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Last Updated: December 28, 2025

Profile for Hong Kong Patent: 1121148


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1121148

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
7,528,143 Nov 16, 2031 Bristol-myers INREBIC fedratinib hydrochloride
7,825,246 Dec 16, 2026 Bristol-myers INREBIC fedratinib hydrochloride
8,138,199 Jun 30, 2028 Bristol-myers INREBIC fedratinib hydrochloride
>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 HK1121148

Last updated: July 28, 2025


Introduction

Hong Kong patent HK1121148 is a key strategic intellectual property asset within the biotech and pharmaceutical industry. As a jurisdiction-specific patent, its scope, claims, and placement in the broader patent landscape directly impact potential commercialization, licensing, and competitive positioning. This analysis examines the patent’s scope, detailed claims, and its alignment within the global patent environment, providing insights for innovators, patent professionals, and strategic decision-makers.


Overview of Patent HK1121148

HK1121148 pertains to a novel pharmaceutical compound, formulation, or medical method, with an inventive step that confers exclusive rights within Hong Kong. While detailed claim language is essential, we consolidate available information to derive the patent's core technical scope.

Its filing date, priority date, assignees, and prosecution history reveal strategic insights into innovation timelines and patent strength. HK1121148’s filing likely involved rigorous examination, emphasizing novelty, inventive step, and industrial applicability, as required by Hong Kong patent laws mirroring those of the UK and other common law jurisdictions.


Scope and Claims:

1. Claims Structure and Language

The claims define the boundaries of the patent’s protection, typically categorized into independent and dependent claims.

  • Independent Claims: Typically cover the core invention—be it a novel compound, composition, or method of use—with broad language to maximize market coverage.
  • Dependent Claims: Narrower, adding specific features, variants, or embodiments, reinforcing patent robustness.

2. Nature of Claims in HK1121148

Based on available patent documentation, the claims likely encompass:

  • Chemical Entities: If the patent pertains to a novel molecule, the claims specify the chemical structure, possibly in Markush form, including particular substituents or stereochemistry.
  • Formulations: Claims may cover pharmaceutical compositions containing the compound, possibly with specific excipients, stabilizers, or delivery systems.
  • Methods of Use: Claims may protect therapeutic methods—e.g., administering the compound for a specific indication or targeting a particular receptor.

3. Claim Scope Analysis

  • Broadness: The independent claims probably aim for maximum coverage, claiming a general class of compounds or methods without overly restrictive limitations.
  • Specificity: Dependent claims narrow scope to particular embodiments for legal robustness against prior art.
  • Potential Limitations: The scope might be limited by the novelty and inventive step over prior art references—pharmaceutical patents often face challenges if the claims are too broad or anticipate known compounds.

4. Claim Strategies

  • Composition of Matter Claims: Dominant in pharmaceutical patents due to their broad protection against generic competitors.
  • Use Claims: Cover specific therapeutic applications, expanding patent lifespan and market exclusivity through method patenting.
  • Formulation Claims: Focused on specific delivery systems or stability-enhancing features.

Patent Landscape and Strategic Considerations

1. Global Patent Environment

The primary jurisdictions relevant to pharmaceutical patent protection include:

  • United States (US): Patent USXXXXXX covers similar compositions or methods. US patent law emphasizes written description and enablement, with particular scrutiny of claim breadth.
  • Europe (EPO): Examines inventive step and sufficiency of disclosure; the scope may differ from Hong Kong, especially regarding polymorphs or formulations.
  • China and Asia: Growing patent filings, especially in China, where patenting of chemical and biotech inventions is increasingly robust.

2. Patent Family and Priority

  • Priority Date and Family: HK1121148 is likely part of an international patent family, claiming priority from earlier PCT applications or foreign filings. The strategic importance lies in establishing priority early to prevent copycat filings or to extend exclusivity.

3. Patentability and Challenges

  • Novelty and Inventive Step: Given the crowded pharmaceutical space, claims must navigate prior art, including existing literature, patents, and known compounds.
  • Potential Challenges: Patent validity could be challenged by prior art disclosures, especially if the compound or use is similar to previously described entities.

4. Competitive Landscape

  • Patent Filings: Pre-existing patents in the same class or therapeutic area—such as blockbuster drugs or major drug candidates—impact freedom-to-operate.
  • Patent Litigation and Licensing: The patent’s strength influences potential licensing deals, litigation strategies, and market exclusivity.

Implications for Stakeholders

Pharmaceutical Companies and Innovators: Should analyze whether HK1121148’s claims offer broad protection or are narrowly tailored. Broad claims suggest high potential market control but may face invalidation risks.

Patent Practitioners: Must scrutinize claim language for scope and validity, considering potential overlaps with existing patents and prior art.

Investors and Business Strategists: Require understanding of the patent landscape to assess risk and value—whether the patent provides robust protection in key markets or warrants further filings.


Key Takeaways

  • Definition of Scope: HK1121148 likely claims a novel chemical entity, its formulations, or therapeutic method, with claim breadth optimized for market and legal strategy.
  • Claims Strategy: Focus on composition-of-matter, use, and formulation claims to maximize protection across jurisdictions.
  • Patent Landscape Position: Competes within a dense patent environment; validation of patent novelty and inventive step is critical.
  • Global Alignment: The patent’s strength depends on consistency with international filings, especially in key markets like the US, Europe, and China.
  • Strategic Actions: Regular patent landscape analyses, monitoring of potential infringers, and diversification through family filings are vital.

FAQs

1. What is the primary focus of patent HK1121148?
It likely covers a novel pharmaceutical compound, its formulations, or therapeutic methods, designed to address specific medical indications.

2. How does the scope of claims influence patent enforceability?
Broader claims provide extensive protection but must be precisely supported by the disclosure to withstand validity challenges. Narrow claims are easier to defend but offer limited market control.

3. Can HK1121148 be challenged or invalidated?
Yes, if prior art demonstrates that the claimed invention lacks novelty or inventive step, the patent could be challenged through legal proceedings or opposition.

4. What is the significance of patent families in this context?
Patent families extend protection internationally, safeguarding innovations across multiple markets, which is essential for global pharmaceutical commercialization.

5. How does HK1121148 compare to patents filed in other jurisdictions?
The scope and strength depend on local patent laws; a patent effective in Hong Kong may require modifications in other jurisdictions to meet specific legal standards.


References

  1. Hong Kong Intellectual Property Department. (n.d.). Patent Examination Guidelines.
  2. World Intellectual Property Organization (WIPO). (2022). Patent Cooperation Treaty (PCT) filings.
  3. European Patent Office. (2022). Guidelines for Examination.
  4. U.S. Patent and Trademark Office. (2022). Manual of Patent Examining Procedure.
  5. Strategic patent analysis reports, available through proprietary databases such as Derwent Innovation or Clarivate.

Conclusion

Hong Kong patent HK1121148 embodies a pivotal safeguard for its assignee’s pharmaceutical innovation. Its claim structure potentially offers broad protection, contingent upon strategic drafting and examination robustness. Its placement within the global patent landscape reflects ongoing competition, necessitating vigilant portfolio management and strategic filing practices. Stakeholders must continually analyze both the patent’s claims and the evolving patent environment to optimize market exclusivity and technological advantage.


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