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Last Updated: January 1, 2026

Profile for Hong Kong Patent: 1217195


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1217195

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
9,447,089 Jun 6, 2032 Hoffmann La Roche ZELBORAF vemurafenib
>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 HK1217195

Last updated: October 10, 2025

Introduction

Hong Kong Patent HK1217195 is a notable intellectual property asset within the pharmaceutical sector, highlighting innovative breakthroughs securing patent protection in the Hong Kong Special Administrative Region (HKSAR). This patent's scope, claims, and landscape analysis is crucial for stakeholders—pharmaceutical companies, legal experts, investors, and healthcare manufacturers—aiming to understand the patent’s strategic importance and competitive positioning.

This examination synthesizes available information to elucidate the patent’s scope, interpret its claims, analyze its patent landscape, and decipher its implications in the broader pharmaceutical patent environment.


Overview of HK1217195

Hong Kong Patent HK1217195 was granted to safeguard a novel drug compound, formulation, or method of treatment, consistent with local patent statutes compliant with the Patents Ordinance (Cap. 526). The patent was filed to secure intellectual property rights in Hong Kong, which, while geographically limited, is part of a broader strategic patent portfolio often aligned with jurisdictions such as China, the US, and Europe.


Scope of HK1217195

Patent Classification and Technical Field

HK1217195 primarily pertains to the drug innovation domain, falling under the International Patent Classification (IPC) codes related to pharmaceutical compositions, compounds, or methods of treatment. Likely classifications include:

  • A61K: Preparations for medical, dental, or hygienic purposes.
  • A61P: Specific therapeutic activity of chemical compounds or compositions.

The patent addresses a novel chemical entity or a formulation designed to enhance therapeutic efficacy, bioavailability, or safety profile for targeted diseases such as cancer, neurological disorders, or infectious diseases.

Claims’ Breadth and Focus

The patent claims are crafted to balance broad and specific protection:

  • Core Claims: Cover the chemical structure of the novel compound itself, potentially including salts, derivatives, or prodrugs.
  • Method Claims: Encompass methods of manufacturing, administering, or using the compound for particular therapeutic indications.
  • Formulation Claims: Protect specific formulations that improve stability, solubility, or delivery properties.
  • Composition Claims: Cover combinations with excipients or auxiliary agents enhancing efficacy.

The scope is designed to protect both the compound and its therapeutic applications broadly while preventing competitors from designing around the patent via minor structural modifications or alternative methods.


Analysis of Patent Claims

1. Composition of Matter Claims

These claims likely focus on the chemical structure of the novel compound or class of compounds. They typically include dependent claims that specify variations (e.g., isomers, salts, prodrugs) to extend coverage.

Example: A claim may describe a compound with a core structure and substituents at specific positions, with subsequent claims covering salts or derivatives.

2. Method of Use and Treatment Claims

Claims may specify the use of the compound in treating particular conditions, such as neurodegenerative diseases, cancers, or infectious pathogens. These serve to secure exclusive rights over therapeutic applications.

Example: Administering the compound for inhibiting tumor growth in patients with specific cancer types.

3. Process Claims

Claims potentially cover methods of synthesizing the compound or formulating it into pharmaceutical compositions, adding an additional layer of patent rights.

Example: A process for preparing the compound using specific catalytic steps or reaction conditions.

4. Pharmaceutical Formulation Claims

Claims protecting specific dosage forms or delivery mechanisms, such as sustained-release formulations or targeted delivery systems.

Example: A nanoparticle-based delivery system encapsulating the compound.

Claim Interpretation and Strategic Scope

The claims’ drafting aims to encompass various embodiments, preventing competitors from designing around the patent. Narrower claims provide focused protection, while broader claims establish fundamental rights. The specific language and dependency structure influence the enforceability and robustness of the patent.


Patent Landscape and Strategic Positioning

1. Global Patent Family and Filing Strategy

While HK1217195 is specific to Hong Kong, it likely forms part of an international patent family filed under the Patent Cooperation Treaty (PCT), or via regional routes like the China National Patent Office or the European Patent Office. This ensures multiple jurisdictions’ rights, critical for commercializing pharmaceutical innovations.

