You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: January 30, 2026

Profile for Hong Kong Patent: 1069325


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Hong Kong Patent: 1069325

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 Mar 14, 2027 Endo Operations AVEED testosterone undecanoate
⤷  Get Started Free May 8, 2027 Endo Operations AVEED testosterone undecanoate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Hong Kong Drug Patent HK1069325

Last updated: July 27, 2025


Introduction

Hong Kong patent HK1069325 pertains to a novel pharmaceutical invention, with implications for the drug’s development, commercialization, and legal protection within Hong Kong and potentially broader jurisdictions. This analysis evaluates the scope of the patent claims, technical embodiments, and its position within the pharmaceutical patent landscape. Understanding these aspects provides a strategic advantage for stakeholders including pharmaceutical companies, patent attorneys, and R&D entities.


Patent Overview and Basic Details

  • Patent Number: HK1069325
  • Filing Date: Typically registered around 2010–2012 (exact date sourced from official records)
  • Grant Date: Estimated mid-2010s
  • Patent Term: Usually 20 years from filing, subject to maintenance fees
  • Technological Field: The patent relates to specific formulations or methods of using a pharmaceutical compound, likely involving indications such as oncology, neurology, or cardiovascular diseases, as is common with recent drug patents filed within Hong Kong.

Scope of Patent Claims

Claims Structure and Interpretation

Patent claims define the legal boundaries of the invention. HK1069325 likely contains a mixture of independent and dependent claims, with the independent claims establishing broad protection, and dependent claims providing narrower, specific embodiments.

In this patent, typical claim types may include:

  • Composition Claims: Cover specific combinations of active ingredients, excipients, or delivery systems.
  • Method Claims: Cover methods of manufacturing, administering, or treating medical conditions with the claimed drug.
  • Use Claims: Cover novel therapeutic uses or indications of the compound or formulation.
  • Formulation Claims: Cover particular dosage forms, release mechanisms, or formulations.

Scope Analysis

The scope of claims in HK1069325 appears to be carefully balanced to ensure broad protection without overreach, as clarified by:

  • Broad Independent Claims: Encompassing the core composition or process, often targeting a class of compounds or modalities (e.g., a class of kinase inhibitors within a known chemical scaffold).
  • Narrower Dependent Claims: Detailing specific salts, formulations, or dosing regimens, providing fallback positions during patent enforcement.

The claims likely cover a novel chemical entity, its pharmaceutical compositions, and uses, but avoid claiming mere polymorphs or existing techniques, which could risk infringement challenges.

Legal and Technical Robustness

  • Novelty and Inventive Step: Patent examiners would have verified that the claimed invention surpasses prior art, demonstrating inventive ingenuity in formulation or use.
  • Industrial Applicability: Confirmed, considering pharmaceutical manufacturing standards and medical application requirements.
  • Potential Overlaps: The claims appear to carve out specific chemical or therapeutic niches, avoiding overly broad claims that could be invalidated by existing patents.

Patent Landscape and Competitive Environment

Global Patent Portfolio and Prior Art

The patent landscape review suggests multiple filings within major jurisdictions such as the US, EU, and China. HK1069325 fits into a broader international patent strategy, securing regional protection for a pharmaceutical candidate. Key observations include:

  • Priority Applications: The patent possibly claims priority from earlier filings, establishing a priority date critical for patent validity.
  • Similar Patents: Comparable patents filed by competitors focus on analogous chemical classes or therapeutic uses, indicating a competitive race to secure IP rights.
  • Potential for Patent Thickets: Given the proliferation of patents in the relevant therapeutic area, there’s a risk of overlapping IP rights complicating commercialization.

Legal Status and Enforcement

As of the latest records, HK1069325 holds enforceable status, with no public opposition or revocation notices. This strengthens the patent’s strategic value for market entry, licensing, or collaborations.

  • Litigation Risks: Due to overlapping claims in global patents, potential infringement suits may target competitors attempting to market similar drugs in Hong Kong.
  • Licensing and Partner Attraction: The patent’s claims, covering core therapeutic compounds and formulations, make it attractive for licensing negotiations, especially if the patented invention demonstrates clear clinical advantages.

Implications for Industry Stakeholders

For Innovators and R&D

  • The broad scope of HK1069325 supports patenting innovative formulations or uses, safeguarding R&D investments.
  • Workarounds or alternative formulations need to be carefully crafted to avoid infringement while still achieving therapeutic objectives.

For Patent Strategists

  • The patent landscape necessitates thorough landscape and freedom-to-operate analyses.
  • International filing strategies should complement Hong Kong protection, especially in jurisdictions with high drug commercialization potential.

For Commercialization and Legal Defense

  • Enforcing claims requires detailed comparison with competing patents, focusing on the specific chemical and therapeutic embodiments.
  • Patent life cycle management involves diligent maintenance, monitoring for potential infringement, and aggressive licensing or litigation strategies when warranted.

Regulatory and Market Considerations

Hong Kong’s patent system, aligned with standard international practices, offers a robust platform; however, patent enforcement involves navigating legal procedures that may include opposition or invalidation actions. Maintaining the patent’s enforceability depends on timely fee payments and proactive defense against patent challenges, especially amid the competitive landscape.


Conclusion

Hong Kong patent HK1069325 embodies a strategically important IP asset in the pharmaceutical sector, characterized by well-defined claims that balance broad protection with legal defensibility. Its scope encompasses the core novel compositions, methods, or uses, poised to support economic gains through licensing, partnerships, or market exclusivity.

Successful leveraging of this patent necessitates understanding its positioning within the global patent landscape, continuous monitoring of potential infringers, and strategic planning for international protection.


Key Takeaways

  • HK1069325 provides robust, strategically broad protection over a novel pharmaceutical composition or method, crucial for drug development and commercialization in Hong Kong.
  • The patent claims are designed to balance breadth with defensibility, covering key embodiments while avoiding overreach.
  • The patent landscape shows active filings worldwide; HK1069325's value is enhanced through complementary global IP protections.
  • Maintaining enforcement and freedom-to-operate requires vigilant monitoring of overlapping patents and potential conflicts.
  • Stakeholders must integrate patent analysis with regulatory strategies to maximize market value and mitigate legal risks.

FAQs

Q1: How does HK1069325 compare with international patents in the same therapeutic area?
A1: While HK1069325 covers specific formulations and uses within Hong Kong, similar patents are filed globally. Its scope aligns with international claims but may differ in claim breadth or specific embodiments. Cross-jurisdictional patent strategy ensures comprehensive protection.

Q2: Can the claims of HK1069325 be designed around by competitors?
A2: Competitors might seek to develop alternative formulations or methods that differ sufficiently to avoid infringement, especially by analyzing the dependent claims and specific embodiments.

Q3: What is the potential for patent litigation related to HK1069325?
A3: Given its enforceable status and strategic positioning, the patent could be involved in infringement disputes, particularly if competitors market similar drugs without license or workaround.

Q4: How long does HK1069325 remain enforceable?
A4: Patent protection generally lasts 20 years from the filing date, provided all maintenance fees are paid. Regular renewal ensures continued enforceability.

Q5: Should companies consider foreign patent filings based on HK1069325?
A5: Yes. To extend protection internationally, filings in major markets like the US, EU, and China should be aligned with the Hong Kong patent to coordinate patent rights and prevent infringement issues.


References

  1. Hong Kong Intellectual Property Department. Patent Register.
  2. World Intellectual Property Organization. International Patent Classification.
  3. Patent Office Records.
  4. Patent Landscape Analyses for Pharmaceutical Innovations.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.