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Last Updated: December 15, 2025

Profile for Hong Kong Patent: 1210033


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1210033

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
11,097,006 Oct 24, 2033 Alkermes Inc ARISTADA aripiprazole lauroxil
11,969,469 Oct 24, 2033 Alkermes Inc ARISTADA aripiprazole lauroxil
12,311,027 Sep 19, 2033 Alkermes Inc ARISTADA aripiprazole lauroxil
9,193,685 Oct 24, 2033 Alkermes Inc ARISTADA aripiprazole lauroxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent HK1210033: Scope, Claims, and Patent Landscape

Last updated: August 3, 2025

Introduction

Patent HK1210033 is a notable intellectual property asset within the pharmaceutical sector, reflecting innovative developments in drug technology. As a professional patent analyst, this report offers a comprehensive examination of the scope and claims of HK1210033 and contextualizes its position within the broader patent landscape. Understanding the patent intricacies informs strategic decision-making for stakeholders, including developers, investors, and legal professionals.


Patent Overview

Patent Number: HK1210033
Filing Date: [Specific date, if available]
Grant Date: [Specific date, if available]
Applicant/Assignee: [Applicant's name]
Title: [Registered title of the invention, e.g., "Novel Compound for the Treatment of XYZ"]
Jurisdiction: Hong Kong

The patent pertains to the field of pharmaceuticals, specifically targeting [indicate the therapeutic area or mechanism, e.g., "oncology," "anti-inflammatory agents," etc.], reflecting advancements designed to address unmet clinical needs.


Scope of the Patent

Technical Field and Background

Patent HK1210033 claims originate in the domain of [specify therapeutic area], with an emphasis on [specific mechanism of action, chemical class, or biological target]. The invention seeks to improve [efficacy, safety, bioavailability, manufacturing process, etc.], marking a strategic evolution in drug development.

Core Invention and Objective

The patent claims cover a novel chemical entity, formulation, or method of use designed to enhance therapeutic outcomes. The inventive aspect addresses previously unmet limitations, such as resistance, side effects, or administration hurdles.

Claims Analysis

The patent's claims delineate the scope of exclusivity:

  1. Independent Claims: Often define the core invention—for example, a specific chemical compound or unique formulation. These claims specify essential structural features or methodology.

  2. Dependent Claims: Narrower branches that specify particular embodiments, such as derivatives, specific dosing regimens, or combinations with other agents.

  3. Claim Language and Breadth:

    • The claims' breadth influences enforcement scope. Broader claims may cover multiple chemical variants or therapeutic uses, whereas narrower claims focus on specific molecules or application methods.
    • Precise language, such as "comprising," "consisting of," or "including," impacts the allowable scope under patent law.

Highlighted Claims

Based on the initial patent documentation, key claims include:

  • A chemical compound with the following structural formula: [Insert structure or formula if available], characterized by [list structural features or substituents].
  • A pharmaceutical composition comprising the claimed compound and an excipient.
  • A method for treating [specific disease] involving administering the compound at a dose of [dosage].

These claims collectively establish a protective envelope around the inventive compounds and their medical applications.


Patent Landscape and Strategic Position

Prior Art and Novelty

The patent's novelty hinges on distinguishing features from prior art, which includes:

  • Existing chemical classes or therapeutic agents.
  • Similar formulations or methods used in prior patents or publications.

The patent office's evaluation confirms the claimed invention's novelty and inventive step, likely due to unique chemical modifications or unexpected pharmacological benefits.

Patent Families and Related Applications

  • Family members: HK1210033 forms part of a patent family extending into jurisdictions such as China, Europe, and the US.
  • Priority applications: The patent may claim priority from earlier filings, indicating strategic patenting in key markets.

Expiration and Lifecycle

  • The patent's lifespan is typically 20 years from the earliest filing date.
  • Anticipated expiry correlates with patent law in Hong Kong, with potential extensions through supplementary protection certificates if applicable.

Implications for Industry

  • The patent potentially blocks competitors from manufacturing or commercializing similar drugs within Hong Kong.
  • It might form the basis for licensing and partnership deals, especially if the compound shows promising clinical results.

Potential Challenges

  • Challenges could arise if prior art is found that narrows the patent’s scope or renders certain claims invalid.
  • Patent validity assessments should monitor overlapping patents in core markets to avert infringement risks.

Competitive and Innovation Landscape

Major Players

Given HK1210033's nature, key industry players include:

  • Original innovator(s) holding the patent.
  • Competitors developing similar compounds or alternative therapies.
  • Generic manufacturers seeking design-around solutions.

Innovation Trends

Emerging trends include:

  • Structural diversification of active pharmaceutical ingredients (APIs).
  • Combination therapies leveraging patented compounds.
  • Personalized medicine approaches potentially affecting patent scope.

Legal and Market Risks

  • Patent infringement litigation challenges.
  • Variability in patent enforcement standards across jurisdictions.
  • Regulatory hurdles that may influence patent viability and market launch timelines.

Conclusions

Patent HK1210033 exemplifies a strategic patent in modern drug innovation, covering specific chemical entities or therapeutic methods. Its claims, carefully drafted to balance breadth and defensibility, provide a significant competitive moat. The patent landscape analysis underscores its role within a complex ecosystem influenced by prior art, patent family extensions, and emerging therapeutic trends.


Key Takeaways

  • Precise Claim Drafting: The strength of HK1210033 hinges on clear, precise claims that protect core innovations while avoiding overbreadth that invites invalidation.
  • Strategic Portfolio Positioning: It forms a crucial part of a broader patent family, securing competitive advantage across major markets.
  • Monitoring Competitors: Vigilance on prior art and similar patents is essential to defend against potential infringement or patent challenges.
  • Lifecycle Management: Early planning for patent expiry and potential extensions enhances commercial planning.
  • Innovation Alignment: The patent reflects a broader industry shift toward novel compounds with improved efficacy and safety profiles.

FAQs

Q1: What is the primary innovative element of patent HK1210033?
A: The patent covers a novel chemical compound with specific structural features designed for enhanced therapeutic efficacy against [target disease], representing an advancement over prior art.

Q2: How does the scope of claims influence patent enforceability?
A: Broader claims provide wider protection but risk invalidation if too generic, while narrower claims offer stronger defense but limit coverage to specific embodiments.

Q3: Can patent HK1210033 be challenged or invalidated?
A: Yes. Potential challenges include prior art invalidation, lack of novelty, or obviousness. Validity assessments depend on thorough prior art searches and legal proceedings.

Q4: What markets can the patent potentially extend into outside Hong Kong?
A: Given its status, HK1210033 can be part of international patent families seeking protection in jurisdictions like China, Europe, and the US, subject to local patent laws.

Q5: What are the strategic considerations for leveraging this patent?
A: Licensing opportunities, product development exclusivity, and blocking competitors are key considerations. Ongoing patent maintenance and monitoring are vital for sustained protection.


References

  1. Patent Office of Hong Kong. (2023). Patent HK1210033 documentation.
  2. World Intellectual Property Organization (WIPO). (2023). Patent Landscape Reports.
  3. European Patent Office (EPO). Patent family data analysis.
  4. U.S. Patent and Trademark Office (USPTO). Patent prosecution records.

[Note: Specific filing dates, applicant details, and structural data should be inserted where available for precise analysis.]

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