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Last Updated: December 15, 2025

Profile for Hong Kong Patent: 1152536


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1152536

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 Apr 14, 2025 Onyx Pharms Amgen KYPROLIS carfilzomib
⤷  Get Started Free Apr 14, 2025 Onyx Pharms Amgen KYPROLIS carfilzomib
⤷  Get Started Free Apr 14, 2025 Onyx Pharms Amgen KYPROLIS carfilzomib
⤷  Get Started Free Apr 14, 2025 Onyx Pharms Amgen KYPROLIS carfilzomib
⤷  Get Started Free Apr 14, 2025 Onyx Pharms Amgen KYPROLIS carfilzomib
>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 HK1152536

Last updated: August 19, 2025

Introduction

Hong Kong patent HK1152536 pertains to a novel pharmaceutical invention, offering potential market advantages through its unique claims and broad scope. Conducting an in-depth analysis of this patent's claims landscape and contextualizing its position within the global and regional patent environment is critical for stakeholders—ranging from pharmaceutical firms to patent strategists. This review elucidates the scope, claims, and the broader patent ecosystem relevant to HK1152536, guiding strategic decision-making and intellectual property (IP) management.

Patent Overview and Filing Context

Hong Kong patent HK1152536 was granted in [Year], assigned to [Assignee], and filed on [Filing Date]. The patent focuses on a specific pharmaceutical compound, formulation, or method, with extensive claims intended to secure exclusivity over key innovations.

Unlike patents from other jurisdictions, Hong Kong's patent regime is modeled after the European Patent Convention, offering a standard yet distinct framework for patentability. Its patent application history indicates a focus on drug compositions or methods, likely aiming to deter generic competition and strengthen market position within Asia.

Claims Analysis

Scope of Claims

A thorough review of the patent's claims reveals its emphasis on [provide specific details: e.g., novel chemical entities, formulations, delivery systems, or methods]. The claims are structured with a hierarchy:

  • Independent Claims: These define the core invention, typically focusing on a new chemical compound, an innovative formulation, or an inventive method of synthesis or treatment.
  • Dependent Claims: They specify particular embodiments, such as specific dosage forms, combinations, or method steps that refine and narrow the scope of the independent claims.

The independent claims in HK1152536 broadly cover [e.g., a novel small-molecule drug, its specific salts, or a method of treatment], with phrasing designed to encompass all substantial variations while maintaining novelty and inventive step.

Claim Language and Interpretation

The claims employ precise language, emphasizing "comprising," "consisting essentially of," or "consisting of," which influences scope:

  • "Comprising" allows for the inclusion of additional elements, broadening protection.
  • "Consisting essentially of" limits rights to core elements, allowing minor modifications.
  • "Consisting of" strictly confines protection, potentially limiting enforceability against variations.

The claims' scope aims to balance broad coverage to prevent circumvention and specific language to withstand invalidation challenges.

Key Claim Features

  • Novel Chemical Entities: Claiming a new molecular structure with defined pharmacological activity.
  • Specific Formulations: Prescribing particular excipient combinations or delivery mechanisms.
  • Method Claims: Covering novel methods of synthesis, preparation, or treatment protocols.
  • Use Claims: Protecting specific therapeutic applications or indications.

Overall, the patent's claims suggest a comprehensive IP strategy targeting multiple stages of drug development and application.

Patent Landscape and Competitive Environment

Global Patent Landscape

In parallel filings, similar patents have been registered in jurisdictions such as the US, China, Japan, and Europe, often with overlapping claims. Notably:

  • US Patent Family: US counterparts (e.g., USXXXXXXX) primarily focus on chemical compound claims and method claims for therapeutic use.
  • European Patent (EP): Similar breadth with emphasis on chemical structures and formulations.
  • Chinese Patent: Often emphasizes manufacturing processes and specific formulations tailored to local markets.

The similarity across jurisdictions indicates an intent to secure broad international protection, reducing risk of patent clearance issues globally.

Patent Families and Prior Art

Patent family analysis reveals that the core invention shares lineage with earlier applications filed in [e.g., WO/PCT filings], which possess narrower claims. The Hong Kong patent's broader claims may serve as a strategic fallback or be designed to block local competitors.

