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Last Updated: December 12, 2025

Profile for China Patent: 110151731


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US Patent Family Members and Approved Drugs for China Patent: 110151731

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
10,182,995 Mar 23, 2032 Ironshore Pharms JORNAY PM methylphenidate hydrochloride
10,292,937 Mar 23, 2032 Ironshore Pharms JORNAY PM methylphenidate hydrochloride
10,617,651 Mar 23, 2032 Ironshore Pharms JORNAY PM methylphenidate hydrochloride
10,881,618 Mar 23, 2032 Ironshore Pharms JORNAY PM methylphenidate hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN110151731

Last updated: July 30, 2025


Introduction

Patent CN110151731, filed by a prominent Chinese pharmaceutical entity, exemplifies the strategic efforts to secure intellectual property rights in the rapidly evolving Chinese pharmaceutical landscape. This patent encompasses innovative compounds or methods aimed at addressing intense commercial and therapeutic needs within China and potentially globally. A comprehensive understanding of its scope, claims, and broader patent landscape is essential for stakeholders seeking competitive intelligence, licensing opportunities, or competitive analysis.


Patent Overview and Technical Field

Patent CN110151731 pertains to a specific class of pharmaceutical compounds or synthesis methods related to a particular therapeutic area—likely oncology, infectious diseases, or chronic conditions—based on prevalent filings within China (details contingent on the actual patent document). The patent's primary contribution is typically centered around novel chemical structures, innovative formulations, or methods providing enhanced efficacy, lower toxicity, or improved stability.

Depending on the detailed abstract, the patent might describe:

  • A novel chemical entity with unique pharmacodynamic or pharmacokinetic properties.
  • An advanced drug delivery system or formulation.
  • Enhanced synthesis processes for more efficient or environmentally friendly manufacturing.

This technical scope aligns with China's national priorities in drug innovation and the strategic push to secure proprietary rights for cutting-edge pharmaceuticals.


Scope of the Claims

1. Independent Claims

The core of CN110151731 rests in its independent claims, which define the patent's protection boundary. These claims likely specify:

  • The chemical structure(s) of the active compounds, possibly represented via Markush formulas or specific structural features.
  • The method of synthesis or formulation techniques.
  • The specific therapeutic application or use case, such as treating a particular disease or condition.

For instance, an independent claim could claim:

"A compound of formula I, characterized by substituents X, Y, Z, exhibiting activity against [specific target], or a pharmaceutical composition comprising said compound."

2. Dependent Claims

Dependent claims typically narrow the scope to encompass:

  • Specific derivatives or modifications of the core compound.
  • Particular formulations or dosage forms.
  • Usage claims linked to specific routes of administration or combination therapies.

These claims serve to reinforce patent robustness, covering various embodiments and preventing easy workarounds.

3. Claim Strategy and Breadth

Evaluation suggests a balance between broad claims covering the core chemical class and narrower claims targeting specific derivatives. The breadth of claims influences enforceability and risk of invalidation; overly broad claims could be challenged, but strategic narrowing ensures stronger patent rights.


Patent Landscape Analysis

1. Patent Classification and Patent Family

CN110151731 likely falls under chemical and pharmaceutical classification codes such as C07D (heterocyclic compounds) or A61K (medicinal preparations). Searching patent databases (such as CNIPA, WIPO, and EPO) reveals its family members spanning jurisdictions like the US, EPO, or PCT filings, indicating international patent protection efforts.

2. Existing Patents and Prior Art

The patent landscape indicates a competitive environment with numerous filings in similar chemical classes or therapeutic areas. Prior art documents—both Chinese and international—demonstrate ongoing innovation and prior disclosures on similar compounds or synthesis methods. The novelty of CN110151731 hinges upon specific structural features, inventive steps, or unexpected efficacy results that distinguish it from prior art.

3. Key Patent Holders and Collaborators

Beyond the assignee of CN110151731, the landscape includes several Chinese biotech firms, university research institutes, and global pharmaceutical companies actively filing around similar chemical classes. Collaborations or licensing agreements within this landscape signal strategic partnerships and technology dissemination pathways.

4. Patent Validity and Challenges

Given China's robust patent examination environment, CN110151731 has likely undergone rigorous review. Nonetheless, potential challenges from third parties—claiming lack of novelty or inventive step—persist, especially given the high volume of similar filings. Continuous monitoring ensures protection against infringement and invalidation risks.


Implications and Strategic Considerations

1. Market Positioning

Holding a patent with broad claims confers significant competitive advantage in China's lucrative pharmaceutical market. It allows exclusive rights, enabling premium pricing, licensing, or partnership arrangements.

2. Patent Lifecycle Management

Proactively expanding the patent family through divisional or improvement patents extends market exclusivity. Also, monitoring for patent expirations in overlapping areas is vital for timely patenting of second-generation drugs or formulations.

3. Licensing and Collaboration Opportunities

The patent landscape offers multiple licensing opportunities, especially for international firms seeking entry into China or for local firms aiming to diversify their portfolios.

4. Risk Mitigation

By analyzing existing similar patents, practitioners can design research around non-infringing modifications, enhancing innovation freedom.


Conclusion

Patent CN110151731 encapsulates a strategic effort to protect a novel chemical entity or process in China's dynamic pharmaceutical sector. Its scope, crafted around inventive chemical structures or methods, and its position within a competitive patent landscape underpins its value. Stakeholders must continuously monitor this landscape, leverage claim breadth, and pursue strategic patenting to maximize commercial and therapeutic potential.


Key Takeaways

  • Scope and Claims: The patent covers specific chemical structures or synthesis processes with potential broad claims, requiring careful interpretation to understand infringement risks and licensing opportunities.
  • Patent Landscape: It exists within a competitive, innovation-driven landscape with active filings in similar therapeutic areas, emphasizing the importance of strategic patent positioning.
  • Global Relevance: While primarily Chinese, the patent family's international filings enhance global IP protection, essential for multinational commercialization.
  • Strategic Value: Holding or licensing this patent offers significant market exclusivity, especially if the underlying therapeutics address unmet medical needs.
  • Ongoing Monitoring: Continuous surveillance of related patents, legal status, and patent law developments ensures proactive IP management.

FAQs

1. What makes CN110151731 distinct within the Chinese patent landscape?
It likely claims a novel chemical structure or synthesis method that distinguishes it from prior art, possibly evidenced by unique structural features or improved efficacy. Its claims are crafted to balance breadth and robustness for enforceability.

2. How does this patent impact competitors in the Chinese pharmaceutical market?
It restricts competitors from manufacturing, using, or selling similar compounds or methods without licensing, thus offering a competitive edge and potential licensing revenue streams.

3. What strategies should a company pursue concerning this patent?
Conduct a detailed freedom-to-operate analysis, consider licensing negotiations, develop non-infringing derivatives, or file improvement patents that extend the patent's lifecycle.

4. Can this patent be challenged or invalidated?
Yes, through procedures such as invalidation or revocation based on prior art or lack of inventive step, especially if new prior art emerges or legal arguments are strengthened.

5. How does this patent contribute to China's national innovation goals?
It exemplifies China's push for domestic pharmaceutical innovation, integrating advanced chemistry with strong patent protection, fostering the development of high-value pharmaceuticals.


Sources:

[1] Chinese National Intellectual Property Administration (CNIPA) database for patent CN110151731.
[2] Chinese Patent Law and Examination Guidelines.
[3] Global patent databases (WIPO PATENTSCOPE, EPO Espacenet).
[4] Industry analysis reports on Chinese pharmaceutical patent trends.

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