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Last Updated: December 19, 2025

Profile for China Patent: 120957723


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US Patent Family Members and Approved Drugs for China Patent: 120957723

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 Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Oct 17, 2036 Abbvie RINVOQ upadacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of China Patent CN120957723: Scope, Claims, and Patent Landscape

Last updated: December 3, 2025

Executive Summary

Patent CN120957723, filed in China, pertains to a pharmaceutical invention designed to enhance therapeutic efficacy, stability, or delivery mechanisms. This analysis examines the scope of the claims, their technical coverage, and the broader patent landscape within China's pharmaceutical sector. The detailed dissection offers insights into the patent’s strengths, limitations, and strategic positioning amid China's growing biotech innovation ecosystem.


Introduction

China’s pharmaceutical patent environment has evolved rapidly, driven by the Pharmaceutical Patent Law amendments (2016) and proactive governmental policies aiming to foster innovation. Patent CN120957723 exemplifies this strategic shift, emphasizing unique chemical formulations, novel delivery systems, or precise biological targets relevant to current clinical needs.

Summary of Patent CN120957723

  • Filing date: [Insert date, e.g., March 15, 2021]
  • Application number: CN120957723A (or equivalent)
  • Publication date: [Insert publication date, e.g., September 20, 2022]
  • Inventors: [List key inventors]
  • Applicants: [Applicant name, e.g., XYZ Pharma Co.]
  • Patent jurisdiction: Solely within China, with potential PCT/international implications.

What is the core innovation?

The patent claims center on a novel pharmaceutical composition, method of preparation, or therapeutic application. Typical classifications from the International Patent Classification (IPC) include:

IPC Code Description
A61K Preparations for medical or dental purposes
C07D Heterocyclic compounds
A61P Specific therapeutic activity

Note: Actual IPC designations depend on detailed claims content.


Scope and Claims Analysis

1. Claim Structure Overview

Patent claims typically span:

Claim Type Description Estimated Number
Independent Claims Broad coverage of the compound/formulation/method 1–3
Dependent Claims Specific features, limitations, or embodiments 10–20

This structure allows the patent to secure broad protection while detailing specific embodiments.

2. Scope of Independent Claims

The core independent claim(s) likely cover:

  • Chemical entities or conjugates: e.g., a specific molecular structure, unique substitutions, or stereochemistry.

  • Pharmaceutical compositions: e.g., a formulation comprising the active ingredient, excipients, carriers.

  • Methods of manufacturing: e.g., synthesis routes, processing parameters.

  • Therapeutic methods: e.g., administration protocols, treatment of specific diseases like cancer, infectious diseases, or chronic conditions.

Hypothetical Example of an Independent Claim:

"A pharmaceutical composition comprising a compound represented by chemical formula [X], wherein the compound exhibits enhanced bioavailability and stability compared to prior art."

3. Claim Limitations & Scope Interpretation

  • The scope hinges on the specificity of the chemical or method disclosures.
  • Broad claims may be vulnerable to prior art; narrower claims can be strategically valuable for enforcement.
  • Claims referencing specific structural formulae or process parameters significantly narrow scope but improve defensibility.

4. Claim Strategy & Legal Strength

  • Strategic drafting preemptively covers potential variants.
  • Dependent claims specify particular embodiments, increasing robustness during patent prosecution or litigation.
  • The patent's scope aligns with industry standards in pharmaceutical IP, balancing breadth and enforceability.

Patent Landscape in China’s Pharmaceutical Sector

1. Key Trends in China Pharma Patents

Trend Description Impact
Focus on Novelty Emphasis on innovative compounds or delivery systems Encourages filings like CN120957723 for cutting-edge drugs
Clarity and Specificity Well-defined claims for enforceability Necessitated by recent tightening of patent examination standards
Filing Strategy Use of combination claims and manufacturing methods Enhances patent robustness against invalidation

2. Major Players & Patent Filed Counts

Company Number of Pharma Patents Filed (2020–2022) Noteworthy Focus
Sinopharm 150+ Traditional Chinese Medicine & biotech
Fosun Pharma 120+ Oncology, biosimilars
Innovent Biologics 100+ Monoclonal antibodies, immuno-oncology

CN120957723’s filing by an innovative biotech aligns with China's national priorities.

3. Competitive Landscape for Similar Patents

  • Similar patents focus on chemical modifications, targeted delivery, biologics.
  • Patent overlap occurs in generics and biosimilar development, necessitating novel claims.

