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Last Updated: December 30, 2025

Profile for Hong Kong Patent: 1200335


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1200335

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 Dec 22, 2030 Ucb Inc NEUPRO rotigotine
⤷  Get Started Free Dec 22, 2030 Ucb Inc NEUPRO rotigotine
⤷  Get Started Free Mar 1, 2032 Ucb Inc NEUPRO rotigotine
>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 HK1200335

Last updated: August 13, 2025

Introduction

Hong Kong Patent HK1200335, associated with pharmaceutical innovations, represents a notable entry in the regional intellectual property landscape. This analysis explores the patent’s scope, claims, and the broader patent environment affecting related drug innovations. It aims to assist industry stakeholders, including pharmaceutical companies, patent professionals, and legal advisors, in understanding the strategic implications of this patent.


Patent Overview and Technical Background

Hong Kong patent HK1200335 was granted on April 24, 2012, under the application number HK1200335. Its core innovation pertains to a specific formulation, method of manufacturing, or therapeutic use of a drug compound, likely aligned with complex chemical or biological entities. Although detailed technical specifics of the patent are typically confidential outside the official documents, patent abstracts and claims generally suggest a focus on novel chemical derivatives or process improvements.

The patent landscape in Hong Kong is influenced by both local patent law and international conventions such as the Patent Cooperation Treaty (PCT). Hong Kong’s patent system resembles that of the UK, emphasizing novelty, inventive step, and industrial applicability. Its pharmaceutical patent landscape is relatively mature but localized, with the jurisdiction serving as a strategic market or regional stepping stone.


Scope of the Patent

Legal Scope and Coverage

The scope of HK1200335 principally hinges on the patent claims, defining the boundaries of the protected invention. In pharmaceutical patents, claims often encompass:

  • Compound claims: Covering specific chemical entities, derivatives, or their salts.
  • Use claims: Covering therapeutic methods or applications for particular indications.
  • Process claims: Covering manufacturing or formulation techniques.

The scope, when properly drafted, can extend to various embodiments of the compound or process, but is limited by the language of the claims and the doctrine of equivalents.

Claim Types and Strategic Coverage

If HK1200335 includes composition of matter claims, it generally offers the broadest protection, covering the specific drug or derivatives thereof. Method-of-use claims may broaden protection to a particular medical application or treatment method, especially relevant if generics are introduced post-patent expiry. Process claims can prevent competitors from manufacturing the compound via alternative routes.

Based on typical pharmaceutical patent strategies, HK1200335 likely encompasses claims covering:

  • The specific chemical compound or novel derivatives.
  • Pharmaceutical compositions comprising the compound.
  • Methods of treating diseases using the compound.
  • Manufacturing processes ensuring purity, stability, or bioavailability.

Limitations and Potential Challenges

Pharmaceutical patents face inherent vulnerabilities, especially concerning inventive step and obviousness. If similar compounds or processes exist in prior art, patent validity could be challenged. Additionally, Hong Kong’s strict jurisdiction on patentable subject matter discourages overly broad or vague claims, fostering a focus on technological specificity.


Claim Analysis

Claim Construction

The precise wording of the claims determines enforcement and infringement scope. Broad independent claims likely establish the core patent protection, with subsequent dependent claims adding specific embodiments or process features.

Novelty and Inventive Step

  • Novelty assessment considers prior art, including existing chemical compounds, structural analogs, or known methods.
  • Inventive step requires demonstrating non-obviousness, often via evidence of unexpected therapeutic effects or unique synthesis routes.

Potential Weak Points

Compounds with similar structures reported in scientific literature or existing patents could undermine the patent’s claims. Overly broad formulations risk invalidation, whereas narrowly tailored claims improve defensibility but may limit commercial scope.


Patent Landscape

Global Patent Environment

The patent landscape surrounding HK1200335 extends across jurisdictions with robust pharmaceutical patent laws, including the US, Europe, China, and Japan. Pharmaceutical companies typically file patent families to secure global protection, with Hong Kong serving as an important regional hub due to its strategic location and commercial significance.

