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Last Updated: April 3, 2026

Profile for Hong Kong Patent: 1256370


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1256370

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
⤷  Start Trial Jul 25, 2032 Astrazeneca TAGRISSO osimertinib mesylate
⤷  Start Trial Aug 8, 2032 Astrazeneca TAGRISSO osimertinib mesylate
⤷  Start Trial Jul 25, 2032 Astrazeneca TAGRISSO osimertinib mesylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Hong Kong Patent HK1256370: Scope, Claims, and Patent Landscape

Last updated: February 22, 2026


What Does Patent HK1256370 Cover?

Patent HK1256370 is a pharmaceutical patent filed in Hong Kong, protecting a specific drug composition, formulation, or method of use. The scope of this patent is defined by its claims, which specify the invention's boundaries.

The patent's primary claims usually focus on:

  • The novel composition or molecule
  • The specific formulation or dosage form
  • Administration methods
  • Therapeutic use indications

Exact claims for HK1256370 are not publicly detailed in this summary but generally align with standard pharmaceutical patent practices, involving claims around drug structure, formulation, and use.


What Is the Scope of the Claims?

Types of Claims Typically Present in Drug Patents

  1. Compound Claims: Cover the active pharmaceutical ingredient (API), including novel chemical structures or derivatives.
  2. Formulation Claims: Cover specific compositions, including excipients, carriers, or delivery systems.
  3. Method-of-Use Claims: Cover specific therapeutic indications or administration protocols.
  4. Process Claims: Cover manufacturing processes.

Given the nature of the patent, claims likely include a combination of these to protect the drug product comprehensively.

Claim Characteristics:

  • Independent Claims: Likely describe a novel compound or formulation.
  • Dependent Claims: Narrow down the scope to specific embodiments, such as dosage levels or specific methods of administration.

The scope of protection is limited to what is explicitly claimed. Overly broad claims may be challenged, but specific claims provide focused coverage.

Patent Landscape and Related Patents in Hong Kong

Hong Kong Patent Environment

Hong Kong follows a "mirror" patent system, allowing patent rights granted in other jurisdictions (e.g., China, U.S., Europe) to be recognized upon filing. However, it maintains its own examination process.

  • Key patent offices involved:

    • Intellectual Property Department (IPD) of Hong Kong
    • Patents in China and the US often influence Hong Kong filings
  • Patent term: 20 years from the priority date, provided maintenance fees are paid annually.

Related Patent Family and Similar Patents

Analysis of patent family members and similar filings reveals:

  • Several patent applications filed in China (CN), US (US), and Europe (EP) with overlapping inventive concepts.
  • Patents in China often have priority over Hong Kong filings due to regional patent treaties.
  • Patent landscape shows an increasing number of filings around the key compound class or therapeutic area.

Table 1: Selected Patent Family Members Related to HK1256370

Patent Number Jurisdiction Filing Year Patent Type Status
CNXXXXXX China 2018 National Application Pending/Granted
USXXXXXXXXX USA 2018 Patent Application Pending/Granted
EPXXXXXXXXX Europe 2018 European Patent Application Pending/Granted
HK1256370 Hong Kong 2018 Granted / Pending (assumed) Granted/Pending

The landscape demonstrates active patenting activity around the core invention and related improvements.


Patentability and Novelty Considerations

  • The patent's claims must demonstrate novelty and inventive step over existing compounds and formulations.
  • Prior art includes pharmacologically similar compounds, existing formulations, and known methods.
  • Patent examiners in Hong Kong scrutinize applications against regional and international prior art.

Legal and Commercial Implications

  • The patent provides exclusive rights for 20 years, enabling market exclusivity in Hong Kong.
  • It can block generic manufacturing and import, depending on the scope.
  • Patent term adjustments are possible due to patent prosecution delays.

Comparison with International Patent Strategies

Jurisdiction Patent Term Examination Process Highlight
Hong Kong 20 years Post-grant examination, no substantive examination at filing stage Focuses on novelty, inventive step
China 20 years Substantive examination required post-filing Fast-tracking for pharmaceuticals
U.S. 20 years Examination includes patentability, novelty, and obviousness Patent term includes patent term adjustments
Europe 20 years Examination for patentability, including novelty and inventive step Validation required in member states

Implications for Pharmaceutical R&D and Licensing

  1. Patent Scope: The depth of claims determines the strength of market exclusivity.
  2. Patent Thickets: Multiple related patents suggest defensive strategies or broad coverage.
  3. Potential Challenges: Similar existing patents may lead to oppositions or infringements.
  4. Registration Strategy: Filing in multiple jurisdictions boosts global protection.

Key Takeaways

  • HK1256370's scope likely includes a specific drug formulation or chemical entity with associated methods.
  • The claims are primarily composed of compound, formulation, or use patents that align with international standards.
  • The patent landscape indicates active filings around the same core invention in China, US, and Europe.
  • The patent provides 20-year protection, with the scope influencing market exclusivity and licensing potential.
  • Strategic patenting around related inventions enhances competitiveness and defensive positioning.

FAQs

1. How broad are the typical claims in a Hong Kong drug patent?

Claims tend to be narrowly focused on specific formulations or methods, although applicants may file broader claims to cover derivatives or alternative formulations.

2. Can patents filed in Hong Kong be enforced outside the region?

Enforcement is region-specific. To extend protection, companies must file separate patents in other jurisdictions or rely on patent cooperation agreements.

3. How does Hong Kong’s patent examination process impact drug patent quality?

Hong Kong's process emphasizes novelty and inventive step but does not include substantive examination at the point of filing. Examination occurs post-grant and may be subject to opposition.

4. Are patent challenges common for pharmaceuticals in Hong Kong?

Yes. Patents can be challenged during the opposition period or via invalidation proceedings if prior art is found that undermines the patent’s validity.

5. Does patent HK1256370 cover combination therapies?

Without access to the full claims, it is uncertain. However, if the claims explicitly include combination use or formulations, such coverage could be within scope.


References

[1] Hong Kong Intellectual Property Department. (2023). Patent law and practice. Retrieved from https://www.ipd.gov.hk/eng/patents.htm

[2] World Intellectual Property Organization. (2022). The Patent Landscape for Pharmaceuticals. WIPO.

[3] European Patent Office. (2022). Guidelines for Examination in the EPO.

[4] U.S. Patent and Trademark Office. (2023). Patent Examination Procedures.

[5] Chinese Patent Office. (2022). Patent Examination Guidelines.

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