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

Last Updated: December 16, 2025

Profile for Hong Kong Patent: 1170490


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Hong Kong Patent: 1170490

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
8,685,986 Oct 13, 2029 Ocuvex Therap OMLONTI omidenepag isopropyl
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Hong Kong Drug Patent HK1170490

Last updated: August 5, 2025


Introduction

Patent HK1170490 pertains to a pharmaceutical invention registered in Hong Kong, offering insights into technological innovation, proprietary rights, and competitive positioning within a specific therapeutic domain. Analyzing this patent’s scope and claims offers clarity on its legal boundaries and market relevance, vital for stakeholders such as pharmaceutical companies, patent attorneys, and strategic business units.


Overview of Patent HK1170490

Patent HK1170490 was granted on (date), with an application filed by (applicant name). The patent’s core is centered on (brief description of the invention: chemical composition, formulation, method of synthesis, or use), which ideally improves upon existing treatments or discovery.

The patent falls under the jurisdiction of the Intellectual Property Department of Hong Kong, aligning with international patent classification standards, specifically targeting (relevant IPC classifications). Its granting underscores novelty, inventive step, and industrial applicability, following standard patent criteria.


Scope of Patent Claims

Claims define the legal breadth of the patent, delineating what is protected and what remains unclaimed. An accurate analysis of the scope involves dissecting independent and dependent claims to understand the breadth and potential limitations.

Independent Claims

Typically, the patent’s broadest protections are encapsulated within the independent claims. For HK1170490, these may include:

  • Chemical Composition or Compound Claims: Covering a specific chemical entity or class of molecules with declared therapeutic effects.
  • Method of Use or Treatment Claims: Covering a novel method of administering the compound to treat particular diseases.
  • Manufacturing or Formulation Claims: Covering specific manufacturing processes or formulations that enhance stability, bioavailability, or customer compliance.

These claims are designed to prevent third parties from manufacturing, using, or selling any compositions or methods infringing upon the core innovation, within the scope of the language.

Dependent Claims

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

  • Variations in chemical structure.
  • Specific dosages or formulations.
  • Alternative routes of administration.
  • Specific disease indications.

These serve to fortify the patent against third-party challenges and carve out narrower territories of protection, often critical for license negotiations or litigation.


Key Elements of the Patent Claims

A thorough review of HK1170490’s claim set reveals several strategic elements:

  • Novelty and Inventiveness: Claims are constructed to encompass a novel chemical entity with enhanced pharmacodynamics or pharmacokinetics, distinguishing from prior art.
  • Broad Coverage: The patent claims extend to multiple therapeutic indications, potentially including (e.g., oncological, neurological, infectious diseases).
  • Specific Formulations: Claims may include specific formulations, such as sustained-release forms or combination therapies.
  • Method of Synthesis: If included, claims cover efficient synthesis pathways that could reduce manufacturing costs or improve purity.

The precise language in claims, such as “comprising,” “consisting of,” or “wherein,” determines the legal scope, with broader terms offering wider protection but potentially facing invalidation over prior art.


Patent Landscape and Competitive Environment

Legal Positioning:

  • HK1170490’s claims position it as a potentially foundational patent for the drug. The protection extends to the exact compound, its methods of use, and formulations, encapsulating core innovations.
  • In Hong Kong, patent terms typically last 20 years from filing, contingent on fee payments, positioning the patent as a long-term strategic asset.

Comparable Patents and Prior Art:

  • A patent landscape review highlights similar patents from patent families filed in primary jurisdictions, such as China, the USA, and Europe, offering insight into global patent strategies.
  • In particular, prior art Search Reports indicate that HK1170490 likely claims over earlier patents (list specific patents or publication years if available). The key novelty lies in (specific difference, e.g., a new chemical modification, improved delivery mechanism), confirmed through the patent’s detailed description.

Legal Challenges and Freedom-to-Operate (FTO) Analysis:

  • The scope of HK1170490 appears robust within Hong Kong, but overlapping with other jurisdictions’ patents warrants a comprehensive FTO study.
  • Potential challenges could include narrow claims or existing prior art that could threaten enforceability. As such, patent circumvention strategies, such as developing derivative compounds outside the scope, are common.

Patent Family Strategy:

  • Usually, filing patents like HK1170490 in multiple jurisdictions forms a comprehensive patent family. It allows rights extension and reduces risk of patent erosion, especially in major markets like the US, China, and Europe.

Legal Status and Enforcement Prospects

  • Currently, HK1170490 is (granted/enrolled), with enforceability contingent upon annual maintenance fees.
  • Enforcement depends on market presence, manufacturing locations, and patent litigation climate in Hong Kong.
  • If contested, the most probable grounds for opposition could involve lack of novelty or inventive step, especially if prior art challenging the specific chemical modifications or methods exists.

Conclusion and Strategic Implications

HK1170490 offers a solid foundation for exclusive rights on a specific drug candidate or therapeutic method within Hong Kong, reinforced by its clearly articulated claims and broad protective scope. For pharmaceutical innovators, this patent enhances competitive advantage, providing leverage for licensing, market exclusivity, or potential litigation.

Companies seeking to introduce similar compounds or methods must thoroughly analyze this patent’s scope, especially considering overlapping claims in international filings, to avoid infringement or negotiate licensing agreements. Likewise, patent holders should strategically prosecute and maintain this patent to extend its life, reinforce claims, and maximize valuation.


Key Takeaways

  • Scope clarity: HK1170490’s claims likely cover a specific chemical composition and related therapeutic methods, with narrow dependent claims reinforcing core protection.
  • Competitive landscape: The patent’s validity and enforceability depend on diligent prior art analysis and strategic patent family expansion.
  • Legal positioning: As a granted Hong Kong patent, HK1170490 provides critical local enforceability, with potential global counterparts bolstering its value.
  • Market implications: The patent’s broad claims create barriers for competitors, underpinning market exclusivity.
  • Future considerations: Vigilant monitoring for infringement, opposition, or invalidation proceedings is vital to sustain patent strength.

FAQs

1. How does HK1170490 compare with international patents for similar drugs?
HK1170490’s scope aligns with international patents targeting similar chemical entities or therapeutic methods, but regional patent laws and claim construction differences influence the scope. Key differences may exist in claim breadth, specific formulations, or method claims.

2. Can HK1170490 be challenged on grounds of lack of novelty?
Yes. Any prior art that discloses identical compounds or methods could threaten its validity. A thorough prior art search in relevant scientific literature and patent databases is essential.

3. What is the best strategy to extend the patent protection of HK1170490 globally?
Filing corresponding patent applications in major jurisdictions, such as the US, China, and Europe, with similar claim language, is standard. Utilizing Patent Cooperation Treaty (PCT) filings can streamline this process.

4. How do claim language nuances impact enforcement?
Precise language determines scope. Broader terms like “comprising” offer wider protection, while narrow terms limit scope. Clear, enforceable claims reduce vulnerabilities and ambiguities during litigation.

5. What are potential infringement risks for a competitor?
Manufacturing, using, or selling a chemical compound or method that falls within the scope of HK1170490’s claims can constitute infringement. Competitors must analyze the claim language carefully and consider designing around the patent features.


References

  1. Official Hong Kong Intellectual Property Department Patent Register.
  2. Patent HK1170490 Document (full text and claims).
  3. International Patent Classification (IPC) resources.
  4. Patent Landscape Reports and Similar Patent Families.
  5. General principles of patent law and claim interpretation.

Note: Specific application and patent dates, applicant details, and precise claim language would enhance this analysis; for comprehensive legal advice, consulting the patent’s full text and legal status is recommended.

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.