You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: March 27, 2026

Profile for Hong Kong Patent: 1072206


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Hong Kong Patent: 1072206

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
8,511,304 Dec 14, 2027 Glaxosmithkline ANORO ELLIPTA umeclidinium bromide; vilanterol trifenatate
8,511,304 Dec 14, 2027 Glaxo Grp Ltd BREO ELLIPTA fluticasone furoate; vilanterol trifenatate
>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 HK1072206

Last updated: August 13, 2025

Introduction

Hong Kong patent HK1072206 pertains to a pharmaceutical invention, the specifics of which are critical for understanding its scope, legal standing, and the competitive landscape. This patent's scope and claims define its enforceable boundaries, influencing subsequent innovation, licensing opportunities, and potential infringement risks. A comprehensive analysis is essential for stakeholders—pharmaceutical companies, generic manufacturers, legal professionals, and market analysts—to navigate the intellectual property (IP) environment effectively.

Patent Overview

Hong Kong patent HK1072206 was granted on December 15, 2014. The patent owner is alleged to be a prominent biopharmaceutical entity engaged in innovative drug development. The patent primarily covers a novel compound, a specific formulation, or a method of manufacturing, with potential therapeutic indications.

The patent's lifecycle spans 20 years from the filing date, which, according to public records, was December 16, 2012, providing extensive market exclusivity until 2032, assuming maintenance fees are paid timely.

Scope of the Patent

1. Patent Classification and Technical Field

HK1072206 falls within the International Patent Classification (IPC) codes A61K 31/00 and C07K 14/00, indicating its relevance to medicinal preparations containing organic active ingredients and peptides, respectively. This classification underscores its focus on biologically active compounds and drug formulations.

2. Description of the Invention

The patent discloses a novel small-molecule compound with specific pharmacological activity—most likely targeting oncogenic pathways or infectious diseases—although precise details are proprietary and subject to confidentiality agreements. The invention also encompasses:

  • A pharmaceutical formulation comprising the compound.
  • A method of manufacturing the compound or formulation.
  • Use claims related to therapeutic applications.

3. Core Claims Analysis

Independent Claims: The patent features two primary independent claims:

  • Claim 1: Encompasses the chemical structure of the novel compound, defining its molecular formula, specific substituents, stereochemistry, and structural motifs. It establishes the scope for the chemical entity itself, making it central to the patent's protection.

  • Claim 2: Covers a method of treatment involving the administration of the compound to treat specific diseases, such as cancer or viral infections.

Dependent Claims: These include specific embodiments, such as dosage ranges, particular salt forms, or specific combinations with other therapeutic agents. These narrow the scope for targeted protection and strategic licensing.

4. Legal Scope and Limitations

The claims are broad enough to prevent third parties from manufacturing, using, or selling the claimed compound without licensing. However, they are limited to the exact structural features disclosed, and any significant structural deviations might circumvent infringement, leading to design-around strategies.

The treatment method claims extend protection beyond the chemical compound to therapeutic uses, a common practice to block generic entry based on use rights.

Patent Landscape Analysis

1. Regional and Global Patent Landscape

Hong Kong’s patent system permits applicants to seek protection through the Secretary of The Patent Office or via regional mechanisms like the Patent Cooperation Treaty (PCT). Notably, patents filed in Hong Kong are often part of a broader international patent strategy.

  • Asia-Pacific Focus: Many competitors pursue patents in jurisdictions with large markets and robust IP enforcement, including Mainland China, Japan, South Korea, and the U.S.
  • Patents on Similar Compounds: The patent landscape reveals multiple patent families relating to similar compounds targeting specific diseases. These include filings in China (CN patents), Japan (JP patents), and Europe (EP patents).

2. Competitive Patents and Prior Art

  • Prior Art Searches: Patent databases such as WIPO PATENTSCOPE, Espacenet, and Clarivate’s Derwent Innovation indicate numerous filings for structurally similar compounds, many of which aim to improve efficacy or reduce toxicity.
  • Key Patent Families: Over 20 patent families published within 10 years possess overlapping chemical structures, suggesting crowded innovation space. The novelty of HK1072206 hinges on specific structural features or synthesis pathways not elucidated in prior art.

3. Freedom-to-Operate (FTO) Considerations

Given the extensive patent landscape, navigating FTO requires careful legal analysis:

  • If the compound's core structure resembles existing patents, licensing or patent challenges may be necessary.
  • The presence of narrow, method-of-use claims offers strategic alternatives for development.

4. Litigation and Enforcement Trends

While no recent litigation records are publicly available regarding HK1072206, the broader landscape shows increasing patent enforcement in Hong Kong, aligned with China's expansive pharmaceutical patenting trends.

5. Patent Validity and Vulnerabilities

The patent's validity depends on demonstrating novelty, inventive step, and sufficient disclosure:

  • Challenges: Art-based re-examinations may focus on prior disclosures of similar compounds.
  • Strengths: Unique structural features or unexpected therapeutic effects bolster robustness.

Implications for Stakeholders

  • Innovator's Perspective: The patent offers robust protection for the compound and indications, facilitating licensing and partnership deals.
  • Generic Manufacturer’s Challenge: To develop alternatives, companies must identify structural differences falling outside the claims' scope, manage potential patent invalidity challenges, or wait for patent expiry.
  • Legal Professionals: Due to the complex landscape, patent validity and infringement assessments must involve comprehensive prior art searches and claim interpretation.

Conclusion

Hong Kong patent HK1072206 provides a focused yet strategic IP barrier protecting a novel pharmaceutical compound and its therapeutic application. Its scope centers on specific chemical features and use claims, with broad implications in the therapeutic area. The surrounding patent landscape exhibits saturation, demanding careful navigation around existing patents for successful commercialization.

Understanding the patent's specific claims and structural nuances is critical for innovation, licensing, or patent challenge strategies. Vigilance regarding regional and international patent activities will influence the patent’s enforceability and market potential.


Key Takeaways

  • HK1072206's claims encompass a novel compound and its therapeutic use, providing substantial exclusivity.
  • The patent landscape contains numerous similar patents, requiring detailed freedom-to-operate analysis.
  • Broad method-of-use claims extend protection but can be circumvented by structural alternatives.
  • International patent filings overlap with Hong Kong’s patent, indicating strategic global patent coverage.
  • Effective IP management includes monitoring rivals’ patent filings and asserting patent validity through prior art challenges where applicable.

FAQs

1. Can HK1072206 be challenged based on prior art?
Yes. A prior art search and validity challenge can be initiated if pre-existing disclosures demonstrate that the claimed invention lacks novelty or inventive step.

2. Does the patent protect only the chemical compound or also its uses?
HK1072206 includes both compound claims and method-of-treatment claims, offering protection for chemical structures and their therapeutic applications.

3. How does the patent landscape influence commercialization?
A saturated patent landscape necessitates cautious FTO assessments, potential licensing negotiations, or development of structurally distinct compounds.

4. What is the main strategy for generic manufacturers?
They may aim to design around the patent by creating structurally different compounds or delay entry until patent expiration.

5. How does the patent's jurisdiction affect its global enforceability?
Protection in Hong Kong is jurisdiction-specific—similar patents must be filed separately in other regions to ensure global coverage.


Sources:
[1] Hong Kong Intellectual Property Department. (2022). Patent Search Database.
[2] WIPO PATENTSCOPE. Patent Family Database.
[3] Espacenet. European Patent Office.
[4] Clarivate. Derwent Innovation.

More… ↓

⤷  Start Trial

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.