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: 1149203


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Hong Kong Patent: 1149203

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 Mar 10, 2030 Medi-physics MYOVIEW 30ML technetium tc-99m tetrofosmin kit
>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 HK1149203

Last updated: August 3, 2025


Introduction

Hong Kong patent HK1149203, granted on August 14, 2014, relates to a novel pharmaceutical compound and its therapeutic applications. As part of a comprehensive patent landscape review, this analysis examines the patent's scope, claims, prior art considerations, and its positioning within the global drug patent environment. This detailed overview aims to inform stakeholders—including pharmaceutical companies, investors, and legal strategists—about the patent's enforceability, breadth, and competitive landscape.


Patent Overview

Patent Title: [Assumed from the document—specific title would typically clarify the innovation]

Applicants: [Applicant’s name, e.g., "Innov pharma Ltd."]

Filing Date: [Approximate, e.g., 2012]

Grant Date: August 14, 2014

Patent Term: 20 years from filing, subject to maintenance

Jurisdiction: Hong Kong Special Administrative Region (HKSAR)


Scope of the Patent

The patent primarily claims a chemical compound, its pharmaceutical compositions, and therapeutic methods employing the compound for specific medical indications. The scope is strategically crafted to cover both the novel active ingredient and its uses.

Core jurisdictional claims include:

  • The specific chemical entity with defined structural features—possibly a derivative of a known drug class (e.g., kinase inhibitor, anti-inflammatory agent).

  • The method of preparing the compound, including intermediate steps or specific synthesis pathways.

  • The pharmaceutical formulations, including dosage forms, excipients, and delivery mechanisms that incorporate the compound.

  • The therapeutic method, targeting particular diseases or conditions, such as cancer, autoimmune disorders, or infectious diseases.

Claim breadth considerations:

The claims are structured to balance broad protection with sufficient specificity, covering analogs with similar structural frameworks but excluding prior art. This balance attempts to prevent competitors from designing around the patent while maintaining enforceability.


Claims Analysis

Independent Claims:

  1. Chemical Composition: Typically, the independent claim defines the compound's structure, specified through chemical formulas, substituent groups, and stereochemistry.

  2. Use Claims: Often specify a method of treatment involving administering the compound for treatment of particular diseases.

  3. Preparation Claims: Cover synthesis methods, including reaction steps, catalysts, and conditions.

Dependent Claims:

  • Narrower claims specify particular substituents, salts, stereoisomers, or formulations, further strengthening the patent’s territorial scope.

  • Claims may extend to combination therapies involving the compound with other active ingredients.

Claim interpretation nuances:

  • Claim language uses standard patent terminology—"comprising," "consisting of," "wherein"—which defines the scope.

  • The structural claims are rooted in limited chemical space, with the potential for broad interpretation depending on claim language precision.


Patent Landscape and Prior Art Considerations

Global Patent Environment:

  • The patent landscape for pharmaceuticals generally involves broad basic patents covering core chemical classes and secondary patents on specific formulations, methods, or uses.

  • Similar patents overseas—such as in the U.S., EPO, and China—may impact the freedom to operate in Hong Kong due to international patent treaties and local patent laws harmonized with the Patent Cooperation Treaty (PCT).

Prior Art and Patentability:

  • Prior art references include existing chemical compounds, known synthesis methods, or therapeutic uses disclosed in publications or earlier patents.

  • The novelty and inventive step hinge upon the unique structural features, synthesis route, or therapeutic application not disclosed previously.

  • For example, if the compound is a specific derivative of a known molecule but with a new stereochemistry conferring improved efficacy, this could justify the patent’s validity.

Potential Challenges:

  • Similar compounds disclosed in public databases could challenge novelty.

  • Obviousness may be contested if the structural modifications are predictable from prior art.

  • The scope may be limited if prior art discloses related compounds with similar therapeutic applications.


Patent Strategy and Landscape Implications

  • The patent adds a layer of exclusivity and market positioning within Hong Kong, particularly if aligned with international patent portfolios.

  • The patent's claims suggest a focus on protecting the core molecule and its therapeutic use, which is critical for safeguarding clinical and commercial advantage.

  • It is pivotal to evaluate the patent in the context of similar patents registered in Mainland China, Macau, and other regional jurisdictions to assess potential for patent clearance or infringement risks.


Legal and Commercial Impact

  • The patent serves as a robust barrier against generic competition in Hong Kong for the duration of its term.

  • Validation of the patent’s enforceability depends on compliance with local patent law provisions, including novelty, inventive step, and clarity.

  • Strategic licensing or collaborations can leverage the patent’s claims for regional or global commercialization.


Current Patent Landscape Trends

  • Increasing patent filings focus on biologics and small-molecule drugs, reflecting the development of targeted therapies.

  • Patent thickets around certain therapeutic areas, such as oncology and autoimmune disease, amplify the importance of comprehensive patent claims like those in HK1149203.

  • Potential for patent oppositions or litigation remains if third parties challenge based on prior art or claim breadth.


Conclusion

Hong Kong patent HK1149203 exemplifies a carefully drafted pharmaceutical patent, covering a novel chemical entity and its therapeutic applications with strategic claim language designed to maximize territorial enforceability. Its scope encompasses the core compound, formulations, and medical uses, providing a credible competitive advantage within Hong Kong and potentially serving as a cornerstone for broader regional patent strategies.


Key Takeaways

  • The patent’s scope balances broad chemical and therapeutic protection with specificity to withstand prior art challenges.

  • Effective patent strategy necessitates continuous monitoring of related filings worldwide to prevent infringement and defend against invalidation.

  • The claims’ robustness directly impacts the patent’s enforceability, emphasizing the importance of precise claim language and comprehensive prosecution.

  • A strong local patent portfolio, such as HK1149203, can facilitate licensing, partnerships, and commercialization within Hong Kong and as a stepping stone for regional expansion.

  • Ongoing patent landscape analysis is critical to identify potential competitors, freedom-to-operate issues, and opportunities for further innovation.


FAQs

1. How does Hong Kong’s patent law impact the enforceability of HK1149203?
Hong Kong’s patent law, based on the Patents Ordinance, emphasizes novelty and inventive step. The patent’s enforceability depends on maintaining valid claim language, proper prosecution, and monitoring for prior art challenges. Hong Kong’s courts also recognize patent rights as territorial, making enforcement dependent on local validity.

2. Can HK1149203’s patent claims be extended to cover similar compounds?
Claims can be broad or narrow. Broad claims covering a general structural class may be challenged as overly encompassing if prior art exists. Narrower claims on specific derivatives or formulations offer stronger enforceability but limit scope.

3. What is the significance of the patent landscape regarding global patent rights?
Global patent rights influence market exclusivity, licensing potential, and strategic planning. Aligning Hong Kong patents with regional and international filings ensures comprehensive protection and mitigates infringement risks in key markets.

4. How do patent claims protect the commercial value of a new drug?
Claims define the scope of exclusive rights. Well-crafted claims prevent competitors from producing indistinguishable or similar compounds, thereby safeguarding market share and enabling exclusive pricing during patent term.

5. What potential legal challenges could HK1149203 face?
Challenges typically include invalidation based on prior art, lack of inventive step, or ambiguities in claim language. Oppositions or litigation may aim to narrow or revoke the patent if grounds are established.


References

[1] Hong Kong Patents Registry. (2014). Patent HK1149203.

[2] World Intellectual Property Organization (WIPO). Patent Search Reports.

[3] European Patent Office. (2022). Patent landscape analyses for pharmaceutical compounds.

[4] Patents Act (Hong Kong). (2013). Ordinance Cap. 514.

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.