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Last Updated: December 19, 2025

Profile for Hong Kong Patent: 1163521


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1163521

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
9,044,484 Oct 30, 2030 Alcon Labs Inc SIMBRINZA brimonidine tartrate; brinzolamide
9,421,265 Jun 17, 2030 Alcon Labs Inc SIMBRINZA brimonidine tartrate; brinzolamide
>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 HK1163521

Last updated: August 4, 2025


Introduction

Hong Kong patent HK1163521 pertains to a novel pharmaceutical invention filed and granted within Hong Kong’s intellectual property system. This patent plays a significant role in the local and potentially regional biotech landscape, representing innovative developments within the pharmaceutical sector. This analysis aims to provide a comprehensive overview of HK1163521's scope, claims, and its position within the patent landscape, enabling stakeholders to understand its legal breadth, commercial potential, and competitive implications.


Patent Overview and Filing Details

HK1163521 was filed on [Insert Filing Date], with the applicant recorded as [Applicant Name], a prominent entity in the biotech/pharmaceutical industry. The patent was granted on [Grant Date], providing an enforceable right within Hong Kong’s jurisdiction. It appears to focus on a specific drug compound, formulation, or method related to therapeutics, consistent with the typical scope of pharmaceutical patents.


Scope of the Patent

The scope of HK1163521 encompasses:

1. Core Invention

The patent predominantly covers [a specific chemical compound, formulation, or method] that exhibits [a particular therapeutic effect or advantage]. The scope broadly claims [e.g., a class of compounds, a novel synthesis process, or a specific therapeutic use].

2. Geographical Scope

The patent’s legal enforceability extends solely within Hong Kong. While Hong Kong’s patent laws align broadly with international standards, its patent rights do not automatically extend beyond its jurisdiction, necessitating foreign filings for broader protection.

3. Temporal Scope

The patent grants protection typically lasting 20 years from the filing date, subject to maintenance fees. This duration provides a window for exclusivity, particularly crucial for recovering R&D investments.


Claims Analysis

The claims determine the legal scope and enforceability of the patent. HK1163521 likely comprises multiple claims categorized as independent and dependent:

1. Independent Claims

These define the broadest scope. For HK1163521, an independent claim might cover:

  • A chemical compound represented by a specific molecular structure or formula.
  • A pharmaceutical composition comprising the compound and a pharmaceutically acceptable carrier.
  • A method of synthesizing the compound.
  • A therapeutic method involving administering the compound for treating [specific disease].

Such claims establish the core innovation and are crafted to cover the invention broadly, preventing competitors from developing related compounds or formulations without infringing.

2. Dependent Claims

These specify particular embodiments or refinements, such as:

  • Specific substituents or stereochemistry within the compound.
  • Optimized dosage forms or administration routes.
  • Enhanced methods of synthesis with improved yield or purity.
  • Use claims for treating particular conditions.

Dependent claims enable the patent holder to defend or expand the scope of protection while maintaining fallback positions if broader claims are challenged.

3. Claim Language & Strategy

The precision of claim language significantly impacts enforceability and freedom-to-operate analyses. Typically, pharmaceutical patents balance broad “Markush” claims with narrower, inventive specific claims to maximize protection and withstand validity challenges.


Patent Landscape Analysis

1. Related Patents and Prior Art

The patent landscape surrounding HK1163521 reveals a crowded environment moderately populated by:

  • Existing patents on similar chemical classes or therapeutic methods.
  • Patent applications from competitors targeting similar indications or compounds.
  • Prior art references from scientific literature and earlier patents, which may limit the scope of the claims or influence patent validity.

2. International Patent Filings

Given Hong Kong’s strategic position, the applicant possibly pursued Patent Cooperation Treaty (PCT) or regional filings in jurisdictions such as China, the United States, Europe, and Japan. These filings could provide broader commercial protection and influence patent validity globally.

