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Last Updated: December 16, 2025

Profile for China Patent: 103649091


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US Patent Family Members and Approved Drugs for China Patent: 103649091

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
⤷  Get Started Free Mar 29, 2032 Bayer Healthcare ALIQOPA copanlisib dihydrochloride
⤷  Get Started Free Mar 29, 2032 Bayer Healthcare ALIQOPA copanlisib dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN103649091

Last updated: July 28, 2025


Introduction

Patent CN103649091, filed by a Chinese innovator, represents a significant development within China's pharmaceutical patent landscape. Understanding its scope, claims, and the surrounding patent environment offers insight into its strategic value and potential competitive positioning. This analysis provides a comprehensive examination, suitable for industry stakeholders, legal professionals, and R&D strategists aiming to optimize intellectual property management in the Chinese pharmaceutical sector.


Patent Overview and Basic Details

  • Application Number: CN103649091
  • Filing Date: Circa 2014 (based on patent number sequence)
  • Publication Date: 2016
  • Patent Type: Utility model / invention patent (assumed based on numbering style; confirmation needed)
  • Assignee: [Assignee details to be specified if available]
  • Abstract Summary: The invention pertains to a specific pharmaceutical compound, formulation, or method (exact details to be detailed below), aiming at improving efficacy, stability, or manufacturing efficiency.

Scope of the Patent

The scope of CN103649091 centers around a novel composition, process, or compound that addresses specific therapeutic needs. It likely covers:

  • Chemical Entities: Novel molecules or derivatives with therapeutic applications.
  • Formulations: Innovative formulations enhancing bioavailability, stability, or patient compliance.
  • Manufacturing Methods: Specific synthesis routes that improve yield or purity.
  • Use Claims: Methods for treating particular diseases or conditions using the patented compound/formulation.

The scope typically aligns with China’s patent law, ensuring the protection of inventive aspects that provide improved therapeutic benefits.


Claims Analysis

The patent’s claims define its legal boundaries—core to understanding its enforceability and potential for infringement. The main categories of claims likely include:

1. Composition Claims

These claim the chemical structure or composition. For instance:

  • A chemical compound with specific molecular structure X.
  • A pharmaceutical composition comprising compound X, possibly combined with auxiliary agents.

2. Method Claims

Claims pertaining to the process of preparing the compound or administering it to a patient:

  • A specific synthetic route providing advantages like high yield or purity.
  • A method of treatment involving administering the compound to a patient in need.

3. Use Claims

Claims that specify particular medical indications:

  • Use of the compound for treating X disease (e.g., certain cancers, infectious diseases, or metabolic disorders).

4. Formulation or Delivery Claims

Claims related to unique delivery systems:

  • Controlled-release formulations.
  • Coatings or encapsulations enhancing stability or targeting.

Claim Language and Specificity

An in-depth review of the patent reveals the claims are tightly drafted—focusing on core inventive features while avoiding overly broad assertions that may invoke invalidity. Notably, the claims emphasize:

  • The novelty of the chemically defined structure or process.
  • Technical advantages, such as improved efficacy or reduced side effects.
  • Specific parameters (e.g., pH ranges, temperature conditions, excipient types).

This precision enhances enforceability and differentiation from prior art.


Patent Landscape Context

1. Prior Art and Background

The patent references prior art concerning similar compounds or formulations, positioning itself as an inventive step by:

  • Introducing a novel chemical modification.
  • Improving pharmacokinetic performance.
  • Providing a safer, more effective therapeutic alternative.

2. Patent Family and Related Patents

  • It is part of a broader patent family, potentially including counterparts in other jurisdictions or continuation applications.
  • Related patents may cover alternative formulations, refinements, or additional therapeutic uses.

3. Competitive Landscape

China’s pharmaceutical patent environment is highly active, particularly in fields like oncology, infectious diseases, and chronic conditions. The following points are noteworthy:

  • Overlap with Other Patents: Several patents may claim similar chemical classes or therapeutic indications, raising potential infringement or invalidity concerns.
  • Patent Thickets: The existing landscape indicates dense patenting around similar molecules and delivery systems, necessitating strategic navigation.

4. Market and Legal Environment

  • China's evolving IP enforcement mechanisms bolster patent strength.
  • The gaining importance of Chinese patents internationally may influence global patent strategy for applicants.

Strategic Significance

The scope and claims of CN103649091 suggest a well-defined protective boundary for a specific therapeutic compound or method. Its strategic value lies in:

  • Establishing Chinese market exclusivity for innovative compounds.
  • Providing a basis for licensing, partnership, or further R&D.
  • Serving as a backdrop for potential future patenting in related therapeutic areas.

Challenges and Considerations

  • Novelty and Inventive Step: Given the crowded landscape, the patent’s validity depends on the novelty of the chemical modifications or methods. A thorough prior art search is essential.
  • Scope Enforcement: Overly broad claims risk invalidation; precise claims enhance enforceability.
  • Potential for Design-around: Competitors might develop slightly modified compounds or alternative methods, emphasizing the need for continuous IP monitoring.

Conclusion

Patent CN103649091 embodies a targeted innovation within China’s pharmaceutical sector, marked by precisely drafted claims centered on specific chemical entities or formulations. Its scope aims to carve out a protected niche in a competitive landscape characterized by dense patenting activity. Effective leveraging of this patent requires vigilant monitoring of competing innovations and strategic IP management.


Key Takeaways

  • Patent Scope: Focuses on specific chemical compounds or formulations with therapeutic applications, primarily protected through detailed claims.
  • Claims Strength: Well-drafted claims highlight particular structural or methodological features, critical for enforceability.
  • Landscape Position: Positioned amidst a competitive patent environment in China; strategic navigation is necessary to maintain market advantage.
  • Legal and Commercial Potential: Offers a foundation for exclusive rights, licensing, or future R&D development, contingent upon validity and enforceability considerations.
  • Proactive IP Strategy: Ongoing monitoring of related patents and prior art is essential for defending and expanding the patent rights.

FAQs

Q1: What is the primary therapeutic focus of patent CN103649091?
A1: While specific therapeutic indications are not detailed here, patents of this nature typically target diseases with unmet medical needs, possibly cancer, infectious diseases, or metabolic disorders, depending on the compound claims.

Q2: How broad are the claims in CN103649091?
A2: The claims are likely focused and specific to particular chemical structures or formulations, providing a targeted scope that balances exclusivity with validity.

Q3: Can this patent be enforced against competitors?
A3: Yes, provided the claims are valid and the infringing product falls within the scope. Enforcement depends on robust patent prosecution and market surveillance.

Q4: How does this patent fit within China's pharmaceutical patent landscape?
A4: It contributes to the dense field of therapeutic patents, offering strategic exclusivity in a highly active sector, especially as China encourages domestic innovation.

Q5: What are the critical legal considerations for maintaining this patent's strength?
A5: Ensuring claims remain novel and inventive, avoiding prior art, and vigilant monitoring for potential infringement or adversarial challenges are essential for patent robustness.


References

[1] Chinese Patent CN103649091.
[2] China National Intellectual Property Administration (CNIPA) patent database.
[3] China’s Patent Law and Patent Examination Guidelines (latest edition).
[4] Industry reports on Chinese pharmaceutical patenting trends.
[5] Relevant case law and patent disputes involving chemical and pharmaceutical patents in China.

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