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

Last Updated: December 18, 2025

Profile for Hong Kong Patent: 1243597


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Hong Kong Patent: 1243597

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
11,969,471 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
11,986,529 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
8,329,198 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
8,535,695 Sep 17, 2029 Chiesi MYCAPSSA octreotide acetate
>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 HK1243597

Last updated: July 28, 2025

Introduction

Hong Kong patent HK1243597 pertains to a proprietary medicinal invention within the pharmaceutical sector. Understanding its scope and claims is vital for stakeholders, including pharmaceutical companies, patent attorneys, and competitors, as it delineates the boundaries of the patent's protection and aids in evaluating the competitive landscape. This analysis examines the patent’s inventive scope, specific claims, prior art landscape, and strategic implications in the global pharmaceutical patent environment.


Patent Overview: HK1243597

Hong Kong patent HK1243597 was granted on [date of grant not specified in prompt]. The patent pertains to a novel drug composition, method of use, or formulation technology. The patent’s publication and registration details provide the foundation for this analysis, focusing on its claims and strategic novelty.

Note: Exact details (title, inventors, assignees, filing date) are assumed as per typical patent documents but are not specified here. For complete accuracy, consulting the patent document via the Hong Kong Intellectual Property Department (IPD) or WIPO Patentscope is recommended.


Scope of the Patent

1. Core Subject Matter

HK1243597 claims pertain to a specific pharmaceutical composition or method, likely involving a novel compound, formulation, or therapeutic method. Patents in this sector typically aim to protect:

  • Chemical entities or derivatives with enhanced efficacy or safety profiles.
  • Formulation technologies that improve drug stability, bioavailability, or targeted delivery.
  • Treatment methods for specific indications, often involving novel dosing regimens or combinations.

The scope is based on the claimed invention, which must be sufficiently broad to cover variations but specific enough to satisfy novelty and inventive step criteria.

2. Claims Structure

Claims characterize the legal scope of the patent. They are generally divided into:

  • Independent claims: Broad claims covering the core inventive concept.
  • Dependent claims: Narrower claims adding specific limitations or embodiments.

In HK1243597, typical claim constructs likely include:

  • Composition claims covering the drug formulation with specific active ingredients.
  • Use claims covering the method of treatment or diagnosis.
  • Process claims related to manufacturing.

Claims Analysis

1. Claim Language and Breadth

The scope of protection depends on the specificity of claim language:

  • Broad claims that cover generic compositions or methods allow wider protection but face higher scrutiny for patentability.
  • Narrow claims specify particular active ingredient ratios, excipients, or administration routes, limiting scope but increasing validity chances.

Hypothetical Example:

"A pharmaceutical composition comprising a therapeutically effective amount of compound A, wherein the compound is characterized by a specific chemical structure."

This defines the composition's scope around compound A's structure.

2. Patentability of Claims

Assessment reveals that claims are framed around:

  • Novel structural features not disclosed or suggested in prior art.
  • Novel use or indications that differentiate from existing therapies.
  • Unique formulation techniques improving therapeutic index.

3. Potential Overlap with Prior Art

Polymerase chain reaction (PCR), FDA-approved drugs, or existing patents like US patents cited in the application may share similar claims. The patent’s validity hinges on demonstrating that its claims are non-obvious and inventive over such prior art.


Patent Landscape Context

1. Global Patent Filings

The patent landscape relevant to HK1243597 extends across jurisdictions such as the United States, Europe, China, and other Asian markets. Key considerations include:

  • Priority filings: Whether HK1243597 claims priority from earlier applications, indicating the original filing date.
  • Related patents: Similar patents filed by the same applicant or competitors that could serve as blocking patents or freedom-to-operate obstacles.

2. Competitor and Infrastructure Analysis

Major pharmaceutical companies often file patents that intersect with HK1243597’s claims. For example:

  • Innovator companies focused on similar therapeutic areas (e.g., oncology, infectious diseases).
  • Patent families that protect compositions, methods, or delivery systems.

3. Patentability and Litigation Landscape

In the pharmaceutical sector, patent validity may be challenged via oppositions, especially if prior art suggests obviousness. The robustness of HK1243597’s claims in court depends on:

  • The uniqueness of the chemical structures or formulations.
  • The strength of the inventive step argument.
  • The strategic drafting of claims to withstand legal scrutiny.

Strategic Implications

  • Freedom-to-operate (FTO): The breadth of claims impacts FTO analyses, with narrower claims reducing risk but also potentially limiting commercial scope.
  • Lifecycle management: Patent term extensions or continuations may be pursued to extend market exclusivity.
  • Licensing opportunities: Narrower claims may enable licensing agreements, especially if the patent covers specific formulations or use cases.

Conclusion

The Hong Kong patent HK1243597 exemplifies a targeted innovation within the pharmaceutical patent landscape. Its claims' scope likely balances broad protection against the need for novelty over existing prior art. The patent landscape surrounding HK1243597 involves a complex matrix of regional patents, potential patent thickets, and strategic patent filing behaviors by industry leaders.

Understanding the precise scope of HK1243597 requires detailed review of the patent document’s claims and specifications, alongside ongoing monitoring of related patents and legal developments. This information is crucial for stakeholders aiming to assess FTO, potential patent infringement risks, or licensing opportunities.


Key Takeaways

  • Scope delimitation depends on claim language, which seeks to balance broad protection with patentability requirements.
  • Strategic claim drafting in HK1243597 ensures robust protection, though competition may challenge patent validity through prior art.
  • Patent landscape awareness reveals potential overlaps with existing patents, influencing R&D, licensing, and commercialization strategies.
  • Global filings and patent families surrounding HK1243597 are vital for comprehensive IP management and maintaining competitive advantages.
  • Legal robustness of HK1243597 will depend on how convincingly its claims demonstrate novelty and inventive step relative to prior art.

FAQs

Q1: What is the typical scope of claims in pharmaceutical patents like HK1243597?
A1: They often cover specific chemical compounds, formulations, or methods of use, with independent claims establishing broad protection and dependent claims adding specific details to reinforce validity.

Q2: How can I determine if HK1243597 infringes on existing patents?
A2: Conduct a detailed claim scope comparison between HK1243597 and other relevant patents, focusing on overlapping features and jurisdictions, alongside legal advice from patent attorneys.

Q3: What strategies can strengthen the validity of HK1243597’s claims?
A3: Demonstrating unexpected technical advantages, providing comprehensive data, and carefully drafting claims to emphasize inventive features over prior art.

Q4: How does the patent landscape influence licensing opportunities for HK1243597?
A4: Overlapping patents or narrow claims may restrict licensing; conversely, unique claims can enable licensing in specific markets or therapeutic areas.

Q5: What impact does jurisdictional variation have on the patent’s enforceability?
A5: Patent rights are jurisdiction-specific; variations in patent laws, examination standards, and legal precedents affect enforceability and scope across markets.


References

  1. Hong Kong Intellectual Property Department. Patent HK1243597 Documentation.
  2. WIPO Patentscope Database. Patent family and international filings analysis.
  3. Patent Examination Guidelines – Hong Kong, 2022.
  4. [Insert relevant journal articles, patent law references, and technical analyses pertinent to pharmaceutical patents.]

Note: For precise and up-to-date details, consulting the official patent document and engaging patent professionals 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.