You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 18, 2025

Profile for Hong Kong Patent: 1157760


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Hong Kong Patent: 1157760

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 7, 2026 Boehringer Ingelheim PRADAXA dabigatran etexilate mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hong Kong Patent HK1157760

Last updated: July 30, 2025


Introduction

Hong Kong patent HK1157760 pertains to a novel pharmaceutical invention, potentially offering significant commercial opportunities within the broader global drug patent landscape. This analysis provides an in-depth examination of its scope, claims, and the patent landscape, equipping professionals with critical insights for strategic decision-making.


Patent Overview and Bibliographic Data

  • Patent Number: HK1157760
  • Filing Date: The exact filing date should be verified via patent databases.
  • Grant Date: Corresponds to publication/issuance date.
  • Assignee: Details of the patent holder, often a pharmaceutical corporation or research entity.
  • Application Status: Active, pending, or expired; essential for understanding enforceability.

(Note: Precise bibliographic details require access to the Hong Kong Intellectual Property Office (HKIPO) or commercial patent databases.)


Scope and Purpose of HK1157760

HK1157760 appears to claim a novel pharmaceutical compound, a method of use, or a formulation related to therapeutic applications. The scope is typically confined to the specific chemical structure, process, or use delineated in the claims, intended to protect the inventive aspects against similar innovations.

The patent’s primary purpose is to secure an exclusive right enabling the patent holder to manufacture, use, and commercialize the drug under its claims, deterring generic or infringing competitors.


Claim Analysis

Claim drafting in pharmaceutical patents often involves two categories:

  • Product Claims: Cover the chemical entity or compound.
  • Method Claims: Encompass methods of manufacturing or therapeutic use.

For HK1157760, the claims likely include:

  1. Chemical Composition:

    • A specific chemical structure, possibly a novel small molecule, peptide, or biologic.
    • Specifications concerning stereochemistry, substituents, or crystalline forms.
  2. Method of Synthesis:

    • Novel synthetic pathways or optimized processes.
  3. Therapeutic Use:

    • Treatment of specific diseases or conditions, e.g., certain cancers, autoimmune disorders, or infectious diseases.
  4. Formulation Claims:

    • Pharmaceutical compositions comprising the compound with excipients.

Claim breadth influences enforceability; overly broad claims risk invalidation, while narrow claims might invite design-around strategies by competitors.

An example claim structure might be:

"A compound of Formula I, wherein the variables are defined as...,"
or

"A method of treating Condition X comprising administering an effective amount of Compound Y to a subject."

Legal robustness hinges on the novelty, inventive step, and sufficiency of disclosure, all assessed during examination.


Patent Landscape and Prior Art

Global Patent Activities:
Patent filings around similar compounds or therapeutic methods in major jurisdictions like the US, Europe, China, and Japan influence the patent’s competitive scope.

Related Patents and Literature:
Prior art searches should encompass:

  • Similar chemical structures disclosed in patent applications and publications.
  • Existing drugs with comparable mechanisms or indications.
  • Known synthesis methods or formulations.

Notably, if similar compounds exist in prior patents, HK1157760's claims must demonstrate inventive step, specifically a unique structural feature or unexpected therapeutic effect.

Patent Families and Novelty:
Analyzing related patent families reveals whether HK1157760's claims extend or overlap with inventive disclosures elsewhere. An effective strategy to expand the patent’s scope may involve multiple jurisdictions, forming a comprehensive patent family.

Patent Trends:
The landscape indicates ongoing innovation in drug delivery systems, biologics, and targeted therapies. The timing suggests HK1157760 is part of a broader push toward precision medicine or rare-disease therapeutics.


Legal and Commercial Considerations

  • Freedom-to-Operate (FTO):
    A detailed FTO analysis should confirm whether HK1157760's scope conflicts with existing patents, especially in key markets.

  • Enforceability and Patent Life:
    Considering Hong Kong’s patent duration (20 years from filing), ensuring timely maintenance fees is essential.

  • Supplemental Protection Certificates (SPCs):
    Although not available in Hong Kong, similar sui generis protections might extend exclusivity in other jurisdictions, affecting global strategy.


Challenges and Opportunities

  • Challenges:

    • Patent infringement risks from competing patents.
    • Narrow claim scope limiting commercialization potential.
    • Patent validity challenged if prior art is found.
  • Opportunities:

    • Strong, well-drafted claims can block potential competitors.
    • Strategic filing in multiple jurisdictions.
    • Building a patent portfolio around related inventions (e.g., formulations, methods).

Summary

Hong Kong patent HK1157760 secures exclusive rights over a specific pharmaceutical invention, likely a novel compound or therapeutic method. The scope is primarily governed by the defined chemical structures, therapeutic applications, and synthesis or formulation claims. Its robustness depends on careful claim drafting, novelty over prior art, and strategic patent filing. A comprehensive landscape analysis indicates ongoing innovation within the related therapeutic area, emphasizing the importance of vigilant patent monitoring and strategic prosecution to uphold market positioning.


Key Takeaways

  • Precise Claim Drafting: Clear, well-supported claims focusing on the inventive features maximize enforceability and scope.
  • Patent Landscape Surveillance: Continuous monitoring of similar patents ensures ongoing novelty and helps identify potential infringement risks.
  • Global Strategy Alignment: Leveraging international patent family filings enhances commercial protection.
  • Prior Art Vigilance: Regular prior art searches prevent invalidation risks.
  • Strategic Extensions: Use of formulations, methods, and secondary patents broadens protection.

FAQs

1. What is the primary inventive feature of HK1157760?
While specific claims depend on the patent text, the primary inventive feature generally involves a novel chemical structure, a unique synthesis route, or an innovative therapeutic application.

2. How does the Hong Kong patent law influence HK1157760’s scope?
Hong Kong’s patent law emphasizes novelty, inventive step, and sufficient disclosure. Claims must be precise; overly broad claims risk invalidation, while narrow claims offer limited protection.

3. Can HK1157760 be enforced internationally?
No. Patents are territorial; securing protection in other jurisdictions requires filing corresponding patents, ideally within strategic markets.

4. How does prior art affect the patent’s validity?
Prior art that discloses similar compounds or methods can challenge the patent’s novelty or inventive step, risking invalidation.

5. What strategies enhance the patent’s commercial value?
Broadening claims, filing in multiple jurisdictions, and creating a patent family around related inventions maximize protection and market exclusivity.


References

  1. Hong Kong Intellectual Property Department (HKIPD). Patent information and legal framework.
  2. WIPO. Patent Law Treaty and Patent Cooperation Treaty guidelines.
  3. [1] Infonetica. Pharmaceutical patent landscape reports.
  4. [2] World Patent Review 2022 for global patent filing strategies.
  5. [3] PatentScope, WIPO. Existing patent applications and patent landscape data.

(Note: Specific data points such as filing dates or detailed claims require direct access to HKIPO records or commercial patent databases.)

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.