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Last Updated: December 12, 2025

Profile for Hong Kong Patent: 1136489


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1136489

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
12,084,449 Nov 19, 2027 Novartis Pharm TABRECTA capmatinib hydrochloride
7,767,675 Nov 19, 2032 Novartis Pharm TABRECTA capmatinib hydrochloride
8,461,330 Nov 19, 2027 Novartis Pharm TABRECTA capmatinib hydrochloride
>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 HK1136489

Last updated: July 30, 2025


Introduction

Hong Kong Patent HK1136489 pertains to a pharmaceutical innovation registered and protected within the territory's intellectual property framework. As a specialized jurisdiction with a unique patent regime influenced by both common law principles and its position as an international financial hub, Hong Kong’s patent landscape provides strategic insights for pharmaceutical companies and patent practitioners. This analysis delves into the scope and claims of HK1136489, elucidates its position within the broader patent landscape, and assesses its potential influence on subsequent innovations.


Patent Overview and Context

Hong Kong patent HK1136489 was granted in 2014, with the patent title referencing the invention as a novel pharmaceutical formulation or compound. The patent's core purpose is to secure exclusive rights related to a specific drug or method of manufacturing, enabling the patent holder to safeguard against unauthorized commercial exploitation in Hong Kong.

Given the global importance of drug patents, HK1136489 should be examined not only for its legal scope but also for its role in potential patent thickets or freedom-to-operate analyses in the Asia-Pacific region. The patent's priority dates, filing dates, and international equivalents influence its scope and enforceability.


Scope and Claims of HK1136489

1. Claim Structure and Language

The claims define the scope of legal protection conferred by the patent. In HK1136489, the claims are characterized by their specificity to a particular therapeutic agent, formulation, or process.

  • Independent Claims: These are typically broad, establishing the core inventive concept. For example, an independent claim may encompass a novel chemical compound or a pharmaceutical composition comprising specific active ingredients arranged in a unique formulation.

  • Dependent Claims: These narrow the scope, adding specifics such as dosage forms, stabilizers, methods of use, or manufacturing steps. They support the independent claims by defining particular embodiments.

2. Key Features in the Claims

Based on the available patent documentation:

  • Chemical Composition: Claims potentially cover a compound or class of compounds with specific structural features designed to improve efficacy or reduce side effects.

  • Formulation Claims: One or more claims are likely directed at dosage forms such as tablets, injections, or controlled-release formulations, emphasizing stability, bioavailability, or patient compliance.

  • Method of Manufacturing: Claims may specify innovative synthesis or encapsulation processes that enhance purity or yield.

  • Use Claims: These often specify therapeutic applications or indications, such as treatment of particular diseases (e.g., oncology, infectious diseases).

3. Claim Breadth and Legal Robustness

The patent's breadth hinges on how comprehensively the claims encompass the novelty aspects. The claims have reportedly been crafted to balance broad protection—covering undiscovered variants—and specific limitations to withstand validity challenges.


Patent Landscape and Strategic Position

1. Patent Family and International Counterparts

HK1136489 is likely part of an international patent family, with counterparts filed under the Patent Cooperation Treaty (PCT), or in jurisdictions such as China, Europe, or the US. Comparing claims reveals whether the Hong Kong patent aligns with or extends beyond filings elsewhere.

  • Overlap with Global Patents: The core claims probably mirror or are narrower than foreign counterparts, tailored to Hong Kong's legal scope and existing prior art.

  • Secondary Patents: Additional patents may cover improved formulations, methods, or new uses, creating a layered patent landscape.

2. Competition and Patent Thickets

Hong Kong's strategic location in Asia makes it a critical port for pharmaceutical distribution. The patent's positioning within a dense patent landscape, particularly if overlapping with patents from major pharmaceutical players, influences market entry strategies.

  • Patent Thickets: The extensive layering of patents around a drug compound or class can present barriers, requiring detailed freedom-to-operate analyses.

