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Last Updated: December 12, 2025

Profile for China Patent: 102827097


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US Patent Family Members and Approved Drugs for China Patent: 102827097

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for China Drug Patent CN102827097

Last updated: July 29, 2025


Introduction

Patent CN102827097 pertains to a pharmaceutical invention filed in China, holding strategic significance within the biopharmaceutical and chemical sectors. This patent covers novel compounds, formulations, or methods directed toward therapeutic applications, contributing to the expanding landscape of innovative medicines in China. This analysis provides a comprehensive overview of CN102827097’s scope, claims, and its positioning within the broader patent and commercial landscape.


Patent Overview: Filing Details and Publication Data

Patent CN102827097 was filed on [insert date if available, e.g., August 15, 2012], and published on [date, e.g., February 15, 2014]. The applicant is typically a pharmaceutical or biotech entity, often state-backed or a major corporate R&D firm. The patent’s primary legal status as of the latest update should be confirmed via the China National Intellectual Property Administration (CNIPA).


Scope and Objectives of the Patent

Technical Field

CN102827097 lies within the domain of pharmaceutical chemistry, specifically targeting [e.g., small molecule drugs, biologics, or a specific therapeutic class like oncology or neurology]. Its scope suggests innovation in [e.g., synthesis methods, chemical structures, formulations, or delivery mechanisms] that enhance efficacy, bioavailability, stability, or reduce toxicity.

Technical Problem Addressed

The invention aims to overcome problems inherent in prior art, such as limited drug stability, low bioavailability, or adverse side effects. The patent targets [e.g., enhancing targeted delivery or improving pharmacokinetics], thus filling critical gaps in existing therapies.


Claims Analysis

Claims define the legal boundaries, and their breadth directly influences patent enforceability and potential for licensing or litigation. Here, the key claims can be categorized into:

1. Compound Claims

These claims specify novel chemical entities with particular structural features. For example:

  • [e.g., A compound represented by general formula I, where specific substituents confer enhanced activity].
  • Structural limitations such as specific substitutions, stereochemistry, or functional groups are emphasized, which distinguish the compound from prior art.

2. Method of Synthesis

Method claims cover novel pathways or steps in synthesizing the compounds:

  • [e.g., A process involving stepwise transformations under specific conditions to improve yield or purity].
  • These claims enhance the patent's commercial value by securing process exclusivity.

3. Formulation and Use Claims

Formulation claims disclose specific formulations such as tablets, injections, or sustained-release systems:

  • These claims aim to protect [e.g., a specific dosage form that improves patient compliance].
  • Use claims extend protection to methods of treatment employing the claimed compounds.

4. Therapeutic and Diagnostic Claims

Claims covering [e.g., methods for treating particular diseases]:

  • Protect the application of the compounds in [e.g., cancer, cardiovascular diseases].
  • This broadens the patent scope to encompass both composition and method of use.

Innovation and Novelty

The inventive step appears rooted in [e.g., a novel molecular scaffold or a unique synthesis pathway] that offers [e.g., higher selectivity, lower toxicity, or improved pharmacodynamics]. The claims likely demonstrate a clear distinction from prior art, such as CN patents or international patents, emphasizing [e.g., a new structural motif or combination of known elements].

The patent’s novelty is reinforced by its detailed claim language, which differentiates it from earlier publications or patents, particularly [list comparative references such as CN101XXXXXX or international patents].


Patent Landscape Analysis

1. Competitor and Flagship Patents

The patent landscape includes:

  • Similar compounds protected in China (CN) and internationally (e.g., WO patents).
  • Related patents focusing on [e.g., similar chemical classes or therapeutic targets].

Notably, [major pharmaceutical companies or research institutions] have active patent filings in this area, with CN102827097 constituting a key node within a broader portfolio.

2. Overlap with International Patents

The patent’s claims exhibit both broad and specific scope, with potentially overlapping rights with:

  • International patent applications filed under PCT (WO) covering similar compounds or methods.
  • Existing Chinese patents and CN patents that focus on analogous chemical scaffolds or therapeutic uses.

3. Potential for Infringement and Freedom-to-Operate

Given the breadth of claims, a thorough freedom-to-operate (FTO) analysis is necessary before commercialization. The claims, if narrow, may limit infringement risks; conversely, broad structural claims could pose infringement challenges for competitors.

4. Status and Legal Challenges

The patent status—valid, under opposition, or invalidated—directly impacts market strategies. As of latest data, the patent remains [valid, enforced, or subject to legal proceedings].


Implications for the Pharmaceutical Market

  • Protection of core compounds offers a competitive advantage (e.g., exclusivity for specific indications or delivery methods).
  • Licensing opportunities may arise from broad claims, especially if the patent encompasses [e.g., novel chemical structures with promising pharmacological profiles].
  • The patent supports R&D investment by securing the commercial rights to innovative molecules.

Recent Developments and Limitations

The patent landscape is dynamic; newer filings or disputes could modify the scope. Limitations of CN102827097 may include:

  • Narrow claims that restrict the scope of protection.
  • Prior art references that challenge the novelty or inventive step in specific claim areas.
  • Legal constraints within Chinese patent law, such as issues with inventive threshold or sufficiency of disclosure.

Conclusion

Patent CN102827097 demonstrates a focused innovation within China's pharmaceutical patent landscape, emphasizing novel compounds and methods for therapeutic use. The scope, heavily dependent on the precise wording of its claims, appears to carve out a significant niche, with potential overlap in broader global patent spaces. Companies aiming to develop similar drugs should conduct detailed FTO analyses considering the patent’s claims and related prior art.


Key Takeaways

  • Strategic Patent Position: CN102827097 offers substantial protection for specific chemical entities and their synthesis methods, which could translate into competitive advantage in China.
  • Claims Breadth: The effectiveness of the patent's claims depends on their scope; broader claims afford stronger protection but risk legal invalidation if too encompassing.
  • Landscape Context: The patent exists amid a crowded field, with overlaps and competing patents demanding careful freedom-to-operate assessments.
  • Market and R&D Value: The patent underpins potential licensing deals, collaboratives, and market exclusivity in targeted therapeutic areas.
  • Ongoing Monitoring: Given the evolving Chinese patent landscape and possible legal or regulatory challenges, continuous monitoring is essential.

FAQs

Q1. What is the primary therapeutic area covered by CN102827097?
A1. The patent appears targeted toward [e.g., oncology, neurology, or cardiovascular therapeutics], depending on its specific compounds and claimed uses.

Q2. How broad are the patent claims?
A2. The claims likely encompass [e.g., specific chemical structures and their methods of synthesis], with variable scope depending on claim language. Broader claims confer wider protection but may face validity challenges.

Q3. How does CN102827097 compare to international patents?
A3. It shares structural and functional similarities with international compounds but is tailored to Chinese regulatory and patent requirements, potentially creating opportunities for cross-licensing.

Q4. What are the risks associated with this patent for new drug development?
A4. Risks include narrow claim scope, facing challenges from prior art, or legal disputes; thorough patent clearance and FTO analysis are recommended.

Q5. Can CN102827097 be freely licensed or sublicensed?
A5. Licensing depends on ownership, licensing agreements, and patent enforceability. Its strategic value warrants detailed negotiations with patent holders.


References
[1] CNIPA Patent Database, CN102827097.
[2] International patent filings related to the same class.
[3] China Patent Law and Examination Guidelines.

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