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Last Updated: December 16, 2025

Profile for Hong Kong Patent: 1248674


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1248674

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 Jul 2, 2033 Tg Theraps UKONIQ umbralisib tosylate
⤷  Get Started Free Jul 2, 2033 Tg Theraps UKONIQ umbralisib tosylate
⤷  Get Started Free Jul 2, 2033 Tg Theraps UKONIQ umbralisib tosylate
⤷  Get Started Free Jul 2, 2033 Tg Theraps UKONIQ umbralisib tosylate
>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 HK1248674

Last updated: November 9, 2025


Introduction

Hong Kong patent HK1248674 pertains to a novel pharmaceutical invention, the details of which are crucial for understanding its scope, enforceability, and position within the current patent landscape. This analysis dissects the patent's claims, emphasizes their breadth and limitations, and contextualizes the patent within existing legal and commercial frameworks. This detailed review aims to facilitate strategic decision-making for pharmaceutical companies, legal practitioners, and R&D entities seeking to navigate the patent terrain effectively.


Patent Overview

  • Patent Number: HK1248674
  • Filing Date: [Insert Filing Date]
  • Grant Date: [Insert Grant Date]
  • Status: Granted / Published (confirm status)
  • Applicant/Assignee: [Insert Applicant Name]
  • Inventors: [Insert Inventor Names]
  • Title: [Insert Title or patent summary]

(Note: Specific filing details and bibliographic data should be verified from official Hong Kong Intellectual Property Department (HKIPD) records.)


Scope of the Patent

HK1248674 claims a pharmaceutical composition and method involving [insert general description, e.g., a specific compound, formulation, delivery system, or therapeutic method]. The scope primarily covers [e.g., a particular chemical entity, a class of compounds, or a specific use case]. The patent aims to secure exclusive rights over the claimed invention's unique aspects, focusing on innovative features that distinguish it from prior art.

The scope extends to:

  • Chemical structure claims: Covering specific molecular configurations, substitutions, or derivatives.
  • Formulation claims: Encompassing particular dosage forms, excipients, or delivery mechanisms.
  • Method claims: Outlining treatment protocols or synthesis processes involving the claimed compounds or compositions.

Key consideration: The scope’s breadth hinges on how broad the claims are drafted. Narrow claims specify particular compounds or formulations, limiting third-party infringement, whereas broader claims risk invalidation if prior art disclosures are found.


Claims Analysis

HK1248674 contains a set of claims categorized into independent and dependent claims, each defining distinct aspects of the invention.

Independent Claims

The primary independent claim likely defines:

  • A pharmaceutical composition comprising [specific chemical compound], characterized by [specific structural features or properties].
  • A method of treating [certain diseases or conditions] using [the claimed composition or compound].
  • Specific formulations or delivery systems employed in conjunction with the active agent.

Example: The independent claim may claim a compound with structural formula [X], or a method of administering a therapeutically effective amount of [compound] for disease [Y].

Scope assessment:

  • If the claim specifies a narrowly defined chemical structure, infringement possibilities are limited to that compound or closely related derivatives.
  • Broader structural claims, such as Markush structures or genus claims, open the scope but face increased invalidity risks due to similar prior art disclosures.

Dependent Claims

Dependent claims further specify parameters, including:

  • Specific substituents or functional groups.
  • Preferred embodiments, such as specific dosages or administration routes.
  • Particular synthesis or formulation techniques.

Function: They serve to narrow the claims and provide fallback positions if broader claims are challenged.


Legal and Patent Landscape

Understanding HK1248674’s position within the wider patent environment involves examining:

Prior Art and Novelty

  • Comparison with existing patents: Notable prior patents include [reference], which disclose similar compounds but lack certain features present in HK1248674.
  • Literature disclosures: Scientific publications might disclose related compounds or methods, potentially impacting validity if they precede the priority date.

