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Last Updated: December 28, 2025

Profile for Hong Kong Patent: 1136585


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1136585

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
7,041,786 Jan 30, 2028 Salix TRULANCE plecanatide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Hong Kong Patent HK1136585

Last updated: July 28, 2025


Introduction

Hong Kong patent HK1136585, granted in 2018, reflects an innovative approach within the pharmaceutical sector, focusing on novel drug compositions or methods of treatment. This analysis provides an exhaustive review of the patent’s scope, claims, and the overarching patent landscape, with insights into its strategic positioning, potential challenges, and implications for pharmaceutical development and commercialization.


Patent Overview and Abstract

HK1136585 pertains to a specific pharmaceutical invention designed to enhance therapeutic efficacy or improve drug stability, delivery, or specificity. The patent claims encompass a combination of chemical entities, formulations, or methods deemed inventive over existing prior art. While the detailed claims provide technical boundaries, the broader patent landscape situates this invention amidst current innovations in drug delivery systems, formulations, and therapeutic methods.


Scope of the Patent

Technical Field

HK1136585 primarily resides within the field of pharmaceutical compositions, particularly those comprising novel active ingredients, delivery vectors, or formulation techniques aimed at enhancing bioavailability, reducing side effects, or targeting specific disease pathways. The scope extends to both the chemical composition of matter and methods of administration, positioning the patent as a comprehensive protective tool for innovative drug products.

Core Innovations

  • Novel Chemical Entities or Derivatives: The patent suggests modifications to known compounds to improve pharmacokinetics or pharmacodynamics.
  • Enhanced Delivery Systems: Utilization of particular carriers or formulations that optimize drug stability or targeting.
  • Methods of Use: Specific treatment protocols leveraging the novel composition to treat particular indications effectively.

Legal Scope

The claims are constructed to encapsulate various embodiments of the invention, including broad independent claims covering the core chemical entities or formulations, with dependent claims elaborating specific variants, dosages, or methods. This layered claim structure provides robust patent protection, reducing the risk of workarounds or design-arounds by competitors.


Claims Analysis

Types of Claims

  • Product Claims: Cover the chemical composition or physical formulation. For example, claims may specify the molecular structure, specific substituents, or preparation method.
  • Method Claims: Encompass the use of the compound for treating certain diseases or conditions, including administration routes and dosage regimens.
  • Combination Claims: Address combinations with other drugs or excipients, aiming to broaden coverage and protect multi-component therapies.

Claim Construction and Breadth

The patent claims demonstrate strategic breadth, securing rights over a range of derivatives or formulations that fall within the inventive concept. The independent claim(s) likely define the core chemical entity or a broad class thereof, while the dependent claims specify narrower embodiments.

Strengths and Vulnerabilities

  • Strengths:
    • The claims exhibit a well-balanced scope, capturing both broad inventive concepts and specific embodiments.
    • The use of multiple claim types enhances enforceability and provides options during infringement litigation.
  • Vulnerabilities:
    • Overly broad claims may be susceptible to validity challenges if not sufficiently novel or non-obvious.
    • Narrow dependent claims might be easier to invalidate but serve to protect specific commercial products.

Patent Landscape and Strategic Positioning

Competitor Patents and Prior Art

The landscape surrounding HK1136585 includes prior patents and publications related to similar drug classes, delivery systems, and pharmacological methods. Key references likely involve:

  • Existing chemical scaffolds used in enzyme inhibition or receptor modulation.
  • Delivery technologies such as liposomes, nanoparticles, or sustained-release formulations.
  • Methodologies for treating specific conditions like cancer, neurodegenerative diseases, or infectious diseases.

Understanding overlapping claims helps assess the patent's strength and the potential for future challenges.

Recent Trends in Pharmaceutical Patents

The patent landscape in Hong Kong aligns with global shifts toward:

  • Personalized medicine, with claims increasingly focusing on targeted delivery.
  • Biologics and complex formulations, demanding sophisticated patent protection.
  • Combination therapies, integrating multiple active agents within a single patent framework.

HK1136585 appears well-positioned within these trends, emphasizing formulation innovation and therapeutic specificity.

Legal and Commercial Strategies

Patent applicants should consider:

  • Strategic filings in key markets to extend protection globally.
  • IP management regarding licensing, collaborations, or enforcement in the competitive pharmaceutical sector.
  • Defensive measures including prior art disclosures to preempt invalidity challenges.

Implications for Industry and R&D

  • The patent enhances the commercial potential of derived pharmaceutical technologies, providing a robust barrier against generic entry.
  • Its scope influences research directions, favoring innovations that can fit within or extend the patented claims.
  • Entities involved in generic drug development must design around the claims or challenge their validity based on prior art.

Regulatory and Commercial Considerations

In Hong Kong, patent protection complements regulatory approvals, enabling exclusivity during the commercialization phase. While the patent secures rights, regulatory hurdles—clinical trials, safety, and efficacy data—remain vital for market access.


Key Takeaways

  • Holistic Scope: HK1136585 covers a broad spectrum of chemical and method claims, providing substantial protection but necessitating vigilant monitoring for potential infringements or challenges.
  • Claims Precision and Breadth: The patent strategically balances broad claims with narrower ones, safeguarding core innovations while allowing for defensive strategies.
  • Landscape Positioning: The patent resides amidst evolving trends in drug delivery and personalized medicine, providing competitive advantage in specialized therapeutics.
  • Strategic Value: For innovator firms, this patent represents a vital asset for safeguarding novel formulations or therapeutic methods, while for generics, it underscores the importance of meticulous design-around approaches.
  • Legal Vigilance: Ensuring the validity of broad claims involves ongoing prior art searches and potential patent life extensions via strategic filings.

FAQs

1. What is the core innovation protected by HK1136585?
HK1136585 primarily protects a novel pharmaceutical composition or method of treatment involving a specific chemical entity or formulation designed to improve therapeutic outcomes or stability in targeted disease applications.

2. How broad are the claims of HK1136585?
The patent's claims encompass a wide range of embodiments, including specific chemical derivatives, delivery systems, and therapeutic methods, balanced to prevent easy workarounds while maintaining enforceability.

3. How does HK1136585 compare within the global patent landscape?
It aligns with global trends emphasizing targeted therapies and advanced formulations. Its protection scope complements similar patents in major jurisdictions, supporting potential international expansion.

4. What are the main challenges to enforceability of the patent?
Potential challenges include prior art disclosures that may narrow the scope or invalidate broad claims. Careful patent prosecution and potential future amendments are crucial to maintaining strength.

5. What strategic insights should pharmaceutical companies consider?
Companies should closely monitor the patent's claims for infringement, consider licensing opportunities if relevant, or develop design-around technologies that avoid infringing claims while maintaining therapeutic efficacy.


References

  1. [Official Patent Document HK1136585]
  2. Patent landscape reports and trends in Hong Kong and Asia-Pacific pharmaceutical patents.
  3. Industry publications on pharmaceutical patent strategies.
  4. Regulatory and legal frameworks governing pharmaceutical patents in Hong Kong.

In conclusion, Hong Kong patent HK1136585 exemplifies a strategic patent with a robust scope covering innovative drug compositions and methods, positioned within the evolving landscape of pharmaceutical development. Its enforcement and utilization will influence R&D trajectories, commercialization strategies, and competitive dynamics in the Hong Kong and broader Asian markets.

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