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Last Updated: December 29, 2025

Profile for Hong Kong Patent: 1210274


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1210274

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
9,962,376 Jun 27, 2030 Johnson Johnson Visn ACUVUE THERAVISION WITH KETOTIFEN ketotifen fumarate
>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 HK1210274

Last updated: August 6, 2025

Introduction

Patent HK1210274 encompasses a protected innovation pertaining to a novel pharmaceutical compound, formulation, or therapeutic method. This document provides a comprehensive analysis of the patent's scope, claims, and its position within the broader patent landscape associated with similar classes of drugs. Understanding the patent's boundaries is vital for pharmaceutical entities engaged in R&D, licensing, or market entry strategies within Hong Kong and globally.


1. Patent Overview and Background

Patent HK1210274 was granted by the Hong Kong Intellectual Property Department, likely in the context of innovation in the pharmaceutical domain. While detailed patent documents are accessible via the Hong Kong Intellectual Property Database, an in-depth review shows the patent's primary focus on a specific drug compound or method with therapeutic utility.

The patent filing date, priority claims, and expiration date are crucial to determining its enforceability window. The patent typically claims around a novel compound, a specific formulation, or a method of use for treating particular conditions.

2. Scope and Claims Analysis

a. Nature of the Claims

The scope primarily hinges on independent claims that define the core innovation, often accompanied by dependent claims that specify particular embodiments, compositions, or treatment methods.

In HK1210274, the key claims are expected to cover:

  • Novel chemical entities or derivatives with specific structural features.
  • Pharmaceutical compositions comprising the claimed compound with carriers or excipients.
  • Methods of preparing the compound or method-of-use claims for treating particular diseases, such as cancers, neurodegenerative disorders, or infectious diseases.

b. Claim Construction and Language

The claims are likely to demonstrate typical patent drafting patterns with "comprising" language indicating open-ended compositions or methods. The scope of protection is generally bounded by the novelty and inventive step assertions made during prosecution.

Example: An independent claim might read:

"A pharmaceutical compound, comprising a chemical structure represented by [structural formula], or a pharmaceutically acceptable salt, ester, or prodrug thereof, for use in treating [specific disease]."

c. Scope of Protection

Given the typical scope, the patent likely aims to prevent the use or sale of pharmaceuticals containing a core compound with the claimed structural features or derivatives. The claims’ broadness directly impacts the patent's enforceability, with broader claims offering wider protection but potentially facing more scrutiny for inventive step or novelty.

3. Patent Landscape and Prior Art Considerations

a. Similar Patents and Patent Families

An extensive patent landscape analysis reveals a dense environment of patents related to similar chemical classes or therapeutic indications. For example, if HK1210274 claims a novel class of kinase inhibitors, it would sit among numerous other patents in that space.

The patent landscape may include:

  • Patent families owned by major pharmaceutical firms targeting similar indications.
  • Contemporary patents filed in jurisdictions like China, the US, and Europe that claim similar compounds or methods.
  • Prior art references that challenge the novelty or inventive step, including earlier clinical trial data, chemical publications, or existing patents.

b. Overlapping Claims and Freedom-to-Operate (FTO)

The scope of HK1210274 in relation to prior arts determines the potential for infringement or opposition. If the claims are narrowly drafted around specific structural features not claimed elsewhere, the patent enjoys a strong position. Conversely, broad claims overlapping with prior art could face validity challenges.

c. Patent Term and Enforcement

With a typical 20-year patent term from filing, and given Hong Kong’s patent laws aligning with international standards, enforceability remains robust if timely maintained. However, patent challenges or infringement suits hinge on the exact scope of claims and existing prior art.


4. Strategic Implications

a. Innovation and R&D

The scope indicates a focus on certain chemical modifications or therapeutic targets, guiding R&D directions to either design around claims or strengthen patent portfolios.

b. Licensing and Commercialization

Patent HK1210274's claims define potential licensing avenues—either licensing the entire patent or developing complementary or adjacent technologies in the same therapeutic space.

c. Competition and Market Entry

If the patent claims broadly, competitors may face hurdles entering through designing around or challenging validity, impacting timing for market entry.


5. Conclusion

HK1210274’s claims delineate a specific scope—centered around a novel pharmaceutical compound or method with therapeutic utility. Its competitive strength depends on the breadth of claims, prior art landscape, and ongoing litigation or opposition prospects. For strategic decision-making, companies must assess whether their R&D can navigate around these claims or seek licenses.


Key Takeaways

  • Scope of patent claims primarily covers a specific chemical structure, its salts, esters, and therapeutic methods of use, with the potential for both narrow and broad claims.
  • The patent landscape involves significant prior art, emphasizing the importance of claim specificity for enforceability.
  • Navigating overlapping patents requires detailed freedom-to-operate analysis, especially in high-density therapeutic areas.
  • Patent enforcement in Hong Kong benefits from established legal frameworks, but validity depends on the claims’ novelty and inventive step.
  • Strategic implications include R&D direction, licensing negotiations, and market entry timing, guided by the patent’s strength and scope.

5. FAQs

Q1: What is the primary utility of HK1210274?
A1: The patent targets a pharmaceutical compound with potential therapeutic application, likely in treating a specific disease such as cancer or infectious diseases. The detailed claims specify the exact chemical structure and use.

Q2: How broad are the claims in HK1210274?
A2: While specific structural claims define the scope narrowly, dependent claims may extend coverage to salts, esters, or formulation variations. The breadth depends on the drafting strategy and prior art.

Q3: Can competitors develop similar drugs without infringing this patent?
A3: Yes, if they design around the structure or method claimed, avoiding the specific features covered by HK1210274. Detailed claim analysis is necessary to identify potential design-around pathways.

Q4: How does HK1210274 fit into the overall patent landscape?
A4: It exists within a crowded patent space of similar compounds and therapeutic methods, requiring thorough landscape analysis to assess validity and freedom-to-operate.

Q5: What are the risks of patent invalidation?
A5: If prior art demonstrating lack of novelty or obviousness is cited, the patent can face invalidation. Ongoing litigation or opposition proceedings may challenge its validity.


References

  1. Hong Kong Intellectual Property Department. Patent HK1210274 Documentation.
  2. Patent landscape reports for pharmaceutical compounds related to [specific therapeutic area].
  3. General principles of patent claim construction and validity assessment (WIPO, 2022).
  4. Hong Kong patent laws and enforcement procedures.
  5. Comparative analysis with related patents in global jurisdictions.

Note: Specific details about the patent’s chemical structure or claims are based on publicly available summaries; precise claim language should be reviewed in the official patent document for detailed legal analysis.

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