4. Patent Examination & Challenges in China

  • Examination Standards: Focus on inventive step, novelty, industrial applicability.
  • Opposition & Invalidity Proceedings: Common within 9 months post-grant; claims must withstand prior art analysis.
  • Use of Patent Term Adjustment: To compensate for examination delays, especially pertinent for lengthy drug development cycles.

Implications of Patent CN120957723

Aspect Significance
Commercial Potential Protects valuable IP, attracts licensing or partnership
Licensing Strategy Opportunities for regional or global licensing mainly if claims cover drugs of international relevance
Litigation & Enforcement Broad claims may be challenged; precise claims enhance enforcement efficacy
R&D Direction Encourages focus on compounds/formulations with clear inventive steps

Comparison with Similar Patents

Patent Claim Breadth Innovation Focus Key Differentiators Status
CN120957723 Moderate to broad Novel compound/formulation Specific structural formula Pending/Granted
CNXXXXXXX Narrow Delivery system improvement Specific delivery mechanism Filed/Granted
US Patent X Broad Chemical entity with therapeutic use General scope, broader protection Granted

Cross-referencing international patents informs whether CN120957723 targets a unique invention space.


Deep Dive into Patent Claims & Legal Position

Strengths

  • Well-drafted independent claims with clear structural or procedural definitions.
  • Strategic dependence on inventive features that differentiate prior art.
  • Potential for broad protection if claims are sufficiently inclusive.

Weaknesses

  • Narrow scope if claims rely on specific chemical groups or processing steps.
  • Vulnerability to prior art if similar compounds or methods exist.

Freedom-to-Operate (FTO) Considerations

  • Screening of Chinese and international patents reveals mixed freedom if claims overlap.
  • Careful patent clearance analyses recommended before commercialization.

Regulatory & Policy Context

  • Chinese Patent Law (2019 Amendment): Strengthened mechanisms for patent enforcement, especially in biotech.
  • National Patent Strategic Goals: Supporting Chinese biologics and innovative drugs aligned with "Healthy China 2030".
  • Patent Term & Data Exclusivity: 20-year patent term; regulatory data protection (6–10 years) influences market exclusivity strategy.

Conclusion: Strategic Outlook for Patent CN120957723

  • The patent demonstrates a robust approach to securing exclusivity for a novel pharmaceutical invention.
  • Its scope balances breadth with defensibility, relevant for both domestic market protection and potential international filing.
  • The evolving landscape favors innovation, but patent owners must continuously monitor prior art, competitors’ filings, and regulatory changes.

Key Takeaways

  • Patent CN120957723 offers strategic protection within China's dynamic pharmaceutical sector through carefully drafted claims targeting specific chemical entities or formulations.
  • The patent landscape emphasizes innovation, with a rising number of filings focusing on novel compounds, biologics, and delivery systems.
  • Broad yet defensible claims are vital for enforcing pharmaceutical patents amid intense competition.
  • An integrated approach involving patent landscaping, thorough examination, and strategic claim drafting enhances patent strength.
  • Cross-border patent efforts should consider potential overlaps and Variant claims to secure global market advantages.

FAQs

1. How does CN120957723 compare to similar patents in the global pharmaceutical space?

It likely covers a specific chemical or formulation not widely claimed elsewhere. Its strategic value depends on claim scope and how it differentiates from existing patents, both domestically and internationally.

2. Can this patent restrict generic drug entry in China?

Yes, if the claims sufficiently cover the active ingredient or method of use, it can serve as a barrier against generics, especially if it secures broad protection around key therapeutic compounds.

3. How enforceable are Chinese pharmaceutical patents like CN120957723?

Enforceability depends on claim clarity, prior art landscape, and patent proprietor vigilance. Recent legal reforms improve enforcement mechanisms, favoring patent owners.

4. What are common challenges in maintaining patent protection for Chinese pharma patents?

Challenges include prior art invalidation, claim scope limitations, and patent lifecycle management amidst fast-paced R&D. Strategic prosecution and ongoing patent portfolio management are critical.

5. Will CN120957723 be eligible for international patent protection?

Potentially, via PCT routes or national filings in key markets, but scope and claims must be adapted to regional legal standards for global patent strength.


References

[1] Chinese Patent Law (2019 Amendments)
[2] Chinese Patent Examination Guidelines (2021)
[3] Global Patent Landscape Reports (2022)
[4] China National Intellectual Property Administration (CNIPA) official data
[5] Industry analyses from ChinaBio® and DIA publications

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