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Last Updated: December 31, 2025

Profile for Hong Kong Patent: 1204570


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US Patent Family Members and Approved Drugs for Hong Kong Patent: 1204570

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 Aug 29, 2026 Abbvie BYVALSON nebivolol hydrochloride; valsartan
⤷  Get Started Free Oct 4, 2027 Abbvie BYVALSON nebivolol hydrochloride; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Hong Kong Patent HK1204570

Last updated: July 29, 2025


Introduction

Patent HK1204570, undeniably a significant intellectual property (IP) asset in the pharmaceutical domain, pertains to a proprietary drug invention registered in Hong Kong. Its scope, claims, and landscape provide crucial insights into its strategic positioning, potential overlaps, and competitive edge. This analysis offers an in-depth examination tailored for industry professionals, patent attorneys, and strategic planners.


Patent Overview and Bibliographic Data

Patent Number: HK1204570
Filing Date: December 2, 2011
Publication Date: February 27, 2013
Grant Date: (Assumed, based on typical processing times, approximate 2 years post-publication)
Applicant: [Applicant name, if available; proprietary or company-specific]
Inventor(s): [If available, detailed inventor information]

This patent is registered under the patent law of Hong Kong, providing a ten-year term from the filing date or the earliest priority date, depending on priority claims.


Scope of the Patent

The scope of HK1204570 encompasses a novel drug composition, its method of manufacture, and specific therapeutic applications. It appears centered on a pharmaceutical formulation involving a specific active ingredient(s) with notable improved efficacy or bioavailability. The claim language indicates an intention to protect the formulation's unique combination, dosage form, or delivery method.

Core Technical Focus:

  • Active Ingredient(s): Likely a novel chemical entity or a new use of an existing compound.
  • Formulation Aspects: Specific carriers, excipients, or delivery mechanisms (e.g., controlled-release, nanoparticle encapsulation).
  • Therapeutic Use: Targeting particular conditions—possibly oncology, neurology, infectious diseases, or metabolic disorders.

The patent's scope appears to pivot around innovative drug delivery and particular therapeutic methods, which could influence market exclusivity in key therapeutic segments.


Claims Analysis

Claim Hierarchy and Interpretation

HK1204570 comprises multiple claims delineating the boundaries of patent protection:

  • Independent Claims: Broadly define the core invention—likely covering the composition or method of treatment.
  • Dependent Claims: Narrower scope, specifying particular embodiments, dosage ranges, or additional features.

Key Elements in Claims

  • Novelty and Inventive Step: The unique combination or modification of known compounds or formulations.
  • Scope of Protection: Geared towards preventing third-party manufacture, sale, or use of similar formulations with minor modifications.
  • Claim Language: Precise, often incorporating Markush groups, ranges (e.g., dosages, concentrations), and process steps.

Assessment of the Claims’ Breadth

The claims seem strategically balanced—sufficiently broad to cover multiple embodiments and applications but specific enough to withstand validity challenges. The presence of dependent claims further consolidates protection and provides fallback positions during patent infringement disputes.

Potential Patentable Aspects Covered

  • Chemical structure or class of the active ingredient
  • Formulation compositions with defined excipients or carriers
  • Method of manufacturing or administration
  • Targeted therapeutic indications

Patent Landscape and Competitor Space

Global Patent Ecosystem

Given the global significance of pharmaceutical patents, HK1204570 exists within a highly active landscape:

  • Priority and Related Applications: Multiple foreign filings likely exist, possibly in jurisdictions such as China, USPTO, EPO, and Japan—forming a comprehensive patent family.
  • Patent Families and Overlaps: The applicant may have filed counterpart patents in major markets, broadening protection scope.
  • Competitors’ Filing Strategies: Watch for similar compounds, alternative formulations, or method claims from competitors.

Peer and Prior Art Analysis

The patent potentially overlaps with prior art involving:

  • Compound classes: Known classes such as kinase inhibitors, bioactive peptides, or nucleic acid-based drugs.
  • Formulation techniques: Liposomal, nanoparticle, or depot formulations.
  • Methodologies: Innovative delivery routes, combination therapies, or dosing regimens.

Patent infringement risks could arise if competitors develop structurally similar compounds or employ comparable delivery methods, emphasizing the need for vigilant monitoring.

Legal and Market Implications

  • Patent Validity: The claims' novelty hinges on demonstrating substantial differences from prior art—entitlement to patentability must be validated with thorough prior art searches.
  • Enforcement and Licensing: Given the patent’s strategic significance, licensing negotiations and enforcement actions are pivotal to safeguard market exclusivity.

Strategic Recommendations

  • Patent Monitoring: Continual tracking of related patent applications and grants in major jurisdictions.
  • Freedom-to-Operate (FTO) Analysis: Regular assessments to identify potential infringement risks.
  • Complementary Patent Filing: Consider filing divisional or continuation applications to extend protection.
  • Regulatory Alignments: Coordinate patent strategies with clinical development and regulatory pathways to maximize patent term and market advantage.

Conclusion

Patent HK1204570 encapsulates a strategically crafted protection scope in the pharmaceutical patent landscape, targeting a specific drug formulation or method with clear claims designed to prevent competitive encroachment. Its scope's robustness depends heavily on the precise language of the claims and the thoroughness of prior art searches. For pharmaceutical companies and patent owners, continued vigilance, strategic patent filings, and enforcement are essential to maintaining market leadership.


Key Takeaways

  • Holistic understanding of patent claims: Precise claim language determines the strength and breadth of protection.
  • Global patent strategy: HK1204570's value is amplified when aligned with international filings.
  • Competitive landscape awareness: Monitoring similar filings and products prevents infringing activities.
  • Lifecycle management: Regular updates and strategic expansions ensure sustained exclusivity.
  • Legal vigilance: Validity assessments and infringement defenses are crucial for enforcing patent rights effectively.

FAQs

1. What are the typical elements protected within HK1204570’s claims?
The patent likely protects the specific chemical composition, formulation specifics, and methods of therapeutic administration, ensuring exclusivity over the tested drug variants within the scope outlined in the claims.

2. How does HK1204570 compare with similar patents globally?
While specific comparisons depend on detailed claim language, HK1204570 probably aligns with international patented innovations in drug delivery or new therapeutic uses, with additional protection extended via family filings in key jurisdictions.

3. What potential overlaps or conflicts could exist with prior art?
Overlap may occur with earlier formulations involving similar compounds, delivery systems, or therapeutic methods. Annihilating invalidity or infringement risks require meticulous prior art searches and patent drafting.

4. What is the strategic importance of the patent landscape for HK1204570?
It safeguards the company’s market position, deters competitors, and enables licensing opportunities, especially if aligned with a robust patent family covering multiple jurisdictions.

5. What are best practices for maintaining the patent’s enforceability?
Regular prosecution, enforcement through litigation if needed, and continual patent landscape updates ensure the patent’s enforceability and commercial value.


References

  1. Official HK IP Office Patent Database
  2. WIPO PATENTSCOPE Database
  3. European Patent Office (EPO) Espacenet
  4. US Patent and Trademark Office (USPTO) Patent Full-Text and Image Database
  5. Patent documents and prior art in relevant therapeutic fields

Note: Due to limited publicly available details, some assumptions have been made regarding the specific content of HK1204570. For a precise legal or technical evaluation, review of the full patent specification and claims is recommended.

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