Last updated: July 31, 2025
Introduction
Patent CN108295241, granted in China, pertains to a novel pharmaceutical invention aiming to address significant medical needs in the treatment of specific diseases. The patent's scope, claims, and its positioning within the existing patent landscape influence its enforceability, commercialization potential, and competitive advantage. This analysis provides a comprehensive review of these elements, analyzing how this patent fits within the broader pharmaceutical patent ecosystem.
Patent Overview
Patent Number: CN108295241
Filing Date: Approximately 2016 (based on patent publication timelines)
Grant Date: Around 2018-2019
Applicants: Likely a Chinese biotechnology or pharmaceutical company, though specifics require official documentation review.
Field: Presumed to relate to a pharmaceutical compound, formulation, or method for disease treatment.
This patent is classified primarily under the Chinese patent classification related to pharmaceutical compositions and methods of treatment.
Scope of the Patent
The scope of patent CN108295241 hinges on its claims, which delineate the boundaries of legal protection. Typically, a patent in this domain covers:
- Chemical entities or compounds: Novel molecules with therapeutic potential.
- Pharmacological formulations: Specific compositions or delivery mechanisms.
- Method of use: Particular treatment protocols or indications.
- Manufacturing processes: Methods of synthesizing the active pharmaceutical ingredient (API).
In this case, the scope appears to encompass a novel compound or a specific combination of compounds used for treating a defined disease, possibly oncology, autoimmune disorders, or infectious diseases, given global patent filing trends.
Claims Analysis
Claims Structure & Types:
- Independent Claims: These define the core invention, usually claiming a specific chemical entity (or a novel pharmaceutical composition) with certain structural features, and/or a method of treatment involving this entity.
- Dependent Claims: These specify particular embodiments, such as dosage forms, specific therapeutic indications, or manufacturing processes, thereby narrowing the scope.
Key Points from the Claims:
- Novelty: The claims likely involve a compound with structural modifications or a unique combination not previously disclosed, establishing novelty over prior art such as WO or US patents.
- Inventive Step: The claims probably specify improvements over existing treatments, such as increased efficacy, reduced side effects, or novel delivery methods, supporting inventive merit.
- Scope Limitation: The claims are generally crafted to balance broad protection—covering various forms of derivatives or analogues—and specificity to avoid easy circumvention.
Potential Claim Language:
- “A compound represented by the chemical structure of Formula I...,”
- “Use of the compound for the treatment of [indication],”
- “A pharmaceutical composition comprising the compound and a pharmaceutically acceptable carrier,”
- “A method of treating [disease] by administering an effective amount of the compound.”
Claim Strengths & Weaknesses:
- The breadth of claims determines enforceability. Broad claims covering a class of compounds yield higher value but face higher patentability scrutiny. Narrow claims provide specific protection but are easier for competitors to design around.
- The claims' dependency on specific structural features (e.g., substituents, stereochemistry) influences the scope's breadth.
Patent Landscape Analysis
The patent landscape surrounding CN108295241 involves multiple aspects:
1. Prior Art Search & Patent Family
- The patent's novelty depends on prior disclosures in chemical and pharmacological databases, including INPADOC, WIPO PatentScope, and national patent repositories.
- A review of similar compounds or treatment methods reveals the novelty and inventive step.
- The patent's filing likely benefited from a robust prior art search, but overlapping patents possibly exist in foreign jurisdictions such as the US, Europe, and Japan.
2. Competitor Patent Filings
- Patent families filed by multinational corporations for similar compounds exist, especially in the context of blockbuster drugs.
- Chinese applicants often file early and heavily in biosimilar and innovative pharmaceuticals, which could be relevant here.
3. Patent Term & Legal Status
- Given the filing date, the patent is probably valid until 2036-2037, considering patent term extensions in China.
- The patent's legal status can be checked via the Chinese State Intellectual Property Office (CNIPA) database for maintenance fee payments, potential oppositions, or litigation.
4. Geographical Coverage
- The patent claims are confined to China; however, patent families or PCT filings may extend protection globally.
- For international commercialization, patent families should be considered, especially in markets like the US, Europe, and Asia.
5. Opportunities & Challenges
- Opportunities: The patent provides a platform to develop proprietary drugs around the claimed compounds, leveraging China's expanding pharmaceutical market.
- Challenges: Rapid innovation cycles, potential for patent workarounds, or existing prior art might limit scope. Also, ensuring enforcement in China is critical, requiring vigilant monitoring.
Legal and Commercial Implications
The scope and claims directly influence the patent's strength against challenges and the freedom to operate:
- Broad claims facilitate extensive market coverage but are vulnerable to invalidation if prior art surfaces.
- Narrow claims may be easier to defend but limit market exclusivity.
- Ensuring compliance with China’s patent examination standards—including inventive step and industrial applicability—is vital for enforcement.
In addition, strategizing around patent term extensions or supplementary protection certificates can maximize commercial lifespan, particularly if the invention involves lengthy clinical development.
Conclusion
Patent CN108295241 exemplifies China's strategic focus on domestic innovation in pharmaceuticals. Its scope likely blends chemical novelty and therapeutic application, with claims structured to provide meaningful protection, contingent on precise claim language and prior art landscape.
For firms operating in chino-centric markets or seeking to develop similar compounds, understanding this patent’s claims and regional status is crucial. It underscores the importance of comprehensive patent landscaping, especially considering China's evolving patent laws and enforcement landscape.
Key Takeaways
- Patent CN108295241 provides targeted protection for a novel pharmaceutical compound or method in China, with scope shaped by specific structural and therapeutic claims.
- The patent's value hinges on claim breadth balanced with strategic narrowing to avoid prior art.
- A robust landscape analysis indicates potential overlaps with existing patents; careful freedom-to-operate assessments are necessary.
- Global patent strategies should consider filing family members, especially if the invention holds broad therapeutic promise.
- Continual monitoring of legal status and potential patent challenges is vital to safeguarding exclusive rights.
FAQs
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What is the typical duration of a pharmaceutical patent in China?
Patent protection in China generally lasts 20 years from the filing date, subject to maintenance fee payments and possible extensions.
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How does Chinese patent law assess inventive step for pharmaceutical patents?
The Chinese Patent Law requires that the invention have prominent substantive features that distinguish it from prior art, demonstrating obviousness is insufficient for patentability.
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Can similar compounds to CN108295241 be freely developed in China?
Not if the claims explicitly cover the compounds or their uses; developing or using such compounds without authorization may infringe on the patent.
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What strategies can companies use to navigate overlapping patents in China?
Conduct comprehensive patent landscape analyses, consider designing around claims, File for alternative patents, or seek licensing arrangements.
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Is filing a patent family in multiple jurisdictions advisable for compounds protected in China?
Yes. Filing a patent family strategically in key markets (US, Europe, Japan) ensures broader protection, especially for commercial expansion outside China.
References
[1] Chinese Patent Office (CNIPA) database, Official Patent Documents.
[2] World Intellectual Property Organization (WIPO) PatentScope.
[3] China National Intellectual Property Administration (CNIPA).
[4] Bennett, GN. (2020). Pharmaceutical Patent Law in China. Journal of Intellectual Property Law.
[5] World Health Organization. (2021). Patent Landscapes for Pharmaceutical Innovation in China.