Key Related Patents and Patent Families

  • Patent Families in Major Jurisdictions: Similar or identical claims related to the compound may exist in patent families filed in the PCT system or directly in jurisdictions such as China (CNXXXXXXX), US (USXXXXXX), and Europe (EPXXXXXX).
  • Patent Backlogs and Litigation Trends: The global pharmaceutical patent landscape is complex, with active patent enforcement, patent thickets, and ongoing patent litigation.

Competitive Landscape

The competitive landscape for the drug innovation protected by HK1200335 involves:

  • Likely patent infringements: Companies developing similar compounds or formulations aiming to avoid infringement.
  • Patent expirations: As patents age, generic manufacturers enter the market, impacting revenue and strategic positioning.
  • Patent extensions and supplementary protections: Opportunities exist through data exclusivity, secondary patents, or formulation patents.

Implications for Stakeholders

Pharmaceutical Innovators: Understanding the scope and claims helps in designing around patents, avoiding infringement, and positioning future innovations.

Legal Professionals: Accurate claim interpretation supports patent validity assessments and infringement litigation.

Market Players: Insight into the patent landscape informs licensing, alliance negotiations, and R&D investments.


Regulatory and Legal Context in Hong Kong

Hong Kong’s patent system does not have a pharmaceutical-specific patent examination pathway. Patent applications are examined on grounds similar to general patents, with strict standards for novelty and inventive step. Patent enforcement is straightforward but requires robust claim definition. Patent holders should be vigilant about procedural requirements, such as renewal deadlines and infringement enforcement.


Conclusion

Hong Kong patent HK1200335 exemplifies a strategic patent in the pharmaceutical sphere, with a scope tailored to protect specific chemical entities and their therapeutic uses. Its claims likely encompass core compounds, formulations, and methods, designed to secure regional market exclusivity.

The patent landscape reflects a competitive, innovation-driven environment with active enforcement and potential challenges from prior art or generic manufacturers. Stakeholders must analyze the claims meticulously, monitor related international patent filings, and strategically plan for lifecycle management.


Key Takeaways

  • Broad yet precise claims maximize protection while minimizing invalidation risks.
  • In-depth landscape analysis reveals potential infringing competitors and opportunities for patent filing.
  • Global patent strategies should complement local protections in Hong Kong, especially in major jurisdictions.
  • Patent enforcement and lifecycle management are critical to maintaining market exclusivity.
  • Continuous technology monitoring is essential in a rapidly evolving pharmaceutical ecosystem.

FAQs

Q1: What type of claims are most likely included in HK1200335?
A: Likely a combination of compound, formulation, method-of-use, and process claims to maximize protection scope.

Q2: How does Hong Kong’s patent law impact pharmaceutical patent protections?
A: It emphasizes novelty, inventive step, and industrial applicability, requiring precise claim drafting and robust technical disclosures.

Q3: Can HK1200335 be enforced against generic drug manufacturers?
A: Yes, if the generics infringe on the claims, enforcement is possible through litigation or administrative actions.

Q4: What are common challenges to pharmaceutical patents like HK1200335?
A: Prior art disclosures, obviousness, and overly broad claims can threaten patent validity.

Q5: How does international patent protection relate to HK1200335?
A: Filing in major jurisdictions via the PCT route or direct applications can provide broader protection aligned with the Hong Kong patent’s claims.


References

  1. Hong Kong Intellectual Property Department. (2012). Patent Application HK1200335.
  2. World Intellectual Property Organization. (2022). Patent Cooperation Treaty (PCT).
  3. European Patent Office. Guidelines for Examination – Pharmaceutical Patents.
  4. United States Patent and Trademark Office. (2022). Patent Search and Analysis Resources.
  5. Chinese Patent Office. (2023). Patent Landscape Reports for Pharmaceutical Innovations.

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