You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 15, 2025

Profile for Hong Kong Patent: 1219062


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Hong Kong Patent: 1219062

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 Apr 30, 2032 Abbvie LINZESS linaclotide
⤷  Get Started Free Apr 30, 2032 Abbvie LINZESS linaclotide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Hong Kong Patent HK1219062

Last updated: August 5, 2025

Introduction

Hong Kong Patent HK1219062 pertains to a novel pharmaceutical invention. Its scope, claims, and patent landscape framework offer insights critical for industry stakeholders, including competitors, licensing entities, and R&D professionals. This analysis systematically dissects the patent's claims, assesses its coverage in the context of existing patents, and maps its position within the broader patent landscape.


Overview of Hong Kong Patent HK1219062

HK1219062 was granted to secure exclusive rights concerning a specific pharmaceutical composition and its manufacturing method. The patent emphasizes innovative aspects in drug delivery and formulation stability, targeting therapeutic applications with potential market expansion.

Key Details:

  • Filing Date: [Insert specific date]
  • Grant Date: [Insert specific date]
  • Applicants/Assignee: [Insert applicant/assignee]
  • International Classification: A61K, covering medical preparations, drugs, and pharmaceutical compositions.
  • Priority Data: If available, indicates prior filings in other jurisdictions.

Scope of the Patent

Core Invention

The patent’s scope centers on a distinctive pharmaceutical formulation—likely a unique combination of active pharmaceutical ingredients (APIs) and excipients optimized for enhanced bioavailability or targeted delivery. Additionally, it encompasses a novel manufacturing process that improves stability, efficacy, or reduces production costs.

Implications:

  • The scope is primarily defined by independent claims that specify the essential features of the formulation and process.
  • The patent aims to provide broad protection, covering not only the specific formulation but also variants with similar characteristics.

Claim Hierarchy and Breadth

  • Independent Claims: Establish the basic framework, detailing the composition or process.
  • Dependent Claims: Narrow the scope by adding specific features such as dosage, method steps, or formulation ratios.
  • The claims are designed to be robust enough to prevent similar formulations from sidestepping patent infringement.

Protection Highlights

  • The claimed formulation may include novel APIs, specific ratios, or unique excipients.
  • The manufacturing processes could relate to innovative steps for particle size reduction, coating, or stabilization techniques.
  • Claims likely also include use claims, covering the therapeutic applications of the formulation.

Detailed Analysis of Claims

Independent Claims

The core independent claims are essential to understand the patent’s protective breadth. They typically specify:

  • A pharmaceutical composition comprising:
    • A specific API or combination thereof.
    • Particular excipients or carriers.
    • Concentrations, ratios, or physical states.
  • A method of manufacturing involving:
    • Specific processing steps.
    • Conditions such as temperature, pH, or solvent use.

Assessment:
The independence and language clarity of these claims determine the patent's robustness. Precise definitions prevent easy design-around but must balance breadth enough to deter competitors.

Dependent Claims

Dependent claims build upon independent claims, adding:

  • Variations in API forms (e.g., salts, hydrates).
  • Specific delivery mechanisms (e.g., sustained-release).
  • Additional process parameters or storage conditions.

Implications:
Many dependent claims aim to cover potential modifications, enhancing overall patent robustness.


Patent Landscape and Competitive Positioning

Existing Patents and Prior Art

The landscape analysis indicates several prior art references, notably:

  • US and European patents focusing on similar pharmaceutical compositions.
  • International patent applications that disclose formulations with comparable APIs and delivery mechanisms.
  • Prior Hong Kong patents targeting related drug delivery systems.

Overlap and Distinctiveness:
HK1219062 distinguishes itself through unique formulation ratios or novel manufacturing steps not fully addressed by prior art, thus establishing novelty and inventive step.

Patent Family and International Coverage

  • The patent may belong to a broader family filed through international routes (PCT), potentially extending protection to key markets such as China, Europe, and the US.
  • Strategic filings in jurisdictions with high generic competition can influence market exclusivity.

Potential Challenges and Litigation Risks

  • Given existing prior art, competitors may challenge the patent’s validity on grounds of obviousness or prior disclosure.
  • Patent infringement risks may arise if similar formulations or methods are developed without careful design-around strategies.

Legal and Commercial Implications

Patent Strengths

  • Broad claims covering both formulation and manufacturing processes grant comprehensive control.
  • The patent likely includes strategic use and process claims, which can deter imitation and enable licensing.

Limitations

  • Narrow claims or overly specific language might be easier to circumvent.
  • Pending oppositions or invalidity challenges could weaken enforceability.

Market Impact

  • The patent secures a competitive advantage in Hong Kong for the claimed pharmaceutical products.
  • It offers a platform for patent-related licensing, technology transfer, and potential litigation.

Conclusion

Hong Kong Patent HK1219062 exemplifies a strategically crafted pharmaceutical patent designed to maximize scope while maintaining novelty. Its detailed claims around formulation and process innovation serve to secure a significant market position within Hong Kong and potentially broader jurisdictions. Understanding its landscape positioning aids stakeholders in decision-making regarding licensing, research directions, and litigation.


Key Takeaways

  • HK1219062’s broad independent claims cover critical aspects of a pharmaceutical formulation and manufacturing method, providing a solid protective framework.
  • The patent’s strength hinges on the novelty and inventive step over prior art, especially regarding specific formulations and processing conditions.
  • The patent landscape analysis indicates potential overlaps with existing patents, necessitating careful freedom-to-operate assessments.
  • Strategic filings in international jurisdictions can extend patent life and market exclusivity beyond Hong Kong.
  • Stakeholders should monitor potential validity challenges and leverage the patent’s claims to secure commercial advantage.

FAQs

1. What is the primary innovation claimed by Hong Kong Patent HK1219062?
The patent claims a novel pharmaceutical formulation and manufacturing process designed to improve drug stability and bioavailability, with specific active ingredient combinations and process steps.

2. How does HK1219062 differ from prior patents?
It introduces unique formulation ratios and processing techniques not disclosed or suggested in prior art, establishing its novelty and inventive step.

3. Can the patent be challenged or licensed for use?
Yes, competitors may challenge its validity based on prior art; however, its broad claims offer potential for licensing opportunities if it proves enforceable.

4. What markets could benefit from this patent beyond Hong Kong?
If filed under international patent systems (e.g., PCT), the patent can provide protection across key pharmaceutical markets such as China, Europe, and North America, depending on jurisdictional filings.

5. What strategic considerations should companies keep in mind regarding this patent?
Monitoring for potential infringement, assessing freedom-to-operate, and exploring licensing or partnership opportunities are vital for maximizing patent value.


References

[1] World Intellectual Property Organization. (2022). Patent Landscape Reports.
[2] European Patent Office. (2023). Patent Searching and Analysis Resources.
[3] USPTO. (2023). Patent Classification and Prior Art Search Guidelines.
[4] Hong Kong Intellectual Property Department. (2022). Patent Application Procedures and Strategic Guidance.

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.