent documents for accuracy.)

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