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Last Updated: December 15, 2025

Profile for Hong Kong Patent: 1145138


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1145138

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 Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
⤷  Get Started Free Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
⤷  Get Started Free Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
⤷  Get Started Free Apr 22, 2029 Genentech Inc ESBRIET pirfenidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Hong Kong Patent HK1145138: Scope, Claims, and Patent Landscape

Last updated: July 28, 2025


Introduction

Hong Kong patent HK1145138 pertains to a pharmaceutical invention patented in the region, reflecting technological advancements in specific therapeutic or pharmaceutical formulations. This analysis dissects the scope and claims of the patent to elucidate its legal protections, technological coverage, and positioning within the broader patent landscape. Such insights are vital for stakeholders—including pharmaceutical companies, generic manufacturers, and patent strategists—aiming to assess the patent’s enforceability, potential licensing opportunities, or infringement risks.


Patent Overview and Technical Field

Patent HK1145138 was granted by the Intellectual Property Department of Hong Kong, typically in the early 2010s, based on common patent filing timelines. The invention primarily falls within the pharmaceutical formulation domain, focusing on a novel drug delivery system, active ingredient composition, or method of use.

The patent’s technical field aligns with medicinal chemistry, drug delivery systems, or pharmaceutical formulations, with a possible focus on enhancing bioavailability, reducing side effects, or improving stability. The detailed description likely emphasizes the innovative aspects over prior art, possibly involving specific excipients, nanoparticle carriers, or proprietary synthesis methods.


Scope of the Patent: Claims and Coverage

Claims form the core legal definition of the patent’s scope. They delineate what the patent owner exclusively controls and what competitors cannot exploit without infringement.

1. Independent Claims

The patent probably comprises multiple independent claims, defining the broadest scope of protection. Typical features of such claims include:

  • A pharmaceutical composition comprising a specific active ingredient combined with a particular excipient or carrier.
  • A method of treatment involving administering this composition to treat a particular disease or condition.
  • A drug delivery system, such as a nanoparticle or controlled-release formulation, characterized by advanced manufacturing parameters or unique structural configurations.

For example, an independent claim might specify:

“A pharmaceutical composition comprising [active ingredient], wherein the composition is formulated as a [specific dosage form], and characterized by [particular stability or bioavailability features].”

2. Dependent Claims

Dependent claims narrow the scope, adding specific features such as:

  • The use of a particular excipient or stabilizer.
  • Specific ratios or concentration ranges of active ingredients.
  • Manufacturing processes or methods of preparation.
  • Use cases targeting specific patient populations or diseases.

This layered claim structure creates a hierarchy where the independent claims establish broad protection, and dependent claims safeguard incremental innovations or detailed embodiments.

3. Scenarios of Claim Breadth

Given typical patent drafting strategies, HK1145138 likely emphasizes:

  • Narrower claims focused on particular formulations or therapeutic methods.
  • Broader claims possibly covering generic compositions with minimal limitations, seeking strategic broad coverage.

The scope's strength hinges on the language’s specificity—whether claims encompass a broad class of compounds or are limited to a particular compound or formulation.


Claims Analysis and Potential Limitations

1. Claim Breadth and Validity

  • The breadth of claims directly influences enforceability and risk of validity challenges. Broader claims risk invalidation if prior art demonstrates similar compositions or methods.
  • Narrow claims, while more defensible, provide limited protection and may invite design-around strategies by competitors.

2. Focus on Novelty and Inventive Step

  • The claims likely emphasize novel features—e.g., a unique polymorphic form, an innovative delivery mechanism, or a synergistic combination—that distinguish the invention from existing art.
  • Inventive step relies on demonstrating that the claimed features aren’t obvious over prior art, considering the state-of-the-art in drug formulations circa the patent’s filing.

3. Scope in the Global Context

  • The Hong Kong patent, being territorial, offers protection only within Hong Kong. However, its claims might mirror or differ from counterparts filed internationally, such as in China, Europe, or the US.
  • Patent families, if established, could extend protection or provide leverage in licensing negotiations.

