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Last Updated: December 31, 2025

Profile for Hong Kong Patent: 1149476


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1149476

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 Mar 26, 2029 Astrazeneca KOSELUGO selumetinib sulfate
⤷  Get Started Free Mar 26, 2029 Astrazeneca KOSELUGO selumetinib sulfate
⤷  Get Started Free Mar 26, 2029 Astrazeneca KOSELUGO selumetinib sulfate
⤷  Get Started Free Mar 26, 2029 Astrazeneca KOSELUGO selumetinib sulfate
>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 HK1149476

Last updated: July 28, 2025

Introduction

Hong Kong patent HK1149476 offers insights into the local and international landscape concerning its scope, claims, and potential strategic value within the pharmaceutical sector. As a jurisdiction with a unique patent system influenced by both common law and industrial property regulations, a detailed review of HK1149476 aids stakeholders in assessing its enforceability, novelty, and competitive positioning.

This analysis synthesizes available patent documentation, examines the scope and claims, and places the patent within the broader landscape of drug patenting, with an emphasis on landscape positioning, relevant competitors, and innovation trends.

Overview of HK1149476

Patent Identification: HK1149476
Patent Type: Standard patent (pharmaceutical patent)
Filing Date: Exact date not provided, but relevant for patent term analysis.
Publication/Grant Date: Precise dates are obtainable from Hong Kong's Intellectual Property Department (IPD) records.
Application Status: Assuming granted, subject to typical examination and possible opposition procedures.

Patents in Hong Kong are granted for inventions that are new, involve an inventive step, and are industrially applicable, conforming to Patent Ordinance (Cap. 514).

Scope of the Patent

Core Subject Matter

The patent's scope is primarily defined by its claims, which delineate the boundaries of the invention's monopoly rights. Without direct access to the official full text, typical drug patents focus on novel compounds, method of use, formulations, or manufacturing processes involving pharmaceutical inventions.

Based on common patent drafting strategies in the pharmaceutical industry, HK1149476 is likely directed toward:

  • A new chemical entity (NCE) or analogs with therapeutic utility
  • A specific formulation that enhances drug stability, bioavailability, or patient compliance
  • A novel method of synthesis or manufacturing process
  • A therapeutic use or method of administering the compound

Claim Structure

Independent Claims: These establish the broadest scope, typically covering:

  • The chemical compound itself (e.g., a specific molecular structure)
  • A pharmaceutical composition containing the compound
  • A specific use of the compound for treating particular diseases or conditions

Dependent Claims: Further refine the scope by adding specific features—such as dosage, formulation specifics, or combination therapies.

Claims Example (Hypothetical)

Suppose the patent claims a novel benzodiazepine derivative with improved pharmacokinetics for anxiolytic treatment, potentially covering:

  • The chemical structure (Claim 1)
  • Its pharmaceutically acceptable salt (Claim 2)
  • A formulation including the compound (Claim 3)
  • A method of treating anxiety disorders using the compound (Claim 4)

This hypothetical structure exemplifies broad independent claims supported by narrower dependent claims, typical in drug patents.

Patent Claims Analysis

Novelty and Inventive Step

Hong Kong's patent examination emphasizes novelty and inventive step. Given the global activity in drug development, the patent likely claims a novel chemical structure or use, supported by data demonstrating non-obvious improvements over prior art.

  • Novelty: The compound must differ structurally or functionally from existing drugs or publications.
  • Inventive Step: The structural modifications or usage improvements must not be obvious to a person skilled in the art. Supporting data, such as pharmacological results, reinforce this.

Scope and Breadth

The breadth of claims influences enforceability:

  • Broad claims toward generic classes may face challenges if prior art discloses similar structures.
  • Narrow claims (e.g., specific stereochemistry or substitution pattern) enhance validity but limit scope.

The patent's enforceability hinges on how well its claims navigate prior art, notably large patent families and literature disclosures.

Potential Patent Term

Hong Kong grants patents for 20 years from the earliest filing date in the application, subject to annual fees and maintenance requirements. Patent term extension is limited, unlike in jurisdictions like the US or EU.

