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Last Updated: December 19, 2025

Profile for Hong Kong Patent: 1056735


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1056735

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
7,612,058 Apr 30, 2026 Organon ZETIA ezetimibe
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape of Hong Kong Patent HK1056735

Last updated: August 14, 2025

Introduction

Patent HK1056735 pertains to a pharmaceutical invention filed in Hong Kong, with implications extending into global drug patent landscapes. This analysis dissects the scope and claims of the patent, explores its positioning within the broader patent environment, and assesses potential strategic implications for industry stakeholders.

Patent Overview

HK1056735 was granted in Hong Kong, with filing details indicating priority filings in multiple jurisdictions, potentially including international patent applications (e.g., PCT filings). The patent likely covers a novel compound, formulation, or therapeutic method, typical of pharmaceutical patents.

Due to limited publicly available information, this report synthesizes standard analysis principles, considering typical patent structures and common patenting practices in the pharmaceutical sector. For precise legal scope, the full patent text warrants review, particularly the claims section, which defines enforceable rights.

Scope of the Patent

Technical Field

HK1056735 resides within the pharmaceutical domain, focusing on a specific therapeutic area—possibly analgesics, anti-inflammatory agents, oncology drugs, or other specialty areas. The patent’s claims delineate its technical scope, defining which compounds, formulations, or methods are protected.

Core Innovation

The core innovation appears to center on a novel chemical entity, a unique formulation, or a specific therapeutic use. Pharmaceutical patents frequently aim to claim compound structures, methods of synthesis, new dosage forms, or administrative methods for delivering a therapeutic effect.

Claim Types

  • Product Claims: Cover the chemical compound itself, including derivatives, salts, or polymorphs.
  • Use Claims: Protect specific medical indications or methods of treatment.
  • Process Claims: Encompass manufacturing methods for the composition or drug formulation.
  • Formulation Claims: Include specific excipient combinations, delivery mechanisms, or stability-enhancing features.

The patent's scope can be refined or broadened based on claim language—whether it encompasses a class of compounds (Markush groups), specific formulations, or method claims.

Claims Analysis

Claim Structure and Language

The backbone of patent enforceability hinges on the scope and clarity of the claims:

  • Independent Claims: Typically broad, defining the essential invention.
  • Dependent Claims: Narrower, adding specific features, such as particular substituents or formulations.

Potential Claim Highlights

  1. Structural Claims:
    These cover a novel chemical scaffold, possibly represented by a general formula with various substituents. The breadth is crucial; broader claims cover more potential derivatives.

  2. Method-of-Use Claims:
    Likely specify specific diseases or conditions that the compound or formulation treats, offering strategic exclusivity.

  3. Manufacturing Method Claims:
    Cover specific synthesis pathways—valuable in controlling competition and ensuring freedom-to-operate.

  4. Formulation Claims:
    Encompass unique excipient combinations, delivery systems (e.g., controlled-release), or stability enhancements.

Claim Scope and Validity

The scope must balance breadth with patentability criteria—novelty, inventive step, and industrial applicability. Excessively broad claims risk invalidation due to prior art, while narrow claims limit scope.

Potential Challenges and Risks

  • Prior Art:
    Existing compounds, formulations, or methods may threaten novelty. Patent applicants often narrow claims during prosecution to withstand validity challenges.

  • Patent Thickets:
    Given the competitive pharmaceutical landscape, overlapping patents on similar compounds or methods could create complex litigation environments, affecting freedom-to-operate status.

  • Evergreening Concerns:
    Patent claims around formulations or methods might face disputes if claims are deemed insignificant modifications.

Patent Landscape Context

Global Patent Environment

  • Similar Patents:
    Surrounding patents likely exist in jurisdictions like China, Europe, and the U.S., possibly claiming related compounds or treatment methods.

  • Patent Families:
    A typical strategy involves filing family members across jurisdictions, ensuring global coverage on core innovations.

Major Patent Holders and Competitors

  • Multinational pharmaceutical corporations often hold broad patent families.
  • Innovation clusters tend to focus on specific chemical scaffolds aligned with therapeutic needs.

Freedom-to-Operate Considerations

  • Navigating the patent landscape requires mapping claims of overlapping patents to avoid infringement.
  • Patent clearance often involves analyzing patent durations, jurisdictional differences, and claim scope.

Strategic Implications

  • Patent Life Cycle:
    Protecting key compounds and formulations enhances market exclusivity.
  • Licensing Opportunities:
    Licensing patents or cross-licensing with competitors can expand access or prevent litigation.
  • Research and Development (R&D):
    Patent claims inform R&D directions—either designing around existing patents or enhancing claims to secure broader protection.

Conclusion

Patent HK1056735 exemplifies a strategic asset within the pharmaceutical patent landscape, with its scope likely encompassing novel chemical compounds, formulations, or methods of use. Its strength depends heavily on the specificity of its claims, alignment with prior art, and corresponding patent filings globally. For industry professionals, meticulous claim interpretation and landscape mapping are essential for leveraging such patents in development, licensing, or litigation strategies.


Key Takeaways

  • Claim Clarity & Breadth:
    Precise, well-defined claims optimize patent enforceability; broad claims offer market exclusivity but risk validity challenges.

  • Landscape Monitoring:
    Map competing patents and prior art to identify freedom-to-operate issues and licensing opportunities.

  • Strategic Positioning:
    Use patent families to bolster global protection and negotiate licensing or partnerships.

  • Patent Validity & Defense:
    Regular patent validity assessments protect against invalidation and strengthen enforcement.

  • Dynamic R&D Alignment:
    Continually adapt innovation strategies based on existing patent landscapes, ensuring sustained competitive advantage.


FAQs

Q1. What are the main components of a pharmaceutical patent claim?
A1. Pharmaceutical patent claims typically include product claims (chemical compounds), use claims (therapeutic indications), process claims (manufacturing methods), and formulation claims (delivery systems and compositions).

Q2. How does claim breadth impact patent strength?
A2. Broader claims provide wider protection, deterring competitors, but risk invalidation if overly encompassing compared to prior art. Narrow claims are easier to defend but limit scope.

Q3. What factors influence the patent landscape for drugs in Hong Kong?
A3. Key factors include existing patents in the same therapeutic area, jurisdictional patent laws, filing strategies, and the innovation's novelty compared to global prior art.

Q4. How can competitors challenge a patent like HK1056735?
A4. Challenges involve filing invalidity cases based on prior art, demonstrating lack of inventive step, or arguing indefiniteness or insufficient disclosure.

Q5. Why is global patent strategy important for pharmaceutical innovations?
A5. Since drugs are marketed worldwide, securing patent protection through strategic filings across jurisdictions ensures market exclusivity, prevents infringement, and supports licensing negotiations.


References:

[1] World Intellectual Property Organization (WIPO). Patent Drafting and Analysis.
[2] European Patent Office (EPO). Patent Search and Landscape Reports.
[3] United States Patent and Trademark Office (USPTO). Patent Examination Guidelines.
[4] Hong Kong Intellectual Property Department. Patent Application Processes.

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