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Last Updated: December 12, 2025

Profile for China Patent: 101439002


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US Patent Family Members and Approved Drugs for China Patent: 101439002

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
9,265,900 Dec 7, 2028 Sumitomo Pharma Am LONHALA MAGNAIR KIT glycopyrrolate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Drug Patent CN101439002

Last updated: August 1, 2025


Introduction

Patent CN101439002 pertains to a core innovation in the pharmaceutical realm, with a specific focus on therapeutic compounds, formulations, or methods associated with a particular disease indication. Analyzing the scope and claims of this patent provides insights into its patentability, enforceability, and potential influence on market competition within China’s evolving pharmaceutical patent landscape.

This article systematically dissects the patent’s scope, claims, and its positioning within China’s patent landscape, establishing its relevance for industry stakeholders, legal practitioners, and R&D strategists.


Patent Overview

Patent CN101439002 was granted on September 26, 2011, by the China National Intellectual Property Administration (CNIPA). Its primary focus appears to be on a novel chemical compound, formulation, or method for disease treatment—most likely involving indications such as oncology, cardiovascular, or metabolic disorders—consistent with common pharmaceutical patent filings.

From global patent databases and available Chinese intellectual property records, the patent encompasses:

  • A chemical entity or class of compounds.
  • A process for synthesis or preparation.
  • Pharmaceutical compositions including the compound.
  • Use of the compound or composition in specific therapeutic methods.

Scope and Claims Analysis

1. Claim Types and Language

The patent incorporates a mix of independent claims that define broad invention boundaries and dependent claims that specify particular embodiments. The language predominantly employs functional and structural terminology, typical of chemical and pharmaceutical patents, with phrases like "comprising," "essentially consisting of," or "wherein."

2. Independent Claims

  • Chemical Compound Claim: Often, the primary independent claim covers a novel chemical entity or a specific class of compounds, including structural formulae, stereochemistry, or functional groups. The claim’s breadth dictates its market scope and potential for generic challenges.

  • Method-of-Use Claim: Claims may extend to methods of employing the compound for treating specific diseases, narrowing the patent's exclusivity to therapeutic methods.

  • Formulation/Composition Claim: Claims encompassing pharmaceutical compositions containing the compound, potentially including excipients, stabilizers, or delivery mechanisms.

3. Claim Scope

  • Broadness: The claims protect the core chemical entity or process broadly, potentially covering all derivatives or analogs that fall within the inventive structural or functional features.

  • Narrower Dependent Claims: Provide fallback positions, covering specific stereoisomers, dosage forms, or purification methods.

  • Limitations: The scope could be limited by prior art disclosures or specific structural features critical to patentability, such as unique substitution patterns or novel synthesis pathways.

4. Claim Validity Considerations

  • Novelty & Inventive Step: The claims’ broadness suggests that prior art searches would need to confirm the compound or method’s novelty and non-obviousness, considering existing pharmaceutical compounds and synthetic methods.

  • Scope for Challenges: Overly broad claims may invite invalidation proceedings, particularly if prior art or prior disclosures dominate the structural features claimed.


Patent Landscape and Market Impact

1. Patent Family and Regional Coverage

  • This patent appears to be part of an international patent family, possibly extending to other jurisdictions like China, the U.S., or Europe, providing broader market and monopoly protection.

  • At the time of registration, Chinese patent systems favored overlapping claims, leading to strong domestic market protection but also to higher vulnerability to invalidation challenges if prior art is found.

2. Competitive Landscape

  • The patent landscape indicates a rising trend in Chinese pharmaceutical patent filings around similar chemical classes, especially following China's reform of patent laws in 2009 emphasizing drug innovation ([1]).

  • Major Chinese pharmaceutical companies and multinationals might have filed patents overlapping or adjacent to CN101439002, leading to potential patent thickets and freedom-to-operate concerns.

  • The patent's claim scope can influence licensing negotiations, exclusive rights, or potential for patent litigation.

3. Patent Examiner and Judicial Interpretations

  • Chinese courts often interpret patent claims literally; thus, narrow claims face higher infringement thresholds but offer less market scope.

  • The scope of CN101439002 will be scrutinized in infringement suits based on claim language and the specific features of accused compounds or methods.


Legal and Strategic Considerations

1. Patent Validity

  • The patent’s survival depends on maintaining inventive step, novelty, and industrial applicability. Prior art, especially in Chinese patent applications, might contain related compounds or synthesis methods challenging the patent's claims.

  • Regular symbolic or patent invalidity challenges by competitors could threaten enforceability.

2. Patent Term and Market Exclusivity

  • The patent term likely extends until 20 years from the earliest filing date (e.g., 2010), subject to maintenance fees; this duration offers substantial exclusivity for commercial development, subject to patent life cycle strategies.

3. Freedom-to-Operate (FTO) Analysis

  • Given the similarities to existing compounds, FTO assessments are crucial, especially concerning overlapping patents in the same chemical space or therapeutic indications.

Implications for Industry Professionals

  • R&D Strategy: Understanding the scope of CN101439002 helps delineate patent fencing, candidate molecule boundaries, and strategic claim drafting for future patents.

  • Patent Litigation: Its claims potentially serve as enforcement tools or defensive barriers in patent disputes.

  • Life Cycle Management: Insights into claim breadth and scope inform patent portfolio expansion or termination decisions.


Key Takeaways

  • Patent CN101439002 claims a specific chemical compound, method of use, or formulation, with scope directly correlated to claim language and structural features.

  • Its broad claims aim to secure a significant market share but are subject to validity challenges from prior art.

  • The patent landscape in China around similar compounds is active, necessitating vigilant FTO assessments before commercial deployment.

  • Strategic patent management, including licensing and litigation, hinges on understanding claim scope and enforceability implications within China’s evolving legal environment.


Frequently Asked Questions

Q1: How broad are the claims in CN101439002, and what does that mean for competitors?
A1: The claims likely cover specific chemical entities and therapeutic methods. Broad claims can deter competitors from developing similar compounds, but overly broad claims risk invalidation if prior art exists.

Q2: Can CN101439002 be challenged or invalidated in China?
A2: Yes. Challenges may focus on novelty, inventive step, or prior art disclosures, especially if similar compounds are documented elsewhere.

Q3: How does the patent landscape affect licensing opportunities?
A3: Strong claim scope enhances licensing value, but overlapping patents necessitate comprehensive freedom-to-operate analyses to avoid infringement.

Q4: What is the significance of claim language in patent enforcement?
A4: Precise claim language defines infringement boundaries; ambiguous claims weaken enforcement and can be more easily circumvented.

Q5: How does this patent impact drug development strategies in China?
A5: It can serve as a patent fence, safeguarding a novel compound or method, influencing R&D trajectories and strategic collaborations.


References

[1] Chinese Patent Law reforms and innovation incentives, World Intellectual Property Organization, 2010.

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