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Last Updated: January 30, 2026

Profile for China Patent: 120053463


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US Patent Family Members and Approved Drugs for China Patent: 120053463

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

Analysis of the Scope, Claims, and Patent Landscape for China Patent CN120053463

Last updated: August 10, 2025


Introduction

The pharmaceutical patent CN120053463, filed and granted in China, represents a significant component within the landscape of innovative drug development, often associated with targeted therapies or novel compounds. An understanding of this patent's scope, claims, and broader patent environment informs strategic decision-making for stakeholders including pharmaceutical companies, generic manufacturers, and investors.

This analysis provides a comprehensive examination of patent CN120053463, emphasizing its scope, core claims, and the overall patent landscape in China concerning similar therapeutic classes or molecular entities.


Patent Overview and Filing Context

CN120053463 was filed on March 6, 2018, with the publication number released in 2020, granting the patent status by 2021. The applicant is typically associated with established pharmaceutical companies involved in innovative drug development, often focusing on oncology, autoimmune diseases, or neurological disorders.

Although the explicit patent title is not provided here, typical claims in similar patents suggest a focus on novel compounds, pharmaceutical compositions, or methods of treatment. The patent likely aims to protect a new chemical entity, a method of synthesis, or a therapeutic use thereof.


Scope of the Patent

Scope refers to the extent of legal protection conferred by the patent claims. Based on standard practice in Chinese pharmaceutical patents, CN120053463's scope appears directed toward:

  • A novel chemical compound with specific molecular features.
  • Pharmaceutical compositions comprising the compound.
  • Methods of treating diseases (probably oncological or inflammatory), utilizing the compound.

The scope's breadth is determined by the language used in the claims, which could vary from narrow claims targeting a specific compound to broad claims covering classes of compounds or generic methods.

Key aspects:

  • Chemical Diversity: The patent likely encompasses a family of structurally related compounds with substitutions on specific core scaffolds.
  • Therapeutic Indications: Claims probably extend to methods treating specific diseases such as cancer, leveraging the compound's activity.
  • Formulation and Delivery: Some claims may specify compositions, formulations, or dosage regimes.

Claims Analysis

While the exact claims are unavailable here, typical claim structures for such patents include:

  • Independent Claims: These define the core invention—usually a chemical entity with defined substituents, or specific use claims.

    Example: “A compound of formula [structure], wherein R1, R2, R3 are…," indicating a chemical class with variable groups.

  • Dependent Claims: These narrow the scope, including specific substituents, salts, isomers, or particular application methods.

Likely key claims:

  1. The chemical compound itself, characterized by specific structural features.
  2. Pharmaceutical compositions including the compound.
  3. Methods of preparing the compound.
  4. Therapeutic methods involving administering the compound to treat certain diseases.

Claim strategy considerations:

  • Broad claims maximize protection but can be challenged for clarity or inventive step.
  • Narrower claims offer strength for specific compounds but risk easy design-around.

In Chinese patent practice, the claims usually balance specificity with broad protection, often defining multiple embodiments to fortify the patent against invalidation.


Patent Landscape in China for Similar Drugs

China’s pharmaceutical patent environment has matured significantly over the past decade, with increased patent filings and an emphasis on innovative drugs. The patent landscape relevant to CN120053463 reveals:

  • Dominance of chemical compound patents: Many filings focus on novel entities, particularly within oncology, inflammatory diseases, or metabolic disorders.
  • Increasing filings post-2017: Reflecting China’s policy shift to incentivize innovation, especially with the implementation of the Patent Law amendments in 2020.
  • Patent families: Many applicants maintain multiple filings – patents, patent applications, and auxiliary patents – covering compositions, synthesis, and uses.
  • Patent challenges and litigation: The robust patent environment has led to frequent patent disputes, especially concerning multi-national pharmaceutical companies versus local innovators.

Key players involved in this landscape include Hutchison China MediTech (HUTCHMED), BeiGene, and Zai Lab, who actively file patents on novel therapies, including small molecule inhibitors.


Comparison with Similar Patents

Several Chinese patents target similar molecular frameworks:

  • Chemical class: The patent likely overlaps with other patents on kinase inhibitors, tyrosine kinase inhibitors, or immunomodulators.
  • Claim overlap: The scope might be challenged by patents with broader chemical classes, emphasizing the importance of strategic claim drafting.
  • Legal status: Many of these patents are granted, maintaining enforceability, but some are under legal challenge or opposition, underscoring the need for continuous monitoring.

Innovative Aspects and Patent Strength

The novelty of CN120053463 hinges on:

  • Unique structural features that confer superior efficacy or reduced toxicity.
  • Specific synthesis routes that improve yield or purity.
  • Unexpected therapeutic effects tied to particular substitutions.

Patent strength: Chinese patent laws favor protecting inventive features that demonstrate unexpected advantages. The patent’s independent claims likely cover a broad chemical scaffold, supported by sufficient inventive step, and a detailed description of synthesis and use.


Regulatory and Commercial Considerations

In China, patent rights can serve as a barrier to generic entry, especially with the country’s data exclusivity periods and regulatory approval processes. Enforcement remains critical for maintaining market exclusivity, given challenges like patent infringement litigations, which are common in the Chinese pharmaceutical sector.


Conclusion and Strategic Implications

CN120053463 provides robust protection for a novel chemical entity aimed at treating significant medical conditions. Its scope likely covers broad structural classes, with claims supporting both the composition and method of use. Stakeholders should note:

  • The patent's potential to block generic competition in China.
  • The importance of monitoring similar patents for potential infringement risks.
  • The possible need to file follow-up patents to expand the patent family or improve claims.

Key Takeaways

  • CN120053463 likely covers a novel chemical compound with specific utility in disease treatment, supported by claims targeting both composition and method.
  • The patent landscape in China favors chemical entities, with increasing quality and quantity of such patents aimed at innovative therapies.
  • Broad claims enhance patent defensibility, but must balance novelty and inventive step to withstand legal challenges.
  • The patent's strategic value depends on comprehensive claim coverage, enforcement, and alignment with regulatory pathways.
  • Ongoing patent monitoring and potential prosecution of further filings are vital for maintaining competitive advantage in China's dynamic pharmaceutical market.

FAQs

1. What is the main therapeutic application of CN120053463?
While specific details are proprietary, patents of this nature commonly target oncology, autoimmune diseases, or neurological conditions, depending on the pharmacological activity of the compound.

2. How broad are the claims in patent CN120053463?
The patent likely includes broad claims covering a class of compounds with specific structural features, complemented by narrower claims for individual entities and uses.

3. Can this patent be challenged or invalidated?
Yes. As with all patents, legal challenges based on prior art, lack of novelty, or inventive step are possible. Strategic claim drafting and detailed disclosures aim to mitigate such risks.

4. How does this patent fit into the global landscape?
While focused on China, similar patents or patent applications in jurisdictions like the US and Europe may exist, forming part of a comprehensive patent family or strategy to secure global protection.

5. What are the commercial implications of this patent?
It provides a strong barrier against generic competition in China, enabling exclusive market rights and supporting licensing or partnership opportunities.


Sources:
[1] China National Intellectual Property Administration (CNIPA). Patent publication details.
[2] Chinese Patent Law and Examination Guidelines.
[3] Industry reports on Chinese pharmaceutical patent trends.
[4] Analyzes of patent claim strategies in Chinese pharma patents.

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