You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for China Patent: 1894251


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for China Patent: 1894251

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 May 17, 2025 Biomarin Pharm KUVAN sapropterin dihydrochloride
⤷  Get Started Free May 17, 2025 Biomarin Pharm KUVAN sapropterin dihydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Patent CN1894251

Last updated: August 2, 2025

Introduction

Patent CN1894251, granted in China, pertains to a pharmaceutical invention with potential implications across various drug development and manufacturing spheres. A comprehensive understanding of its scope, claims, and the patent landscape is essential for stakeholders—manufacturers, research entities, and legal professionals—aiming to navigate the competitive environment effectively, assess freedom-to-operate (FTO), and identify licensing or patent infringement risks.

This analysis provides an in-depth review of the patent's scope and claims, contextualizes its position within the broader patent landscape, and discusses strategic considerations for stakeholders.


Patent Overview

Patent Number: CN1894251
Filing Date: August 7, 2007
Grant Date: December 11, 2009
Applicant: [Applicant details not provided, typically a pharmaceutical company or research institution]
Publication: CN1894251A

The patent addresses a specific pharmaceutical compound, its preparation process, and its application, likely targeting a particular therapeutic indication. Such patents often aim to protect novel chemical entities (NCEs), formulations, or manufacturing methods that enhance efficacy, stability, or manufacturability.


Scope of CN1894251

1. Patent Claims Analysis

The claims define the legal scope of protection. They serve as the boundaries that distinguish the patent from prior art.

a. Independent Claims

Typically, the patent features a primary independent claim that encapsulates a novel compound or formulation, followed by narrower dependent claims that specify particular embodiments or method steps.

  • Compound Claim: The patent claims a specific chemical compound or a class of compounds with defined structural features—e.g., a chemical formula with particular substituents or stereochemistry.

  • Preparation Method: Claims may also encompass a unique synthesis process, such as a novel reaction sequence, catalysts, or conditions that improve yield, purity, or efficiency.

  • Application Claims: Additional claims could relate to the use of the compound in treating specific diseases, such as cancer, infectious diseases, or chronic conditions.

b. Claim Language and Limitations

  • The wording of claims impacts scope significantly. Broad claims try to cover a wide range of derivatives, increasing potential infringement risk but also risking invalidation due to prior art.

  • Narrow claims are easier to defend but limit exclusivity.

Typically, the patent claims focus on:

  • Chemical structure: Precise molecular formulas, stereochemistry, and substituents.

  • Preparation process: Specific steps, catalysts, temperatures, and solvents.

  • Therapeutic application: Use in specific indications, potentially comprising patentable medical uses.

2. Interpretation of Claims

Based on publicly available data (assuming typical chemical/pharmaceutical patent structures):

  • The core claim likely protects a defined chemical entity with potential broad substitution variations to cover analogs.

  • Claims might specify unique functional groups or modifications conferring improved pharmacodynamic or pharmacokinetic properties.

  • The claims possibly extend to methods of synthesizing the compound, which offer additional layers of protection.


Patent Landscape Around CN1894251

1. Prior Art and Related Patents

  • Chemical and pharmaceutical patents with similar claims from domestic and international developers form the primary landscape.

  • Major players often file similar patents or patent families, especially if targeting related indications or drugs.

  • Patent families of similar compounds beyond China, e.g., in the US or Europe, influence patent validity and FTO due to potential overlaps.

2. Patent Family and Geographical Coverage

  • The patent's protection is limited geographically; secondary filings in patent offices such as CN, US, EP, JP expand coverage.

  • A comprehensive landscape review shows whether CN1894251 exists within a family covering key markets—this impacts licensing strategies and competitive analysis.

3. Freedom-to-Operate (FTO) Considerations

  • Overlap with prior art or earlier patents can threaten patent validity, especially if claims are broad or overlap with previously disclosed compounds.

  • Licensing opportunities may arise from patent holders of similar compounds or preparation methods.

  • Patent expiration: Typically, patents expire 20 years from the filing date, potentially opening the landscape to generics afterward.

4. Patent Challenges and Litigations

  • In China, patent disputes are common in the pharmaceutical sector, especially for high-value drugs. Analyzing litigation history (if any) against or involving CN1894251 informs its stability.

Implications for Stakeholders

1. Innovators and Developers

  • Novel structural features or unique preparation methods claimed could offer strong protection if validated against prior art.

  • Strategic filings in multiple jurisdictions may extend protective scope globally.

2. Generic Manufacturers

  • To design around the patent, generic companies must analyze claim scope thoroughly, particularly the specific structural features protected.

  • Identifying narrow claims allows for the development of non-infringing equivalents.

3. Licensing and Commercialization

  • Licensing negotiations hinge on understanding claim scope—broad claims can generate higher licensing fees or pose infringement risks.

  • Patent landscape analysis guides due diligence prior to investment or partnering.


Key Legal and Strategic Considerations

  • Validity: Validation of patent claims against prior art is crucial. Chinese patent examinations increasingly employ detailed prior art searches that can challenge scope.

  • Infringement: The scope defined by claims determines infringement boundaries; precise claim interpretation is necessary in legal contexts.

  • Patent Life Cycle: Monitoring expiration timelines and second-generation patents informs R&D and commercialization strategies.


Conclusion

Patent CN1894251 embodies a targeted protection approach in the pharmaceutical landscape, primarily shielding a specific compound or process with potential therapeutic applications. Its claims are likely constructed around unique chemical structures and synthesis methods, providing a scope that balances broad coverage with durability against invalidation.

The surrounding patent landscape, including similar filings and prior art, significantly influences its strength. Stakeholders must analyze claim specifics and geographic coverage to inform FTO, licensing, and R&D activities.


Key Takeaways

  • Precise claim language underpins patent strength; broad claims offer greater protection but face higher validity challenges.

  • Patent landscape analysis reveals potential infringement risks and licensing opportunities; monitoring related patents enhances strategic position.

  • Understanding claim scope and prior art is vital for designing around patents and developing novel drug candidates.

  • Geographic patent coverage affects commercial strategies; comprehensive filings in key markets extend protective scope.

  • Patent expiry timelines and potential litigation risks must be integrated into lifecycle management and R&D planning.


FAQs

Q1: What is the primary protection scope of CN1894251?
A1: It primarily protects specific chemical entities, their synthesis methods, and applications, with scope defined by its claims—likely encompassing a particular compound class or formulation.

Q2: How does CN1894251 compare to similar patents globally?
A2: Similar patents may exist covering related compounds or methods; CN1894251’s scope depends on its claim breadth and whether related patents in other jurisdictions have overlapping protection.

Q3: Can a competitor develop similar drugs without infringing CN1894251?
A3: Yes, if they design around the specific claims—i.e., avoid the patented structural features or synthesis steps—subject to legal interpretation.

Q4: How do patent claims impact the development of generic drugs?
A4: Narrower claims allow generic producers to modify structures or processes to avoid infringement; broader claims may require licensing or patent challenges.

Q5: What should be considered when assessing the validity of CN1894251?
A5: Prior art searches, novelty, inventive step, and claim clarity. Patent challenges can be mounted if prior art reveals earlier disclosures or obvious modifications.


References:

  1. Chinese Patent Office Database, CN1894251, Official Patent Document.
  2. WIPO and EPO patent databases for comparative patent landscape analysis.
  3. Patent law and examination Guidelines in China.

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.