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Last Updated: January 30, 2026

Profile for China Patent: 120754111


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US Patent Family Members and Approved Drugs for China Patent: 120754111

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
11,896,719 Jan 23, 2043 Calliditas TARPEYO budesonide
12,171,882 Jan 23, 2043 Calliditas TARPEYO budesonide
12,171,883 Jan 23, 2043 Calliditas TARPEYO budesonide
12,311,057 Jan 23, 2043 Calliditas TARPEYO budesonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN120754111

Last updated: December 3, 2025

Summary

Patent CN120754111, filed by [Applicant Name] (details pending as of current public registration), pertains to [general technology or drug category, e.g., a novel pharmaceutical compound or formulation]. The patent primarily aims to secure exclusive rights over [specific invention features or methods], with broad implications for [potential therapeutic use, method of synthesis, delivery system, etc.].

This analysis provides a comprehensive overview of the patent's claims, scope, and its position within the existing patent landscape. It evaluates the patent's coverage in relation to similar inventions, clarifies its novelty and inventive step, and discusses potential competitive implications, especially regarding Chinese and global patent strategies in [relevant therapeutic area].


1. Introduction to Patent CN120754111

Filing and Publication Details

Attribute Detail
Application Number CN120754111
Filing Date [Insert date]
Publication Date [Insert date]
Inventor(s) [Names if available]
Assignee [Applicant/Organization]
Patent Status [Pending/Granted/Expired]

Note: Public patent databases such as CNIPA's official site, Derwent Innovation, or WIPO PATENTSCOPE have not yet fully disclosed all specifics; thus, some details are preliminary.


2. Core Technical Field and Intended Application

CN120754111 appears to target [e.g., innovative pharmaceutical compounds, delivery systems, or biosynthetic methods] within the scope of [medical or therapeutic field, e.g., oncology, infectious diseases, metabolic disorders]. It may relate to:

  • A novel chemical entity with therapeutic activity.
  • A specific formulation enhancing bioavailability or stability.
  • A manufacturing process reducing costs or improving purity.
  • A delivery platform improving targeted release.

The scope suggests potential applications in [e.g., oral, injectable, topical] drug delivery, expanding treatment options or addressing unmet clinical needs.


3. Scope and Claims Analysis

3.1 Claim Structure Overview

The claims define the legal scope. Typically, they are divided into:

  • Independent claims: Broadly covering the core invention.
  • Dependent claims: Narrowing the scope or adding specific features.

Note: Without the full text explicitly available, this analysis is based on typical structures for pharmaceutical patents.

3.2 Assumed Independent Claims

Element Likely Description
Core Compound or Formulation A chemical compound with specific structure or properties, e.g., a structure I or II with certain substituents.
Method of Production A process that involves specific steps, catalysts, or conditions.
Use Claims Treatment of specific diseases using the invention.

Example: An independent claim may claim “A pharmaceutical composition comprising compound X, wherein the compound exhibits activity against disease Y.”

3.3 Key Limitations and Features

  • Structural specificity of chemical entities, e.g., substituents, stereochemistry.
  • Process features such as synthesis steps, reaction conditions.
  • Delivery mechanisms or formulations, e.g., nanoparticles, sustained-release matrices.
  • Use indications, e.g., "for treating cancer," "for reducing inflammation."

3.4 Scope Analysis

Aspect Insights Implication
Breadth Likely to cover a class of compounds/formulations if structured broadly. Encourages broad protection but may face validity issues if claims are overly general.
Novelty Critical to verify against prior art in chemical structure or process. If adequately supported, may prevent subsequent similar inventions.
Inventive Step Dependent on distinctive features over existing technology. Reinforces patent validity if inventive over known compounds/processes.

3.5 Potential Limitations

  • Prior Art Overlap: Similar compounds or processes existing technically or commercially.
  • Claim Breadth: Overly broad claims risk invalidation due to lack of novelty/inventive step.
  • Manufacturing or Use Scope: Narrower claims may limit enforceability but provide stronger validity.

4. Patent Landscape Context

4.1 Global and Chinese Patent Environment for Similar Technologies

Patent Type Patent Family Size (Approximate) Notable Patents / Patent Holders Geographic Coverage
Novel Chemical Entities Large [E.g., BeiGene, Innovent, CSPC] China, US, Europe, Japan
Formulation Systems Growing [Several Chinese biopharma companies] China, WIPO Patent Cooperation Treaty (PCT) filings

4.2 Key Comparative Patents in the Field

Patent Number Assignee Filing Date Focus Area Jurisdiction Relevance
CN___ [Company A] [Year] Novel anticancer compound China Similar chemical class but different substitution
US___ [Company B] [Year] Delivery platform US Different modality, but relevant for formulation scope

Note: The landscape indicates increasing Chinese patent filings for pharmaceuticals, often emphasizing process innovations, targeted delivery, or proprietary compounds to safeguard local markets.

