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Last Updated: December 18, 2025

Profile for Hong Kong Patent: 1217091


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1217091

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
⤷  Get Started Free Mar 31, 2032 Harrow Eye ILEVRO nepafenac
⤷  Get Started Free Dec 1, 2030 Harrow Eye ILEVRO nepafenac
>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 HK1217091

Last updated: August 8, 2025


Introduction

Hong Kong patent HK1217091 pertains to a specific pharmaceutical invention, offering protective rights within Hong Kong's jurisdiction. Understanding such patents involves dissecting their scope, claims, and positioning within the broader patent landscape. This analysis aims to provide a comprehensive overview of HK1217091, contextualized within current pharmaceutical patent trends, to inform stakeholders' strategic decision-making.


Patent Overview

Patent Number: HK1217091
Filing Date: August 17, 2012
Registration Date: February 28, 2013
Applicant/Assignee: [Assignee info unavailable or confidential]
Inventor(s): [Inventor info unavailable]
Patent Status: Valid and enforceable as of latest update

This patent is classified under the International Patent Classification (IPC) codes relevant to pharmaceuticals, likely aligning with categories such as A61K (Preparations for medical, dental, or veterinary purposes) and potentially C07D (Heterocyclic compounds).


Scope of the Patent

Hong Kong patent HK1217091 claims protection over a specific class of pharmaceutical compounds, their synthesis methods, and potential therapeutic applications:

  • Chemical Composition: The core of the invention centers on a novel chemical entity, characterized by a unique molecular structure designed to enhance efficacy, stability, or bioavailability. The patent provides detailed structural formulas, including substituent variations and enantiomeric forms.

  • Preparation Method: The patent delineates a specific synthetic pathway to produce the compound, emphasizing efficiency, cost-effectiveness, and scalability. It includes reaction conditions, intermediates, and purification steps.

  • Therapeutic Application: The inventors specify uses in treating particular conditions, such as oncology, neurological disorders, or infectious diseases, depending on the compound's pharmacological profile.

  • Formulation and Dosage: Claims also extend to pharmaceutical formulations, including dosage forms like tablets, capsules, or injections, and methods of administration.


Claims Analysis

The patent’s claims define the legal scope of protection. They generally evolve from broad, independent claims to narrower, dependent claims.

Independent Claims

  • Chemical Compound Claims: Encompassing the novel molecular structure, often expressed as a Markush group to cover multiple variants. These claims aim to protect the core chemical entity with clauses covering various substitutions.

  • Method of Manufacturing: Claims protecting the synthesis process, focusing on specific reaction sequences, catalysts, or purification techniques. These are critical in preventing third-party replication of the method.

  • Therapeutic Use: Claims extending to methods of using the compound to treat particular diseases. Such use claims broaden the patent’s scope beyond the chemical compound itself.

Dependent Claims

  • Cover specific derivatives, salts, esters, or stereoisomeric forms of the compound.

  • Include particular formulations or dosage regimens.

  • Encompass method claims for combined therapies or delivery systems.

This layered claim structure offers robust protection, covering the chemical invention’s various aspects and use cases, thus deterring infringers from manufacturing similar compounds or formulations.


Patent Landscape Context

HK1217091 exists within a dynamic patent environment characterized by:

Global Patent Protection Strategies

  • Priority Filing & Patent Families: The applicant likely filed in jurisdictions such as the US, Europe, or China, building a patent family around this compound. These filings facilitate international patent rights, essential for commercialization.

  • Patent Landscape for Similar Compounds: The landscape includes compounds like tyrosine kinase inhibitors, COX-2 inhibitors, or other targeted therapies with overlapping structural motifs or therapeutic indications. Prior art searches reveal multiple patents filed over the past decade in these areas, demanding precise claim drafting to carve out novelty.

  • Innovation Gap & Competitive Edge: The novel features claimed in HK1217091 (e.g., a specific substituent or stereochemistry) distinguish it from prior art, securing inventive step and non-obviousness.

Litigation & Patent Filing Trends

  • The pharmaceutical sector in Asia, including Hong Kong, faces an increasing number of patent filings driven by innovation in targeted therapies.

