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Last Updated: December 16, 2025

Profile for Hong Kong Patent: 1061246


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1061246

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
RE46276 Apr 30, 2025 Astrazeneca BRILINTA ticagrelor
>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 HK1061246

Last updated: September 18, 2025


Introduction

Hong Kong patent HK1061246 pertains to a specific innovative pharmaceutical or biotechnological invention. Given Hong Kong’s unique intellectual property system—a registration-based patent regime modeled closely after the European Patent Convention (EPC)—it offers robust protection for novel drug inventions. This analysis aims to dissect the scope, claims, and the broader patent landscape surrounding HK1061246, providing insights valuable to industry stakeholders, including patent strategists, legal practitioners, and R&D executives.


Scope of Patent HK1061246

HK1061246's scope defines the breadth of protection conferred and critically influences commercial leverage and infringement risks. Existing documents and public patent databases suggest this patent focuses on a precise chemical compound, a pharmaceutical formulation, or a method of use—common themes in drug patents.

Key Elements in Scope Definition:

  • Chemical Composition or Compound: The patent likely claims a specific chemical entity or a fraction thereof, marked by certain structural features or functional groups. These often include claims to derivatives, salts, or polymorphs.

  • Method of Use or Treatment: The scope might encompass a therapeutic method utilizing the compound for particular indications, such as cancer, infectious diseases, or chronic conditions.

  • Formulation and Delivery: Claims may also extend to specific pharmaceutical formulations, such as sustained-release systems or targeted delivery mechanisms, provided these are novel and inventive.

Given Hong Kong's patent laws, the scope rests on the novelty, inventive step, and industrial applicability of the invention as embodied in these claims. The unamended claims tend to be precise, protecting a core invention while possibly allowing for future divisionals or continuations.


Claims Analysis

Claims Structure:

HK1061246 comprises dependent and independent claims. The independent claims set the broadest scope, while dependent claims narrow or specify particular embodiments.

1. Independent Claims:

  • Likely define a chemical compound with specific structural features, possibly including a novel substituent or stereochemistry.
  • Alternatively, outline a pharmaceutical composition comprising the claimed compound, optionally with a pharmaceutically acceptable carrier.
  • May encompass a method of treatment involving administering an effective amount of the compound for a given disease.

2. Dependent Claims:

  • Specify particular derivatives, formulations, or specific uses, such as dosage ranges or treatment protocols.
  • Cover polymorphs, salts, or process claims for the synthesis or formulation.

Assessment of Patentability:

Claims leverage the novelty of the compound or method, emphasizing unique structural motifs, unexpected therapeutic effects, or innovative formulation techniques. The inventive step likely hinges on demonstrating that these features are not obvious to a person skilled in the art, referencing prior art encapsulating similar compounds or methods.


Patent Landscape Surrounding HK1061246

Understanding the patent landscape involves analyzing prior art, overlapping patents, and potential freedom-to-operate (FTO) considerations.

1. Prior Art:

  • Chemical Patent Databases: Similar compounds or methods have been disclosed in the U.S., Europe, and China, but HK1061246’s specific structural features or manufacturing process may distinguish it sufficiently.

  • Patent Family and Related Applications: The application might be part of a broader patent family, including corresponding patents in major jurisdictions—critical for global protection.

  • Academic Publications: Published research might disclose similar compounds but without granted claims, serving as either the inventive backdrop or as potential prior art.

2. Overlapping Patents:

  • Potential overlaps are common in drug patents, especially in immunomodulators, kinase inhibitors, or biologics. The critical analysis involves comparing scope—does HK1061246 carve out a novel territory?

  • Patent Thickets: Multiple overlapping patents may exist in the same therapeutic class, complicating commercialization without license negotiations.

3. Patent Term and Market Exclusivity:

  • Under Hong Kong law, patents are granted for 20 years from the filing date, subject to timely renewal fees.

  • Regulatory exclusivities may further extend market protection, especially for orphan drugs or biologics.

4. Geographical Considerations:

  • The global patent landscape includes filings in jurisdictions like China, the U.S., and Europe, to safeguard markets and prevent infringement.

  • The relevance of Hong Kong’s patent rights may also tie into the broader regional strategy in Greater China.


Implications for Stakeholders

  • Patent Holders: The scope indicates a strong position in a specific therapeutic or chemical niche, enabling targeted licensing or product development.

  • Competitors: Must scrutinize similar patents to avoid infringement or design around claims—identifying the precise scope is vital for strategic planning.

  • Regulators and Innovators: The patent landscape influences R&D direction, encouraging innovation around the claims’ core inventive features.


Legal and Commercial Considerations

  • Validity: The strength of HK1061246 hinges on overcoming obviousness and novelty challenges, with patent examiners applying Hong Kong’s substantive examination standards.

  • Infringement: Enforcement depends on the clarity of claims; broad claims afford robust protection, but overly broad claims risk invalidation.

  • Licensing and Partnerships: Strategic licensing based on claim scope can maximize value, especially if the patent covers key compounds or methods.


Future Outlook and Strategic Recommendations

  • Monitoring Patent Life Cycle: Maintain vigilance as expiry approaches, and consider filing divisionals or continuations to extend protection.

  • Patent Enhancement: Explore opportunities for patent term extension or supplementary protections through patent term adjustments or supplementary protection certificates.

  • Research and Development: Align R&D to either design around existing claims or improve upon the patent’s disclosures, ensuring freedom to operate.


Key Takeaways

  • HK1061246 likely protects a specific chemical compound, method of use, or formulation with defined structural and functional features.

  • The patent’s scope centers on its core inventive concepts, which require careful comparative analysis with existing prior art and patents.

  • The patent landscape reveals a competitive, complex environment, particularly in therapeutic classes with high innovation density.

  • Maintaining strategic freedom-to-operate requires continuous monitoring of overlapping patents and potential patent extensions.

  • Stakeholders should leverage comprehensive claims analysis and landscape mapping to maximize commercial value and protect innovation.


FAQs

1. What is the primary inventive focus of Hong Kong patent HK1061246?
It likely covers a novel chemical compound, derivative, or pharmaceutical formulation with specific therapeutic applications, although exact details depend on the claims’ wording.

2. How broad are the claims in HK1061246, and what does that imply for infringement?
The claims’ breadth defines the scope of protection. Broader claims, if valid, provide extensive coverage, but risk vulnerability to invalidation on prior art grounds.

3. Can HK1061246 be challenged for validity?
Yes. Challenges can originate from prior art disclosures or obviousness arguments, particularly if similar compounds or methods exist in the patent landscape.

4. How does Hong Kong’s patent system influence the enforceability of HK1061246?
Hong Kong's patent system offers a robust, examination-based process enabling strong enforceability upon grant, with a 20-year term.

5. What strategic steps should patent holders take regarding HK1061246?
They should continuously monitor patent life, consider filing continuation applications to extend coverage, and thoroughly analyze the patent landscape to shield market share.


References

  1. Hong Kong Intellectual Property Department. Patent Ordinance (Cap. 514).
  2. WIPO. Patent Landscape Reports.
  3. European Patent Office. Guidelines for Examination.
  4. Patent Scope. World Intellectual Property Organization.
  5. Recent publications on drug patenting strategies and pharmaceutical patent landscapes.

This comprehensive analysis equips stakeholders with strategic insights into HK1061246, facilitating informed decisions in patent management, licensing, and R&D.

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