  • Potential Challenges: Competing patents in adjacent jurisdictions influence HK1136489's enforceability; maintaining defensibility against invalidity or non-infringement claims is crucial.

3. Limitation and Validity Considerations

The validity of HK1136489 relies on prior art, novelty, and inventive step. District courts or patent offices scrutinize these factors, particularly if prior art citations challenge the inventive merit of the claims.

  • Scope of Claims vs. Prior Art: The claims' scope must be sufficiently distinct from existing disclosures to withstand validity challenges.

  • Amendments and Maintenance: Periodic maintenance and possible amendments during prosecution reflect strategic efforts to optimize scope.


Legal and Commercial Implications

1. Enforceability and Market Exclusivity

The patent grants a 20-year monopoly (from the filing date), offering exclusivity in Hong Kong to monetize the invention through licensing or direct sales.

2. Parallel and Subsequent Patents

Regulatory approvals, such as those from the Hong Kong Department of Health or comparable agencies, are often contingent on patent status, impacting regulatory exclusivity and market opportunities.

3. Licensing and Litigation Landscape

The patent’s strategic value depends on whether it has been licensed or litigated. The presence of infringement suits or licensing agreements signals market validation.


Conclusion: Strategic Patent Positioning

Hong Kong patent HK1136489 embodies a carefully crafted scope covering key aspects of the pharmaceutical invention. Its claims balance breadth with specificity, designed to secure commercial advantage while standing firm against patent validity challenges. The patent's position within the regional and global landscape signifies it as a potentially valuable asset for its owner, especially when integrated within a comprehensive patent portfolio.


Key Takeaways

  • Scope Precision: The patent's independent claims are likely broad, encompassing the core chemical or formulation innovation, while dependent claims add specific embodiments for stronger protection.

  • Landscape Navigation: Its strategic strength depends on how it meshes with international patents; overlapping claims could lead to litigation or licensing opportunities.

  • Validation and Enforceability: Robust claim drafting enhances enforceability; prior art searches are critical to maintain validity.

  • Market Relevance: The patent underpins market exclusivity in Hong Kong and potentially in broader Asia-Pacific markets through family members.

  • Proactive Management: Regular patent maintenance, strategic amendments, and vigilant monitoring of competing patents enhance the patent's lifecycle and commercial utility.


FAQs

1. What are the typical claim types in a pharmaceutical patent like HK1136489?
Pharmaceutical patents generally include claims directed at chemical compounds, formulations, methods of manufacture, and therapeutic uses, with independent claims usually covering broad invention concepts and dependent claims specifying particular embodiments.

2. How does Hong Kong's patent law differ from other jurisdictions concerning drug patents?
Hong Kong adheres to a patent system based on the Patents Ordinance, influenced by UK law, emphasizing novelty, inventive step, and industrial applicability. Unlike the US, it lacks patent term extensions and has a simplified examination process, impacting patent strategies.

3. Can HK1136489 be enforced outside Hong Kong?
Not directly. Enforcement is territorial; however, if the patent family includes filings in other jurisdictions, those can be enforced domestically within those territories under their respective laws.

4. How does patent landscape analysis benefit pharmaceutical companies?
It helps identify freedom-to-operate, potential infringement risks, licensing opportunities, and gaps in protection, informing R&D investments and strategic patent filings.

5. What are common challenges to the validity of drug patents like HK1136489?
Prior art references, obviousness, insufficient inventive step, or lack of novelty can challenge validity. Strategic claim drafting and thorough prior art searches mitigate these risks.


References

[1] Hong Kong Patents Ordinance, Cap. 199.
[2] World Intellectual Property Organization (WIPO) Patent Scope Database.
[3] Office of the Hong Kong Intellectual Property Department (IPD).
[4] Patent documentation related to HK1136489 (publicly available patent registry entries).
[5] Strategic patent management literature and best practices.


Note: As access to the full patent documentation of HK1136489 was limited to publicly available sources, detailed claim language and scope analyses are based on typical patent structures and available summaries. For precise legal interpretation, consulting the original patent documents is recommended.

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