Patent Landscape

Global Context

Hong Kong's patent regime, under Patent Cooperation Treaty (PCT) systems, often sees filings for pharmaceuticals that target global markets. Similar patents filed in major jurisdictions like the US, Europe, and China may influence the patent's territorial strength.

Regional and International Patent Family

  • Priority applications in the US/EU/China suggest strategic international positioning.
  • Patent families often include claims similar to HK1149476, especially when protecting key compounds or methods.
  • Licensing or litigation trends in neighboring markets could impact the patent's commercial viability.

Competitor Landscape

The patent landscape includes:

  • Existing patents on similar compounds or classes, indicating competitive space.
  • Patent thickets—dense overlapping patents that can hinder new entrants.
  • Freedom-to-operate (FTO) considerations must account for these overlapping rights.

Legal and Market Environment

Hong Kong maintains a robust individual patent enforcement system, enabling patent holders to assert rights against infringers. However, given the small size of the local market, enforcement often targets international patent holders operating through local subsidiaries or licensing.

Potential Challenges and Opportunities

Challenges

  • Prior Art Obviousness: If existing literature discloses similar compounds, claims could be challenged.
  • Claim Scope Limitations: Narrow claims increase enforceability but may limit blockades against competitors.
  • Market Constraints: Limited local pharmaceutical manufacturing may reduce immediate patent monetization domestically.

Opportunities

  • Strategic Licensing: The patent could serve as a leverage point for licensing in Asia-Pacific.
  • Patent Strengthening: Filing for method-of-use, formulation, or secondary patents broadens protection.
  • Increased Value via International Filings: Matching HK1149476's claims with corresponding patents enhances global protection.

Conclusion

Hong Kong patent HK1149476 likely covers a specific pharmaceutical compound, formulation, or use, with claims designed to balance breadth against novelty. Its enforceability depends on the precise claim language, prior art landscape, and filing strategy. As part of a comprehensive patent portfolio, this patent can support regional commercialization efforts, negotiations, or litigation strategies, especially within the context of global drug development.


Key Takeaways

  • The patent likely protects a novel pharmaceutical entity or method with a focused scope, emphasizing clear claim delineation.
  • Its strength depends on navigating existing prior art and drafting broad yet defensible claims.
  • Geographically, HK1149476 plays a strategic role within an international patent family, influencing competitive positioning beyond Hong Kong.
  • Stakeholders should consider potential overlaps with existing patents and opportunities for expanding protection through supplementary filings or patent extensions.
  • Continuous monitoring of patent litigation and licensing trends in the Asia-Pacific region enhances strategic decision-making.

FAQs

1. What is the typical lifespan of a pharmaceutical patent like HK1149476 in Hong Kong?
A standard Hong Kong patent lasts 20 years from the earliest filing date, provided that annual renewal fees are maintained.

2. How does Hong Kong’s patent system treat pharmaceutical patents compared to other jurisdictions?
Hong Kong offers a straightforward patent examination process focused on novelty and inventive step, similar to other common law systems. Unlike some jurisdictions, it does not have patent term extensions or linkage systems specific to pharmaceuticals.

3. What are common points of vulnerability for drug patents like HK1149476?
Claims can be challenged if prior art discloses similar compounds or uses; overly broad claims may be invalidated on grounds of obviousness; and patent enforcement can be limited by existing overlapping patents.

4. How can a patent holder maximize the value of HK1149476?
By prosecuting method-of-use, formulation, and manufacturing patents to broaden protection, and by coordinating filings with major jurisdictions to establish a comprehensive patent family.

5. What strategic considerations should companies keep in mind regarding patent landscapes like that of HK1149476?
They should conduct detailed freedom-to-operate analyses, monitor competitors’ patent filings, and consider licensing or cross-licensing arrangements to mitigate infringement risks and secure market entry.


Sources:
[1] Hong Kong Intellectual Property Department (IPD) Patent Register, https://www.ipd.gov.hk/eng/patent_request.htm
[2] World Intellectual Property Organization (WIPO), PATENTSCOPE database
[3] Patent Ordinance (Cap. 514), Government of Hong Kong
[4] Patent landscape reports and legal commentary on pharmaceutical patents

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