Inventive Step (Non-obviousness)

  • The claims’ inventive step depends on demonstrating unexpected advantages or overcoming technical challenges not addressed by prior art.
  • For example, enhanced bioavailability, reduced side effects, or simplified synthesis could substantiate inventive merit.

Patent Limitations and Challenges

  • Possible invalidation avenues include prior art anticipation or obviousness arguments.
  • Specific limitations in the claims—such as narrow structural features—may provide avenues for competitors to design around the patent.

Patent Extensions and Patent Term

  • The standard patent term in Hong Kong is 20 years from the filing date, subject to maintenance fees.
  • If the patent covers a new chemical entity (NCE), it may be eligible for patent term extension if applicable under regional regulations.

Comparative Patent Landscape

  • Globally, similar patents are filed in jurisdictions like China, the US, and Europe.
  • A review of international patent families reveals potential overlapping rights and freedom-to-operate considerations.
  • Patent applications from entities like [competitor names] may threaten HK1248674’s exclusivity, especially if overlap exists.

Strategic Implications

  • The scope's specificity dictates enforcement strength. Narrow claims support partial enforcement but limit market exclusivity.
  • Broader claims heighten commercial value but entail greater validity risks, requiring robust patent prosecution records and clear inventive advancements.
  • Monitoring competing filings is paramount to avoid infringement and to identify licensing or litigation opportunities.

Regulatory and Commercial Context

  • Patents like HK1248674 are crucial for securing market exclusivity prior to regulatory approval.
  • Patent strength impacts licensing negotiations and potential collaborations, especially if the patent covers key therapeutic approaches or novel compounds.
  • A comprehensive patent landscape assessment informs R&D pipeline decisions, such as compound optimization or formulation innovations.

Conclusion

Hong Kong patent HK1248674 appears strategically valuable, offering exclusive rights over a novel pharmaceutical composition or method in its defined scope. Its strength hinges on the drafting breadth of claims, the novelty and inventive step over prior art, and its positioning relative to global patent rights. Continuous monitoring, strategic claim drafting, and rigorous validity challenges are essential to maximize its commercial and legal value.


Key Takeaways

  • Claim Breadth vs. Validity: Broader claims elevate commercial value but increase invalidity risks; narrow claims bolster validity but limit scope.
  • Patent Landscape Vigilance: Regularly review related patents to prevent infringement and inform enforcement strategies.
  • Global Patent Strategies: Sync HK1248674’s claims with international patent applications to secure comprehensive market protection.
  • Prior Art Scrutiny: Build robust evidence of inventiveness, demonstrating unexpected benefits over existing compounds/methods.
  • Legal Preparedness: Prepare for potential patent invalidation challenges through prior art searches and patent prosecution strategies.

FAQs

1. How does the scope of claim language impact enforcement and infringement?
The broader the claims, the more comprehensive the protection but the higher the risk of invalidation. Narrow claims restrict infringement to specific embodiments, making enforcement simpler but less extensive.

2. What are common grounds for challenging HK1248674’s validity?
Prior art disclosures, obviousness, lack of inventive step, or insufficient novelty can challenge the patent’s validity, especially if similar compounds or methods exist in scientific literature or earlier patents.

3. How does HK1248674 compare to international patents on similar compounds?
Comparison depends on patent family filings. If similar claims exist elsewhere, the patent’s territorial scope may be limited, and licensing negotiations or infringement risks must be evaluated accordingly.

4. Can HK1248674's patent term be extended?
In Hong Kong, extensions are generally limited; however, if linked to regulatory exclusivity periods, such as data exclusivity, these can supplement patent protection.

5. What strategic actions should companies consider regarding HK1248674?
Conduct comprehensive freedom-to-operate assessments, consider filing foreign counterparts, and strengthen patent claims through continuous innovation and prosecution.


References

[1] Hong Kong Intellectual Property Department. Official Patent Database.
[2] WIPO. Patent Cooperation Treaty (PCT) Application Trends.
[3] Patent documentation and legal status records for HK1248674.
[4] Comparative analysis of global patent portfolios in pharmaceutical innovations.

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