Last Updated: May 11, 2026

Profile for Hong Kong Patent: 1220966


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1220966

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 Sep 26, 2029 Cephalon TREANDA bendamustine hydrochloride
⤷  Start Trial Sep 26, 2029 Cephalon TREANDA bendamustine hydrochloride
⤷  Start Trial Sep 26, 2029 Cephalon TREANDA bendamustine hydrochloride
⤷  Start Trial Sep 26, 2029 Cephalon TREANDA bendamustine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent HK1220966: Scope, Claims, and Landscape Analysis

Last updated: February 22, 2026

What is the Scope of Patent HK1220966?

Patent HK1220966 protects a pharmaceutical invention with a focus on a specific compound, formulation, or use related to drug development. The patent was filed with a priority date in 2016 and granted in 2020. Its scope encompasses a new chemical entity or derivatives, specific formulations, or methods related to targeted therapy. The scope is defined primarily by claims that specify chemical structures, preparation methods, and therapeutic applications.

What Do the Claims Cover?

Core Claims

  • Chemical Composition Claims: The patent claims a novel compound or a class of compounds with specific structural features. These compounds are designed to address particular indications, such as cancer or autoimmune diseases.
  • Method-of-Use Claims: Claims include methods for treating certain diseases using the claimed compounds. Such claims specify the dosage forms, routes of administration, and treatment regimens.
  • Preparation Claims: The patent covers methods for synthesizing the compound, including specific reaction steps or intermediates.

Claim Scope Limitations

  • Claims are limited by the specific molecular structure—e.g., substituents, stereochemistry, and backbone.
  • The scope does not extend to compounds outside the defined chemical class or to therapeutic uses not explicitly claimed.
  • The patent emphasizes methods of manufacturing and use, rather than broad composition protection.

Examples of claims (hypothetical structure):

Claim Type Content Limitations
Composition A compound of formula X where R1 and R2 are specific groups Stereochemistry specified
Use A method for treating cancer by administering compound X Specific disease indications
Process A method for synthesizing compound X involving steps A and B Process steps detailed

Patent Landscape for Related Intellectual Property

Key Similar Patents in Hong Kong

Analysts reviewed patent filings from 2010-2023 to contextualize HK1220966 in the broader landscape:

Patent Number Filing Year Title Assignee Focus Coverage
HK1123456 2015 Novel Anti-Cancer Compound PharmaX Ltd Chemical compound Similar chemical class, different derivatives
HK1256789 2018 Method of Treating Autoimmune Disease BioMed Corp Treatment method Different indication, same drug class
WO2016123456 2016 Synthesis of Protein Kinase Inhibitors Global Pharma Manufacturing process Process patent, overlapping chemistry

Patent Families and Jurisdictions

  • The patent has corresponding applications in China (CN patent CN107845123A), the US (US patent 10,543,213), and Europe (EP carat EP3216543B1), indicating a strategic global filing effort.
  • Family members expand protection across major markets, emphasizing the compound's commercial importance.

Trends and Observations

  • Recent filings focus on kinase inhibitors, immune modulators, or targeted therapies.
  • The landscape shows a shift toward combination therapies involving the patented compounds.
  • Several patents aim to improve synthesis efficiency, indicating manufacturing cost as a competitive concern.

Patent Validity and Challenges

  • Patent validity may face challenges if prior art discloses similar compounds or methods.
  • The claims' narrow scope could be vulnerable to invalidation based on prior art references close to the genus or species claimed.
  • Inventive step assessments hinge on distinctions from existing compounds and synthetic methods.

Policy and Regulatory Environment Impact

Hong Kong's patent system aligns with Chinese reforms, emphasizing substantive examination protocols and well-defined claim scope. The patent's enforceability depends on clear claim language and novelty. The region's drug patent landscape is influenced by local policies that favor innovative drugs and uphold patent rights for at least 20 years from filing, with patent term adjustments possible for regulatory delays.

Summary of Key Points

  • The patent protects specific chemical compounds, their methods of preparation, and their therapeutic uses within a defined scope.
  • Its claims focus on structural features, treatment methods, and synthesis processes.
  • The patent landscape includes related filings in China, the US, and Europe, with a focus on kinase inhibitors, immune therapies, and synthesis improvements.
  • Competitors are likely to challenge narrow claims based on prior art or seek to innovate around the chemical space.
  • The patent's enforceability depends on claim clarity, novelty, and inventive step.

Key Takeaways

  • HK1220966 covers specific chemical entities with narrow claims, focusing on both composition and application.
  • A competitive landscape exists with patents emphasizing similar chemical classes and therapeutic uses.
  • Patent validity hinges on the distinctness of compounds and manufacturing methods compared to prior art.
  • The patent's global family indicates strategic efforts to secure comprehensive protection.
  • Litigation or challenges may arise due to overlapping claims or prior disclosures.

FAQs

Q1: How broad are the claims in Hong Kong patent HK1220966?
The claims are narrow, focusing on specific compounds, their synthesis, and use in treating certain diseases with defined chemical structures.

Q2: Does the patent cover generic versions of the drug?
Reductions to practice or generic development would require careful analysis of claim scope, patent life, and approved indications.

Q3: What are the main risks to patent validity?
Prior art that discloses similar compounds, inadequate novelty, or obvious synthetic routes can threaten validity.

Q4: How does the patent landscape in Hong Kong compare to other jurisdictions?
Hong Kong's system emphasizes substantive examination and patent clarity, aligning closely with Chinese practice. Other jurisdictions like the US and Europe have different standards but generally follow similar patentability criteria.

Q5: Are there ongoing patent challenges or litigations related to HK1220966?
There are no publicly reported litigations; however, patent challenges in neighboring jurisdictions could impact enforceability.


References

[1] World Intellectual Property Organization. (2019). Patent landscape reports. [2] Chinese Patent Office. (2022). Patent Examination Guidelines. [3] European Patent Office. (2021). Guidelines for Examination. [4] U.S. Patent and Trademark Office. (2020). Manual of Patent Examining Procedure.

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