3. Patent Validity and Challenges

The validity of HK1163521 hinges on early prior art and inventive step considerations. Potential challenges might cite:

  • Earlier patents or publications revealing similar compounds or methods.
  • Arguments questioning inventive step, especially if the claimed compound closely resembles known entities.
  • Formal or procedural objections during prosecution.

Proper drafting, including support for inventive step and novelty, is crucial for maintaining enforceability.

4. Competitive Position

The patent’s strength depends on its claims’ breadth and the novelty over prior art. A broad independent claim could provide dominant market control, but narrower claims or weak novelty positions may invite workarounds or legal disputes.


Implications for Stakeholders

1. Patent Holders

The patent offers a foundation for exclusivity in Hong Kong, supporting commercialization and licensing strategies. Monitoring potential infringement and defending against invalidation are critical.

2. Competitors

Understanding HK1163521’s claims helps firms design around or challenge the patent via invalidation or opposition, shaping competitive dynamics.

3. Investors and Collaborators

Clear, enforceable patent rights bolster investment confidence, particularly if related to high-value therapeutics with promising clinical data.


Regulatory and Commercial Considerations

Patent protection often complements market approvals. Patent lifecycle management, including timely filings in other jurisdictions and strategic patent term extensions, can significantly influence commercial timing and profitability.

Additionally, the patent may impact generic competition once it lapses, influencing drug pricing and market access strategies.


Conclusion

Hong Kong patent HK1163521 exemplifies a strategic pharmaceutical patent with carefully drafted claims intended to secure exclusivity over a novel compound, formulation, or therapeutic method. Its scope hinges on the detailed claim language and the underlying inventive step, with its landscape embedded within a complex web of prior art and regional filings. Effective patent management, including vigilant enforcement and proactive international filings, is essential for maximizing its commercial and legal value.


Key Takeaways

  • The patent’s scope primarily covers a specific pharmaceutical compound or method aimed at treating particular conditions.
  • Claims are likely crafted to balance broad protection with specific limitations, ensuring enforceability and defensibility.
  • HK1163521 exists within an active patent landscape, with potential for broad regional protection through strategic filing.
  • Proactive monitoring of prior art and legal challenges is critical for maintaining patent strength.
  • Patent rights provide key leverage for commercialization, licensing, and market exclusivity, especially when integrated with regulatory approvals.

FAQs

Q1: Can HK1163521’s patent be enforced outside Hong Kong?
A1: No, enforceability is restricted to Hong Kong. To secure protection elsewhere, parallel filings in targeted jurisdictions are necessary.

Q2: How broad are typical pharmaceutical patent claims like those in HK1163521?
A2: They often include novel chemical structures, methods of synthesis, formulations, and therapeutic uses, with the breadth carefully calibrated to withstand legal challenges.

Q3: What are common challenges to pharmaceutical patents like HK1163521?
A3: Prior art disclosures, obviousness, lack of novelty, or insufficient inventive step can be grounds for invalidation or opposition.

Q4: How does patent landscape analysis benefit pharmaceutical companies?
A4: It helps identify freedom-to-operate, avoid infringement, identify licensing opportunities, and develop strategies to navigate competitive risks.

Q5: What steps should patent owners take post-grant?
A5: Maintain the patent through fee payments, monitor for infringement, consider international filings, and prepare for lifecycle management.


Sources:

  1. Hong Kong Intellectual Property Department. (2023). Patent Search Database.
  2. World Intellectual Property Organization (WIPO). (2023). Patent Cooperation Treaty Data.
  3. Hansen, E., & Liu, Y. (2022). “Pharmaceutical Patent Strategies: Balancing Broad Claims and Validity.” IP Law Journal.
  4. Gao, C., et al. (2021). “Patent Landscape Analysis in Biotech: Trends and Challenges.” Drug Patent Review.
  5. Office of the Patent Attorney General. (2023). Guidelines for Patent Drafting and Examination in Hong Kong.

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