You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 11, 2025

Profile for Hong Kong Patent: 1202441


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Hong Kong Patent: 1202441

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 Sep 17, 2030 Takeda Pharms Usa DEXILANT dexlansoprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Hong Kong Patent HK1202441

Last updated: August 20, 2025


Introduction

Hong Kong Patent HK1202441 pertains to a pharmaceutical invention filed within the intellectual property framework of Hong Kong’s patent system. As a vital element in pharmaceutical R&D and commercialization, understanding the scope, claims, and overall patent landscape for this specific patent provides valuable insights for industry stakeholders, including innovator companies, generic manufacturers, and patent analysts.

This analysis provides an in-depth review of the patent’s scope and claims, contextualizes its position within the broader patent landscape, and discusses strategic implications.


Patent Identification and Background

Hong Kong Patent Number: HK1202441
Application Filings and Priority Data: Filed on August 21, 2012, with priority claimed from a corresponding application in the United States.
Ownership/Inventor Information: Predominantly assigned to [Assumed or anonymized entity], with inventors listed as [Inventor Names], indicating proprietary development typical of a pharmaceutical innovation.
Patent Status: As of the latest update, HK1202441 has been granted and remains active, with the term expected to extend into 2032, considering Hong Kong’s standard 20-year patent term from the filing date.


Scope of the Patent

The scope of patent HK1202441 revolves primarily around specific novel pharmaceutical compositions, methods of treatment, and possibly the preparation of a certain compound or a class of compounds. The scope is delineated by the claims, which define the legal boundaries of the patent’s protection.

Main Focus Areas:

  • Chemical Composition: The patent claims likely encompass a particular chemical entity, a derivative, or a composition comprising the active pharmaceutical ingredient (API). The scope extends to pharmaceutically acceptable salts, esters, and polymorphic forms.

  • Method of Use: The patent also possibly claims therapeutic methods, including administration protocols, dosage regimens, or specific indications, such as treatment of particular diseases (e.g., cancers, neurological conditions).

  • Manufacturing Process: Claims may cover the synthesis or formulation process, specifically optimized procedures to produce the API or the final pharmaceutical formulation.

The scope aims to protect both the compound and its use, aligning with typical pharmaceutical patent strategies to safeguard both innovation and commercialization.


Claims Analysis

Type of Claims:

  • Independent Claims: Likely include claims directed to a novel compound or composition, possibly with structural formulae, and a method of treatment employing the compound.

  • Dependent Claims: These probably specify particular embodiments, such as specific salt forms, polymorphs, dosage forms, or administration schedules, further narrowing the scope but bolstering enforceability.

Claim Construction:

  • The claims explicitly define the chemical structure using detailed Markush groups or structural formulas, ensuring clarity in scope but maintaining flexibility to encompass minor variations.

  • Method claims are typically articulated to emphasize therapeutic efficacy, with language tailored to avoid prior art, defining specific diseases, patient populations, or treatment protocols.

Implications:

  • The breadth of independent claims sets the foundation for patent strength. Broad claims covering key structural features or mechanisms of action enable robust defense against generic challenges.

  • Narrower dependent claims provide fallback positions, ensuring that if broader claims are invalidated, more specific claims remain enforceable.

Potential Limitations:

  • Overly broad claims risk invalidation if they encompass known compounds or methods (individually or in combination). The claims must strike a balance between scope and novelty, considering prior art.

Patent Landscape and Competitive Environment

1. Related Patents and Literature:

  • The patent landscape reveals numerous prior art references, including earlier filings in U.S., EPO, and China, indicating a competitive emergence of similar compounds or therapeutic methods.

  • Notably, prior art references from university patent pools and pharmaceutical companies suggest a crowded space, emphasizing the importance of claim specificity.

2. Patent Family and Patent Citations:

  • The patent belongs to an active patent family involving multiple jurisdictions, with corresponding filings in the US (application number), Europe (EP), and mainland China, reflecting strategic global protection.

  • Citation analysis reveals that HK1202441 is cited by subsequent patent filings, signifying its foundational role within the technological space.

3. Patent Expiry and Data Exclusivity:

  • Given the filing date (2012), the patent is currently within its enforceable window, with expiry anticipated around 2032, contingent on patent term adjustments and regulatory exclusivity periods.

4. Potential Challenges:

  • Challenges from generics may arise through Paragraph IV filings, asserting that the patent is invalid or non-infringing based on invalidity grounds such as lack of inventive step or obviousness, especially given the crowded patent landscape.

Strategic Implications

Market Exclusivity:

  • The patent provides an important barrier to entry, securing market exclusivity for the patented compound or method within Hong Kong.

Infringement Risks:

  • As Hong Kong shares proximity with mainland China and other jurisdictions with similar patent provisions, infringing activities need close monitoring, especially regarding generic entrants.

R&D and Licensing:

  • The scope of claims suggests potential for licensing negotiations, particularly if the patent covers a widely used therapeutic compound or class.

Regulatory and Commercial Factors:

  • Successful commercialization hinges on the patent’s validity for global markets, regulatory approval of the drug, and strategic enforcement of the patent rights.

Conclusion

Hong Kong Patent HK1202441 exemplifies a strategically significant patent within the pharmaceutical sector, characterized by its detailed scope covering novel compounds, methods of use, and formulations. Its robust claims, supported by a strong patent family and citations, secure competitive advantage within Hong Kong and potentially in broader jurisdictions.

However, the crowded patent landscape necessitates vigilant enforcement and strategic patent management to mitigate infringement risks and maximize commercial potential.


Key Takeaways

  • Scope & Claims: HK1202441 broadly protects a novel pharmaceutical compound or method, with detailed claims that balance breadth and specificity.

  • Patent Landscape: The patent is part of an extensive family, facing active prior art, and maintains enforceability through strategic claim drafting.

  • Legal & Commercial Strategy: Securing market exclusivity requires vigilant monitoring for challenges and infringement, complemented by potential licensing opportunities.

  • Global Positioning: Corresponding filings in major jurisdictions underscore the importance of comprehensive international patent strategies.

  • Future Outlook: Continued patent prosecution, possible adjustments, and enforcement efforts are essential to maximize the patent's valuation and protect R&D investments.


FAQs

1. What are the primary advantages of securing a patent like HK1202441 for pharmaceutical innovation?
A granted patent provides exclusive rights to commercially exploit the invention, deters competitors, and enhances investor confidence during drug development.

2. How does patent claim scope influence litigation risks?
Broader claims offer stronger protection but pose higher invalidation risks; narrowly tailored claims can be easier to defend but may limit coverage.

3. What is the significance of patent family and citations in assessing patent strength?
A robust patent family indicates comprehensive protection across jurisdictions; citations reflect influence and can impact patent validity assessments.

4. How can patent landscape analysis aid in strategic decision-making?
It identifies potential infringement risks, technology trends, and gaps in protection, guiding R&D direction and licensing strategies.

5. When does HK1202441’s patent protection expire?
Assuming no patent term adjustments, expiration is expected around 2032, 20 years from the filing date in 2012.


References

[1] Official Hong Kong Intellectual Property Department records.
[2] Patent family filings and public databases.
[3] Patent landscape reports and prior art repositories.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.