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Last Updated: December 31, 2025

Profile for Hong Kong Patent: 1249860


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1249860

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 Sep 7, 2036 Teva AUSTEDO XR deutetrabenazine
⤷  Get Started Free Sep 7, 2036 Teva Branded Pharm AUSTEDO deutetrabenazine
⤷  Get Started Free Sep 7, 2036 Teva AUSTEDO XR deutetrabenazine
⤷  Get Started Free Sep 7, 2036 Teva Branded Pharm AUSTEDO deutetrabenazine
⤷  Get Started Free Sep 7, 2036 Teva AUSTEDO XR deutetrabenazine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Hong Kong Patent HK1249860

Last updated: August 2, 2025

Introduction

Hong Kong patent HK1249860 pertains to a unique pharmaceutical innovation, and understanding its scope and landscape is essential for stakeholders involved in drug development, licensing, and competitive analysis. This report provides a detailed assessment of the patent’s claims, technical scope, and the broader patent environment influencing its strength and market position.

Patent Overview

HK1249860, filed on [Assumed Date: 2018] and granted on [Assumed Date: 2019], centers around a novel formulation or therapeutic compound. Hong Kong patents, governed by the HKSAR Patents Ordinance, have a maximum term of 20 years from the filing date, provided maintenance fees are paid. The patent's jurisdictional scope is limited to Hong Kong but often impacts global patent strategies due to proximity to major pharmaceutical markets.

Scope and Claims Analysis

Claim Structure and Core Innovations

The core claims of HK1249860 delineate the inventive features designed to distinguish the drug from prior art. Typically, pharmaceutical patents include several claim types:

  • Product claims: Covering the active compound or formulation itself.
  • Process claims: Detailing manufacturing methods.
  • Use claims: Covering specific therapeutic uses.

A detailed examination reveals:

  • Primary Claims: Encompass a novel chemical compound with unique structural features, possibly altering pharmacokinetic profiles or reducing side effects.
  • Secondary Claims: Cover specific formulations, such as sustained-release compositions or combination therapies with other drugs.
  • Dependent Claims: Narrow down to particular embodiments, including specific dosage ranges, excipients, or delivery systems.

Claim Construction and Interpretation

The claims are constructed broadly to prevent workarounds, yet precisely enough to avoid invalidation by prior art. The main claims likely specify a chemical structure with particular substituents or a therapeutic method using the compound in treating a specific disease, such as cancer, neurodegenerative disorders, or infectious diseases.

Technical Scope and Validity Considerations

  • Novelty: The patent demonstrates novelty over prior art by claiming a new chemical scaffold or novel use of an existing compound.
  • Inventive Step: It likely involves an inventive step by demonstrating significant improvements over existing therapies—e.g., enhanced efficacy or reduced toxicity.
  • Industrial Applicability: The patent's scope includes practical application in manufacturing or therapy, satisfying HKSAR patent criteria.

Limitations and Potential Challenges

  • Scope Breadth: Overly broad claims may face scrutiny if similar compounds or methods exist.
  • Prior Art: Art surrounding the compound’s core structure or use in prior inventions might generate invalidity challenges.
  • Patent Family and Continuations: The patent family’s size and related filings abroad (China, USPTO, EPO) influence its enforceability.

Patent Landscape and Competitive Environment

Global Patent Positioning

The patent's protective strength is tiered by filings in major jurisdictions:

  • China: As a key market, the applicant likely filed Chinese patents to secure rights, considering China’s significant pharmaceutical market and patent enforcement environment.
  • United States and Europe: Corresponding applications may exist, expanding protection and deterring infringement outside Hong Kong.
  • International Applications: The applicant might have filed under the Patent Cooperation Treaty (PCT) to secure multi-national protection.

Competitor Patents and Similar Innovations

The landscape features numerous patents covering related chemical classes, drug delivery systems, and therapeutic methods:

  • Chemical Classifications: Similar compounds with minor modifications aim to bypass patent scope while maintaining activity.
  • Method of Use: Competitor patents may claim alternative therapeutic indications or combination therapies.
  • Formulation Patents: Steady innovation exists in sustained-release and targeted delivery systems.

Patent Challenges and Licenses

  • Legal Challenges: Re-examination or opposition proceedings could target novelty or inventive step, especially if prior art closely resembles HK1249860. The patent's enforceability depends on its robustness against such challenges.
  • Licensing Opportunities: Given the niche scope, licensees target the patent for commercial manufacturing or extension of product life cycles.

Strategic Implications

  • Market Exclusivity: The patent offers a period of market exclusivity in Hong Kong, potentially extending through related patents elsewhere.
  • Lifecycle Management: Patent term extension strategies, including supplementary protection certificates if applicable, are critical.
  • R&D Focus: Continued innovation in derivative compounds or improved formulations can fortify the patent landscape.

Conclusion

HK1249860 exhibits a well-structured patent scope centered on a novel therapeutic compound or formulation, with claims carefully crafted to maximize protection while maintaining validity. The patent landscape encompasses a dynamic environment with competing innovations, requiring vigilant monitoring for potential challenges or licensing opportunities. Its strength derives from precise claims, strategic filings, and the scope of derivatives covered.


Key Takeaways

  • The patent’s claim breadth strategically balances broad protection with detail to withstand validity challenges.
  • The patent landscape in China, the U.S., and Europe plays a crucial role in the global commercial viability of the invention.
  • Competitors are active in developing similar compounds or delivery systems, highlighting the importance of vigilant IP management.
  • Ongoing patent filings and prosecutions determine long-term patent strength and licensing prospects.
  • Strategic lifecycle management, including patent extensions and new filings, enhances market exclusivity.

FAQs

Q1: How broad are the claims in Hong Kong patent HK1249860?
A: The claims encompass a specific chemical compound or formulation with some breadth to cover derivatives and use cases, balanced against requirements for novelty and inventive step.

Q2: Does the patent protect only in Hong Kong?
A: Yes, as a Hong Kong patent, enforceability is limited to Hong Kong, but the applicant likely filed corresponding applications in other jurisdictions for broader protection.

Q3: What are common challenges to the validity of such pharmaceutical patents?
A: Prior art describing similar compounds or uses, lack of inventive step, or overly broad claims can threaten validity.

Q4: How does the patent landscape influence commercialization strategy?
A: A robust patent portfolio across key markets supports licensing, prevents infringement, and extends product lifecycle.

Q5: What future patenting strategies should applicants consider?
A: Continuous innovation with new derivatives, method claims, and formulation patents, along with strategic filings in emerging markets, bolster long-term protection.


References

[1] Hong Kong Patents Ordinance, Cap 514.
[2] WIPO Patent Landscape Reports.
[3] Patent search databases and applicant disclosures (assumed or illustrative).

Note: Due to the hypothetical nature of this analysis—assuming standard patent characteristics and procedures—specific details about HK1249860 may vary. For precise legal assessment, direct examination of the patent document is recommended.

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