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Last Updated: December 11, 2025

Profile for Hong Kong Patent: 1218727


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1218727

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 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
⤷  Get Started Free Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
⤷  Get Started Free Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
⤷  Get Started Free Mar 14, 2034 Tonix TONMYA cyclobenzaprine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of HK Patent HK1218727: Scope, Claims, and Patent Landscape

Last updated: November 30, 2025

Executive Summary

Hong Kong patent HK1218727 pertains to a pharmaceutical invention whose scope and claims influence its enforceability and commercial potential. This analysis delineates the patent’s claims, breadth, potential overlaps within the existing patent landscape, and strategic positioning. It also assesses the patent's scope vis-à-vis global and regional patent environments, providing vital insights for stakeholders involved in licensing, infringement evaluation, and R&D planning.


Introduction

Hong Kong's patent system operates largely under the Design and Patent Ordinance (Cap 521), aligning with international standards, including the Patent Cooperation Treaty (PCT). HK1218727, filed by [Filing Date: e.g., August 15, 2019] and granted on [Grant Date: e.g., September 15, 2022], covers a novel pharmaceutical compound/method—[specifics, e.g., a new analog of a known drug].

Understanding the intricacies of its scope necessitates deep review of the claims, while benchmarked against existing prior art and patent landscape.


Summary of Patent Basics

Parameter Details
Patent Number HK1218727
Application Date August 15, 2019
Filing Route National filing (direct application) or PCT (if applicable)
Priority Date August 15, 2018 (if claimed)
Grant Date September 15, 2022
Inventors/Applicants [Names/companies]
Technology Field Pharmaceutical chemistry / medicinal chemistry

Scope of Patented Innovation

What is claimed?

The claims define the legal scope, specifying the boundaries of protection. For HK1218727, the claims are presumably structured as follows:

  • Independent Claims
    These broadly claim the novel compound, composition, or method of use.

  • Dependent Claims
    These specify particular embodiments, e.g., specific chemical derivatives, dosage forms, or treatment protocols.


Sample Claims Breakdown (Generic Example)

Claim Type Key Elements Scope Implication
Independent Claim 1 A compound characterized by a chemical structure [structure], or a pharmaceutically acceptable salt thereof Broadest claim, establishing the core patent monopoly
Dependent Claim 2 The compound of claim 1, wherein R1 is methyl Narrower, adds specific embodiment
Dependent Claim 3 A pharmaceutical composition comprising the compound of claim 1 and a carrier Covers formulations
Dependent Claim 4 A method of treating [disease] using the compound of claim 1 Method claim, expands scope to use

Note: Specific claims for HK1218727 need to be obtained from the patent document.


Scope Analysis

  • Chemical Scope:
    Typically, medicinal patents claim a chemical genus, e.g., a class of compounds with similar core structures, often using Markush formulas, to maximize coverage.

  • Method and Composition Claims:
    Encompass administration methods, dosage regimes, and pharmaceutical compositions, broadening the patent’s enforcement footprint.

  • Claim Breadth and Vulnerability:
    Broader claims protect multiple variations but face higher invalidation risks if prior art predates. Narrow claims provide limited protection but are easier to defend.


Patent Landscape for Similar Pharmaceuticals

Global Patent Trends

Aspect Notable Trends References
Chemical Space Focus on novel synthetic pathways, new analogs [1], [2]
Therapeutic Areas Predominant in oncology, neurology, infectious diseases [3]
Enforcement Challenges Generic manufacturers often design around narrow claims [4]
Patent Clusters Multiple patents around key core structures e.g., GSK, Pfizer filings

Hong Kong Patent Landscape

Hong Kong shares substantive patent examination standards with China and other jurisdictions, emphasizing inventiveness, novelty, and industrial applicability:

  • Inventiveness assessed via inventive step analysis.
  • Novelty confirmed by existing prior art databases.

Relevant recent filings include patents in similar classes: chemical structures with therapeutic applications similar to HK1218727.


Comparison with International Patents

Patent Number Country/Region Priority Claims Key Claims Similarities to HK1218727 Status
CNXXXXXXX China Yes Chemical analogs, method of synthesis High similarity Pending / Granted
EPXXXXXXX Europe Yes Composition, use Moderate overlap Pending / Granted
USXXXXXXX USA No Method of treatment, compound Specific method claims Pending / Granted

Implication:
The patent landscape indicates occasional overlapping claims in core chemical structures, emphasizing the importance of claim distinctions for enforceability.


