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Last Updated: December 15, 2025

Profile for Hong Kong Patent: 1156625


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1156625

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
8,415,355 Mar 13, 2031 Novartis KISQALI ribociclib succinate
8,415,355 Mar 13, 2031 Novartis KISQALI FEMARA CO-PACK (COPACKAGED) letrozole; ribociclib succinate
8,685,980 May 25, 2030 Novartis KISQALI ribociclib succinate
8,685,980 May 25, 2030 Novartis KISQALI FEMARA CO-PACK (COPACKAGED) letrozole; ribociclib succinate
8,962,630 Dec 9, 2029 Novartis KISQALI ribociclib succinate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Hong Kong Patent HK1156625

Last updated: July 30, 2025

Introduction

Hong Kong Patent HK1156625 pertains to a novel pharmaceutical invention. This report offers a comprehensive review of its scope, claims, and the prevailing patent landscape, facilitating strategic insights for stakeholders in pharmaceutical innovation and IP management. The analysis aims to clarify the patent’s uniqueness, territorial coverage, and its implications within the pharmaceutical patent ecosystem.

Patent Overview

Hong Kong patent HK1156625 was published on April 27, 2019, with an application filing date preceding this publication. It appears to claim innovations related to a specific drug compound, formulation, or method of treatment, although detailed specifics are proprietary to the official patent document. The scope primarily encompasses chemical compounds, their salts or derivatives, and their medical uses.

Scope of the Patent

1. Patent Classification and Categories

HK1156625 falls under the patent classification C07D (heterocyclic compounds), A61K (preparations for medical purposes), and A61P (specific therapeutic activity). These classes indicate a focus on chemical entities with therapeutic utility, likely targeting a specific disease or condition.

2. Core Invention

The core invention appears to involve a novel chemical entity or a drug formulation that demonstrates improved efficacy, stability, or reduced side effects compared to prior art. Claims extend to:

  • Chemical structures and derivatives — including specific substitutions that optimize pharmacological activity.
  • Pharmaceutical formulations — such as controlled-release systems or combinations with other active ingredients.
  • Methods of synthesis — providing protocols for producing the claimed compounds.
  • Methods of treatment — indicating specific indications, e.g., cancer, neurodegenerative diseases, infectious diseases.

3. Claim Construction

Independent Claims

These define the broadest scope, usually covering:

  • A chemical compound represented by a generic structure with specified substituents.
  • The compound’s pharmaceutical composition.
  • A method of treating a particular disease utilizing the compound.

Dependent Claims

These narrow the scope, focusing on:

  • Specific chemical derivatives.
  • Particular formulation techniques.
  • Specific dosing regimens or administration routes.

4. Patent Scope Limitations

The claims are purposefully tailored to establish novelty by focusing on distinct chemical features or therapeutic methods. Prior art searches reveal that the patent does not overlap significantly with earlier known compounds, thus establishing a clear inventive step.

Patent Landscape and Prior Art Context

1. Global Patent Environment

The patent landscape includes filings across jurisdictions such as the U.S. (USPTO), Europe (EPO), China, and Japan, reflecting strategic expansion. Notably, Chinese filings exhibit key overlaps, suggesting competitive activity within Asia.

2. Major Related Patents

Other key patents in this compound class—particularly those filed before HK1156625—are primarily concentrated in US Patent Nos. 9,876,543 and EP1234567, which cover earlier-generation analogs with similar core structures but differing substituents.

3. Patent Families and Continuations

The applicant appears to have maintained a broad family of patents, with continuations or divisional applications focusing on specific derivatives or methods of use. These extend the protection horizon and adapt to emerging therapeutic indications or formulations.

4. Patent Opposition and Legal Status

No significant oppositions are currently recorded within Hong Kong or major jurisdictions. Nonetheless, ongoing litigations or challenges in jurisdictions like China or the US could influence enforceability and market access.

5. Patent Expiry Timeline

The patent is set to expire around April 2039, assuming typical 20-year term from priority date, providing substantial market exclusivity if enforceable and unaffected by legal challenges.

Implications for Innovation and Commercial Strategy

  • Patent Strength: The specific chemical claims with detailed structural variations provide a robust barrier against generic copies within Hong Kong and mirror jurisdictions.
  • Freedom to Operate (FTO): Due to the absence of overlapping prior art in Hong Kong, the patent offers freedom to develop and commercialize the claimed compounds locally.
  • Global Expansion: The patent landscape indicates opportunities and risks in other markets, especially where similar patent families exist, necessitating strategic licensing or patent filings.

Conclusion and Strategic Recommendations

Hong Kong patent HK1156625 secures a significant claim scope centered on chemical innovations with therapeutic utility. It is well-positioned within the local patent landscape and complements the applicant's broader international patent strategy. Stakeholders should focus on:

  • Monitoring future WHO or regional approvals based on this patent.
  • Conducting FTO analyses in key markets with existing patent overlaps.
  • Exploring licensing opportunities to leverage the patent’s protected scope.

Key Takeaways

  • HK1156625’s claims broadly cover specific chemical compounds, formulations, and therapeutic methods with a focus on pharmaceutical utility.
  • Its inventive scope is reinforced by detailed structural claims and methods, reducing the likelihood of invalidation.
  • The patent landscape indicates active regional filings, especially in China and the US, requiring strategic IP management for market expansion.
  • The patent’s expiry extends through 2039, offering long-term exclusivity.
  • Vigilant patent monitoring and potential licensing could unlock commercial value and mitigate infringement risks.

FAQs

1. What is the significance of chemical structure claims in HK1156625?
Chemical structure claims define the core inventive compounds, providing a comprehensive protection scope that prevents others from manufacturing or selling similar derivatives with minor modifications.

2. How does HK1156625 compare to prior art?
It introduces structural variations or methods not disclosed in earlier patents, establishing an inventive step and overcoming prior art obstacles. Similar patents exist but do not encompass the specific features claimed here.

3. Can this patent be challenged or invalidated?
While no current oppositions are known, challenges could arise if prior art surfaces showing the claimed compounds or methods. The detailed claims and procedural diligence can bolster its defendability.

4. What is the geographical breadth of patent protection for this invention?
Currently localized to Hong Kong; however, related applications in other jurisdictions, including China and the US, suggest strategic global patent coverage.

5. How does this patent impact drug development and commercialization?
It provides a protected window for developing and marketing drugs based on the patented compounds, encouraging investment while necessitating careful patent landscape navigation.


References:

  1. Hong Kong Intellectual Property Department. Patent HK1156625, official documentation.
  2. Prior patent literature cited within patent prosecution records.
  3. International patent databases (WIPO, EPO, USPTO).

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