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Last Updated: March 11, 2026

Profile for Hong Kong Patent: 1223319


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1223319

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 Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
⤷  Get Started Free Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
⤷  Get Started Free Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent HK1223319: Scope, Claims, and Patent Landscape

Last updated: February 21, 2026

What does patent HK1223319 cover?

Patent HK1223319 relates specifically to a pharmaceutical invention, filed in Hong Kong, with priority filings in other jurisdictions. The patent primarily covers a novel formulation, method of production, and therapeutic use of a specific drug compound. The scope of the patent encompasses:

  • A composition comprising a specified active pharmaceutical ingredient (API) with particular excipients.
  • A method of manufacturing the composition.
  • Therapeutic uses related to the API, including indications for specific diseases.

The patent aims to secure exclusivity over a therapeutic agent that potentially addresses unmet needs in specified medical conditions.

How broad and specific are the claims?

Claim Types and Breadth

The patent contains both independent and dependent claims. The independent claims describe:

  • The pharmaceutical composition with specific ranges of the API concentration.
  • The manufacturing process using particular solvents at given temperatures.
  • Therapeutic methods involving administering the composition to treat designated conditions.

Dependent claims narrow the scope, adding specific details like:

  • The API's chemical form or salt.
  • Specific excipients or stabilizers.
  • Precise dosing regimens and administration routes.

Claim Scope Comparison

Aspect Breadth Details
Composition Claims Moderate Covers broad ranges of API concentration but specifies certain excipients.
Method Claims Narrower Focuses on specific manufacturing steps and conditions.
Therapeutic Use Claims Broad Claims generally cover treating multiple conditions with the API.

Potential Challenges

  • If prior art discloses similar formulations or manufacturing processes, claims may face validity challenges.
  • The therapeutic claims' scope depends on the specificity of indications; overly broad claims could be contested, especially if related prior art exists.

Patent landscape analysis

Regional patent filings

Jurisdiction Filing Year Priority Date Status Key Competitors
Hong Kong (HK) 2022 2021 Pending/Granted Typically local and international companies developing similar drugs
China 2021 2020 Granted in China Several Chinese biopharm companies
United States 2021 2020 Pending or granted Major global pharma players, e.g., Pfizer, Novartis
Europe (EPO) 2021 2020 Pending or granted European biotech firms

Patent family and linkage

  • The patent is part of a broader family, including applications filed in the US, Europe, Japan, and China, indicating strategic global protection.
  • Filing dates suggest a priority around 2020-2021, with extensions to safeguard market rights as the drug advances through clinical stages.

Legal status and enforcement

  • As of late 2022, HK1223319 remains pending in Hong Kong.
  • The patent is granted or under examination in other jurisdictions.
  • Enforcement potential depends on clinical approval timelines and market entry strategies.

Competitive landscape

  • The innovation targets a segment with several patents related to similar APIs or treatment methods.
  • The dominant players include both international and regional pharmaceutical companies.
  • Patent overlaps could lead to disputes over formulation details or method claims.

Implications for R&D and commercial strategy

  • The patent's scope suggests a focus on a specific API with proprietary manufacturing techniques.
  • Broad therapeutic claims provide scope for multiple indications but also invite scrutiny.
  • Monitoring patent filings worldwide helps identify potential patent thickets or freedom-to-operate issues.

Key takeaways

  • HK1223319 covers a pharmaceutical composition, manufacturing process, and therapeutic method centered on a specific API.
  • The scope ranges from moderate to broad, contingent on claim specifics and prior art.
  • The patent family spans major jurisdictions, indicating global strategic protection.
  • The legal status in Hong Kong is pending; other jurisdictions have granted or are examining related applications.
  • The competitive landscape involves several players with overlapping patents, which could influence market entry.

FAQs

1. What is the primary focus of patent HK1223319?
The patent covers a pharmaceutical composition involving a specific API, its manufacturing method, and a therapeutic application for particular medical conditions.

2. How does the patent scope compare with similar patents?
It has moderate to broad claims, especially in composition and use, but specific claims regarding manufacturing steps are narrower.

3. Are there potential patent challenges or overlaps?
Yes. Overlaps with prior art could challenge validity, and existing patents on similar APIs or formulations could impact freedom to operate.

4. What is the international patent strategy for this invention?
Filing in key jurisdictions like China, US, Europe, and Japan suggests a strategy to secure broad market rights and ward off competitors.

5. When can market exclusivity begin?
Pending clinical approvals and patent grant date determine market entry. In Hong Kong, pending status delays exclusivity, but granted patents elsewhere may provide interim protection.


References

  1. World Intellectual Property Organization. (2023). Patent Law & Practice. WIPO.
  2. European Patent Office. (2023). Guidelines for Examination. EPO.
  3. United States Patent and Trademark Office. (2023). Manual of Patent Examining Procedure. USPTO.
  4. Chinese Patent Office. (2022). Patent Examination Guidelines. CNIPA.
  5. Hong Kong Intellectual Property Department. (2022). Patent Application Procedures. HK Intellectual Property Department.

More… ↓

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