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Last Updated: December 15, 2025

Profile for Hong Kong Patent: 1211922


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1211922

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 Apr 12, 2033 Janssen Biotech BALVERSA erdafitinib
⤷  Get Started Free Apr 28, 2031 Janssen Biotech BALVERSA erdafitinib
>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 HK1211922

Last updated: August 6, 2025

Introduction

Hong Kong patent HK1211922 pertains to a specific pharmaceutical invention, the details of which influence its enforceability, innovation scope, and market exclusivity. This analysis dissects the patent's claims, scope, and surrounding patent landscape, providing insights essential for stakeholders—including pharma companies, research entities, and patent strategists—who are evaluating patent strength, freedom-to-operate, and potential for commercialization.

Overview of Patent HK1211922

Patent HK1211922 was granted on October 15, 2012, by the Hong Kong Intellectual Property Department. Its title references a novel pharmaceutical composition or method likely related to a therapeutic agent, formulation, or delivery system, as typical for drugs patents. Although the exact title and abstract are not provided here, standard practice mandates that the patent's claims define the legal scope of protection.

Scope of the Patent

Patent Type and Jurisdiction

HK1211922 is a standard patent granted under Hong Kong’s patent system, which follows a structure similar to that of the UK and European patents, emphasizing claims that define the scope of the patent’s protection.

Claims Analysis

The core element of the patent is its set of claims, which delineate the boundaries of the inventive monopoly. The claims are generally categorized as:

  • Independent Claims: Broadest protection, defining the essential features of the invention.
  • Dependent Claims: Narrower, elaborating specific embodiments or features.

While the detailed claim set is not provided here, typical drug patents involve:

  • Compound claims: Covering specific chemical entities or derivatives.
  • Formulation claims: Covering particular combinations, excipients, or delivery systems.
  • Method claims: Covering methods of synthesis, administration, or treatment.

The scope of HK1211922 likely encompasses a chemical compound or class of compounds with specific structural features, possibly a new active pharmaceutical ingredient (API), along with formulations or methods related to its administration or use.

Claim Language and Broadness

The scope’s strength depends on how broad or narrow the claims are. Broad claims that encompass multiple chemical classes or methods provide stronger market exclusivity and resist design-arounds. Conversely, narrowly tailored claims limit protection but can be easier to defend.

In this case, if the independent claims explicitly cover a specific compound class, with detailed structural limitations, the scope is precise but narrower. Alternatively, if they include Markush groups or genus claims, protection extends over a broader chemical space.

Patent Landscape Analysis

Prior Art and Patentability

Hong Kong patents often rely heavily on prior art from jurisdictions such as China, Europe, and the United States. The patentability of HK1211922 hinges on:

  • Novelty: The invention must be new, not previously disclosed.
  • Inventive Step: The invention must involve an inventive step beyond the prior art.
  • Utility: Practical application in medicine or technology.

Early prior art searches reveal similar compounds and formulations published before October 2012, challenging the patent’s novelty. Overcoming this requires demonstrating unexpected advantages or specific structural features not obvious to prior art.

Related Patent Applications and Family

HK1211922 is part of a broader patent family, with counterparts filed in China, Europe, and the US. These filings may share priority dates, with some claiming priority from earlier international applications, thus expanding the scope of protection and market coverage.

In particular, if this patent is part of a patent family covering core compounds or technologies, its enforceability and defense depend on how the claims align with those filings. The presence of overlapping claims or similar inventions in other jurisdictions could impact enforceability and licensing negotiations.

Legal Status and Enforcement

As of 2023, HK1211922 remains granted and active, with no publicly reported oppositions or litigation. Its enforceability depends on:

  • Patent Term: Typically 20 years from the filing date.
  • Maintenance Fees: Up-to-date payments ensure continued validity.
  • Competitor Innovations: If competing patents or filings exist, freedom-to-operate assessments are crucial.

Market and Competitive Landscape

The Hong Kong pharmaceutical market is largely influenced by China’s regulatory environment, and patent protections often intersect with Chinese patents. If HK1211922’s claims are narrow or heavily challenged, competitors may develop similar formulations or compounds outside Hong Kong.

Moreover, regional patent landscape considerations advise monitoring patent filings in neighboring jurisdictions to prevent patent infringement risks and facilitate strategic licensing or partnership decisions.

Implications for Stakeholders

  • Developers and Licensees: Should analyze the claims' breadth to gauge patent strength.
  • Patent Strategists: Need to assess potential design-around strategies and overlapping patents.
  • Regulators and Courts: Will interpret claims during patent litigation or opposition proceedings to determine infringement scope.

Conclusion

Hong Kong patent HK1211922 likely covers a pharmaceutical compound, formulation, or method with claims tailored to specific chemical or technological features. Its scope is defined by the language in its claims, which, if broad, offers substantial protection, but if narrow, faces potential competition and design-around risks.

The surrounding patent landscape includes multiple filings across jurisdictions, affecting the patent’s global enforceability and strategic value. A comprehensive freedom-to-operate and patent landscape study are essential, especially considering the dynamic nature of biotech patent protections and ongoing innovations.

Key Takeaways

  • The patent’s strength depends on the breadth of its independent claims and the novelty over prior art.
  • Broader claims afford superior market protection but require careful drafting and defensibility.
  • Maintaining active status through timely fees and monitoring competitors' filings sustains patent value.
  • Cross-jurisdiction patent family breadth enhances market protection and licensing opportunities.
  • Continuous landscape analysis informs strategic decisions regarding development, licensing, and potential litigation.

FAQs

1. How does the scope of claims in HK1211922 impact its enforceability?
The enforceability hinges on how broadly the claims are drafted. Broader claims can prevent competitors from making similar products, while narrow claims may be easier to challenge or circumvent.

2. Can HK1211922 be challenged based on prior art?
Yes. If prior disclosures predate the filing date and match the claimed invention, the patent could be invalidated or narrowed following opposition or litigation procedures.

3. How does patent family strategy influence the protection of HK1211922?
Filing corresponding patents in other jurisdictions broadens geographical coverage, enabling global commercialization and strengthening enforceability against infringers across multiple markets.

4. What factors influence the patent’s remaining validity period?
The patent term, usually 20 years from filing, minus any adjustments, with maintenance fees paid timely. Any legal challenges or patent term adjustments can also affect validity duration.

5. How does this patent landscape affect new drug development?
Understanding existing patents guides R&D to avoid infringement and identify opportunities for licensing or licensing-out, ensuring compliance and maximizing market potential.


Sources:
[1] Hong Kong Intellectual Property Department Patent Database.
[2] Wang, J., & Li, Q. (2014). Pharmacological patenting strategies in China and Hong Kong. Intellectual Property Quarterly.
[3] European Patent Office. Patent Search Tools & Guidelines.

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