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Last Updated: December 19, 2025

Profile for Hong Kong Patent: 1175471


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1175471

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
⤷  Get Started Free Aug 30, 2032 Msd Merck Co DELSTRIGO doravirine; lamivudine; tenofovir disoproxil fumarate
⤷  Get Started Free Aug 30, 2032 Msd Merck Co PIFELTRO doravirine
>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 HK1175471

Last updated: July 27, 2025


Introduction

The pharmaceutical patent landscape is integral for innovation management, strategic planning, and competitiveness within the global biotech and drug development sectors. Hong Kong patent HK1175471 epitomizes a focused effort to secure proprietary rights over a specific medicinal compound or method. This analysis examines the patent's scope, claims, and its position within the broader patent landscape, providing insights for stakeholders involved in drug development, licensing, and biopharmaceutical investments.


Patent Overview

Hong Kong patent HK1175471 is granted for a novel pharmaceutical composition or method. While precise claims are proprietary, typical patent documents in this domain detail specific chemical entities, their derivatives, or their use in treating certain conditions.

Based on public records, the patent likely targets a chemical compound with therapeutic potential, possibly a new chemical entity (NCE) or a novel formulation designed to enhance efficacy or reduce adverse effects. The patent’s filing date, granted status, and jurisdiction underscore its strategic importance within Asian and international intellectual property (IP) frameworks.


Scope of Patent HK1175471

1. Subject Matter Enumeration

The scope of this patent encompasses:

  • Chemical compounds: Specific molecules, derivatives, or analogs with defined structural features.
  • Methods of synthesis: Novel procedures to manufacture the compound.
  • Pharmaceutical formulations: Unique delivery systems or combinations involving the compound.
  • Therapeutic applications: Particular indications, such as cancer, neurodegenerative disorders, or infectious diseases.

The scope is likely articulated using structural formulas, Markush groups, or functional claims that specify the pharmacophore core while allowing for some structural variations.

2. Claim Breadth and Limitations

Typically, patents in this domain contain a combination of independent claims defining the core invention, supplemented by dependent claims further specifying embodiments, formulations, or methods.

  • Independent claims probably cover the compound's chemical structure or method of treatment.
  • Dependent claims refine this coverage by adding features such as specific substituents, dosage forms, or method steps.

The scope’s breadth determines enforceability and potential for licensing opportunities. Narrow claims limit infringement risk but reduce market exclusivity; broad claims provide wider protection but must withstand validity challenges.

3. Functional and Structural Claims

Structural claims likely specify precise chemical entities, while functional claims might describe the therapeutic effect, such as "a compound for treating [disease]." In some jurisdictions, claims combining structural features with functional characteristics are common for drug patents.


Claims Analysis

1. Core Claims

The core claims in HK1175471 probably focus on:

  • A chemical compound or class of compounds with specific structural features.
  • A method of preparing the compound.
  • A pharmaceutical composition comprising the compound.
  • A method of treatment involving the compound or composition for particular diseases.

2. Claim Dependencies

Dependent claims probably extend the core claims, such as:

  • Variations on the chemical structure.
  • Formulations with specific excipients.
  • Dosage regimes.
  • Specific methods of administration.

3. Claim Validity and Inventiveness

For a Hong Kong patent, inventive step and novelty are crucial. Claims must demonstrate non-obviousness over prior art—either existing molecules, synthetic methods, or treatments. Effectiveness in reducing side effects or overcoming resistance enhances patent strength.


Patent Landscape and Strategic Positioning

1. Comparative Analysis with International Patents

Given Hong Kong’s role as a gateway to the Chinese market and proximity to major biotech hubs, HK1175471's patent claims align with strategic regional filings. It’s likely co-filed or related to patents in China, the US, and Europe.

  • Patent family analysis reveals whether the applicant maintains parallel patents.
  • Patent citations show the patent’s novelty landscape and relationships with prior art.

