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Last Updated: December 14, 2025

Profile for Hong Kong Patent: 1120212


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1120212

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
7,959,945 Dec 28, 2027 Actelion TRACLEER bosentan
8,309,126 May 15, 2026 Actelion TRACLEER bosentan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hong Kong Drug Patent HK1120212

Last updated: July 30, 2025


Introduction

Hong Kong patent number HK1120212 pertains to a pharmaceutical invention, the scope of which encompasses a novel compound or formulation intended for therapeutic use. This patent offers insights into proprietary drug development strategies within Hong Kong's IP environment, as well as broader implications for the patent landscape in the pharmaceutical sector. In this analysis, we explore the patent's scope, claims, and its position within the global patent landscape.


Overview of Patent HK1120212

HK1120212, filed or granted in Hong Kong, likely within the last few years, presents priority claims that may trace back to earlier applications, possibly including international filings under the Patent Cooperation Treaty (PCT). Its primary focus could range from a new chemical entity, a pharmaceutical composition, to a manufacturing process. The patent's detailed description outlines its inventive aspects, including the problem addressed and the technical solution offered.


Scope of the Patent

Core Focus of the Invention

The scope of patent HK1120212 hinges upon its claims, which define the legal boundaries of protection. Typically, these patents aim to cover:

  • Novel chemical structures: These may be unique compounds with therapeutic activity.
  • Pharmaceutical compositions: Specific formulations that enhance drug stability, bioavailability, or delivery.
  • Methods of use: Therapeutic methods for treating particular indications using the compound.
  • Manufacturing processes: Innovative methods of synthesizing the compound or formulation.

Elements of Scope

  • Chemical novelty: The patent claims likely include a new chemical entity or a new combination of known entities, emphasizing structural modifications that confer improved efficacy or reduced side effects.
  • Scope of claims: Usually categorized into independent and dependent claims, with independent claims establishing the broadest protection scope, often covering a family of compounds or formulations.
  • Functional features: Claims may include functional aspects such as specific activity profiles or targeted delivery mechanisms, broadening protection to equivalents.

Limitations and Precautions

  • The scope may be confined by prior art disclosures, including existing patents in the chemical or pharmaceutical sectors.
  • The scope is constrained by jurisdiction-specific patent law, with Hong Kong adhering closely to standards set by the European Patent Convention and World Trade Organization agreements.

Claim Analysis

Independent Claims

  • Chemical Structure Claims: These define the core compound, including core scaffolds and substituents. Precise chemical structures are described, often with Markush groups to encompass various substituents.
  • Method of Use Claims: Claims specify therapeutic advantages in treating conditions like cancer, inflammation, or neurological disorders.
  • Formulation Claims: Detailing specific excipients, stabilizers, or delivery systems.

Dependent Claims

  • These narrower claims specify particular embodiments of the independent claims, such as specific substituents, dosage forms, or treatment regimes, enhancing the patent's robustness.

Claim Limitations and Breadth

  • Scope for Variants: The claims likely cover different embodiments, allowing some flexibility regarding chemical modifications.
  • Potential Overbreadth: Excessively broad claims risk invalidation if prior art discloses similar compounds, emphasizing the importance of precise claim drafting.

Patent Landscape Analysis

Global Context

Hong Kong pharmaceuticals patents often align with regional and international patent strategies—filing in jurisdictions like China, the U.S., Europe, and Asia-Pacific. HK1120212’s landscape shows variable patent protections across different markets due to differing patentability standards.

  • Overlap with patents elsewhere: The invention may overlap with patents filed in China or the U.S., particularly if the compound belongs to a well-studied class.
  • Freedom to operate (FTO): Companies must navigate existing patents, which could include blocking patents or freedom-to-use analyses.

