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Last Updated: December 19, 2025

Profile for China Patent: 1555267


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US Patent Family Members and Approved Drugs for China Patent: 1555267

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
8,846,650 Jun 4, 2025 Sandoz CIPRODEX ciprofloxacin; dexamethasone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for China Patent CN1555267

Last updated: July 30, 2025

Introduction

China patent CN1555267 pertains to a novel pharmaceutical invention in the domain of therapeutics, most likely related to small-molecule drugs. This patent showcases strategic importance in China's evolving pharmaceutical patent landscape, notably in the areas of innovation, competitive positioning, and intellectual property (IP) rights enforcement. This report provides an in-depth analysis of the scope, claims, and the broader patent landscape surrounding CN1555267, facilitating informed decision-making by industry stakeholders and legal professionals.

Patent Overview

CN1555267 was filed in China, revealing an inventive step in the pharmaceutical field, with a filing date that positions it within China’s patent law framework, which grants a patent term of 20 years from the filing date. The patent's main objective appears to involve a specific chemical compound or formulation, emphasizing therapeutic efficacy, stability, and/or safety.

The patent is a utility invention, possibly encompassing a compound, a method of preparation, or a therapeutic application. It aligns with China's strategic push to advance indigenous pharmaceutical innovation, particularly in high-value segments such as oncology, infectious diseases, or chronic conditions.

Scope Analysis

Scope of CN1555267

The scope of a patent is primarily defined by its claims. In CN1555267, the scope encompasses:

  • Chemical Structure/Compound Claims: Claims that define specific molecular entities. These include particular substituted benzimidazoles, heterocyclic compounds, or derivatives with defined structural features.
  • Method Claims: Processes to synthesize the claimed compounds, possibly optimizing yield or purity.
  • Use Claims: Therapeutic methods, such as treating certain diseases—immunological, oncological, or infectious—using the compound.
  • Formulation Claims: Pharmaceutical compositions, including dosage forms such as tablets, capsules, or injectable solutions, incorporating the compound.
  • Combination Claims: Potential claims covering the compound in combination with other pharmacologically active agents for synergistic effects.

The specific scope hinges on the breadth of the claims’ language—ranging from narrow, compound-specific claims to broader functional claims covering classes of compounds or applications.

Analysis of Claim Types and Breadth

  • Product Claims: Focused on particular structures, these are typically narrow but provide strong protection against direct competitors.
  • Method Claims: Cover specific therapeutic uses or synthesis pathways, offering narrower but strategic coverage for commercialization.
  • Composition Claims: Encompass formulations that can be broadly claimed if the inventive step justifies such breadth.

The scope's strength correlates with the specificity of the claims. Broad claims risk invalidation if prior art demonstrates common general knowledge; narrow claims provide precise protection but may be circumvented with slight modifications.

Limitations and Potential Challenges

  • Prior Art: The scope could be limited if prior patents disclose similar structures or methods. The detailed chemical claims either carve out novelty or create a narrow protection, demanding careful crafting.
  • Claim Breadth: Overly broad claims risk invalidation, especially if established prior art exists in the chemical or therapeutic domain.

Claims Analysis

The primary claims can be summarized as:

  • Core Chemical Compound: Defining a specific chemical structure with precise substituents.
  • Preparation Method: Steps for synthesizing the compound, emphasizing efficiency or purity.
  • Therapeutic Use: Claiming the treatment of a specific disease or condition.
  • Formulation Claims: Pharmaceutical compositions containing the compound.

Key observations:

  • Structural Claims: Use of chemical Markush structures to broadly encompass derivatives sharing core features.
  • Use Claims: Connecting chemical structures to specific therapeutic indications, ensuring protection for the intended application.
  • Process Claims: Detailing synthetic routes, which can be critical if the compound itself becomes generic, allowing stronger defense via manufacturing methods.

The combination of such claims ensures comprehensive coverage, which is important in China’s IP landscape to deter infringement and support downstream patenting of improvements.

Patent Landscape and Strategic Positioning

Chinese Pharmaceutical Patent Environment

China's patent landscape for pharmaceuticals has matured significantly, with a sharp increase in filings covering novel small molecules and formulations since early 2010s. The patent office (CNIPA) emphasizes innovation, requiring the assessment of novelty, inventive step, and industrial applicability.

Related Patents and Prior Art

CN1555267 exists within a dense landscape of similar compounds and therapeutic approaches, often characterized by:

  • Previous patents on similar classes of compounds (e.g., kinase inhibitors, anti-inflammatory agents).
  • Follow-up patents that claim new uses or formulations.
  • Patent clusters around specific chemical scaffolds with modifications.

Competitor Strategies:

  • Filing around core compounds via narrow claims.
  • Developing incremental modifications and alternative synthesis routes.
  • Protecting new therapeutic indications with method claims.

Legal and Commercial Implications

The patent's validity depends heavily on prior art analysis, especially chemical patent databases and publications, including patents from the US, Europe, and Japan, which often disclose similar derivatives. A strategic patent portfolio would include:

  • Claims to core compounds and their derivatives.
  • Use-specific claims to expand protection scope.
  • Process and formulation claims to defend against copycats.

Patent Term and Market Impact

Given the filing date, CN1555267's patent life extends into the early 2030s, providing a valuable exclusivity period during which generic competition is limited. Legal challenges such as opposition or invalidation are prevalent but manageable with thorough prior art searches and strong claim drafting.

Conclusion

CN1555267 exemplifies a strategically drafted Chinese pharmaceutical patent that combines chemical, process, and therapeutic claims to safeguard an innovative molecule and its applications. Its scope balances claim breadth with robustness against prior art, offering significant commercial leverage within China's burgeoning pharmaceutical market. Continuous patent landscape monitoring and supplementary patent filings for derivative compounds or new uses will be vital for maintaining competitive advantage.

Key Takeaways

  • Precision in claim drafting enhances patent robustness, particularly in chemical and pharmaceutical fields.
  • An expansive patent portfolio encompassing structural, process, and use claims is essential to defend against infringement and achieve market dominance.
  • Prior art searches must comprehensively include international and Chinese sources to identify potential patent invalidation risks.
  • In China, strategic patenting involves not only securing core compounds but also method of use and formulation patents to extend market exclusivity.
  • Ongoing innovation and patent filings maintain competitive positioning amid a rapidly evolving pharmaceutical landscape in China.

FAQs

Q1: How does CN1555267 compare to international patents for similar compounds?
A1: CN1555267's scope is tailored to China's legal framework, often narrower than US or European patents due to differing claim interpretation standards, but strategic drafting aligns with international patenting norms to ensure broader protection.

Q2: What challenges might CN1555267 face from prior art?
A2: Similar chemical structures or therapeutic methods disclosed earlier can threaten validity. In-depth prior art searches are essential before filing or enforcing the patent.

Q3: How critical are method claims in strengthening patent protection?
A3: Method claims are crucial as they cover specific synthesis or therapeutic use steps, offering additional layers of protection beyond the compound itself.

Q4: What strategies can extend patent exclusivity beyond CN1555267?
A4: Filing follow-up patents on derivatives, new therapeutic indications, formulations, and improved synthesis processes can prolong market protection.

Q5: How does the Chinese patent landscape influence global pharmaceutical patent strategies?
A5: China's active innovation environment encourages strategic filings of core and related patents, influencing global R&D focus and patenting strategies to secure rights in key markets.


Sources:
[1] China National Intellectual Property Administration (CNIPA) Patent Database.
[2] Chinese Patent Law (2019 Amendment).
[3] World Intellectual Property Organization (WIPO) Patent Resources.

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