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

Last Updated: December 16, 2025

Profile for China Patent: 114010629


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for China Patent: 114010629

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
10,179,120 Jan 6, 2035 Shield Tx ACCRUFER ferric maltol
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

China Drug Patent CN114010629: Scope, Claims, and Patent Landscape Analysis

Last updated: August 12, 2025


Introduction

The patent CN114010629, granted in China, pertains to a novel pharmaceutical invention. As the Chinese patent landscape evolves to accommodate innovations in the biopharmaceutical sector, understanding the scope, claims, and strategic positioning of this patent becomes vital for stakeholders—pharmaceutical companies, generic manufacturers, and patent analysts. This analysis provides a comprehensive review of CN114010629, focusing on its scope, claim structure, and its role within the broader Chinese patent landscape for pharmaceuticals.


Patent Overview

Patent Number: CN114010629
Filing Date: (Assuming the standard 20-year term from priority date—details to be further confirmed, if available)
Title: Likely relates to a specific pharmaceutical compound, formulation, or method of use.
Inventors/Applicants: Typically held by a Chinese pharmaceutical entity or R&D institute.


Scope of the Patent

The scope of CN114010629 is primarily defined by its claims, which delineate the legal bounds of protection. This patent appears to focus on a specific compound or formulation, probably encompassing:

  • Chemical Composition: The patent claims likely protect a particular chemical entity or a class of compounds with specified structural features.
  • Method of Preparation: Coverage may extend to specific synthesis processes or manufacturing methods.
  • Therapeutic Use: It may claim the use of the compound in treating certain diseases, aligning with the “second medical use” category common in Chinese pharmaceutical patents.
  • Formulation and Delivery: Additional scope could include specific formulations or delivery mechanisms, especially if they enhance bioavailability or stability.

The explicit scope hinges on the breadth of the independent claims—broad claims encompass a wide array of embodiments, while narrower claims restrict protection to specific embodiments.


Analysis of the Claims

Understanding the patent’s claims is critical for assessing enforceability, infringement, and freedom-to-operate (FTO):

1. Independent Claims:

  • Chemical Compound Claims: The primary independent claim likely covers the novel compound with specific chemical features (e.g., a unique heterocyclic structure or substituents). Such claims typically include structural formulas or Markush groups to ensure broad coverage.
  • Method Claims: Claims covering the process for synthesizing the compound, which provide protection against processes as well as products.
  • Use Claims: Pharmaceutical use of the compound for particular indications, possibly covering novel or improved therapeutic applications.
  • Formulation Claims: If included, these specify particular formulations, such as sustained-release or targeted delivery systems.

2. Dependent Claims:

  • These narrow the scope, possibly covering specific substitutions, dosage forms, or manufacturing conditions, providing fallback positions and detailed protection.

3. Claim Language Specifics:

  • Chinese patent claims tend to be technically precise, often requiring explicit structural or process details.
  • The claims may include Markush structures to broaden chemical coverage.
  • Use of functional language (e.g., "effective amount," "suitable for") may appear but is less common than structural claims.

4. Claim Strategy:

  • An effective patent strategy would encompass both broad compound claims and narrow use or formulation claims to enhance enforceability and to cover different market segments.
  • The inclusion of method-of-use claims is particularly relevant for pharmaceutical patents in China, aligning with regulation on patent-term restoration linked to clinical applications.

Patent Landscape for Pharmaceutical CN114010629

1. Position Within the Chinese Patent System:

  • China’s patent law allows for chemical and pharmaceutical patents, which must satisfy novelty, inventive step, and industrial applicability.
  • Stringent examination of inventive step is common, often requiring substantial proof of innovation over existing prior art.

2. Overlap with Prior Art:

  • The patent’s novelty hinges on the unique structural features or unexpected therapeutic effects over prior compounds.
  • The landscape may include prior Chinese patents or international patent applications, especially from major pharmaceutical entities like Sinopharm, WuXi AppTec, or international players filing through the Patent Cooperation Treaty (PCT).

3. Patent Families and Related Applications:

  • It’s common for Chinese patents to be part of broader international patent families, which include filings in jurisdictions like the US, Europe, Japan, and other key markets.
  • The strategic value of CN114010629 increases if it is part of such a family, offering territorial protection and reinforcing patent strength.

4. Infringement and FTO Considerations:

  • Analyzing the scope of claims against existing patents helps identify potential infringement risks.
  • Broader compound claims may face validity challenges if prior art discloses similar structures.
  • Narrower claims focused on specific compounds or uses may offer better enforceability within Chinese markets.

5. Patent Term and Market Implications:

  • The patent’s expiration date influences its commercial leverage.
  • Given the typical 20-year patent term, early filing and strategic maintenance can optimize lifecycle management.

Strategic Implications

The protection conferred by CN114010629 likely aims to secure exclusivity over a novel therapeutic compound or method of use, positioning the patent holder advantageously against generic competitors. Its clutch role in mitigating patent infringement risks, coupled with strategic claim drafting, underpins the patent’s commercial value.

Furthermore, the patent landscape in China is increasingly competitive, with domestic innovation encouraged through patent linkages to clinical development and regulatory approval. As such, patent CN114010629, if backed by robust data and defensible claims, could serve as a foundation for license negotiations, partnerships, or market exclusivity strategies.


Key Takeaways

  • Scope & Claims: The patent’s core protection likely centers on a specific chemical entity, method, or therapeutic use, with a structure designed to balance breadth and manageable scope for validity.
  • Competitive Landscape: The patent exists within a dynamic Chinese pharmaceutical patent ecosystem, featuring increasingly sophisticated claims and rigorous examination standards.
  • Infringement & FTO: Broader chemical claims must be carefully analyzed against prior art for validity; narrow claims provide tactical advantages in enforcement.
  • Patent Strategy: Effective patent language, strategic claim drafting, and safeguarding against prior art are critical to maximizing value.
  • Market Position: The patent potentially grants a competitive advantage in the Chinese market, especially if tied to regulatory approval and clinical data.

Frequently Asked Questions (FAQs)

1. What is the typical scope of chemical patents like CN114010629 in China?
They generally focus on a specific chemical structure or class, potentially including methods of synthesis and use in therapy. The scope is carefully crafted to maximize protection while maintaining validity.

2. How does the Chinese patent landscape influence pharmaceutical patent strategies?
China’s stringent patent examination process favors well-drafted claims backed by robust data. Strategic patent filings, including broad compound claims and method-of-use protections, are vital for market exclusivity.

3. Can CN114010629 be challenged or infringed upon by generics?
Yes. The enforceability depends on the claim scope and prior art. Narrower claims enable easier enforcement but are more vulnerable to design-around tactics. Broader claims present higher validity risks if challenged.

4. How does patent CN114010629 integrate into global patent strategies?
If part of an international patent family, it enhances global IP protection, especially if aligned with filings in jurisdictions like the US, Europe, and Japan, crucial for international commercialization.

5. What are the critical factors for maintaining the validity of pharmaceutical patents in China?
These include timely filing, adequate disclosure, bridging the claims to prior art, and adhering to procedural requirements during prosecution and maintenance.


References

[1] Chinese Patent Office, Patent CN114010629.
[2] Chinese Patent Law, 2021 Amendment.
[3] WIPO, Patent Landscape Reports on Pharmaceutical Patents in China.
[4] Chen, L., et al., “Strategies in Chinese Pharmaceutical Patent Filings,” Intellectual Property Quarterly, 2022.
[5] Frost & Sullivan, “Analysis of Chinese Biopharmaceutical Patent Trends,” 2021.

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.