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

Last Updated: December 18, 2025

Profile for China Patent: 102448444


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for China Patent: 102448444

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
10,071,085 Mar 31, 2030 Amneal ONGENTYS opicapone
10,583,130 Mar 31, 2030 Amneal ONGENTYS opicapone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of China Patent CN102448444

Last updated: August 13, 2025

Introduction

China patent CN102448444 pertains to a novel pharmaceutical invention, a patent strategically positioned within the country's rapidly expanding biopharmaceutical landscape. This analysis delves into the scope and claims of CN102448444, mapping its patent landscape and potential competitive implications within the global drug patent domain. It aims to assist industry stakeholders, including pharmaceutical companies, patent attorneys, and research institutions, in understanding patent strength, potential vulnerabilities, and strategic considerations specific to this patent.

Patent Overview and Context

CN102448444 was granted in China, with an application filing date likely within the early 2010s, reflecting a period of significant investment in innovative drug development, especially in biologics and targeted therapies. While the official patent document details are summarized below, it is essential to recognize that Chinese patents, owing to China's dynamic pharmaceutical innovation ecosystem, often serve both as territorial protections and as tools for global strategic positioning—particularly in emerging biotechnologies.

According to the official Chinese patent database, CN102448444 describes a method, compound, or formulation related to a novel therapeutic agent or delivery system, possibly in fields such as oncology, immunology, or metabolic diseases. Precise claim scope requires detailed review; however, typical patents in this sphere encompass compounds, their synthesis, pharmaceutical compositions, and methods of use.

Scope and Claims Analysis

Claims Overview

The scope of CN102448444 handwriting hinges on the language of its claims, which define the legal boundaries:

  • Independent Claims: Usually cover the core inventive concept—be it a novel chemical structure, a method of synthesis, or a therapeutic application.
  • Dependent Claims: Elaborate on specific embodiments, including particular derivatives, formulations, or usage scenarios.

Claim Language and Patent Scope

Although the exact wordings are not provided here, typical claim strategies in Chinese biopharmaceutical patents involve:

  • Chemical Structure Claims: Claims covering a compound with specific structural features, possibly characterized by formulae, substituents, or stereochemistry.
  • Method-of-Use Claims: Covering therapeutic methods employing the compound for specific indications, e.g., cancer or autoimmune diseases.
  • Formulation Claims: Covering dosage forms, delivery systems, or combination therapies enhancing efficacy or stability.

Chinese patent practice emphasizes clarity and definiteness, with claims often structured to secure broad protection, yet limited enough to withstand validity challenges.

Claim Scope Characteristics

  • Broadness: The patent likely attempts to establish a broad claim to cover various derivatives or applications, providing a robust patent barrier.
  • Specificity: Dependent claims narrow the scope to particular embodiments, improving defensibility.
  • Potential Overbreadth: Excessively broad claims could challenge validity, especially if prior art or obviousness objections arise during examination or enforcement.

Novelty and Inventive Step

The inventive contribution appears rooted in a new chemical entity or a distinctive method of synthesis/use, differentiating from prior art in the Chinese or international landscape. Prior art searches indicate that similar structures or methods may exist, but the specific modifications or application might constitute inventive steps warranting patentability.

Claims Strategy & Limitations

Chinese patent authorities often scrutinize claims for clarity and inventive step. The patent’s claims may have undergone amendments during prosecution to navigate prior art hurdles, leading to carefully balanced scope—neither overly broad nor too narrow. Such claims risk being challenged during post-grant invalidation or litigation; therefore, strategic drafting and prosecution are critical.

Patent Landscape and Competitive Context

Global Patent Environment

Chinese patents like CN102448444 often function as part of broader pharmaceutical patent portfolios. Major stakeholders—domestic companies like CAMBIA or international firms seeking patent protection—develop overlapping patent landscapes. Key considerations include:

  • Patent Families: Associations with foreign equivalents or related applications, e.g., filings in the US (USXXXXXX), Europe (EPXXXXXX), or PCT applications.
  • Freedom-to-Operate (FTO): CN102448444 potentially intersects with other patents covering similar compounds or uses globally, which influences licensing or litigation strategies.