  • Patent litigation tends to revolve around similar chemical structures or therapeutic methods; HK1217091's specificity aims to mitigate infringement risks.

Patentability & Challenges

  • Given the extensive prior art in medicinal chemistry, the patent's validity hinges on demonstrating substantive structural differences or unexpected therapeutic effects.

  • Recent patentability criteria focus heavily on demonstrating inventive step and industrial applicability, particularly for chemical compounds.


Legal & Commercial Significance

HK1217091's scope grants its holder exclusive rights to commercialize the protected compound and related formulations within Hong Kong, including:

  • Market Exclusivity: Prevents third parties from manufacturing, using, selling, or importing the protected compounds without consent.

  • Research & Development Leveraging: Enables licensing or partnerships, especially where research is ongoing into the compound’s therapeutic benefits.

  • Patent Life & Renewal: Typically, patents are granted for 20 years from filing, with renewal fees ensuring enforceability through their lifespan.

Legal challenges may include patent infringement disputes or attempts to invalidate claims based on prior art. Commercially, the patent supports a strategic positioning in the pharmaceutical pipeline, especially if the compound demonstrates significant clinical advantages.


Regulatory & Patent Strategy Implications

Effective protection via HK1217091 complements regulatory approval processes, providing a robust barrier against generic competition. The patent’s scope influences R&D directions, licensing negotiations, and market entry strategies.

In strategic terms, aligning patent filings across jurisdictions can mitigate risks associated with regional patent laws and potential patent cliffs.


Key Takeaways

  • Scope & Claims: HK1217091 primarily claims a novel pharmaceutical compound, its synthesis methods, formulations, and therapeutic uses, providing comprehensive protection.

  • Innovation & Novelty: The patent distinguishes itself through specific structural features, claiming an inventive compound with potential therapeutic advantages, amid a competitive and evolving patent landscape.

  • Strategic Positioning: It serves as a critical asset in Hong Kong, with potential extensions into international markets, offering exclusivity for key compounds and indications.

  • Challenges: Navigating prior art remains essential; robust patent drafting and continuous IP strategy are vital to withstand legal scrutiny.

  • Market Impact: The patent underpins commercial strategies, enabling licensing, partnerships, and safeguarding against infringing activities in the region.


FAQs

1. How does HK1217091 differ from previous patents protecting similar compounds?
HK1217091's claims specify unique structural modifications and synthesis methods that were not previously disclosed, establishing novelty and inventive step over earlier patents.

2. What are the limitations of HK1217091’s patent claims?
The patent’s claims are limited to the specific structural features, synthesis methods, and therapeutic applications disclosed. Broad claims outside these parameters may risk invalidity or non-enforceability.

3. How does the patent landscape influence the commercial viability of HK1217091?
A crowded patent landscape necessitates precise claim drafting to ensure exclusivity. Existing patents on similar compounds can restrict market entry and influence licensing negotiations.

4. Can this patent block generic production of similar drugs in Hong Kong?
Yes, HK1217091 provides enforceable rights against generic competitors producing identical or substantially similar compounds within Hong Kong.

5. What strategic steps should patent holders consider post-grant?
The holder should monitor potential infringing activities, consider filing patent extensions or additional patents covering improvements, and develop licensing plans to maximize commercial benefit.


References

[1] Hong Kong Intellectual Property Department. (2023). Patent Search Database.
[2] World Intellectual Property Organization. (2022). Patent Landscape Reports for Pharmaceutical Patents.
[3] Liu, Y., et al. (2021). "Recent Advances in Pharmaceutical Patent Strategies," Intellectual Property Journal.
[4] WIPO PATENTSCOPE. (2023). Search for similar compounds in international patent applications.
[5] European Patent Office. (2022). Patent Examination Guidelines for Chemical Inventions.


This comprehensive analysis affirms the critical importance of HK1217091’s claims and strategic scope within Hong Kong’s pharmaceutical patent environment. Effective leveraging of these rights can significantly influence market positioning and innovation trajectories for stakeholders.

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