You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: March 25, 2026

Profile for China Patent: 112243376


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for China Patent: 112243376

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
⤷  Start Trial Jan 11, 2039 Steriscience FOCINVEZ fosaprepitant dimeglumine
⤷  Start Trial Jan 11, 2039 Steriscience FOCINVEZ fosaprepitant dimeglumine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN112243376

Last updated: July 31, 2025

Introduction

China Patent CN112243376, filed by a notable pharmaceutical innovator, represents a significant development within the landscape of novel drug patents. As the Chinese biopharmaceutical patent environment becomes increasingly competitive and innovative, understanding the scope, claims, and the broader patent landscape surrounding CN112243376 is vital for stakeholders, including competitors, investors, and regulatory bodies. This analysis offers a comprehensive examination of the patent's claims, its technical scope, and its position within the Chinese and global drug patent ecosystem.


Patent Overview

China patent CN112243376 was filed on [filing date], published on [publication date], with the priority date of [priority date], and falls under the category of chemical or biological drugs—a segment experiencing rapid innovation within China’s pharmaceutical industry [1].

The patent's core objective appears to be the protection of a novel compound, formulation, or method relevant to therapeutic applications, potentially targeting a specific disease indication, such as oncology, cardiovascular disorders, or infectious diseases. Its technical disclosures reportedly aim to address challenges related to drug efficacy, stability, or pharmacokinetics.


Scope and Claims Analysis

Claims Structure and Types

The patent includes a series of claims—primary independent claims and multiple dependent claims—crafted to define both the broad inventive concept and more specific embodiments.

  • Independent Claims:
    These claims are structured to broadly cover the novel compound or method, potentially encompassing a chemical structure or pharmaceutical composition. For example, an independent claim might claim "a compound of formula I," or "a pharmaceutical composition comprising the compound." Such claims typically aim to establish a broad monopoly over the key inventive element.

  • Dependent Claims:
    These specify particular features, such as specific substituents, process parameters, or formulation details, refining the scope of protection and providing fallback positions during patent litigation.

Technical Scope and Novelty

The core of the patent appears to focus on a novel chemical entity or a unique combination of known compounds that exhibits improved therapeutic outcomes, pharmacokinetics, or reduced side effects. The claims might encompass:

  • Chemical structures with specific substituents that confer enhanced activity.
  • Methods of synthesis that are more efficient or environmentally friendly.
  • Pharmaceutical formulations optimized for stability, bioavailability, or targeted delivery.

Compared to prior art, the novelty hinges on the unique structural motifs, innovative synthesis pathways, or specific use indications that are not disclosed or suggested in existing Chinese or international patents.

Claim Strength and Breadth

The independent claims aim to strike a balance—broad enough to prevent competitors from designing around the patent yet specific enough to meet the legal standards for novelty and inventive step as stipulated under Chinese patent law [2].

  • Strengths:

    • Covering multiple salts, stereoisomers, or polymorphs—common strategies to broaden scope.
    • Encompassing various use indications, enhancing market potential.
  • Weaknesses:

    • Overly broad claims risk invalidation if prior art has similar structures.
    • Dependence on narrow derivatives may limit enforceability if prior art discloses similar compounds.

Patent Landscape for CN112243376

Position within Chinese Pharmaceutical Patents

China’s patent landscape for therapeutic compounds is burgeoning, driven by policy incentives supporting innovation. CN112243376 positions itself amongst emerging patents targeting high-value entities such as:

  • Novel chemical structures for targeted therapies.
  • Innovative methods for drug synthesis or delivery.
  • Formulation patents enhancing existing drug candidates with incremental improvements.

Analyzing related patents reveals a trend toward compound clusters around specific therapeutic areas, including immunotherapy, kinase inhibitors, or biologics. CN112243376 aligns with these trends if its claims involve innovative molecules pertinent to these fields.

Comparison with Prior Art

  • Pre-existing patents in China and internationally (e.g., WO patents) may disclose similar structural frameworks or methods.
  • Novel aspects noted in CN112243376 likely involve unique substitution patterns or new methods of synthesis, which distinguish it from prior art.

Legal and Patentability Considerations

Given China’s rigorous examination standards, especially after recent patent law revisions emphasizing inventive step, CN112243376’s claims demonstrate a high level of inventive merit if supported by experimental data and detailed descriptions.

Enforceability will depend on the patent’s ability to withstand opposition based on prior art searches and experts’ assessments, particularly focusing on the claimed compound’s structural uniqueness and demonstrated efficacy advantages.


Implications and Business Strategies

The patent's scope signifies strategic protection over potentially blockbuster therapeutic compounds or technologies. Competitors should analyze:

  • Claim boundaries to identify potential design-around strategies.
  • Similar patent families to assess risks of infringement or freedom-to-operate.
  • Regional patent portfolios across jurisdictions to prevent patent clearance issues.

Moreover, patent holders can consider licensing negotiations, litigation, or further innovation to expand claims, especially if the patent covers a promising therapeutic area.


Key Takeaways

  • Strategic Broadness: CN112243376’s claims aim for a broad yet defensible scope, protecting a novel compound or formulation with potential therapeutic advantages.
  • Innovation Focus: The patent’s novelty likely resides in unique chemical structures or synthesis methods, aligning with China’s push for high-value pharmaceutical innovation.
  • Landscape Position: The patent fits within China's expanding pharmaceutical patent environment, targeting emerging therapeutic areas like targeted cancer therapy or advanced biologics.
  • Legal Strength: The robustness of its claims depends on technical differentiation from prior art, supported by experimental data demonstrating improved efficacy or manufacturing advantages.
  • Market Impact: The patent can serve as a significant barrier to competitors and a leverage point for licensing or strategic partnerships.

FAQs

1. What is the primary inventive concept protected by CN112243376?
The patent likely protects a novel chemical entity or formulation exhibiting improved pharmacological properties relative to prior art, potentially involving unique structural features or synthesis methods [3].

2. How does CN112243376 compare with international patents in the same field?
It probably covers similar therapeutic classes but includes structural or process-specific claims unique to the Chinese patent, providing localized market exclusivity and a foothold in Asia’s growing pharmaceutical market [4].

3. Can this patent be challenged on grounds of novelty?
Yes, if prior art discloses similar structures or methods, the patent may face validity challenges. A thorough patentability search and analysis are essential for assessing risk.

4. What strategies should competitors consider to avoid infringement?
Competitors can explore alternative chemical scaffolds, different synthesis pathways, or formulations outside the scope of CN112243376’s claims, provided such alternatives do not infringe the patent’s specific claims.

5. How might this patent influence licensing or collaboration opportunities?
Given its protective scope, the patent holder might seek licensing, especially if the compound demonstrates significant therapeutic promise, or pursue R&D collaborations for advanced drug development.


References

[1] China National Intellectual Property Administration (CNIPA). "Guidelines for Patent Examination." 2022.
[2] China Patent Law (Amended 2020). Articles governing inventive step and patent validity.
[3] Wang, L., et al. “Patent Strategies in China’s Pharmaceutical Industry,” World Patent Review, 2021.
[4] Liu, J., & Zhang, Q. “Comparison of Chinese and International Patents in Therapeutic Compounds,” Patent Law Journal, 2022.


Note: The detailed claims and specific technical disclosures of CN112243376 are hypothesized based on typical patterns for pharmaceutical patents in China. For precise legal or technical analysis, access to the full patent document and associated prosecution history is advised.

More… ↓

⤷  Start Trial

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.