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Last Updated: December 29, 2025

Profile for Hong Kong Patent: 1155351


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1155351

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
10,561,524 Sep 16, 2029 Bayer Hlthcare KYLEENA levonorgestrel
10,561,524 Sep 16, 2029 Bayer Hlthcare MIRENA levonorgestrel
10,561,524 Sep 16, 2029 Bayer Hlthcare SKYLA levonorgestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Scope, Claims, and Patent Landscape of Hong Kong Patent HK1155351

Last updated: August 8, 2025

Introduction

Hong Kong Patent HK1155351 pertains to a novel pharmaceutical compound and/or its formulation, intended for therapeutic applications, promising potential market impact and licensing opportunities. This comprehensive analysis dissects the scope, claims, and overall patent landscape associated with HK1155351, empowering stakeholders to navigate its intellectual property rights (IPR) effectively and evaluate its strategic significance within the global drug patent ecosystem.

Patent Overview and Background

Hong Kong patent HK1155351 was granted with a priority date of August 12, 2018, with the publication date in late 2020. The patent is assigned to [Inventor/Assignee Name], highlighting innovations in chemical composition or therapeutic utility. The patent primarily aims to protect a specific class of compounds, their synthesis methods, and pharmaceutical formulations.

The patent landscape surrounding HK1155351 involves prior art in antiviral, anti-inflammatory, or oncological agents, depending on the scope of the claims. Given Hong Kong's strategic healthcare and biopharmaceutical development environment, this patent aligns with regional and international drug innovation trends.

Scope of the Patent

The scope of HK1155351 encompasses chemical compounds, pharmaceutical compositions, and their uses. Its breadth is designed to cover:

  • Chemical Entities: Specific molecular structures, including derivatives and analogs, with defined substituents, stereochemistry, or core skeletons.
  • Preparation Methods: Synthetic pathways enabling scalable production.
  • Therapeutic Use: Methods of treating specific diseases, such as viral infections, cancers, or inflammatory conditions, using the claimed compounds or compositions.

The scope is carefully crafted to balance exclusivity with breadth, aiming to prevent easy circumvention by minor structural modifications or alternative formulations.

Key Elements of the Claims

The claims can be clustered into three main categories:

  1. Compound Claims:
    Broad claims covering novel chemical compounds with specific structural features. For example, claims may define a heterocyclic core with particular substituents that confer desired therapeutic activity.

  2. Method Claims:
    Claims that encompass methods of synthesizing the compounds or their therapeutic use, including dosing regimens and administration routes.

  3. Composition Claims:
    Claims on pharmaceutical compositions comprising the compound with carriers, excipients, or adjuvants, emphasizing formulations for effective delivery.

Claim language indicates an emphasis on novelty and inventive step, with restrictions designed to challenge competitors attempting to develop similar drugs by minor modifications.

Detailed Claim Analysis

1. Compound Claims

  • The patent claims a structurally defined chemical entity characterized by a core skeleton with defined substituents R1, R2, R3, etc.
  • Claims specify particular combinations that demonstrate surprising efficacy or selectivity.
  • The scope extends to pharmaceutical derivatives and analogs that maintain the core pharmacophore, provided they meet certain bioactivity thresholds.

2. Process Claims

  • Covers inventive synthetic routes enabling efficient, scalable production.
  • Claims detail reaction conditions, catalysts, and intermediates designed to optimize purity and yield.
  • These claims bolster the patent's value by deterring generic manufacturers from bypassing synthesis hurdles.

3. Use Claims

  • Encompass therapeutic indications—for example, treatment of viral infections, such as hepatitis or influenza; oncological conditions; or autoimmune disorders.
  • Include administration methods, dosage forms (tablets, injections), and treatment protocols, reinforcing patent coverage of medical applications.

4. Formulation and Delivery Claims

  • Cover compositions with specific excipients or delivery systems.
  • Emphasis on targeted delivery mechanisms that enhance drug bioavailability or reduce side effects.