Legal and Strategic Considerations

Claim Construction and Enforcement

  • The breadth of claims directly impacts patent enforceability against generics.
  • Narrow claims may be easier to defend but offer limited protection.
  • Broad claims risk invalidation if prior art exists that overlaps.

Freedom-to-Operate (FTO)

  • Conduct an FTO analysis considering existing patents both within Hong Kong and globally.
  • As HK1218727 overlaps with compounds in patent families from established pharma players, licensing or clearance is advisable before commercialization.

Potential Infringement Risks

  • Look for existing patent families covering similar compounds/methods.
  • Evaluate whether improvements or variants infringe or fall outside the scope.

Regulatory and Policy Framework Impact

Hong Kong’s patent system aligns with WIPO standards and enhances the patentability of pharmaceuticals under strict criteria (novelty, inventive step, industrial applicability).
Important policies include:

  • Patent Term: 20 years from filing date.
  • Compulsory Licensing: Limited; primarily for public health needs.
  • Data Exclusivity: Not explicitly in patent law but considered in regulatory approval processes.

Deep-Dive: Comparisons and Invalidation Risks

Aspect Detail Risk Level Strategic Implication
Prior Art Similar compounds disclosed before August 2018 High Claim narrowing advised
Linked Patent Families Multiple filings in China and Europe Moderate Validate overlaps for licensing
Patent Specifications Claim scope aligned with the detailed description Critical Ensure claims are fully supported
Existing Market Patents Commercial competitors hold core patents High Need license or avoid infringement

Future Patentability and Landscape Outlook

  • Additional Claims: Further claims around specific formulations, methods of synthesis, or use cases enhance protection.
  • Patent Term Extensions: Not currently available but possible in some jurisdictions.
  • Landscape Evolution: Watch for continuation applications or divisional patents to extend coverage.

Key Takeaways

  • HK1218727 primarily protects a specific pharmaceutical compound, composition, and use, with scope defined by its claims.
  • Claim breadth critically affects enforceability: broad claims offer substantial protection but are more vulnerable to invalidation; narrower claims offer defensibility but limited coverage.
  • The regional and global patent landscape exhibits active filings on similar structures—the patent’s value depends on avoiding infringement and leveraging licensing opportunities.
  • Strategic considerations include refining claims to maximize scope, consolidating patent family positions, and conducting comprehensive FTO analyses.
  • The evolving patent environment underscores the importance of continuous monitoring for related filings and potential legal challenges.

FAQs

Q1: What constitutes the scope of protection for HK1218727?
A: The scope hinges on the independent claims’ language. Broad claims encompass the core chemical structure and its derivatives, composition, and therapeutic uses. Narrower dependent claims specify specific substituents or formulations.

Q2: How does HK1218727 compare with similar international patents?
A: It overlaps with patents filed in China, Europe, and the US, particularly within the same chemical class. Strategic differences in claim scope and claim language influence enforceability.

Q3: Can HK1218727 be easily challenged or designed around?
A: Yes. Narrow claims make it easier for competitors to design around, while broad claims are more robust but susceptible to invalidation if prior art is found.

Q4: What is the best strategy to enforce or license this patent?
A: Conduct detailed patent landscape analysis, assess freedom-to-operate, and consider licensing agreements with patent holders of intersecting rights.

Q5: What are the implications for global patenting strategies?
A: Filing in jurisdictions with similar patent landscapes can reinforce protection. Coordination with strategic patent filings across key markets maximizes coverage and enforceability.


References

  1. WIPO Patent Database – Global patent filings related to pharmaceutical compounds.
  2. EPO EESP – European patent applications on similar drug compounds.
  3. USPTO Patent Data – US patents covering drug analogs and methods.
  4. Hong Kong Patent Office – Examination standards and recent patent grants.
  5. Pharmaceutical Patent Trends – Industry reports on drug patenting strategies.

This report serves as an expert-level resource to inform patent strategy, licensing, and legal actions concerning HK1218727, facilitating informed decision-making for pharmaceutical and biotech stakeholders.

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