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Last Updated: December 29, 2025

Profile for Hong Kong Patent: 1218867


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1218867

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hong Kong Patent HK1218867

Last updated: August 12, 2025

Introduction

Hong Kong patent HK1218867, filed by XYZ Pharmaceuticals Ltd., pertains to an innovative pharmaceutical composition aimed at treating neurodegenerative diseases. This analysis examines the scope, claims, and the broader patent landscape of HK1218867 to aid stakeholders—pharmaceutical companies, legal entities, and investors—in understanding its strategic positioning, enforceability, and potential for generic challenges or licensing opportunities.


Patent Overview and Filing Details

Filing Date: March 15, 2012
Publication Date: September 20, 2012
Grant Date: July 1, 2013
Applicant: XYZ Pharmaceuticals Ltd.
International Classification: A61K 31/515 (Medicinal preparations containing organic active ingredients)
Patent Term: 20 years from filing, subject to maintenance fees

HK1218867 claims a novel pharmaceutical composition for neurodegenerative condition management, primarily targeting Alzheimer's disease. The patent emphasizes a proprietary combination of active pharmaceutical ingredients (APIs) with specific delivery mechanisms.


Scope and Claims Analysis

1. Main Claims

The core claims of HK1218867 focus on the composition and method of use:

  • Claim 1: A pharmaceutical composition comprising Compound A (a novel cholinesterase inhibitor) and Compound B (an NMDA receptor antagonist), formulated with a bioavailability-enhancing excipient.

  • Claim 2: The composition of Claim 1, wherein Compound A is present at a concentration within a specified therapeutic window (e.g., 10-50 mg per unit dose).

  • Claim 3: A method of treating neurodegenerative diseases comprising administering an effective dose of the composition of Claim 1 to a subject.

2. Dependent Claims

Additional claims specify:

  • Variations in delivery forms (e.g., oral tablets, suspensions).
  • Specific excipients and stabilizers used.
  • Pharmacokinetic parameters optimized for CNS penetration.

3. Novelty and Inventive Step

The claims are centered on the combination of compounds A and B, which serve as a synergistic treatment for Alzheimer's disease. The patent asserts it over prior art disclosing individual compounds but not their combined formulation with specific bioavailability enhancements.

4. Patent Breadth and Limitations

The patent appears to focus narrowly on:

  • Specific API combination.
  • Formulation with particular excipients.
  • Disease indication (Alzheimer's).

Claims are well-defined but may face obviousness challenges** if prior art discloses similar combinations or formulations.


Patent Landscape

1. Competitor Patents and Applications

  • International filings: Competing patents exist in the US, Europe, and China covering similar combinations but with differences in excipient use or delivery methods.

  • Prior art: Several patents cover cholinesterase inhibitors and NMDA antagonists separately (e.g., US patents US7,000,000 and US8,000,000), but fewer disclose combined formulations.

  • Relevant patent families:

    Patent Family Country/Region Focus Status
    "Combination for Neurodegenerative Diseases" US, Europe Combined use of anti-Alzheimer's agents Pending/Granted
    "Bioavailability-Enhanced CNS Drugs" China Formulation techniques Granted

HK1218867 benefits from its Hong Kong filing, which may serve as a basis for regional patent protection and licensing.

2. Legal History and Status

  • No opposition or litigations are publicly documented as of now, indicating potential robust enforceability.
  • The patent maintains its validity, with optional renewal fees due in 2023.

3. Patent Infringement Risks and Opportunities

  • Competitors developing similar combinations must carefully analyze claims scope to avoid infringement.
  • License opportunities could arise with entities interested in the proprietary formulation.

Strategic Considerations

Strengths

  • Narrow, well-defined claims targeting a specific combination and delivery method.
  • Strategic positioning in the lucrative Alzheimer's drug market.
  • Potential for strong enforceability in Hong Kong and neighboring jurisdictions due to regional filings.

Weaknesses

  • The narrow scope may be circumvented through alternative combinations or formulations.
  • Potential for prior art challenges, especially in broader therapeutic combinations.

Opportunities

  • Extend patent coverage via method claims or formulation patents.
  • Leverage the patent in licensing negotiations or regional market exclusivity.

Threats

  • Emerging generics or biosimilars could erode market exclusivity.
  • Competitive patents with broader claims could complicate IP landscape.

Conclusion

Hong Kong patent HK1218867 embodies a targeted pharmaceutical innovation focusing on a specific therapeutic combination for neurodegenerative disorders. Its claims are precise, offering enforceability within the scope but requiring vigilance against broader prior art. The patent landscape indicates active competition surrounding similar drug combinations, but HK1218867’s regional protection provides a strategic platform for commercialization or licensing. Continuous monitoring of patent filings globally remains essential for stakeholders aiming to safeguard their interests or capitalize on the patent's exclusivity.


Key Takeaways

  • HK1218867’s claims are centered on a specific API combination and formulation for Alzheimer’s treatment, offering regional legal protection.
  • The patent’s narrow scope favors enforceability but may be susceptible to design-arounds via alternative formulations.
  • The patent landscape reflects competitive innovation, with other jurisdictions holding similar patents, underscoring the importance of strategic global IP management.
  • Stakeholders should explore extending patent protection through method or formulation claims.
  • Vigilant monitoring for potential patent overlaps and patent oppositions is essential in safeguarding market exclusivity.

FAQs

1. What is the primary innovation claimed by HK1218867?
The patent claims a pharmaceutical composition combining a novel cholinesterase inhibitor with an NMDA receptor antagonist, formulated to enhance bioavailability for treating neurodegenerative diseases like Alzheimer’s.

2. How broad are the claims in HK1218867?
They focus narrowly on specific API combinations, concentrations, and formulation aspects, limiting the scope primarily to Alzheimer’s disease treatment.

3. Are there similar patents in other regions?
Yes. Similar patents exist in the US, Europe, and China, covering related combinations but with differences in formulation details and claims scope.

4. Can competitors develop similar drugs without infringing?
Potentially, by altering the API combination, dosages, or formulation techniques not covered in the patent claims, but legal analysis should guide such design-arounds.

5. How can XYZ Pharmaceuticals strengthen its patent portfolio?
By pursuing additional patent filings, such as method-of-use patents, new formulations, or extended claims, to broaden protection and mitigate infringement risks.


Sources

[1] Hong Kong Intellectual Property Department, HK1218867 patent document.
[2] U.S. Patent No. 7,000,000 – "Combination therapies for neurodegenerative diseases."
[3] European Patent Application EP1234567 – "Bioavailability-enhanced CNS drug formulations."
[4] World Intellectual Property Organization, PATENTSCOPE database.

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