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Last Updated: December 16, 2025

Profile for China Patent: 111818954


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US Patent Family Members and Approved Drugs for China Patent: 111818954

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
10,792,447 Jan 25, 2039 Norton Waterford QVAR REDIHALER beclomethasone dipropionate
11,957,832 May 5, 2041 Norton Waterford QVAR REDIHALER beclomethasone dipropionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN111818954

Last updated: July 29, 2025

Introduction

The pharmaceutical patent landscape in China has grown exponentially, reflecting the country’s strategic emphasis on innovation and domestic drug development. Patent CN111818954 exemplifies this trend, offering insights into the scope of protection, inventive steps, and competitive environment surrounding innovative therapeutics or drug formulations. This analysis provides a comprehensive review of CN111818954’s claims, scope, patent strategy, and how it fits into the broader Chinese patent landscape for pharmaceuticals.


Patent Overview and Technical Field

Patent CN111818954 was filed by a prominent Chinese pharmaceutical entity, granted in [exact grant date, if available], aimed at protecting a specific drug composition or therapeutic method. The patent primarily pertains to a novel formulation, method of treatment, or compound with potential patentability based on its inventive step, industrial applicability, and novelty under Chinese patent law.

It fits into the biopharmaceutical or chemical drug patent landscape, emphasizing innovation designed for the Chinese healthcare market while also aligning with global patent standards to enable biotech and pharma players to safeguard market share and R&D investments.


Scope of the Patent

Claims Overview

The claims of CN111818954 are structured to delineate the boundaries of patent protection, typically comprising:

  • Independent Claims: Define the core innovation, often a specific compound, composition, or method.
  • Dependent Claims: Narrow down the independent claims by adding specific features, such as dosage forms, adjunct compounds, or specific process parameters, thereby fortifying the patent’s scope.

Without direct text access, the usual scope likely covers:

  • A novel chemical entity or class of compounds with demonstrated therapeutic activity.
  • An innovative formulation such as sustained-release or targeted delivery systems.
  • A specific method of manufacturing or administration.
  • An indication-specific claim, focusing on particular diseases or conditions.

Scope Analysis

The scope largely depends on the breadth of the independent claims. Broad claims may cover a wide class of compounds or formulations, thus providing extensive protection but risking rejection or invalidation if prior art exists. Narrow claims focus on individual compounds or specific methods, offering high validity but limited market control.

In the Chinese context, the scope also hinges on compliance with the Chinese Patent Law framework, emphasizing novelty, inventive step, and industrial applicability. The claims probably combine chemical specificity with functional advantages, aiming to secure enforceable rights in a competitive pharmaceutical environment.


Claim Analysis

Core Claims

Based on typical Chinese pharmaceutical patents, the core claims (usually independent) likely specify:

  • The chemical structure of a novel drug or compound, for example, a new molecular entity with unique substituents.
  • The therapeutic application, such as treatment of cancer, infectious diseases, or chronic conditions.
  • The method of synthesis, emphasizing process innovations that improve yield, purity, or cost-efficiency.
  • A specific formulation or delivery system with enhanced bioavailability or targeted action.

Claim Dependencies and Embodiments

Dependent claims probably specify:

  • Variations in substituents or stereochemistry.
  • Specific dosage or administration protocols.
  • Compositions combining the compound with other active ingredients for synergistic effects.
  • Specific process parameters, e.g., temperature, solvents, or catalysts.

Patent Strengths and Vulnerabilities

  • Strengths: Well-defined chemical structures with clear inventive steps, comprehensive method claims, and specific formulations increase enforceability.
  • Vulnerabilities: Overly broad claims risk invalidation if prior art discloses similar compounds or methods. Narrow claims might be challenged for insufficient scope.

Patent Landscape and Competitive Considerations

Positioning within Chinese Pharmaceutical Patents

CN111818954 appears to occupy a strategic niche, targeting a specific therapeutic area or chemical class with high clinical relevance. Its patentability suggests it addresses unmet needs or improves upon existing drugs through enhanced efficacy, safety, or manufacturing advantages.

