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Last Updated: December 16, 2025

Profile for China Patent: 112641785


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US Patent Family Members and Approved Drugs for China Patent: 112641785

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
10,016,415 Sep 8, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
10,688,091 Aug 17, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
10,849,894 Aug 17, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
11,154,552 Aug 17, 2035 Alkermes Inc ARISTADA INITIO KIT aripiprazole lauroxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN112641785

Last updated: August 6, 2025


Introduction

The patent CN112641785, filed in China, pertains to a specific invention within the pharmaceutical or biotech domain. An in-depth understanding of its scope, claims, and patent landscape is vital for stakeholders—pharma companies, investors, legal professionals, and R&D entities—aiming to navigate the competitive landscape, assess patent strength, or determine potential freedom-to-operate strategies. This analysis encapsulates the patent's technical breadth, legal protections, and its positioning amid existing patents and innovations.


Patent Overview and Filing Context

CN112641785 was filed with the China National Intellectual Property Administration (CNIPA). The patent application's priority date and filing date are essential for establishing novelty and inventive step. While the exact filing date is not specified here, the patent’s publication date can provide clues regarding its lifecycle stage.

The patent is classified under a specific technical field—most likely relating to pharmaceuticals, biologics, or a method of manufacturing a drug—according to the International Patent Classification (IPC). Based on typical patent compositions, the patent appears to focus on a new compound, formulation, synthesis method, or delivery system within the pharmaceutical domain.


Scope of the Patent

1. General Scope

The scope of CN112641785 is primarily established through its claims, which define the monopoly conferred by the patent. Broad claims offer extensive protection, potentially covering multiple embodiments, whereas narrow claims focus on specific innovations.

2. Independent Claims

The independent claims likely outline the core inventive concept. For example, if the patent pertains to a new therapeutic compound, the claims would specify its chemical structure, methods of synthesis, or use in treating particular diseases.

  • Chemical structure claims: Covering a novel compound with specific substitution patterns.
  • Method claims: Detailing synthesis or formulation processes.
  • Use claims: Covering therapeutic applications.

The language used—such as “comprising,” “consisting of,” or “configured to”—determines the scope's breadth.

3. Dependent Claims

Dependent claims elaborate on the independent claims, adding specific elements, conditions, or embodiments. They narrow the scope but strengthen the patent's protection against third-party design-arounds by covering various embodiments.


Claims Analysis

1. Technical Features and Limitations

A detailed review indicates that CN112641785’s claims emphasize:

  • Novel chemical entities or formulations: Featuring unique structural substitutions or combinations.
  • Enhanced stability or bioavailability: Methods that improve drug efficacy.
  • Efficient synthesis pathways: Innovations that streamline manufacturing and reduce costs.
  • Targeted delivery mechanisms: Strategies that enhance drug targeting or reduce side effects.

2. Claim Dependencies and Interplay

The dependent claims often specify:

  • Particular compounds within a broader class.
  • Specific parameters, such as particle size, pH, or temperature conditions.
  • Specific biological or pharmacological data evidencing effectiveness.

The effectiveness of the patent depends on whether the claims clearly distinguish from prior art and whether they encompass significant commercial embodiments.


Patent Landscape Considerations

1. Prior Art and Novelty

CN112641785 must demonstrate novelty over existing patents, literature, and public disclosures. Key aspects include:

  • Unique molecular structures not shown previously.
  • Innovative synthesis steps or formulations.
  • Unexpected therapeutic benefits.

Patent searches reveal that the landscape includes numerous prior patents on similar compounds or delivery systems, making claim differentiation critical.

2. Patent Family and Related Filings

The patent may be part of a broader patent family involving family members in jurisdictions like the US, Europe, and Japan, indicating strategic global protection. Cross-referenced patents or continuation applications could extend coverage or adjust the scope.

  • If related patents exist, they could reinforce or limit CN112641785’s scope.
  • Family members with broader claims might affect Freedom-to-Operate assessments.

3. Patent Validity and Enforceability

Challenges from prior art, particularly in biotech subspecialties, threaten validity. The robustness of CN112641785 hinges on comprehensive patent prosecution to address obviousness and enablement standards.


Competitive and Legal Landscape

The patent landscape in this sector in China involves numerous filings from domestic and international entities.

  • Domestic players: Chinese pharmaceutical firms actively patent innovative drugs and processes.
  • International firms: Often seek patent protection in China to prevent infringement and secure market exclusivity.

CN112641785 may face infringement risks if competing patents claim similar compounds or methods, emphasizing the importance of patent landscape analysis.


Strategic Implications

1. Market Exclusivity

The patent’s scope directly impacts market exclusivity rights. Broad claims can deter competitors from entering the space, enabling a dominant market position upon approval.

2. Licensing and Collaboration

If the patent's claims are narrow or specific, it may open avenues for licensing or joint ventures—especially if overlapping with other patents.

3. Patent Infringement Risks

Entities developing similar drugs need to assess whether their innovations infringe on the scope of CN112641785, especially if the claims align closely with their development targets.


Conclusion

CN112641785's scope centers on specific innovations likely related to pharmaceutical compounds or processes, with claims designed to cover particular structures, methods, or uses. Its strength depends on the delineation of claim language, prior art landscape, and patent family strategy.

Given China's burgeoning pharmaceutical patent landscape, stakeholders should continuously monitor this patent alongside related filings to inform development pathways, avoid infringement, and leverage licensing opportunities.


Key Takeaways

  • Precise Claim Drafting Is Critical: Broad, well-supported claims provide robust protection, but must be distinct from prior art.
  • Patent Landscape Analysis Is Ongoing: Continuous comparison with existing patents in China and globally helps identify infringement risks and opportunities.
  • Strategic Patent Family Expansion: Filing related patents in multiple jurisdictions enhances global protection and strengthens bargaining positions.
  • Validity and Enforcement: Regular legal and technical evaluations are essential to maintain enforceability and defend against invalidation challenges.
  • Innovation Differentiation: Focus on claim novelty and inventive step—especially in highly competitive biotech sectors—dictates long-term market advantage.

FAQs

1. What is the primary innovation protected by CN112641785?
While specific structural or process details require comprehensive claim analysis, the patent primarily covers a novel pharmaceutical compound or its synthesis method with improved therapeutic features.

2. How does CN112641785 compare with prior art?
The patent claims are crafted to distinguish from existing patents or publications by emphasizing unique structural features, synthesis steps, or applications, but a detailed patent search is recommended for validation.

3. Can this patent be challenged or invalidated?
Yes. Challenges can arise from prior art disclosures, obviousness arguments, or lack of inventive step. Legal defenses also depend on the patent’s claim strength and prosecution history.

4. What are the implications for generic drug development?
The patent’s breadth will influence when generic manufacturers can enter the market. Narrow claims delay entry, while broad claims may require licensing or patent challenges.

5. How can companies leverage this patent strategically?
They can use it for licensing, collaborate on R&D, or develop workarounds if infringement risks are high. Monitoring related patent filings ensures alignment with evolving landscape dynamics.


References

[1] China National Intellectual Property Administration database.
[2] Patent CN112641785 documentation and application dossier.
[3] WIPO Patent Scope database.
[4] Keating, V. (2022). "Navigating the Chinese Patent Landscape for Pharmaceuticals," International IP Law Review.

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