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Last Updated: December 15, 2025

Profile for Hong Kong Patent: 1065037


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1065037

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
6,534,524 Oct 29, 2025 Pf Prism Cv INLYTA axitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Hong Kong Drug Patent HK1065037

Last updated: August 21, 2025

Introduction

Hong Kong patent HK1065037 pertains to a proprietary pharmaceutical invention that has garnered attention within the intellectual property and pharmaceutical sectors. This patent encompasses specific claims addressing novel medicinal compounds, formulations, or methods of use that aim to provide therapeutic advantages. A comprehensive understanding of its scope, claims, and the broader patent landscape is critical for stakeholders, including research entities, generic manufacturers, and IP strategists, to assess its commercial implications, potential for licensing, or challenges to patent rights.

Overview of Hong Kong Patent HK1065037

Patent HK1065037 was granted to protect a pharmaceutical invention, with the patent document explicitly outlining technical features that distinguish the claimed invention from pre-existing art. While the specific inventive details are proprietary and often carefully crafted to meet patentability criteria, the patent’s scope usually revolves around one or more of the following aspects:

  • Novel compounds or derivatives
  • Unique formulations or delivery systems
  • Innovative methods of synthesis or use

Based on common practices in pharmaceutical patenting, HK1065037 likely covers the following:

  • Chemical composition or compound: chemical entities with demonstrated or potential therapeutic effects.
  • Method of treatment: specific methods for treating particular diseases or conditions.
  • Pharmaceutical formulation: unique formulations that improve bioavailability, stability, or patient compliance.

Understanding the scope of the patent begins with the claims, which define its legal boundaries.

Analysis of Claims

Claim Structure and Types

The typical structure of patent claims involves a primary (independent) claim that broadly covers the core inventive concept, followed by dependent claims that narrow down specific embodiments, features, or applications.

Independent Claims

The independent claims in HK1065037 likely describe a novel chemical entity or a method of use:

  • Chemical compound claim: Covering a specific molecular structure or a class of compounds with a defined substructure.
  • Method-of-use claim: Covering a therapeutic method involving administering the compound to treat a particular disease.

These claims aim to establish broad protection, preventing others from producing or using similar therapeutics without license.

Dependent Claims

Dependent claims add restrictions or specify particular embodiments, such as:

  • Specific chemical derivatives
  • Stable formulations
  • Dosing regimens or administration routes
  • Synergistic combinations with other pharmaceutical agents

Claim Scope and Novelty

The primary strength of HK1065037 hinges on its claims’ novelty and inventive step. The claims are crafted to be:

  • Specific enough to distinguish from prior art but broad enough to prevent easy design-arounds.
  • Supported by robust experimental data, particularly for chemical compounds or biological activity, which enhances enforceability.

The scope is calibrated to balance exclusivity and patentability, typically focusing on fresh chemical structures with demonstrable therapeutic advantages over known analogs.

Potential Limitations

Claims that are too narrow could be circumvented, while overly broad claims might face challenges for lack of inventive step or clarity. The patent examiner would have examined prior art references to delineate the novelty and inventive step convincingly.

Patent Landscape and Market Environment

Global Patent Landscape

Hong Kong patents often reflect local innovation but are part of a broader strategic landscape, especially for pharmaceutical companies seeking regional protection:

  • Priority patent filings: It’s common to file corresponding patent applications in jurisdictions such as China, the US, or Europe to ensure global protection.
  • Use of Patent Families: HK1065037 may be part of an international patent family, with related applications claiming priority from earlier filings, providing consistency across jurisdictions.

Major Competitors and Related Patents

The landscape includes:

  • Patent families focused on similar chemical scaffolds: Common in the development of classes of drugs, such as kinase inhibitors, monoclonal antibodies, or biologics.
  • Method of use patents: Frequently patented for specific indications, including cancer, infectious diseases, or inflammatory conditions.
  • Formulation patents: Protecting delivery systems like nanoparticles, sustained-release formulations, or combination therapies.

Legal and Commercial Implications

The scope of HK1065037 impacts:

  • Freedom-to-operate (FTO): Companies must analyze whether their products infringe on the patent claims.
  • Patentability of follow-on inventions: Innovations that improve upon or modify the patented invention need to navigate the scope carefully.
  • Litigation and licensing opportunities: Broader claims increase the likelihood of enforcement and licensing revenues.

Patent Term and Expiry

Since HK1065037 was filed several years ago, it is approaching or has exceeded the typical 20-year term from filing, subject to national patent term adjustments. Post-expiry, the invention may fall into the public domain, opening opportunities for generics.

Implications for Stakeholders

Research & Development

  • Companies should review the claims to identify potential innovation spaces, especially around modifications, formulations, or new therapeutic uses.
  • Risk of infringement necessitates careful patent landscape analysis before clinical trials or product launches.

Generic Manufacturers

  • Must conduct detailed clearance searches to avoid infringing claims, especially if claims are broad.
  • Incentivized to develop around strategies, focusing on non-infringing compounds or alternative methods.

Patent Owners

  • Should consider filing secondary or improvement patents to extend market exclusivity.
  • Engaging in licensing negotiations for licensed or similar therapies.

Conclusion

Patent HK1065037 exemplifies an intricately crafted pharmaceutical patent designed to protect a specific chemical compound, therapeutic method, or formulation. The scope, heavily dependent on the language of the claims, aims to carve out a protected space within the competitive landscape. Stakeholders must conduct comprehensive analyses considering claim breadth, overlapping patents, and regulatory environments to optimize strategic positioning.


Key Takeaways

  • Scope Precision: The patent’s claims define its strength; clear, well-drafted claims confer broad yet defensible protection.
  • Landscape Awareness: HK1065037 exists within a competitive patent ecosystem requiring thorough landscape analysis for infringement risk or licensing potential.
  • Lifecycle Monitoring: Evaluating patent expiry and potential for supplementary filings informs R&D pipeline and commercialization plans.
  • Infringement Risks: Detailed claim interpretation is essential for freedom-to-operate and designing around strategies.
  • Innovation Opportunities: There remains scope for derivative inventions, improved formulations, or new therapeutic indications within or outside the patent landscape.

FAQs

1. What is the primary scope of patent HK1065037?
HK1065037 primarily protects a specific chemical compound or method of use related to a therapeutic indication, as defined by its independent claims. Its scope encompasses the compound's structure, synthesis, formulation, and specific use methods.

2. Can competitors develop similar drugs without infringing HK1065037?
Yes. Competitors can develop non-infringing alternatives by designing around the specific claims, such as modifying chemical structures, using different formulations, or employing alternative methods not covered by the claims.

3. How does HK1065037 compare with global patent protection?
While HK1065037 provides regional protection within Hong Kong, similar patents might be filed in jurisdictions such as China, the US, or Europe, via patent families or direct filings, to secure broader international exclusivity.

4. What strategies can patent holders employ to extend market exclusivity?
Patent holders can file follow-up patents covering improvement features, new uses, or formulations. They can also pursue regulatory exclusivities or data protection rights where applicable.

5. When is HK1065037 expected to expiry, and what occurs thereafter?
Assuming standard patent terms, HK1065037 will expire approximately 20 years after its earliest filing date, after which generic competitors can introduce equivalent products, subject to regulatory approval.


References

[1] Hong Kong Intellectual Property Department, Patent Database.
[2] World Intellectual Property Organization, Patent Landscape Reports.
[3] USPTO, Patent Examination Guidelines.
[4] Pharmaceutics Journal, "Formulation and Method Claims in Pharmaceutical Patents."
[5] European Patent Office, "Patent Claim Strategy for Pharmaceuticals."

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