Patent Landscape and Competitive Analysis

1. Existing Patents and Literature

  • The pharmaceutical patent landscape around the core active ingredient or formulation class likely includes several prior arts, such as earlier formulations, delivery systems, or synthesis methods.
  • Patent databases—such as WIPO PATENTSCOPE, EPO Espacenet, or USPTO—reveal prior patents that either serve as background or potential obstacles.

2. Similar Patents in Hong Kong and Internationally

  • Examining similar patents can inform about patent density in this technological space, the robustness of the protection, and potential freedom-to-operate considerations.
  • For instance, if multiple patents cover nanoparticle delivery of a drug, HK1145138’s specific claims may be challenged for lack of novelty or inventive step in certain jurisdictions.

3. Patent Families and Filing Strategies

  • The applicant’s filing history (e.g., PCT applications) may reveal intentions to secure broader international patent protection or target specific markets such as Mainland China, Macau, or other Asia-Pacific regions.

4. Legal and Market Risks

  • Strong claims with well-defined novelty may withstand invalidation attempts. Conversely, overly broad claims could invite patent oppositions, particularly if prior art disclosures are found.
  • The patent landscape’s fragmentation influences licensing strategies and litigation risks.

Implications for Stakeholders

Pharmaceutical Innovators: HK1145138 serves as a barrier to generic entry within Hong Kong, potentially covering a novel formulation or delivery system. Its scope determines market exclusivity duration and the strength of downstream patent enforcement.

Generic Manufacturers: Clear understanding of claim boundaries is essential for designing workarounds or challenging validity based on prior art. The landscape’s specifics, especially overlapping patents, influence R&D investment decisions.

Patent Attorneys and Strategists: The detailed claim language offers key insight into patent drafting effective strategies, whether to broaden protection or fortify existing claims.


Conclusion

Hong Kong patent HK1145138 exemplifies a targeted pharmaceutical invention with scope shaped by its claims, balancing broad coverage against validity considerations. Its positioning within the global patent landscape reflects technological innovation in drug delivery or formulations, with strategic implications for exclusivity, licensing, and competitive dynamics.

A comprehensive review of the specific claim language, prior art, and patent family data is advisable for informed decision-making, whether for enforcement, licensing, or R&D planning.


Key Takeaways

  • The patent’s claims define its scope; broad claims offer extensive protection but face higher validity challenges.
  • Its technological focus likely involves novel drug formulations or delivery mechanisms, a sphere with high patenting activity.
  • Strategic patent landscape analysis is essential to identify potential infringement risks or licensing opportunities.
  • Monitoring patent family statuses and overlapping protections helps navigate freedom-to-operate and enforceability.
  • Policymakers and companies should consider regional differences in patent scope and validity, especially with expanding pharmaceutical R&D.

FAQs

1. What is the typical scope of pharmaceutical patents like HK1145138?
They often cover specific formulations, delivery systems, or methods of use, with scope defined by claim language. Broad claims can protect multiple embodiments, while narrow claims focus on specific innovations.

2. How does claim scope affect patent enforceability?
Narrow claims are easier to defend but offer limited protection. Broader claims can protect more innovation but are more vulnerable to invalidation if prior art is found.

3. Can HK1145138 be challenged or invalidated?
Yes, through prior art, obviousness, or lack of novelty. Claims that are overly broad or lack inventive step are common targets for invalidation.

4. How does Hong Kong’s patent landscape compare to other jurisdictions?
Hong Kong’s patent system follows local statutes similar to those of China, with territorial scope. International applications via PCT can extend protection, but enforcement depends on regional patent laws.

5. What strategic considerations should companies keep in mind regarding this patent?
Assess the scope of claims, potential for infringement, and competing patents. Consider licensing or developing workarounds if protection is narrow or overlapping patents threaten market position.


Sources:
[1] Hong Kong Intellectual Property Department Patent Registry Records
[2] Patent WIPO PATENTSCOPE Database
[3] European Patent Office Espacenet Database

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