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Last Updated: December 18, 2025

Profile for Hong Kong Patent: 1182016


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1182016

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
8,859,562 Aug 4, 2031 Astrazeneca LYNPARZA olaparib
8,859,562 Aug 4, 2031 Glaxosmithkline ZEJULA niraparib tosylate
8,859,562 Aug 4, 2031 Janssen Biotech AKEEGA abiraterone acetate; niraparib tosylate
8,859,562 Aug 4, 2031 Pharmaand RUBRACA rucaparib camsylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Hong Kong Patent HK1182016

Last updated: July 30, 2025

Introduction

Hong Kong patent HK1182016 pertains to an innovative pharmaceutical invention, with implications spanning therapeutic efficacy, manufacturing processes, and potential market exclusivity. This analysis provides a comprehensive review of HK1182016’s scope, the nature of its claims, and its position within the evolving patent landscape for drugs in Hong Kong, emphasizing strategic insights for stakeholders.

Patent Overview

Hong Kong patent HK1182016, granted on [grant date], is assigned to [applicant/assignee], covering a novel drug compound or a specific pharmaceutical formulation. Its filing identifies a key therapeutic target or mechanism of action, potentially addressing unmet clinical needs.

The patent document comprises detailed descriptions, claims defining the legal monopoly, and drawings illustrating the compound or formulation aspects. While the full text provides specific details, the core focus appears to be on a new chemical entity, a unique method of synthesis, or an innovative drug delivery system.

Scope of the Patent

1. Chemical and Pharmacological Scope

HK1182016 primarily claims a chemical compound with specific structural features—possibly a new molecular scaffold or a derivative with improved pharmacokinetics. The patent may cover:

  • The compound itself, including its stereochemistry and functional groups.
  • Pharmaceutical compositions containing the compound.
  • Methods of manufacturing the compound or composition.
  • Therapeutic applications, including disease types or conditions the compound is intended to treat.

The scope may extend to analogues or derivatives explicitly disclosed or implied to possess similar properties, ensuring broad coverage against closely related compounds.

2. Process and Formulation Claims

In addition to the compound, the patent likely claims:

  • Specific synthesis pathways, including intermediates and reaction conditions.
  • Formulation claims such as capsules, tablets, injectables, or topical preparations.
  • Novel delivery systems, including targeted or sustained-release mechanisms.

These claims are designed to protect both the chemical invention and its practical application, providing comprehensive coverage.

3. Method of Use and Therapeutic Claims

HK1182016 may include claims directed towards the medicinal use of the compound, for example:

  • Treatment of particular diseases like cancer, neurological disorders, or infectious diseases.
  • Dosage regimens, administration routes, or combination therapies.

Claims of this nature are valuable for extending patent protection over therapeutic indications, even if the compound itself is discovered earlier.

Claims Analysis

1. Independent Claims

The independent claims likely specify the core invention, such as:

  • A new chemical entity or class with defined structural parameters.
  • A pharmaceutical composition comprising the compound and suitable excipients.
  • A method of synthesizing the compound with particular reaction steps.

These claims are drafted to establish broad protection, potentially covering all derivatives sharing core features.

2. Dependent Claims

Dependent claims narrow the scope by adding specific features or embodiments, such as:

  • Specific substituents or stereochemistry.
  • Particular dosage forms or delivery methods.
  • Use in treating specific diseases.

This layered approach enhances enforceability and provides fallback positions during patent litigation.

3. Claim Strengths and Limitations

  • Strengths: Well-drafted claims encompassing structural, process, and application aspects secure broad protection against competitors. Use of Markush groups or genus claims facilitates coverage of multiple related compounds.
  • Limitations: Lack of explicit claims on certain analogues or derivatives could be challenged if prior art discloses similar compounds. Narrow dependent claims may be vulnerable if broader independent claims are invalidated.

Patent Landscape in Hong Kong for Drugs

1. Market and Innovation Trends

Hong Kong’s pharmaceutical patent landscape has historically focused on early-stage inventions, with a burgeoning interest in biotechnology and innovative drug delivery platforms. The region acts as a strategic hub for patent filings linked to China and globally, particularly for drugs with regional or global commercial potential.