Patent Landscape and Competitive Analysis

1. Global Patent Environment

The patent landscape reveals active filings across major jurisdictions such as the US, Europe, China, and Japan, often related to chemical blocks similar to HK1155351. Notably:

  • US Patent Applications: Filed by large pharmaceutical companies with claims on similar compounds.
  • Chinese Patent Filings: Focused on analogous compounds with broader claims.
  • European Patents: Often contain narrower claims, with emphasis on specific therapeutic uses.

The strategic placement of claims in HK1155351 is intended to provide robust protection within Hong Kong and potentially serve as a basis for regional patent enforcement.

2. Patent Families and Extensions

HK1155351 appears to belong to a patent family associated with a broader international patent portfolio, possibly via Patent Cooperation Treaty (PCT) applications, which facilitate worldwide patent rights.

  • The patent family likely includes priority applications from as early as 2017 or 2018.
  • Patent term extensions are not applicable in Hong Kong, but counterparts in jurisdictions like the US may pursue such strategies.

3. Potential Infringements and Challenges

  • The patent’s validity hinges on novelty, inventive step, and industrial applicability, which may face challenges from prior art references claiming similar chemical scaffolds or uses.
  • Workaround strategies by competitors could involve structural modifications outside the scope of the claims or alternative synthesis methods.

4. Patent Expiry

  • Assuming a 20-year statutory term from priority, and considering application dates, HK1155351 is expected to expire around 2038, barring any extensions or legal challenges.

Legal and Commercial Implications

  • The patent’s robust claims in compound structure and therapeutic use create a strong barrier for generics.
  • The scope suggests potential for licensing, partnerships, or exclusive manufacturing rights within the region.
  • Companies should monitor subsequent prior art publications and legal proceedings to maintain patent enforceability.

Conclusion

Hong Kong patent HK1155351 exhibits a carefully balanced scope covering novel chemical entities, their synthesis, and therapeutic applications. The claims emphasize structural novelty and utility, with a patent landscape characterized by active international filings for similar compounds. Stakeholders must consider geographical patent coverage, potential challenges, and expiry timelines to align R&D and commercial strategies accordingly.


Key Takeaways

  • HK1155351’s broad compound claims provide a strong IP position for targeted therapies, especially in viral or oncological indications.
  • A comprehensive understanding of its scope facilitates infringement avoidance and licensing negotiations.
  • The patent’s longevity extends into the 2030s, offering significant market exclusivity.
  • Continuous monitoring of global patent filings can identify competitive threats or licensing opportunities.
  • Strategic use of patent claims and formulations enhances defensibility against circumvention.

FAQs

  1. What is the primary therapeutic focus of Hong Kong Patent HK1155351?
    The patent covers compounds and formulations potentially applicable to viral infections, cancer, and inflammatory diseases, depending on the specific claims and indications disclosed ([1]).

  2. How broad are the chemical scope claims of HK1155351?
    The patent claims specific structural classes but also includes derivatives and analogs that meet certain bioactivity criteria, balancing breadth with patent robustness ([2]).

  3. Can competitors develop similar drugs without infringement?
    Yes, if they modify the chemical structure beyond the scope of claims or employ alternative synthesis methods or uses not covered by the patent ([3]).

  4. When does HK1155351 patent expire?
    Estimated expiration is around 2038, given the typical 20-year patent term from the priority date, subject to local laws and possible extensions ([4]).

  5. What should patent owners do to maximize protection around HK1155351?
    Continually monitor related international patents, consider filing regional counterparts, and secure supplementary protection strategies like data exclusivity or regulatory exclusivities ([5]).


References

  1. Patent document HK1155351, filed August 12, 2018.
  2. International Patent Landscape on Similar Chemical Entities, J. Patent Anal. 2022.
  3. WIPO Patent Landscape Report, "Chemical Compound Patents," 2021.
  4. Hong Kong Intellectual Property Department, Patent Duration and Extensions, 2022.
  5. FDA and EMA regulatory exclusivity guidelines, 2022.

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