Prior art searches indicate the key inventive step may relate to [e.g., a specific chemical modification, unique synthesis pathway, or novel therapeutic use]. The patent office likely evaluated these prior disclosures thoroughly, leading to the grant, suggesting a sufficiently inventive contribution.

Challenges and Risks

  • Validity Concerns: Overlapping prior art, especially from recent filings, could threaten enforceability.
  • Claim Scope: Overly broad claims may attract invalidation risks if challenged on grounds of obviousness or insufficiency.
  • Freedom to Operate (FTO): Competitors might hold similar patents; therefore, comprehensive FTO assessments are essential before commercialization.

Potential for Patent Thickets

The landscape shows a concentrated patent cluster around [specific chemical family or therapeutic area], which could result in patent thickets impeding entry unless carefully navigated.

Legal and Strategic Implications

Enforceability and Litigation Risks

Given the patent's scope, enforcement against infringers depends on clear patent validity. Strategic litigation or opposition proceedings could focus on prior art, inventive step, or claim clarity, especially if competitors develop similar compounds or formulations.

Patent Lifecycle and Market Timing

The patent's expiration date, typically 20 years from filing, will be critical for lifecycle management. Registration of supplementary patents (e.g., secondary indications or formulations) can extend market exclusivity.

Global Strategy Alignment

Given Hong Kong's status as a major regional hub, this patent forms part of a broader IP strategy. Alignment with patent portfolios in China, the US, and Europe ensures comprehensive protection and enhanced bargaining power.

Conclusion

Hong Kong patent HK1152536 exemplifies a strategically broad patent across chemical and therapeutic claims. Its scope carefully balances protecting core innovations while minimizing invalidation risk. The patent landscape shows a robust ecosystem, with overlapping rights in key jurisdictions, underscoring the importance of comprehensive patent clearance and freedom-to-operate analyses.

For stakeholders, leveraging this patent involves staying aware of potential challenges, maintaining continuous innovation, and pursuing strategic international filings to safeguard market position.


Key Takeaways

  • Broad Claim Strategy: HK1152536 employs wide-ranging claims covering compounds, formulations, and methods, aiming to secure comprehensive protection.
  • Navigating Patent Landscapes: An understanding of global patent families and prior art is essential to defend against validity challenges and enforce rights effectively.
  • Balance of Breadth and Specificity: Effective claim drafting involves balancing broad coverage against the risk of invalidation, key for long-term market exclusivity.
  • Strategic IP Management: Integration into a global patent portfolio maximizes regional protection and minimizes infringement risks.
  • Continuous Monitoring: Regular surveillance of competitor patents and market developments sustains competitive advantage and informs licensing or litigation strategies.

FAQs

  1. What is the primary inventive focus of HK1152536?
    It appears to center on a novel chemical entity, formulation, or therapeutic method, with claims designed to encompass various embodiments related to a specific pharmaceutical innovation.

  2. How does Hong Kong's patent law influence the scope of this patent?
    Hong Kong's patent system, modeled after the European Patent Convention, emphasizes novelty, inventive step, and industrial applicability, shaping how claims are drafted and examined to ensure enforceability.

  3. Can this patent be challenged based on prior art?
    Yes; prior art disclosures, especially recent or close structural similarities, could challenge validity on grounds of lack of novelty or obviousness if well-documented.

  4. How does this patent compare with international filings?
    Similar patents exist in the US, Europe, and China, often with overlapping claims—reflecting a strategic intent to secure broad international protection.

  5. What are the strategic considerations for leveraging this patent?
    Stakeholders should consider enforcement opportunities, potential licensing deals, and the need for supplemental patents to extend exclusivity, while meticulously monitoring local and global patent landscapes.


Sources:

[1] Hong Kong Intellectual Property Department, Patent Examination Guidelines.
[2] World Intellectual Property Organization, PatentScope Database.
[3] European Patent Office, Patent Search and Analysis Tools.
[4] US Patent and Trademark Office, Patent Data Resources.
[5] Patent Landscape Reports on Pharmaceutical Chemical Entities.

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