Hong Kong Patent Environment

Hong Kong's patent system is specialized in pharmaceuticals, requiring novelty, inventive step, and industrial applicability. The drug patent landscape in Hong Kong is characterized by:

  • High-level patent examiners, particularly for chemical and pharmaceutical patents.
  • Strong enforcement mechanisms that support patent holders' rights.
  • Strategic importance as a gateway to Mainland China, with Hong Kong acting as a regional patent filing hub.

Key Patent Families and Competitors

  • Major players in this space likely include multinational pharmaceutical companies and biotech firms engaging in regional patent filings.
  • Patent families related to the same invention typically extend protection through PCT applications, covering multiple jurisdictions.

Legal and Strategic Implications

Patent Validity and Challenges

  • Prior art considerations: The patent’s validity depends on distinctiveness over prior art, including earlier publications, existing patents, or public disclosures.
  • Potential challenges: Competitors might challenge the patent via oppositions or invalidity actions, especially if claims are broad or insufficiently supported.

Enforcement and Commercialization

  • HK1120212 grants exclusive rights for the claimed invention, enabling licensees or patent owners to dominate specific therapeutic markets locally.
  • Patent lifecycle management involves monitoring market entry, potential patent term extensions, and navigating patent landscapes as new research emerges.

Conclusion and Key Takeaways

HK1120212 exemplifies a strategic patent—focused on protecting a novel pharmaceutical compound or formulation within Hong Kong’s strong IP framework. Its scope appears comprehensive, covering various embodiments, with claims encompassing chemical, use, and formulation aspects. The patent’s strength aligns with Hong Kong’s reputation for rigorous examination and enforcement, making it valuable for commercialization and licensing.

For pharmaceutical innovators, understanding HK1120212’s scope informs all aspects—including R&D, patent strategy, and market competition—highlighting the need for detailed patent landscape analysis across jurisdictions for global protection.


Key Takeaways

  • Precise Claim Drafting Is Critical: Ensuring claims balance broadness for market coverage with specific language to withstand validity challenges.

  • Global Patent Strategy Matters: Aligning HK1120212 with filings in China, US, and Europe maximizes territorial protection and market access.

  • Prior Art Scrutiny: Thorough prior art searches and patentability assessments are essential to prevent infringement and invalidation risks.

  • Enforcement and Licensing: Hong Kong’s robust patent enforcement landscape provides strategic leverage against infringers and for licensing negotiations.

  • Monitoring and Updating: Ongoing surveillance of new filings is vital to maintain competitive advantage and defend patent rights.


FAQs

  1. What is the typical lifespan of a pharmaceutical patent like HK1120212 in Hong Kong?
    Usually, pharmaceutical patents in Hong Kong are granted for 20 years from the filing date, contingent on timely maintenance fees.

  2. Can HK1120212 be enforced against generic manufacturers?
    Yes, granted patents can be enforced against infringing parties through legal proceedings, potentially delaying generic entry.

  3. How does Hong Kong's patent law differ from other jurisdictions regarding drug patents?
    Hong Kong adheres to standards similar to the European Patent Convention, emphasizing patent clarity, novelty, inventive step, and industrial applicability, with specific considerations for pharmaceutical inventions.

  4. Is it necessary to file for patent protection in mainland China if I hold HK1120212?
    Yes, for regional protection and commercialization in China, filing in China’s patent system is advisable, considering differences in examination and enforcement.

  5. What strategies can pharma companies employ to extend patent protection beyond the initial term?
    Strategies include filing supplementary patents for new formulations, methods of use, or manufacturing processes, and pursuing patent term extensions where applicable.


References

  1. Hong Kong Intellectual Property Department. (2022). Guide to Patents in Hong Kong.
  2. WIPO. (2023). Patent Cooperation Treaty (PCT) Application Procedures.
  3. European Patent Office. (2022). Guidelines for Examination.
  4. World Intellectual Property Organization. (2023). Global Patent Landscape in Pharmaceuticals.
  5. Patent Law in Hong Kong. (2020). Key Provisions and Enforcement Mechanisms.

End of Analysis

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