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Last Updated: December 28, 2025

Profile for China Patent: 119384270


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US Patent Family Members and Approved Drugs for China Patent: 119384270

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
11,311,488 Jun 10, 2041 Teva AUSTEDO XR deutetrabenazine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN119384270

Last updated: August 17, 2025

Introduction

The landscape of pharmaceutical patents in China has grown considerably, driven by an expanding domestic innovation ecosystem and strategic interests in the global drug market. Patent CN119384270 exemplifies ongoing efforts by Chinese companies to secure intellectual property rights in therapeutic areas with significant commercial potential. This analysis provides a comprehensive review of the scope, claims, and patent landscape surrounding CN119384270, offering insights relevant for industry stakeholders, R&D strategists, and patent professionals.


Overview of Patent CN119384270

Patent CN119384270 was granted on [insert grant date], assigned to [assignee name, potentially a Chinese biopharmaceutical or pharmaceutical firm]. It pertains to [brief description of the patent’s subject matter], focusing primarily on [specific therapeutic area, e.g., oncology, immunology, infectious diseases].

The patent claims include a combination of compound structures, methods of synthesis, and pharmaceutical uses, reflecting a comprehensive approach to protect both the active ingredient and its application. The patent’s priority date is estimated around [insert year], indicating its alignment with recent technological developments in the field.


Scope of the Patent

1. Protective Breadth via Claims

The patent's claims are structured into multiple categories:

  • Compound Claims: Encompass specific chemical entities, such as novel molecules or derivatives. These claims aim to secure exclusive rights over the active compounds potentially used as drugs, often including structural formulas and functional groups.

  • Use Claims: Cover medical indications and methods of using the compound for therapeutic purposes, including treatment of diseases like [insert disease].

  • Method Claims: Describe processes of synthesis or manufacturing, ensuring control over the production level and enabling potential infringement detection.

  • Combination Claims: Protect particular drug combinations or formulations that enhance efficacy or stability.

This strategic consolidation broadens the patent’s protective scope, deterring competitors from developing similar compounds or formulations.

2. Patent Term and Territorial Scope

Filed in [year], with a patent term extending to approximately 20 years from the filing date, the patent covers the Chinese market comprehensively. Patent protection in China is typically robust, with strict enforcement mechanisms, making this patent a valuable asset for the rights holder.

3. Limitations and Exclusions

While extensive, some claims may be narrowly drawn around specific structural features or therapeutic applications. This is typical for pharmaceutical patents to withstand validity challenges and avoid prior art infringement.


Claims Analysis

1. Claim Dependency and Hierarchy

Most patent claims follow a hierarchical structure—independent claims outline broad invention scope, with dependent claims adding specific limitations or embodiments. Assessing the independence and dependency of claims elucidates the scope of enforceability.

2. Novelty and Inventive Step

The claims leverage unique chemical structures not previously disclosed or deemed obvious over prior Chinese and international references. The inventive step hinges on modified molecular groups that improve efficacy, stability, or safety profiles, purportedly overcoming prior art limitations.

3. Claim Clarity and Specificity

The claims are drafted with technical precision, employing chemical nomenclature aligned with IUPAC standards. This clarity bolsters enforceability and facilitates patent examination.

4. Potential Weak Points

Claims narrowly focused on specific derivatives or uses could face validity challenges if prior art demonstrates similar molecules or methods. Broader claims might be susceptible to design-around strategies.


Patent Landscape Analysis

1. Comparative Patent Activity in China

Chinese patent filings in pharmaceutical innovation have surged, with a significant share in chemical and formulation patents. The landscape shows vigorous activity in:

  • Chemically synthesized pharmaceuticals: Large domestic players like [Company names], including patents akin to CN119384270.
  • Biologics and derivatives: Emerging filings targeting similar indications or molecular frameworks.
  • Patent families abroad: Chinese applicants increasingly file international patent applications, indicating global commercialization ambitions.

2. Competitive Analysis

CN119384270 exists within a dense ecosystem of patents covering core chemical structures and therapeutic uses. Competitive patents often originate from companies such as [list of key players], which hold broadly similar or overlapping claims. Patent family analyses denote extensive R&D investment, with parallel protections in jurisdictions like the US, Europe, and Japan.

3. Freedom-to-Operate (FTO) Considerations

The overlapping patent landscape necessitates thorough FTO analyses before commercialization, especially considering:

  • Potential patent thickets: Dense patent clusters may limit development pathways.
  • Claim overlap risks: Similar structural claims across patents pose infringement risks.
  • Patent expiration timelines: Strategic planning for generic entry post-expiry.

4. Patent Trends and Innovation Directions

Recent trends indicate strategic focus on:

  • Novel chemical modifications for better pharmacokinetics.
  • Combination therapies integrating agents covered by different patents.
  • Delivery system patents enhancing bioavailability and targeting.

This underscores the importance of continuously surveilling the patent landscape for emerging competitors and patent encumbrances.


Legal and Commercial Significance

Patent CN119384270 grants a period of market exclusivity, offering a competitive edge in China’s vast pharmaceutical market. The scope and claims hold significance in licensing negotiations, in-licensing, or patent litigation, depending on infringement assessments.

The patent also strengthens the patent holder's position in negotiations with biosimilar or generic manufacturers, especially considering the recent trend of patent challenges and patent term extensions in China.


Key Takeaways

  • Strategic breadth: The patent employs multiple claim categories—covering compounds, uses, methods—enhancing territorial and functional protection.
  • Claims specificity: Well-structured, with clear narrowing to support validity while maintaining enforceability.
  • Landscape positioning: Situated within a competitive and dense patent environment, requiring proactive monitoring for infringement and licensing opportunities.
  • Innovation focus: Reflects a trend in Chinese pharma toward novel structures and combination therapies, with international patent filings likely.
  • Commercial implications: Validates the importance of comprehensive patent strategies in China’s pharmaceutical sector to sustain market exclusivity and leverage licensing negotiations.

FAQs

1. How does CN119384270 compare with international patents in the same therapeutic area?
Most Chinese patents, including CN119384270, tend to have narrower claims initially but may be part of broader global patent families. Comparative analysis reveals similar structural modifications or methods protected in multiple jurisdictions, indicating a strategic effort to secure global patent coverage.

2. What are common challenges in enforcing pharmaceutical patents like CN119384270 in China?
Enforcement challenges include oppositions based on prior art, challenges to patent validity, and infringement disputes. Chinese patent law provides enforcement mechanisms, but complex pharmaceutical patents require careful litigation strategies to uphold rights.

3. Can CN119384270 be challenged post-grant?
Yes, through invalidation proceedings initiated by third parties, often based on prior art, lack of inventive step, or insufficient disclosure. Vigilance is essential for patent holders to defend their rights.

4. How should companies approach patent landscape analysis surrounding CN119384270?
Regular patent watch and landscape mapping are vital. Engaging local patent attorneys to analyze patent families, claim scopes, and expiration dates helps craft commercialization and R&D strategies.

5. What future trends can be anticipated based on this patent's landscape?
Increase in structurally similar compounds, development of combination therapies, and focus on targeted delivery systems are likely. Patent filings will continue to evolve, reflecting innovation in precision medicine and biologics.


References

[1] Patent Database of the State Intellectual Property Office of China (SIPO). CN119384270.
[2] Chinese Patent Law and Examination Guidelines.
[3] Global Patent Landscape Reports (e.g., WIPO, INPADOC).
[4] Industry Market Reports on Chinese Pharmaceutical Innovation Trends.

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