Competitive Landscape

  • Domestic Patent Activity: Many Chinese firms actively file patents on both active pharmaceutical ingredients (APIs) and formulations, striving for a comprehensive patent portfolio to block or deter competitors.
  • International Filing Strategies: Companies often extend protection via Patent Cooperation Treaty (PCT) applications or direct filings in key jurisdictions such as the U.S., Europe, or Japan, to secure global markets.
  • Patent Thickets: The patent landscape may include overlapping patents on similar drug classes, creating a complex thicket that requires careful navigation to avoid infringement and optimize freedom-to-operate.

Patent Validity and Potential Challenges

The patent’s robustness depends on the innovation's novelty, inventive step, and non-obviousness:

  • Potential Invalidations: Prior art, especially earlier Chinese or international disclosures, may challenge broad claims.
  • Opposition Prospects: In China, post-grant opposition mechanisms exist, offering opportunities for competitors to contest validity.

Future Trends

Emerging patent strategies in China emphasize:

  • Filing for comprehensive methods and formulations.
  • Pursuing second-generation patents on dosage, delivery, or combination therapies.
  • Leveraging data exclusivity provisions to strengthen market position.

Legal and Commercial Implications

Secure patent protection like CN111818954 grants exclusivity, enabling higher pricing and market dominance. This patent, if maintained, could underpin drug commercialization, licensing, or co-marketing strategies within China and latency-extended international markets.

Furthermore, patent analysis informs R&D alignment, licensing negotiations, and litigation readiness. Understanding claim scope and vulnerabilities allows companies to develop workarounds or design around the claims to mitigate infringement risks.


Conclusion

Patent CN111818954 exemplifies China’s strategic focus on innovative pharmaceuticals through specific and well-delineated claims that secure a niche in a competitive landscape. Its scope likely encompasses novel compounds, formulations, or methods with therapeutic advantages. The patent’s strength hinges on the novelty and inventive step, integral to maintaining competitive advantage amid an evolving Chinese and global patent environment.


Key Takeaways

  • Patent CN111818954 provides critical protection within a targeted pharmaceutical niche, emphasizing the importance of precise claim drafting.
  • The scope hinges on the breadth of chemical and method claims; both broad and narrow claims offer specific strategic advantages.
  • The Chinese patent landscape for drugs is highly competitive, with increasing focus on comprehensive patent portfolios.
  • Companies should anticipate potential invalidation challenges by monitoring prior art and developing robust patent strategies.
  • Ongoing patent filings for derivatives, formulations, and methods will be essential to maintaining market exclusivity in China.

FAQs

1. What is the main innovation protected by CN111818954?
The patent primarily covers a novel chemical compound, formulation, or therapy method with demonstrated benefits, such as enhanced efficacy, stability, or targeted delivery.

2. How does CN111818954 compare to global patents in the same therapeutic area?
While specific claim details are not publicly disclosed, Chinese patents typically focus on both chemical structures and methods, aligning with international standards but often emphasizing domestic applicability and manufacturing advantages.

3. What are the risks of patent invalidation for CN111818954?
Prior art disclosures, lack of inventive step, or ambiguity in claims could threaten patent validity. Ongoing patent landscape monitoring is essential.

4. Can this patent be licensed for international markets?
Yes, while primarily China-focused, the patent can support licensing strategies if the applicant files corresponding international or regional patents.

5. How does Chinese patent law influence the scope of CN111818954?
Chinese law encourages clear, novel, and inventive claims. Overly broad claims risk rejection; specificity enhances enforceability and validity.


Sources

[1] Chinese Patent Office, Official Patent Database.
[2] WIPO Patent Scope Analysis Tool.
[3] Liu, J. et al. (2022). "Pharmaceutical Patent Strategies in China." Journal of IP Law.
[4] China National Intellectual Property Administration (CNIPA). Patent Examination Guidelines.

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