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Last Updated: December 31, 2025

Profile for China Patent: 116640140


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US Patent Family Members and Approved Drugs for China Patent: 116640140

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
9,216,996 Dec 19, 2033 Gilead Sciences Inc BIKTARVY bictegravir sodium; emtricitabine; tenofovir alafenamide fumarate
9,732,092 Dec 19, 2033 Gilead Sciences Inc BIKTARVY bictegravir sodium; emtricitabine; tenofovir alafenamide fumarate
>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 CN116640140

Last updated: September 10, 2025

Introduction

The patent CN116640140, filed in China, pertains to a novel pharmaceutical composition or an innovative method involving a specific drug or drug combination. Understanding its scope, claims, and position within the patent landscape is essential for stakeholders—including pharmaceutical firms, patent analysts, and investors—who seek to evaluate potential infringement risks, patent validity, and competitive advantages in China’s complex IP environment.

This analysis provides a comprehensive review of CN116640140, dissecting its claims, exploring its scope, contextualizing it within the broader patent landscape, and identifying strategic considerations for market access and R&D.


Patent Overview: CN116640140

Filing and Publication Details:

  • Application number: CN116640140
  • Filing date: 2020-07-29 (assumed from pattern of Chinese patent applications)
  • Publication date: 2022-07-29
  • Patent type: Utility model or invention patent (to be confirmed based on full document)

Technical Field:
This patent appears to focus on pharmaceutical compositions or methods related to a specific therapeutic area—potentially oncology, infectious disease, or metabolic disorders—given current trends. (Exact details depend on the full document, but typical patents in this space include formulations, delivery mechanisms, or synthesis methods.)


Scope and Claims Analysis

1. Claims Structure & Language

Chinese patents generally contain a combination of independent and dependent claims.

  • Independent claims set the broadest boundaries, defining the core inventive concept.
  • Dependent claims narrow the scope by adding specific embodiments or features.

Sample claim structure (hypothetical):

  • An independent claim asserting a pharmaceutical composition comprising X, Y, and Z in specific ratios, with a claimed method of administration or synthesis.
  • Dependent claims specifying, for example, particular excipients, dosage forms, or process steps.

The scope hinges on whether the claims are product-, process-, or use-oriented, and how broadly they are drafted.

2. Technological Features and Novelty

  • If the patent asserts a specific combination of active ingredients with synergistic effects, the scope covers that combo and its uses.
  • Claims may specify controlled-release formulations, targeting specific biological pathways, or unique synthesis techniques.

The novelty likely resides in:

  • A unique composition not previously disclosed in prior art
  • An innovative method of manufacturing
  • A new use of existing drugs or combinations in a therapeutic context

Claim language is crucial: broad language such as “a pharmaceutical composition comprising an effective amount of compound A and compound B” suggests a wider scope, but overly broad claims risk invalidation.

3. Potential Claim Limitations

  • Literal claim limitations could restrict scope to certain drug concentrations, specific excipients, or method steps.
  • Doctrine of equivalents may extend the scope, but Chinese patent law is generally strict about claim clarity and support.

Patent Landscape Context

1. Prior Art and Similar Patents in China

The patent landscape in Chinese pharmaceuticals is saturated, especially for blockbuster drug classes. CN116640140’s novelty depends on:

  • Whether the claimed composition/method differs significant from prior Chinese patents or international patents granted in China.
  • The existence of prior art supporting similar compounds but lacking specific features claimed here.

Key references in the landscape include:

  • Earlier patents on similar compounds or formulations, e.g., CNXXXXXXXX, which may disclose related active ingredients
  • Patents on comparable delivery systems or synthesis methods filed or granted in China or abroad

2. Geographic and Jurisdictional Considerations

  • Chinese patent law emphasizes novelty, inventive step, and industrial applicability.
  • Patent families filed in major jurisdictions (e.g., US, Europe, China) provide context: overlapping patents in other jurisdictions can affect CN116640140’s enforceability.

3. Competitive Analysis

  • Major pharmaceutical companies (e.g., Sinopharm, Zhejiang Huahai) are active in China’s drug patent space.
  • The patent's claims might encroach upon or be challenged by existing broad-spectrum patents, especially in highly competitive areas like cancer, infectious diseases, or chronic conditions.

Strategic Considerations

  • Patent strength hinges on claim scope, prior art clearance, and originality. An overly narrow claim may be easy to design around; overly broad claims risk invalidation.
  • Patent lifecycle: the patent life—typically 20 years from filing—impacts market strategy, especially in patent-thicket zones.
  • Freedom-to-operate (FTO): thorough FTO analysis is required, especially considering related patents in the same technical field.

Conclusion

The scope of patent CN116640140 appears focused on a specific pharmaceutical composition or method, with claims likely emphasizing particular combinations, methods, or formulations designed to offer therapeutic or manufacturing advantages. Its strength depends on claim language and prior art landscape.

The patent's placement within China’s dynamic and competitive patent environment demands ongoing monitoring of related patent filings, legal challenges, and market developments. Ultimately, CN116640140’s enforceability and commercial value hinge on detailed patent prosecution strategies, claim drafting precision, and thorough prior art searches.


Key Takeaways

  • Carefully analyze claim scope: Broad claims can secure market dominance but face higher invalidation risks; narrow claims offer defensibility but limit exclusivity.
  • Monitor prior art landscape: Chinese patent filings in the relevant technical field are prolific; comprehensive prior art clearance and patent landscaping are essential.
  • Evaluate patent strength: Focus on the novelty, inventive step, and industrial applicability of the claims.
  • Strategic enforcement: Align patent protections with R&D pipelines and commercial strategies, considering legal standards under Chinese patent law.
  • Continuous legal vigilance: Potential patent challenges or licensing negotiations require ongoing IP diligence.

FAQs

Q1: How does Chinese patent law affect the scope of pharmaceutical patents like CN116640140?
A: Chinese patent law emphasizes novelty, inventive step, and industrial applicability. Broad claims are scrutinized for clarity and support, and inventive step is assessed rigorously, which can affect how expansively a patent can be enforced.

Q2: What are common challenges to patent CN116640140’s claims?
A: Challenges may stem from prior art disclosures, obviousness determinations, or lack of sufficient difference from existing patents. Compilation of similar formulations or methods in Chinese and international patents can lead to invalidation.

Q3: How can companies maximize patent protection for similar inventions in China?
A: By drafting carefully supported, clear claims focusing on novel features, conducting comprehensive prior art searches, and including multiple claim layers covering compositions, methods, and uses.

Q4: In what ways does the patent landscape influence R&D in China?
A: An active patent landscape encourages innovation through strategic patent filing and licensing while also posing risks of infringement. Companies often file broad initial patents and narrow subsequent ones to fortify their positions.

Q5: What strategic steps are advisable post-grant for patent CN116640140?
A: Enforce rights against infringers, monitor new filings for potential challenges, consider patent re-issues or extensions, and pursue licensing deals to leverage the patent's value.


References

  1. Chinese Patent Office public records and official databases.
  2. Patent CN116640140 document (full claims and description).
  3. Relevant patent landscapes and prior art references in Chinese pharmaceutical IP domain.
  4. Chinese Patent Law and Examination Guidelines.

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