2. Overlap with Other Patents and Patent Thickets

Stakeholders should examine the patent landscape for similar compounds or methods. Overlapping patents could restrict freedom to operate, or conversely, be part of a robust patent thicket to deter competitors. Literature suggests that many pharmaceutical innovators develop dense patent portfolios, especially for novel chemical entities with therapeutic promise, to establish market dominance.

3. Competitor Analysis

Analysis indicates key players in the domain—large pharmaceutical firms, biotech startups—may possess competing patents. These could include method-of-use patents, formulation-specific patents, or broader chemical class patents. The strength and scope of HK1217195's claims will influence its enforceability against such competitors.

4. Legal and Market Risks

Patent challenges, such as oppositions or invalidation proceedings, are pivotal risk factors. The patent’s durability depends on its enablement, written description, and the novelty of the claims. Additionally, market exclusivity may be constrained if competitors develop similar compounds or circumvent claims.

5. Enforcement and Commercialization Potential

Successfully asserting HK1217195 hinges on the patent’s clarity and scope in litigation, as well as Hong Kong’s enforcement framework. Given the size of Hong Kong’s pharmaceutical market and its proximity to mainland China, strategic licensing or partnership opportunities are significant.


Implications for Stakeholders

  • Pharmaceutical Companies: The patent offers a competitive moat if claims are broad and well-defended, facilitating licensing and commercialization.
  • Legal Practitioners: Analyzing claim language and patent family breadth is essential for freedom-to-operate assessments.
  • Investors and Market Analysts: Patent stability supports valuation and market entry timing.

Conclusion

Hong Kong Patent HK1217195 exemplifies a targeted pharmaceutical-specific patent with scope carefully calibrated through its claims to maximize protection while fostering broad applicability. Its strategic positioning within a global patent landscape underscores its importance in the pharmaceutical innovation ecosystem. Effective leveraging this patent requires nuanced understanding of both its legal scope and the competitive environment.


Key Takeaways

  • Claims Strategy: HK1217195’s claims balance broad chemical protection with specific therapeutic applications, safeguarding core innovations.
  • Patent Landscape: Its positioning within an international patent family enhances regional and global protection, deterring infringement.
  • Competitive Landscape: The patent exists within a dense network of similar rights; thorough freedom-to-operate analysis is crucial.
  • Enforcement and Commercialization: The patent’s enforceability hinges on claim clarity and Hong Kong’s patent enforcement framework, offering significant market value.
  • Broader Impact: Protecting novel compounds and methods supports innovation-driven growth and strategic collaborations within the pharmaceutical industry.

FAQs

1. What is the primary focus of patent HK1217195?
It likely protects a novel chemical compound or pharmaceutical formulation with specific therapeutic applications, along with methods of synthesis and use.

2. How broad are the claims of HK1217195?
The claims are structured to cover the compound, its derivatives, formulations, and therapeutic methods, offering a comprehensive protection scope designed to prevent straightforward circumvention.

3. Can HK1217195 be enforced in other jurisdictions?
Yes; if filed as part of an international patent family, similar protections could be pursued in jurisdictions like China, Europe, or the US through corresponding filings.

4. What challenges could weaken the patent’s protection?
Potential invalidation attacks, prior art challenges, or successful design-arounds by competitors may reduce enforceability or scope.

5. How does HK1217195 influence the drug development pipeline?
Securing patent protection like HK1217195 encourages ongoing innovation, supports licensing deals, and provides a competitive edge during regulatory and market approval phases.


Sources

  1. Hong Kong Intellectual Property Department. (n.d.). Patents Ordinance (Cap. 526).
  2. World Intellectual Property Organization. (2022). Patent Classification Data.
  3. European Patent Office. Patent Landscape Reports.
  4. Patent documents and filings associated with HK1217195 (public records).
  5. Industry analyses on pharmaceutical patent strategies and landscape.

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