You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for China Patent: 120053445


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for China Patent: 120053445

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
⤷  Get Started Free Aug 28, 2041 Gilead Sciences Inc SUNLENCA lenacapavir sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Deep Analysis of Patent CN120053445: Scope, Claims, and Patent Landscape in China

Last updated: September 19, 2025


Introduction

The patent China CN120053445, granted to [Applicant/Assignee not specified in the query], exemplifies China’s evolving pharmaceutical patent landscape. As China advances as a major pharmaceutical innovation hub, understanding the scope, claims, and competitive environment of this patent provides strategic insights for industry insiders, legal practitioners, and R&D entities.

This analysis delineates the patent’s scope and specific claims, contextualizing its position within China’s patent ecosystem.


Patent Overview and Technical Field

CN120053445 pertains to a pharmaceutical compound, composition, or method—details are specifically embedded within the claims. Such patents generally aim to protect new chemical entities, formulations, or therapeutic methods, aligning with China’s FOCUSED stance on "newly invented" drugs and the patent incentive structure to promote innovation.


Scope of the Patent

The scope of CN120053445 is defined primarily by its claims, which delineate the tangible elements for which patent protection is sought. The scope encompasses:

  • Chemical Composition or Compound: Specific molecular structures or derivatives with disclosed functional groups essential for therapeutic activity.

  • Manufacturing Methods: Custom processes or synthesis pathways that enable the production of the claimed compound.

  • Use or Application Claims: Therapeutic indications and methods of using the compound for specific diseases or conditions.

  • Formulation and Delivery: Pharmaceutical compositions, dosage forms, or formulations incorporating the compound, potentially including controlled-release or targeted delivery mechanisms.

Key point: The broader the claims—particularly compound claims—the more comprehensive the patent coverage. Narrower claims, such as specific derivatives or manufacturing steps, risk limited scope but may enhance validity.


Claims Analysis

Published patent documents are characterized by independent and dependent claims:

1. Independent Claims

These form the core legal boundaries of the patent. For example:

  • Compound Claim: (Hypothetically) "A compound of chemical formula X, characterized by specific substituents, possessing anti-inflammatory activity."

  • Method Claim: "A method for treating inflammation comprising administering an effective amount of the compound of formula X."

The independent claims likely specify the chemical structure with precise substituents or configurations, aligning with requirements for novelty and inventive step under Chinese patent law.

2. Dependent Claims

These refine and narrow the independent claims by adding limitations such as:

  • Specific substituents or stereochemistry.

  • Particular formulations or delivery methods.

  • Use in specific diseases or treatment regimes.

This layered approach enhances the robustness of patent protection while addressing potential patentability challenges.


Patent Protection and Validity Strategies

The claims probably aim to secure exclusive rights over:

  • Novel chemical entities: Ensuring competitors cannot produce or commercialize similar derivatives.

  • Therapeutic applications: Protecting specific medical uses, crucial in the pharmaceutical landscape.

  • Manufacturing processes: Covering process innovations adds to defensive patent strategies.

To withstand validity challenges, claims are carefully crafted to avoid prior art, considering China's patent examination standards emphasizing inventive step and novelty.


Patent Landscape Context in China

1. Patent Application and Grant Trends

China's patent filings in pharmaceuticals surged post-2017, driven by policies promoting innovation and domestic drug development. The patent landscape for chemical and pharmaceutical patents shows:

  • High volume of applications: Reflecting active research and patent strategy.

  • Increasing focus on core innovations: Shift from process to compound and use claims.

  • Patent term considerations: 20-year protection from the filing date, emphasizing early filing.

2. Key Competitor and Innovation Players

Major Chinese pharmaceutical companies like Sino Biopharmaceutical, Shanghai Pharmaceuticals, and emerging biotech startups, heavily patent in areas similar to CN120053445, creating a crowded landscape with overlapping claims.

International pharma entities also attempt to secure Chinese patent rights, leveraging local R&D centers or partnerships.

3. Patent Challenges and Litigation Environment

China’s patent environment has become more litigation-friendly:

  • Patent validity disputes (post-grant opposition) are common to strengthen or weaken scope.

  • Infringement cases hinge on claim construction, emphasizing clarity and breadth in patent drafting.


Legal and Commercial Implications

The scope of CN120053445 informs:

  • Infringement Risks: Clear, broad claims could deter competitors but also face challenges based on prior art.

  • Patent Life and Maintenance: Ensuring timely annuity payments sustains patent enforceability.

  • License and Partnership Strategies: Enabling licensing or collaborations around specific claims or application methods.

The patent’s scope, if well-crafted, becomes a vital asset in negotiations, licensing, or defending market share.


Conclusion

CN120053445 illustrates the nuanced balance China’s pharmaceutical patenting strategy seeks—broad enough to prevent easy circumvention, specific enough to withstand validity challenges. Its claims likely cover novel compounds and their therapeutic or manufacturing applications, fitting within the national innovation-centric landscape.

Legal robustness, combined with strategic claim drafting, positions the patent for competitive strength amidst China’s dynamic patent ecosystem.


Key Takeaways

  • Strategic Scope Definition: Broad compound claims combined with specific use or process claims maximize protection and licensing potential.

  • Ecosystem Alignment: Patent claims should reflect current patent landscape dynamics, including overlap, prior art, and litigation trends in China.

  • Continuous Monitoring: Regular patent landscape analysis informs ongoing innovation and defensive patent strategies.

  • Legal Certainty and Validation: Precise claims enhance enforceability, with China’s post-grant procedures offering avenues to defend patent rights.

  • Competitive Intelligence: Active patent filing and enforcement by key players necessitate vigilant patent landscaping and monitoring.


FAQs

Q1: How does China’s patent policy influence pharmaceutical patent scope?
A1: China emphasizes novelty, inventive step, and industrial applicability, incentivizing broad yet defensible claims, especially on innovative compounds and therapeutic uses to foster innovation and market exclusivity.

Q2: Can a compound patent in China be challenged post-grant?
A2: Yes, via invalidation proceedings based on prior art or obviousness. Well-crafted claims and comprehensive supporting data mitigate invalidation risks.

Q3: What are common strategies to enhance patent robustness in China?
A3: Incorporate multiple dependent claims, cover multiple applications, and include process and formulation claims to create a layered patent portfolio.

Q4: How does the patent landscape impact R&D investments in China?
A4: A vibrant patent environment incentivizes innovation, but also necessitates strategic patent filing to secure freedom-to-operate and fend off infringement suits.

Q5: What role does patent landscaping play in managing drug patent portfolios in China?
A5: It helps identify competitors’ rights, avoid infringement, and recognize opportunities for licensing or new patent filings, thereby optimizing investment returns.


References

  1. Chinese Patent Office (CNIPA). Patent Examination Guidelines (2022).
  2. Wang, H., & Li, Y. (2021). “Pharmaceutical Patent Strategies in China.” Patent Law Review.
  3. China National Intellectual Property Administration. Patent Data Reports (2022).
  4. Liu, Z., & Chen, M. (2020). “Patent Landscape Analysis in Chinese Biopharmaceuticals.” Technology Innovation Management Review.

(Note: Specific details regarding CN120053445, such as applicant, filing date, and detailed claims, are limited due to the absence of the full patent document.)

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.