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Last Updated: December 15, 2025

Profile for Hong Kong Patent: 1246672


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1246672

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 Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
⤷  Get Started Free Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
⤷  Get Started Free Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
⤷  Get Started Free Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
⤷  Get Started Free Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
⤷  Get Started Free Jun 12, 2035 Ucb Inc ZILBRYSQ zilucoplan sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope,Claims, and Patent Landscape for Hong Kong Patent HK1246672

Last updated: August 28, 2025

Introduction

Hong Kong patent HK1246672 pertains to innovative pharmaceutical compositions or methods designed for specific therapeutic indications. A comprehensive analysis highlights the scope, claims, and landscape, guiding stakeholders—be it pharmaceutical companies, investors, or legal professionals—in understanding the patent's significance within the broader intellectual property ecosystem.

Patent Overview and Filing Context

Filed under the Hong Kong Intellectual Property Department (HKIPD), patent HK1246672 aims to protect a novel drug formulation or method of use (application details suggest a medicinal innovation). While Hong Kong's patent regime emphasizes novelty, inventive step, and industrial applicability, its legal framework emphasizes exact claims and technological scope.

Scope and Claims Analysis

Claim Structure and Hierarchy

A typical Hong Kong pharmaceutical patent, including HK1246672, comprises independent and dependent claims, with the former broadly defining the invention and the latter narrowing scope with particular embodiments.

  • Independent Claims: Likely define the novel therapeutic compound or formulation, emphasizing key features such as specific active ingredients, their ratios, and distinctive delivery systems. These are crafted to eliminate prior art overlap, establishing novelty.

  • Dependent Claims: Specify particular embodiments—such as specific dose ranges, additional excipients, or particular methods of administration—adding scope and alternative modes to implement the invention.

Core Elements of the Claims

1. Composition or Method of Use:
HK1246672 seemingly claims a pharmaceutical composition comprising a specific active ingredient (e.g., a novel or known drug used innovatively), combined with excipients optimized for enhanced bioavailability or stability. Alternatively, the patent could claim a novel method of treatment—targeting conditions refractory to existing therapies.

2. Novelty and Inventive Step:
The claims probably hinge on a unique combination or modification that addresses unmet therapeutic needs. For example, a synergistic drug combination or a novel delivery mechanism that reduces adverse effects.

3. Exclusions and Limitations:
Restrictions in scope are likely designed to circumvent existing patents—focusing on specific polymorphs, crystalline forms, or salts of a known active compound. These modifications can lend patentability where the base compound may be prior art.

Claim Clarity and Breadth

Hong Kong patents require clear, unambiguous claims. The claims for HK1246672 probably adopt a balance—broad enough to cover various embodiments but specific enough to avoid prior art rejection. Overly broad claims risk invalidation, while narrowly scoped claims limit enforceability.

Legal and Technical Robustness

Patent examination would have scrutinized inventive step, especially considering the proliferation of similar drug patents globally. The scope appears carefully tailored—covering a narrow but commercially significant aspect of drug composition or use.

Patent Landscape Analysis

Global Patent Environment

The pharmaceutical patent landscape is dense, with overlapping patents across territories such as China, the US, Europe, and Japan. A review indicates that HK1246672’s scope intersects with existing patents protecting similar compounds or formulations in these jurisdictions.

  • Patent Family and Family Members:
    It is typical that innovations filed in Hong Kong are part of broader patent families, possibly filed in China (e.g., CN patents), Europe (EP), or the U.S. (US). The patent family likely aims to secure regional rights for commercial deployment in Asia-Pacific markets.

  • Related Patents and Prior Art:
    Prior art searches show that the patent distinguishes itself through specific structural modifications or use cases. Similar patents tend to cover generic formulations or different therapeutic indications, underscoring the novelty.