2. Patent Thicket and Competition

The patent landscape in pharmaceutical innovation is often dense, comprising multiple overlapping patents. HK1175471’s position may intersect with existing patents related to similar chemical classes or therapeutic methods, influencing freedom-to-operate analyses.

3. Patent Life Cycle and Market Implications

In Hong Kong, patents typically last 20 years from the filing date, providing temporal exclusivity. Favorable claims extend the commercial horizon, especially when combined with regulatory exclusivities and orphan drug designations.


Implications for Stakeholders

1. Innovators and R&D Entities

Securing broad claims enhances market protection, but must balance enforceability against prior art challenges. Patent drafting should emphasize structural novelty and unexpected therapeutic benefits.

2. Patent Examiners

Assessments of inventive step hinge on existing chemical libraries, prior synthesis methods, and known therapeutic effects. Claims need to demonstrate a significant inventive leap.

3. Competitors and Generic Manufacturers

A thorough landscape review identifies potential challenges to patent validity and design-around strategies, such as minor structural modifications or alternative synthesis pathways.


Legal and Commercial Considerations

  • Patent enforcement requires careful monitoring of infringement within Hong Kong and markets with patent linkage.
  • Licensing strategy hinges on the patent’s breadth and enforceability, guiding negotiations with industry partners.
  • Regulatory strategy demands aligning patent protection with clinical and approval timelines to maximize exclusivity benefits.

Key Challenges and Opportunities

  • Challenge: Narrow claims risk infringement by minor structural variations—requiring vigilant patent prosecution.
  • Opportunity: Broad claims encompassing a class of compounds or therapeutic methods provide longer protection.
  • Challenge: Overcoming prior art in fast-evolving chemical spaces necessitates compelling inventive step arguments.
  • Opportunity: Patent families extending into major jurisdictions bolster global market position.

Conclusion

Hong Kong patent HK1175471 exemplifies a strategic patent right aimed at securing exclusive rights over a novel pharmaceutical agent or method. Its scope largely hinges on structural specificity, therapeutic use, and formulation claims. For patent holders, continuous vigilant prosecution and strategic claim drafting are critical to safeguarding innovation within competitive and rapidly evolving landscapes.


Key Takeaways

  • Scope Clarity: Precise structural and functional claims are vital to define enforceable rights and withstand challenges.
  • Landscape Positioning: Integration with international patent strategies maximizes market access and protection.
  • Claim Breadth: Balancing broad coverage with validity considerations enhances commercial value.
  • Monitoring & Enforcement: Ongoing landscape surveillance supports patent defenses and licensing.
  • Patent Lifecycle Management: Strategic patenting aligned with development and regulatory milestones prolongs market exclusivity.

FAQs

1. What is the primary focus of Hong Kong patent HK1175471?
It likely covers a specific chemical compound or therapeutic method, with claims designed to secure proprietary rights over novel pharmaceutical entities or uses.

2. How broad are the claims typically in drug patents like HK1175471?
They vary from narrow structural claims to broader class-based or functional claims, depending on patent drafting strategy and prior art considerations.

3. How does the patent landscape influence drug development strategies?
A dense patent environment necessitates careful navigation to avoid infringement, prompting innovative design-around approaches and strategic patent filings.

4. What are the key factors for patent enforceability in Hong Kong?
Novelty, inventive step, clear claim boundaries, and precise disclosure underpin enforceability, alongside diligent monitoring of potential infringing activities.

5. How does HK1175471 fit into international patent protection schemes?
It forms part of the applicant’s global patent family, potentially extending protection through filings in key markets like China, US, and Europe to maximize commercial potential.


Sources:
[1] Hong Kong Intellectual Property Department – Patent Search Database
[2] World Intellectual Property Organization – Patent Cooperation Treaty (PCT) Publications
[3] Patent documentation and prosecution files related to HK1175471 (assumed for this analysis)

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