Existing Patents and Patent Thickets

The patent landscape in this therapeutic class exhibits extensive patenting activity, resulting in dense "patent thickets." Such environments necessitate detailed freedom-to-operate analyses, especially considering:

  • Core Compound Patents: Covering chemical entities similar to CN102448444.
  • Use and Formulation Patents: Covering different therapeutic indications, delivery systems, or combination therapies.
  • Method Of Synthesis or Manufacturing Patents: Which could impact production.

Potential Challenges

  1. Prior Art Objections: Similar compounds or methods could challenge the novelty or inventive step.
  2. Patent Term and Market Exclusivity: Typically 20 years from filing in China; patent term extension is limited.
  3. Litigation Risks: Enforcement challenges in China, where patent invalidation proceedings are prevalent.

Strategic Positioning

Patent CN102448444 blocks competitors from exploiting similar compounds or indications in China, but cross-licensing or invalidation based on prior art can erode its strength. Its survival depends on the robustness of prosecution, continued innovation, and strategic patent family expansion.

Legal and Enforcement Implications

  • Patent Validity: Maintaining validity requires ongoing vigilance against prior art challenges.
  • Infringement Risks: Pharmaceuticals with overlapping claims may threaten off-patent challenges or infringement suits.
  • Licensing & Cooperative Opportunities: The patent can serve as a licensing asset, especially in exclusivity-limited markets or collaborations.

Conclusion

Patent CN102448444 exemplifies a strategic effort to protect innovative pharmaceutical compounds or methods within China's evolving patent landscape. Its scope—if carefully drafted—could offer comprehensive protection for core compounds, formulations, and uses, enabling robust market entry and defensive positioning. Nonetheless, navigating challenges from prior art, maintaining validity, and integrating this patent within a broader international portfolio remain critical for stakeholders.


Key Takeaways

  • Scope & Claims: The patent likely covers a novel compound, method of use, or formulation. Its breadth strategically balances protection with defensibility, emphasizing innovation over prior art.
  • Patent Landscape: It exists within a densely patent-cluttered environment, necessitating comprehensive freedom-to-operate assessments.
  • Strategic Significance: For domestic and international firms, CN102448444 serves as a critical IP asset for market entry, licensing, or defensiveness.
  • Legal Considerations: Vigilant monitoring for validity challenges, licensing opportunities, and potential infringement is essential.
  • Global Strategy: Coupling this patent with international counterparts enhances global patent coverage, maximizing commercial protection.

FAQs

1. What is the primary inventive aspect of CN102448444?
While the exact claims are proprietary, the patent typically covers a novel chemical structure, formulation, or method of use that differentiates it from prior art, likely involving structural modifications or therapeutic applications.

2. How does CN102448444 compare to similar patents internationally?
Its scope may be aligned or expanded through corresponding filings under the Patent Cooperation Treaty (PCT), but Chinese patents often serve as core territorial rights, with subsequent national phase filings expanding global protection.

3. What risks exist for patent invalidation in China?
Challenges may arise from prior art, obviousness, or lack of novelty—particularly if similar compounds or methods are documented in existing literature or patents.

4. How can patent CN102448444 be leveraged commercially?
It can serve as a basis for licensing, partnership agreements, or establishing a proprietary position in the Chinese pharmaceutical market.

5. What strategic steps should stakeholders take regarding this patent?
Continuous patent monitoring, potential prosecution of further filings, enforcement activities, and alignment with broader patent portfolios are critical for maximizing value.


Sources:

[1] Chinese Patent Office Official Database, CN102448444
[2] WIPO PCT Patent Landscapes
[3] China National Intellectual Property Administration (CNIPA) Guidelines

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.