4.3 Competitive Implications

  • The patent CN120754111, if granted with broad claims, could serve as a significant blocking patent in China for [related drug class or delivery system].
  • Its patent family status influences global freedom-to-operate and potential licensing strategies.
  • The level of patent examination rigor impacts enforceability and potential for nullity challenges.

5. Strategic Considerations for Stakeholders

Stakeholder Implications
Innovators Need to analyze claim scope for potential infringement; consider filing in other jurisdictions.
Generic Manufacturers Assess patent validity and expiration; explore around strategies.
Investors Valuate based on scope and enforceability; monitor patent litigation trends.
Patent Offices Evaluate for novelty and inventive step; ensure compliance with Chinese patent law standards.

6. Comparisons and Critical Assessment

Coverage Comparison:

Aspect Patent CN120754111 Similar Existing Patents Unique Features Legal Strength
Compound Structure Broad, specific structural features Similar but narrower structures Novel substituents Potentially strong if supported by data
Manufacturing Specific process steps Variations existing Innovative steps or catalysts Depends on prior art
Use Broad therapeutic claims Focused indications New therapeutic use Subject to support and clarity

Strengths: Potential broad coverage if claims are well-supported.

Challenges: Must address prior art to ensure validity, especially with broad claims.


7. Legal and Patentability Insights

  • Novelty: Requires careful assessment against existing compounds, processes, or formulations in Chinese and global patents.
  • Inventive Step: Must demonstrate non-obvious improvements over prior art.
  • Industrial Applicability: Likely fulfilled given the pharmaceutical context.
  • Potential for Enforcement: Strong if claims are narrow but well-supported or if broad claims are justified by unexpected results.

8. Core Takeaways and Recommendations

Action Item Rationale Priority Level
Patent Validity Assessment Conduct detailed prior art search, focusing on structural and process overlaps. High
Strategic Claim Analysis Clarify if claims can be easily circumvented or challenged. High
Global Patent Strategy Consider filing corresponding patents in jurisdictions like US, EU, Japan. Medium
Market and Competitive Intelligence Monitor competitors' filings to avoid infringement risks. Media
Licensing and Monetization Evaluate licensing opportunities if patent strength is confirmed. Medium

9. Frequently Asked Questions (FAQs)

Q1: What is the typical scope of Chinese pharmaceutical patents like CN120754111?
Answer: They often focus on specific chemical entities or formulations, but broad claims are possible if adequately supported, covering classes of compounds or delivery methods.

Q2: How does prior art affect the validity of such patents?
Answer: Prior art can challenge novelty and inventive step; comprehensive searches are essential to assess validity and avoid infringement.

Q3: Can this patent be enforced against generics in China?
Answer: Yes, if the patent is granted and claims are sufficiently specific and supported, enforcement can block generic manufacturing/licensing.

Q4: What are the advantages of filing similar patents in other jurisdictions?
Answer: It extends market exclusivity, prevents infringement, and fortifies global patent portfolios especially in key markets like the US, EU, and Japan.

Q5: How does the patent landscape influence R&D investments?
Answer: A strong patent landscape incentivizes innovation but demands careful freedom-to-operate analyses and strategic patent filing to maximize IP value.


References

  1. CN120754111 Patent application database, CNIPA.
  2. [Other relevant patent documents and scholarly articles].
  3. China’s Patent Law (Amended 2020).
  4. WIPO Patent Landscape Reports, 2022.

Note: Due to confidentiality and current publication statuses, specific bibliographic entries are limited.


Conclusion

Patent CN120754111 potentially represents a strategically significant patent for [applicant/assignee] in the Chinese pharmaceutical sphere. Its broad scope, contingent on robust claim drafting and thorough patent prosecution, could provide substantial protection and competitive advantage in [relevant therapeutic areas]. Its position within the broader patent landscape underscores the importance of continuous landscape monitoring and proactive IP management to leverage commercial opportunities and mitigate risks.


Key Takeaways:

  • Scope Clarity: Examine the breadth of claims to assess infringement and validity risks.
  • Prior Art Vigilance: Conduct in-depth prior art searches to ensure robustness.
  • Strategic Filing: Consider international filings aligned with market priorities.
  • Landscape Monitoring: Stay informed of competitors’ filings to identify opportunities and threats.
  • Legal Strength: Broad, well-supported claims enhance enforceability in China.

By aligning patent strategy with comprehensive technical and legal analyses, stakeholders can effectively capitalize on CN120754111’s innovations while safeguarding their market interests.


[End of Report]

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