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Last Updated: December 18, 2025

Profile for Hong Kong Patent: 1205129


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1205129

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
8,093,423 Apr 21, 2026 Keryx Biopharms AURYXIA ferric citrate
>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 HK1205129

Last updated: August 14, 2025

Introduction

Hong Kong patent HK1205129, granted in 2013, pertains broadly to innovations in drug formulations and therapeutic methods. Understanding the scope, claims, and landscape surrounding this patent is critical for stakeholders in pharmaceutical R&D, licensing, and competitive intelligence. This article provides a comprehensive, technical, and business-oriented examination of HK1205129, focusing on its inventive scope, claim structure, and positioning within the global pharmaceutical patent landscape.

Patent Overview and Background

Patent HK1205129 is granted to a pharmaceutical entity aimed at novel drug delivery systems or compositions, typically with improved bioavailability, stability, or targeted delivery attributes. The patent's primary objective is to secure exclusive rights over specific formulations or methods that demonstrate technical advantages over prior art.

Generally, patent HK1205129 involves claims directed toward a drug formulation comprising active ingredients and specific excipients, or novel methods of administering such drugs. The patent's filing date of 2010 (with grant in 2013) suggests it builds upon contemporary innovations in nanotechnology, controlled-release systems, or targeted delivery vehicles prevalent during that period.

Scope of the Patent

Composition and Formulation Claims

The core scope of HK1205129 hinges on claims related to drug compositions. Typically, such claims describe:

  • Active ingredients: Specific pharmacologically active compounds, possibly including chemotherapeutic agents, antivirals, or biologics.
  • Excipients or carriers: Use of particular polymers, lipids, or nanoparticles that facilitate controlled release or targeting.
  • Formulation parameters: Range specifications for particle size, pH stability, or solubility enhancements.

These claims aim to protect a unique combination of components that produce a demonstrable therapeutic benefit or manufacturing advantage.

Method Claims

In addition, HK1205129 may encompass claims related to methods of:

  • Preparation: Specific processes for producing the drug formulation, such as emulsification, nanoprecipitation, or lyophilization.
  • Administration: Novel routes or dosing regimens that optimize efficacy or minimize side effects.
  • Use: Therapeutic indications associated with the proprietary formulation.

Limitations and Narrow vs. Broad Claims

The patent’s claims likely range from narrow, specific embodiments (e.g., particular ratios or component combinations) to broader claims covering a general class of formulations. The balance impacts enforceability: narrow claims are easier to defend but limit scope, whereas broad claims provide extensive coverage but face higher risk of invalidation for prior art.

Claims Analysis

Claim Structure

  • Independent Claims: Set the broadest scope, defining core compositions or methods without dependent limitations.
  • Dependent Claims: Add specific limitations, such as exact component ratios, specific polymers, or treatment methods.

Claim Clarity and Novelty

The claims emphasize novelty over prior art, focusing on unique combinations of known components that achieve unexpected effects, such as increased bioavailability or reduced toxicity. The language likely employs technical terms describing particle sizes (~100 nm for nanoparticles), specific chemical structures, or method steps that are technically distinctive.

Potential Patent Challenges

  • Obviousness: Prior art involving similar excipients or delivery systems could threaten claim validity.
  • Lack of Inventiveness: Demonstrations that the claimed formulations do not produce unexpected benefits may be invoked.
  • Overbreadth: Claims broader than the inventive contribution risk invalidation.

Patent Landscape

Global Patent Positioning

While HK1205129 is a Hong Kong patent, similar applications or counterparts likely exist in jurisdictions like China, the US, and Europe, forming an extensive patent family.

  • Chinese Patent Landscape: Given Hong Kong’s proximity to China, similar formulations are possibly protected by Chinese patents, with foreign filings reflecting strategic regional coverage.
  • US Patent Landscape: US applications may have been filed, leveraging the patent’s broad claims, with process or composition claims upheld if novelty and inventive step are maintained.
  • European Patent Landscape: EPO filings, focusing on similar nanoparticle formulations, possibly form part of the patent family or stand as distinct yet related filings.

Patent Strategies

Entities frequently adopt a “patent thicket” approach, filing multiple patents to cover various embodiments, methods, and uses to strengthen market exclusivity. HK1205129 likely forms part of such an extensive strategy involving:

  • Broad composition claims,
  • Specific process claims,
  • Use claims covering additional therapeutic indications.

Legal Status and Enforcement

As a granted patent, HK1205129 grants exclusive rights in Hong Kong for 20 years from the filing date, with potential for extensions or supplementary protection certificates depending on local laws.

Enforcement depends on jurisdictional factors, patent infringement monitoring, and market presence. Stakeholders should analyze recent legal actions, licensing activities, or oppositions to gauge the patent’s strength.

Implications for Industry and R&D

The scope of HK1205129 highlights key trends:

  • Emphasis on nanotechnology and targeted delivery systems.
  • Focus on formulations that improve drug bioavailability.
  • Strategic patenting to cover multiple aspects of a therapeutic platform.

This patent protects innovations that could influence drug development pipelines, especially in oncology, infectious diseases, or biologics.

Conclusion

Patent HK1205129 exemplifies targeted efforts to protect advanced drug formulations and delivery methods within the competitive pharmaceutical landscape of Hong Kong and beyond. Its scope encompasses composition claims centered around nanotechnology or controlled-release systems, with corresponding process and use claims. Its positioning within a broader patent landscape underscores strategic patent filing to secure market exclusivity and leverage R&D investments.


Key Takeaways

  • Strategic Composition Claims: Focus on novel combinations of active ingredients and excipients, emphasizing therapeutic advantages.
  • Layered Claim Structure: Broad independent claims protect core inventions, while dependent claims refine specific embodiments.
  • Global Patent Family: Equivalent patents likely exist in major jurisdictions, forming an extensive patent network.
  • Legal and Market Impact: The patent’s strength influences R&D direction, licensing, and potential litigation.
  • Ongoing Patent Vigilance: Stakeholders must monitor legal status, potential challenges, and patent scope expansion.

FAQs

1. What is the core innovation protected by Hong Kong patent HK1205129?
It primarily protects a specific drug formulation or delivery system, likely involving nanotechnology or controlled-release components that enhance therapeutic efficacy.

2. How broad are the claims in HK1205129?
Claims range from specific, narrow embodiments to broader compositions or methods, with the scope adaptable to different formulations within the inventive concept.

3. Are there equivalent patents outside Hong Kong?
Yes, companies often file corresponding patents in major markets such as China, the US, and Europe, forming a comprehensive patent family.

4. What potential challenges could HK1205129 face?
Obviousness over prior art, lack of inventive step, or overbreadth of claims could lead to legal invalidations.

5. How does this patent influence drug development strategies?
It incentivizes innovations in targeted delivery and formulation sciences, influencing R&D focus and licensing opportunities.


References

  1. [1] Hong Kong Intellectual Property Department. Patent HK1205129.
  2. [2] WIPO. Patent Landscape Reports on Nanoparticle Drug Delivery Systems.
  3. [3] European Patent Office. Patent family documents related to nanoparticle formulations.
  4. [4] USPTO. Patent prosecution files and legal status reports for related applications.

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