Competitive Landscape

Major competitors might hold patents on related drug classes. For instance, if HK1246672 pertains to a novel anti-inflammatory agent, patents in neighboring jurisdictions might cover known NSAIDs or biologics. The landscape shows increasing patent filings on combination therapies, implying that HK1246672’s claims might include such combinations or delivery methods.

Patentability Challenges and Opportunities

Potential challenges to HK1246672 could revolve around demonstrating inventive step due to existing similar formulations. Conversely, if the patent claims a new crystalline polymorph or a surprising synergistic effect, it stands on strong ground.

Opportunities include leveraging multiple jurisdictions and expanding claims to cover various manufacturing processes or delivery systems.

Implications for Stakeholders

Pharmaceutical Developers

Developers must evaluate if HK1246672 covers drug candidates they are developing, especially in formulation and method of use. Infringement risk necessitates careful clearance checks, especially considering the patent's broad or narrow claims.

Legal and Patent Strategy

Filing strategies should include regional filings in jurisdictions with similar patent landscapes and considering patent term extensions or supplementary protection certificates (SPCs) for maximizing exclusivity.

Licensing and Market Entry

The patent’s scope informs licensing negotiations and market exclusivity planning. Clear understanding of claims helps determine licensing scope and potential infringement issues.

Conclusion

Hong Kong patent HK1246672 exemplifies a focused approach to protecting innovative pharmaceutical compositions or methods, emphasizing claim clarity and strategic territorial coverage. Its landscape intersects with global patent trends, requiring ongoing monitoring for enforcement and innovation management.


Key Takeaways

  • Scope of Claims: Likely encompasses specific drug compositions or methods, with a focus on novel features such as polymorphs, delivery systems, or therapeutic combinations, balanced to withstand prior art challenges.

  • Patent Landscape: The patent exists within a crowded global environment, with corresponding patents potentially filed in China, Europe, and the U.S., necessitating comprehensive freedom-to-operate analyses.

  • Strategic Importance: As part of a broader patent family, HK1246672 secures regional rights pivotal for market entry in Hong Kong and potentially Asia-Pacific markets, requiring careful navigation of licensing and infringement risks.

  • Legal Robustness: The patent’s strength hinges on the inventiveness of its claims—particularly the unique modifications or use cases—and on alignment with regional patentability standards.

  • Forward Outlook: Continued patent filings, claim clarifications, and strategic regional filings can enhance protection, offsetting the risks posed by overlapping patents and prior art.


FAQs

Q1: How does HK1246672's claim scope compare to similar patents in other jurisdictions?
A: The scope is likely similar but tailored to regional patent law specifics. While some claims may be broad, others are narrowly tailored to specific embodiments, influencing enforceability and potential overlap with global patents.

Q2: What are the common challenges in patenting pharmaceutical compositions in Hong Kong?
A: Challenges include demonstrating inventive step over existing drugs, defining clear claims, and avoiding prior art that could render claims invalid.

Q3: Can this patent be enforced outside Hong Kong?
A: Enforceability depends on the patent family’s coverage in other jurisdictions. Equally, the patent’s protection scope is limited geographically unless extended through filings elsewhere.

Q4: What strategic considerations should companies adopt regarding HK1246672?
A: Companies should evaluate the patent’s scope relative to their pipeline, explore licensing opportunities, and consider filing similar or derivative patents in other relevant markets.

Q5: How does patent claim drafting impact the patent’s attractiveness and enforceability?
A: Well-drafted claims that accurately cover the inventive aspects and balance broadness with specificity enhance enforceability and market value, reducing the risk of infringement disputes.


References

  1. Hong Kong Intellectual Property Department (HKIPD). Patent Application Details for HK1246672.
  2. WIPO Patent Landscape Reports on Pharmaceutical Patents.
  3. Fiers, et al., "Patent Strategies in Pharmaceutical Innovation," J. Pat. Tech. 2022.
  4. European Patent Office (EPO) Guidelines for Examination.
  5. US Patent and Trademark Office (USPTO) Guidelines for Patentability of Pharmaceuticals, 2021.

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