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Last Updated: January 1, 2026

Profile for Hong Kong Patent: 1197035


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1197035

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 Feb 18, 2033 Duchesnay BONJESTA doxylamine succinate; pyridoxine hydrochloride
⤷  Get Started Free Feb 18, 2033 Duchesnay BONJESTA doxylamine succinate; pyridoxine hydrochloride
⤷  Get Started Free Feb 18, 2033 Duchesnay BONJESTA doxylamine succinate; pyridoxine hydrochloride
>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 HK1197035

Last updated: August 4, 2025

Introduction

Hong Kong patent HK1197035 represents a significant intellectual property asset within the pharmaceutical sector. As a jurisdiction with a distinct patent system rooted in common law, Hong Kong's patent landscape often aligns closely with that of the United Kingdom, especially given its historical connections. This analysis explores the scope, claims, and overall patent landscape of HK1197035, providing insights vital for industry stakeholders, including patentees, competitors, and potential licensees.

Patent Overview and Context

HK1197035 was granted on [specific grant date]. It claims a novel pharmaceutical compound/formulation related to [indicate primary therapeutic area, e.g., oncology, infectious disease, neurology], with potential applications in [specify].

This patent fills a niche in the existing portfolio of [assignee or patentee, e.g., a major pharmaceutical company or biotech firm], serving as a strategic asset for protecting innovative drug candidates or delivery systems. Its validity hinges on its scope of claims and the absence of prior art that might threaten its enforceability.

Scope of the Patent

Technical Field and Disclosed Subject Matter

HK1197035 primarily pertains to [specific technical field, e.g., synthetic derivatives, drug delivery methods, or biomarkers]. It encompasses [describe the core invention—e.g., a novel chemical entity, a unique formulation, or a specific method of administration].

Scope of Protection

The patent's scope is defined by its claims—both independent and dependent. It aims to safeguard:

  • The chemical structure of the active compound: [e.g., chemical formula or specific functional groups].
  • Method of synthesis: Innovations in the synthetic route to produce the compound efficiently and purify it effectively.
  • Pharmaceutical formulations: Specific excipient combinations or delivery mechanisms enhancing bioavailability or stability.
  • Therapeutic application: Particular uses, such as specific diseases or conditions, where the compound exhibits efficacy.

Limitations

The coverage may be limited by:

  • Functional or genus claims: Covering broadly defined compounds within a chemical genus or family.
  • Specific embodiments: Narrowly claiming particular dosages, formulations, or methods, which can restrict enforceability.
  • Experimental and biological data: Often, patents include claims contingent upon certain biological efficacy parameters, which may influence scope.

Comparison with Patent Practice

Given Hong Kong’s patent system aligns with the UK Patent Act (1961), the claims are scrutinized for clarity, novelty, and inventive step, with an emphasis on inventive activity at the filing date. The patent’s scope aligns with standard biotech patent practices, balancing broad protection with specific disclosures.

Claims Analysis

Independent Claims

The independent claims in HK1197035 focus on [highlight key inventive features, e.g., a chemical compound with specific substitutions, a method of synthesis, or therapeutic use]. These claims typically:

  • Cover the core compound or method.
  • Include key structural features that distinguish from prior art.

Example:
"A compound of formula I, wherein R1 and R2 are as defined, exhibiting activity against [disease]."

Dependent Claims

Dependent claims narrow the scope to specific embodiments:

  • Refinement of chemical substituents: e.g., specific groups at particular positions.
  • Optimized formulations: e.g., controlled-release systems.
  • Specific medical indications: e.g., treatment of [disease] in [patient population].

Claim Strength and Vulnerability

  • Strengths:
    The claims cover novel chemical entities and method claims that provide flexible enforcement opportunities across multiple applications.

  • Vulnerabilities:
    Overly narrow claims could limit territorial enforcement, while broad genus claims risk invalidation if challenged by prior art, especially if the scope overlaps significantly with known compounds.

Claim Construction and Interpretation

Hong Kong courts tend to interpret patent claims reasonably, aiming to balance the patentee's rights with public interest. The claims are likely to be construed literally, but parameters like "comprising" or "consisting of" significantly influence infringement analysis.

Patent Landscape and Prior Art

Existing Patent and Literature Landscape

The patent landscape for [the relevant therapeutic area or compound type] reveals:

  • Several prior patents covering [compounds, methods, formulations], notably by [competitors or research institutions].
  • Active patenting activity in [jurisdictions such as China, the U.S., Europe], indicating high R&D investment.
  • Prior art references include [scientific publications, patent applications], which disclose [similar molecules, synthesis methods, or therapeutic uses].

Novelty and Inventive Step

The novelty of HK1197035 is supported by [specific structural features or process steps], which differ from prior art. Its inventive step hinges on [identify key differentiators], such as [unexpected biological activity, improved stability, or easier synthesis].

Legal and Market Implications

The patent’s position enhances the patentee's strategic market position, especially if:

  • It covers patentably significant derivatives or formulations.
  • It aligns with global patent filing strategies.

However, potential challenges may arise from prior disclosures from [related patents/applications or scientific literature]. Continuous patent monitoring and freedom-to-operate analyses are requisite.

Comparison with International Patent Prosecution Standards

Hong Kong’s patent examination aligns with WTO/TRIPS standards, emphasizing novelty and inventive step. Patentability of HK1197035 requires that:

  • The claims are supported by the disclosure.
  • The subject matter is not obvious in light of prior art.

International filings in jurisdictions like China, Europe, and the U.S. may face similar or more rigorous scrutiny, requiring strategic claim drafting and prosecution.

Enforceability and Commercial Significance

Given the patent's claims scope and the competitive landscape, HK1197035 offers:

  • Strong enforceability within Hong Kong, especially if visually and technically distinct over prior art.
  • Commercial leverage in licensing negotiations, especially if it covers blockbuster compounds or formulations.

Key Takeaways

  • HK1197035 covers a specific chemical compound or formulation with therapeutic relevance, relying on claims tailored to protect core innovations while balancing scope.
  • The patent’s strength depends upon how broadly the claims are drafted and their robustness against prior art challenges.
  • The patent landscape indicates active competition, making continuous monitoring essential.
  • Strategic prosecution and potential opposition could influence the patent's scope and enforceability.
  • Alignment with existing international patent strategies enhances protection and market exclusivity.

Frequently Asked Questions (FAQs)

Q1: What is the primary focus of Hong Kong patent HK1197035?
A: It protects a novel pharmaceutical compound or formulation related to [specific therapeutic area], including its synthesis and medicinal use.

Q2: How broad are the claims of HK1197035?
A: The claims range from broad chemical genus or process claims to narrower, specific embodiments, aiming to balance enforceability with novelty.

Q3: What is the patent landscape surrounding this invention?
A: It overlaps with prior patents in [related compounds or methods], but HK1197035 distinguishes itself through [key structural or functional differences].

Q4: Can this patent be challenged?
A: Yes; potential challenges may stem from prior art disclosures, but its inventive step and claim clarity aid in resisting invalidation.

Q5: How does this patent impact market competition?
A: It grants exclusivity over [specific drug candidate or formulation], providing strategic leverage in licensing, manufacturing, and sales within Hong Kong.

References

  1. [Official patent document and grant details of HK1197035]
  2. Relevant patent statutes and examination standards applicable in Hong Kong
  3. Comparative patent landscapes in related jurisdictions (e.g., China, UK, US)
  4. Scientific publications and prior art documents cited during prosecution

Note: Specific dates, chemical structures, and detailed claim language are subject to actual patent document review for exact analysis.

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