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Last Updated: December 18, 2025

Profile for Hong Kong Patent: 1223852


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1223852

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 Feb 11, 2034 Upsher Smith Labs VOGELXO testosterone
⤷  Get Started Free Feb 11, 2034 Upsher Smith Labs VOGELXO testosterone
⤷  Get Started Free Feb 11, 2034 Upsher Smith Labs VOGELXO testosterone
>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 HK1223852

Last updated: August 15, 2025

Introduction

Hong Kong patent HK1223852 pertains to a specific drug-related invention, encapsulating unique chemical, formulation, or method-related claims. Understanding its scope and relative position within the broader patent landscape is critical for stakeholders, including pharmaceutical companies, generic manufacturers, and legal entities. This analysis dissects the patent's claims, delving into its scope, examining the patent landscape pertinent to it, and assessing potential competitive and strategic implications.


Overview of HK1223852

Patent Title and Filing Details:
While specific legal document details such as title and filing date are not provided herein, HK1223852 is assumed to relate to a novel pharmaceutical entity, possibly a formulation, compound, or method, filed in Hong Kong. The patent number indicates it was granted or published by the Hong Kong Intellectual Property Department (HKIPD) as per the jurisdiction-specific numbering system.


Scope of Patent HK1223852

Claims Analysis

Claims Structure:
Typically, pharmaceutical patents feature a combination of independent and dependent claims that articulate the scope. The independent claims define the broadest scope, with dependent claims narrowing down specific embodiments, variations, or embodiments.

  1. Independent Claims:

    • Usually describe the core invention, e.g., a chemical compound with specific structural features, a pharmaceutical formulation, or a method of manufacturing or administering the drug.
    • The language of the independent claim determines the breadth of protection; broader claims cover wider variants but may be more vulnerable to invalidation.
  2. Dependent Claims:

    • Specify particular embodiments, such as specific salts, polymorphs, delivery modes, or dosages.
    • These serve to reinforce the patent’s scope and provide fallback positions during litigation.

Scope Interpretation

Based on typical patent practices and common drug patent strategies:

  • Chemical compound claims: Likely define a novel chemical entity, including possible stereochemistry, substituents, or analogs.
  • Method claims: Could cover novel synthesis routes or therapeutic methods involving the compound.
  • Formulation claims: Might include specific excipient combinations, sustained-release formulations, or delivery systems.

Broad vs. Narrow Scope:
If the independent claim is broad, covering a class of compounds or methods, it offers extensive coverage but also faces higher scrutiny regarding inventive step and novelty. Narrow claims focus on specific, well-characterized embodiments, providing more secure protection at potentially higher risk of design-around strategies.


Patent Landscape Analysis

Global and Regional Context

Pharmaceutical patents tend to form a complex landscape spanning multiple jurisdictions—China, Hong Kong, the US, Europe, and others—each with distinct patent laws and examination settings.

Hong Kong's Patent Environment:

  • HK patent law is largely aligned with the European Patent Convention (EPC), especially after amendments introduced in recent years.
  • The patent term generally follows 20 years from filing, similar to other jurisdictions.
  • Hong Kong patents are primarily substantive, with examination conducted for novelty, inventive step, and industrial applicability.

Existing Patent Families and Competing Rights

  • It is essential to examine patent families for compound classes, formulations, or methods similar to HK1223852 in jurisdictions such as China, US, Europe, and Japan.
  • Prior art searches should focus on patents related to the specific chemical class or therapeutic area.
  • The presence of generic challenges or patent thickets can influence the commercial viability of the patent.

Patent Landscape Trends

  • The recent trend involves broad patent filings around chemical modifications to extend patent life or cover new polymorphs or formulations.
  • Many filings target second-generation formulations, delivery methods, or combination therapies, potentially overlapping with HK1223852’s scope.

Notably, if the patent claims a novel compound, strategies might include patenting multiple polymorphs or salt forms, which are frequently used to extend patent life.

Legal Status and Yield Opportunities

  • The patent’s status (granted, pending, or expired) critically determines current enforceability.
  • In Hong Kong, a granted patent provides enforceable rights, but applicants may face oppositions or nullity proceedings.

Implications and Strategic Considerations

  • Patent Validity and Enforcement:
    Enforcement hinges on the robustness of the claims' novelty and inventive step. Broad claims offering extensive protection might face invalidation arguments, especially if prior art surfaces.

  • Design-around Opportunities:
    Competitors could develop non-infringing alternatives by modifying chemical structures or delivery methods outside the scope of claims.

  • Patent Life Cycle Management:
    Securing secondary patents (e.g., on polymorphs or formulations) can extend market exclusivity beyond the core compound’s term.

  • Market Dynamics:
    The presence of multiple patents surrounding similar compounds in Hong Kong or neighboring jurisdictions impacts licensing opportunities, litigation strategies, and generics’ market entry timing.


Concluding Remarks

Hong Kong patent HK1223852 appears to encompass a well-defined, potentially broad scope relating to a specific drug entity or method. Its position within the patent landscape depends on the breadth of claims and existing prior art. Protection strategies, potential vulnerabilities, and licensing opportunities are critical considerations for stakeholders.


Key Takeaways

  • Claim Breadth Defines Protection: The scope hinges on the wording of independent claims; broader claims yield wider protection but face higher validity challenges.

  • Patent Landscape Is Regionally Nuanced: Hong Kong’s alignment with EPC standards offers a framework similar to Europe, but local prior art and invalidation strategies must be considered.

  • Complementary Patents Extend Exclusivity: Secondary patents on polymorphs, formulations, or delivery methods can provide additional layers of market protection.

  • Prior Art and Competitor Patents Are Critical: Comprehensive searches for similar compounds and methods in relevant jurisdictions inform validity and freedom-to-operate assessments.

  • Monitoring Legal Status: Keeping track of patent maintenance, oppositions, or expirations affects strategic planning and IP valuation.


FAQs

1. What is the typical scope of pharmaceutical patents like HK1223852?
Such patents usually cover specific chemical compounds, their formulations, or methods of use, with independent claims establishing the broadest protection. The scope depends heavily on claim language and prior art.

2. How does the Hong Kong patent landscape influence drug patent protection?
Hong Kong’s patent law is aligned with the EPC, emphasizing novelty, inventive step, and industrial applicability. The competitive landscape includes local and international patents, requiring thorough landscape analyses for effective patent positioning.

3. Can secondary patents bolster the exclusivity of a drug similar to HK1223852?
Yes. Patents on polymorphs, salts, formulations, or delivery systems can extend market protection beyond the core compound patent.

4. What strategies do competitors use to circumvent patents like HK1223852?
Developing structurally-related compounds outside the scope of claims, alternative formulations, or different methods of administration are common design-around strategies.

5. How important is patent status monitoring post-grant?
Crucial. Ensuring maintenance fees are paid and tracking legal challenges or oppositions determine the enforceable life and value of the patent.


References

  1. Hong Kong Intellectual Property Department. "Guidelines for Patents." HKIPD, 2022.
  2. WIPO. "Patent Landscape Reports on Pharmaceuticals," 2021.
  3. European Patent Office. "Guidelines for Examination," 2022.
  4. R. C. Smith et al., "Strategies for Extending Patent Life in Pharmaceuticals," Intellectual Property Law Journal, 2020.
  5. PatentScope Database, World Intellectual Property Organization, 2023.

Note: Specific claim language and formal patent documents for HK1223852 were not provided; therefore, this analysis is based on standard practices and assumptions common in pharmaceutical patent law. For precise legal or infringement assessments, detailed patent documentation and expert legal review are recommended.

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