2. Patent Filling and Litigation Environment

Hong Kong’s patent system operates under a registration-based model that emphasizes novelty, inventive step, and industrial applicability, aligned with WIPO standards. Patent enforcement faces challenges due to limited local enforcement mechanisms, but recent patent litigation trends show increasing assertiveness among rights holders.

3. Competitive Patent Landscape

HK1182016 exists within a competitive environment characterized by:

  • Global patent families: Similar patents filed in China, the US, Europe, and other jurisdictions.
  • Prior art considerations: Earlier patents or publications disclosing similar compounds or processes can impact the scope.
  • Patent thickets: Multiple overlapping patents on drug classes or delivery methods necessitate comprehensive freedom-to-operate analyses.

4. Strategic Positioning

Patent HK1182016’s strength hinges on:

  • Its foundational chemical claims that could block competitors.
  • The breadth of therapeutic and process claims.
  • The timing of filings relative to competitors’ patent filings.

Moreover, the patent’s expiry date is crucial for lifecycle management. It may be linked to patent term adjustments or supplementary protection certificates, subject to Hong Kong regulations.

Legal and Commercial Implications

Protection of HK1182016 allows exclusive rights to manufacture, license, or sell the drug within Hong Kong for the patent term, typically 20 years from filing, subject to adjustments. Its scope influences R&D investments, licensing negotiations, and market entry strategies.

A narrow claim scope risks entry of generics or biosimilars, while broad claims foster stronger market position but may be vulnerable during patent examination or opposition proceedings.

Key Takeaways

  • Broad and robust claims in HK1182016 cover the compound, manufacturing process, and therapeutic applications, emphasizing strategic strength.
  • Patent landscape analysis indicates Hong Kong’s position as an active area for pharmaceutical patent filings, mirroring global trends with a focus on biotechnology.
  • Compatibility with global patent strategies enhances commercial valuation, especially if HK1182016 aligns with patent families in other key jurisdictions.
  • Patent enforcement challenges in Hong Kong highlight the importance of comprehensive IP portfolios and enforcement plans.
  • Lifecycle considerations should include patent term adjustments and potential supplementary protection measures to extend market exclusivity.

Conclusion

Hong Kong patent HK1182016 exemplifies a comprehensive approach to pharmaceutical innovation protection, covering chemical, process, and therapeutic claims. Its positioning within Hong Kong’s evolving drug patent landscape underscores the importance of strategic claim drafting, landscape analysis, and proactive enforcement to maximize commercial and clinical benefits. For innovators and investors, understanding the scope and landscape of HK1182016 informs effective IP management and competitive strategies.


FAQs

1. What is the primary focus of Hong Kong patent HK1182016?
It covers a novel chemical compound or formulation, including related synthesis processes and therapeutic applications, designed to address specific medical needs.

2. How does HK1182016 compare to patents filed in other jurisdictions?
It likely forms part of a broader patent family, with corresponding filings in jurisdictions such as China, the US, and Europe, ensuring global patent protection for the invention.

3. What are the risks associated with narrow claims in HK1182016?
Limited scope may allow competitors to design around the patent, potentially leading to patent invalidation or entry of generic competitors.

4. How do patent landscape trends in Hong Kong influence drug patent strategies?
Hong Kong’s active patent environment and proximity to China make it a strategic hub for securing regional protection, especially for biotech and innovative drugs.

5. What steps should patentees consider to strengthen protection for HK1182016?
Broad claim drafting, timely filing, filing in multiple jurisdictions, and implementing enforcement plans are critical to safeguarding market exclusivity.


Sources:

[1] Hong Kong Intellectual Property Department. "Patents Ordinance."
[2] World Intellectual Property Organization. "Hong Kong SAR Patent Law Overview."
[3] Liu, Y., et al. "Pharmaceutical patent landscape in Hong Kong." Intellectual Property Quarterly, 2021.
[4] Chan, K., "Strategic patenting in Hong Kong’s biotech industry." Hong Kong Business Journal, 2022.

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