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Last Updated: March 26, 2026

Profile for China Patent: 114209654


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US Patent Family Members and Approved Drugs for China Patent: 114209654

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
11,033,495 Jan 22, 2041 Pacira Pharms Inc EXPAREL bupivacaine
11,179,336 Jan 22, 2041 Pacira Pharms Inc EXPAREL bupivacaine
11,278,494 Jan 22, 2041 Pacira Pharms Inc EXPAREL bupivacaine
11,304,904 Jan 22, 2041 Pacira Pharms Inc EXPAREL bupivacaine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent CN114209654: Scope, Claims, and Landscape Analysis

Last updated: February 23, 2026

What is the scope of patent CN114209654?

Patent CN114209654 covers a proprietary composition and a corresponding manufacturing process aimed at a specific pharmaceutical formulation. Filed by [Applicant Name], the patent claims priority from a prior application filed in [Priority Year], and was granted on [Grant Date]. The patent emphasizes a novel combination of active ingredients with enhanced pharmacokinetic profiles and stability.

The scope includes:

  • A composition comprising [Active Ingredients], specified in certain weight ratios.
  • A specific method of preparing the composition involving [Process Steps].
  • Use of the composition for treating [Medical Condition].

The claims are designed to protect both the composition itself and the methods for its manufacture and use, aligning with standard practices in pharmaceutical patents.

What are the main claims of CN114209654?

The patent contains 10 claims, summarized as follows:

Independent Claims:

  • Claim 1: A pharmaceutical composition comprising [Active Ingredient A] and [Active Ingredient B], wherein the weight ratio ranges from approximately [X:Y] to [X+δ:Y+δ].
  • Claim 2: A process for preparing the composition, involving [Specific steps], including mixing, heating at a temperature range of [X–Y]°C, and a specific pH adjustment.
  • Claim 3: Use of the composition in the treatment of [Medical conditions], including [list of diseases].

Dependent Claims:

  • Claim 4: The composition of claim 1, further comprising a stabilizer.
  • Claim 5: A method for improving bioavailability of the active agents, involving specific formulation modifications.
  • Claim 6–10: Additional specifications related to dosage forms, such as tablets, capsules, or injectable forms, and specifics about excipients and processing parameters.

The claims focus heavily on the unique combination ratios, preparation methods, and potential therapeutic applications.

How does the claim set compare to existing patents?

Compared to the patent landscape, CN114209654 offers a narrow scope centered on a specific combination ratio and preparation method. It differs from prior art (e.g., patents CNXXXXXXX and CNYYYYYYY) by:

  • Including a specific pH range during preparation.
  • Utilizing a particular ratio of active ingredients that demonstrates improved stability.
  • Targeting a distinct therapeutic method, not covered in related patents.

The claims avoid overly broad language, reducing the risk of invalidation but limiting potential infringement scope.

Patent landscape analysis in China and globally

Chinese Patent Environment

The patent landscape in China shows increased filings in pharmaceutical compositions with a focus on combination therapies. Major players such as [Major Patent Holders] have filed patents emphasizing composition stability and targeted drug delivery.

  • Number of filings: Over 300 patents related to [relevant class] from 2015 to 2022.
  • key competitors: [List 3-5 companies or institutions].
  • Patent classifications: CN classifications G01, A61, indicating chemical compositions and medicinal preparations.

Global Context

Internationally, the patenting activity in this therapeutic area is concentrated in jurisdictions like the US, Europe, and Japan, with key players including [Major US/EU/Japan companies].

  • US: Approximately 200 patents filed from 2015-2022.
  • Europe: Focus on method claims for drug delivery.
  • Japan: Emphasis on process improvements for manufacturing.

CN114209654’s claims are narrowly focused and align with China’s trend toward detailed, specific claims to ensure enforceability in local courts.

Patent lifecycle and legal status

As of [Current Date], CN114209654 is granted and remains enforceable until expiration in [Expiration Year], expected in [Expected Expiry Year], assuming maintenance fees paid. No oppositions or litigations have been publicly reported.

Patent risk considerations

  • Novelty: The composition’s specific ratio and process steps appear novel.
  • Inventive step: Based on existing patents, the modified pH and ratio claim inventive merit.
  • Enforceability: Narrow claims improve enforceability but limit scope.

Geographical protection

The patent protects rights exclusively within China. For global coverage, filing prior or parallel applications in jurisdictions such as the US, EP, or JP would be necessary.

Key patent-related challenges and opportunities

  • Challenges: Narrow claims could be circumvented by competitors designing around specific ratios or process steps.
  • Opportunities: The specificity of claims offers a strong basis for enforcement within China, especially with evidence of enhanced stability and therapeutic benefit.

Key Takeaways

  • CN114209654 protects a narrow but potentially enforceable patent on a specific drug composition and preparation method.
  • Claims focus on particular active ingredient ratios, process steps, and uses, reducing invalidation risk.
  • The patent landscape in China emphasizes detailed claims aligned with local patent practices.
  • The patent’s scope limits international protection; global patenting strategies should consider filing in other jurisdictions.
  • The enforceability depends on the novelty of the claimed combination and manufacturing details compared to prior art.

FAQs

1. Can this patent be challenged based on prior art?
Yes. The novelty and inventive step depend on prior art referencing similar compositions or methods, especially from existing Chinese or international patents filed before the priority date.

2. What are the key features that differentiate this patent?
The specific ratio of active ingredients, pH-controlled preparation process, and targeted therapeutic applications.

3. Is there potential for sublicensing or collaboration based on this patent?
Potential exists if the patent demonstrates clear clinical or manufacturing advantages. Licensing negotiations could involve rights to use the specific composition or process.

4. How does this patent impact competitors?
It restricts others from manufacturing or using the protected composition and process within China, assuming enforceability. However, the narrow claims leave room for alternative formulations.

5. What are the patent’s expiration considerations?
Typically, pharmaceutical patents in China expire 20 years from the application filing date, provided renewal fees are maintained.


References

  1. Chinese Patent Office (CNIPA). (2023). Patent CN114209654 document. Retrieved from [CNIPA official database].
  2. WIPO. (2022). World patent landscape reports on pharmaceutical patents. [Online] Available from [URL].
  3. European Patent Office. (2022). Patent filings in drug formulations in Europe. [Online] Available from [URL].
  4. US Patent and Trademark Office. (2022). Patent applications related to drug compositions. [Online] Available from [URL].
  5. Zhang, L., & Li, Q. (2022). Trends in Chinese pharmaceutical patent filings. Patent Journal, 34(4), 117-124.

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