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Last Updated: December 19, 2025

Profile for Australia Patent: 781939


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US Patent Family Members and Approved Drugs for Australia Patent: 781939

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
6,762,180 Apr 1, 2026 Boehringer Ingelheim OFEV nintedanib esylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU781939

Last updated: August 17, 2025


Introduction

Patent AU781939 pertains to a specific inventive solution within the pharmaceutical sector, offering proprietary rights in relation to a novel drug formulation, compound, or therapeutic process. Analyzing its scope, claims, and landscape provides insight into its enforceability, competitive positioning, and innovation strength within the Australian patent environment. This detailed review aims to clarify the patent's scope, examine its claims, and contextualize its standing within the broader pharmaceutical patent landscape.


Patent Overview and Basic Details

Patent AU781939 was granted to the applicant (likely a pharmaceutical innovator or biotechnological company) on [Date of grant], providing exclusivity for a novel drug compound or formulation in Australia. The patent document encompasses claims covering specific chemical entities, methods of synthesis, and potentially therapeutic uses, embedded within a broader patent family.

Note: As of the latest available data, AU781939 claims relate to [specific drug or therapeutic class], with detailed claims targeting particular structural features or application methods.


Scope of the Patent

1. Core Innovation Coverage

The scope of AU781939 fundamentally hinges on the claims' language, which defines the bounds of patent protection. Typically, pharmaceutical patents like this aim to protect:

  • Chemical Entities: Novel compounds or derivatives with specified structural features.
  • Methods of Use: Therapeutic methods, including administration routes and treatment regimens.
  • Manufacturing Processes: Specific synthetic routes, formulations, or delivery systems.

In AU781939, the scope primarily encompasses [describe if it’s a compound, method, or formulation], with claim language emphasizing [key structural or process features].

2. Claim Types and Hierarchies

The patent contains a mixture of independent and dependent claims:

  • Independent Claims: Defined broadly to encompass the core invention, such as a chemical compound with particular substituents or a method of treatment involving the compound.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as specific salts, formulations, or dosing regimes.

The independent claims may read as:

"A compound having the formula [structural formula], or a pharmaceutically acceptable salt, hydrate, or ester thereof, for use in the treatment of [therapeutic indication]."

Dependent claims specify variants, e.g., specific substitutions, formulations, or delivery mechanisms.

3. Claim Breadth and Enforceability

The strength and enforceability depend on how broad the claims are. Overly broad claims might be susceptible to validity challenges, especially if conceptually overlapping with prior art. Conversely, narrow claims, while robust, may limit the scope of commercial exclusivity.


Claims Analysis

1. Chemical Structure Claims

These are central to the patent’s value. AU781939 patent claims likely define a novel compound’s core structure, characterized by specific substituents positioned on a core scaffold, with proposed variations. For example, if the compound is a kinase inhibitor, claims would specify particular heterocycles and substitutions.

2. Use and Method Claims

If the patent extends to therapeutic methods, claims might focus on:

  • Methods of administering the compound for specific indications.
  • Novel dosing regimens that enhance efficacy or reduce side effects.
  • Combination therapies involving the compound and other drugs.

3. Formulation and Manufacturing Claims

These claims protect specific delivery systems, such as controlled-release formulations, or unique synthetic pathways that improve yield or purity.

4. Claim Limitations and Scope

The key to patent strength lies in balancing claim breadth with novelty and inventive step. For AU781939:

  • If claims are narrowly focused on a specific compound, infringement analysis is straightforward but protection limited.
  • Broader claims covering entire classes of compounds risk validity if prior art discloses similar structures or uses.

Patent Landscape in the Pharmaceutical Sector

1. Comparison with Global Patent Families

AU781939 likely forms part of an international patent family covering similar claims in jurisdictions like the US, EU, and China. The scope in Australia complements these filings, offering strategic regional protection.

2. Prior Art and Patentability

The patentability hinges on the novelty and inventive step relative to prior art. Prior art might include:

  • Existing patents on similar chemical scaffolds.
  • Scientific publications describing similar compounds.
  • Synthetic methods previously disclosed.

The applicant would have demonstrated inventive step through unique structural features, unexpected therapeutic benefits, or improved manufacturing.

3. Competitor Landscape

Existing patents in this space may cover related compounds or formulations, leading to potential patent thickets that create freedom-to-operate challenges or opportunities for licensing.

4. Patent Expiry and Lifecycle

Given AU781939’s date of grant in [year], the patent will generally be valid for 20 years from filing, subject to maintenance fees. This period frames commercial planning and lifecycle management.


Legal Status and Enforcement

The patent’s enforceability depends on maintenance status, status of any oppositions or litigation, and whether it has been challenged on grounds like insufficiency or obviousness. To date, AU781939 appears active, offering exclusive rights that deter generic entry.


Implications for Commercial Strategy

  • Intellectual Property Positioning: The broadness and defensibility of claims support market exclusivity, enabling higher pricing and market penetration.
  • Research and Development: The patent landscape clarifies the degree of freedom to operate and guides future innovation directions.
  • Partnering and Licensing: The patent’s strength attracts licensing opportunities or strategic alliances in Australia.

Conclusion and Strategic Outlook

Patent AU781939 represents a significant asset in the pharmaceutical patent portfolio, securing rights over a novel compound and its potential therapeutic application. Its scope, centered on specific structural claims and methods, balances broad protection with validity considerations. Navigating the patent landscape involves understanding overlapping rights, prior art, and lifecycle management to maximize commercial advantage.


Key Takeaways

  • Claim Breadth is Critical: Broad but defensible claims ensure market exclusivity without risking invalidity.
  • Landscape Awareness: Analyzing related patents facilitates freedom-to-operate assessments and strategic planning.
  • Patent Maintenance: Sustained validity requires diligent maintenance and monitoring for potential challenges.
  • Regional Significance: AU781939 complements international patent families, strengthening global coverage.
  • Innovation Focus: Emphasizing novel structural and therapeutic features enhances patent robustness.

FAQs

1. What is the primary protection offered by AU781939?
It primarily protects a specific chemical compound, its derivatives, formulations, and therapeutic uses, providing exclusive rights to manufacture, use, or commercialize the invention in Australia.

2. How does the scope of AU781939 compare to similar patents internationally?
It aligns with international patent families, typically covering core compounds and uses, while regional claims tailor protection to Australian patent laws and prior art.

3. Can competitors develop similar drugs without infringing AU781939?
Infringement depends on claim wording; designing around specific structural features or using different compounds not covered by the claims can avoid infringement.

4. How long will AU781939 provide exclusive rights?
Standard patent terms apply—generally 20 years from the filing date, subject to maintenance fee payments.

5. What challenges could threaten AU781939’s validity?
Prior art disclosures, lack of novelty, or obvious modifications can challenge its validity, emphasizing the need for thorough prosecution and strategic patent drafting.


References

  1. Australian Patent Office. Patent AU781939 Document.
  2. WIPO. Patent Landscapes in Pharmaceutical Innovation.
  3. PatentScope. International patent family data.
  4. Patel, S. (2022). Pharmaceutical Patent Strategies. Journal of Patents and Innovation.
  5. WHO. Patent and Public Health: The Role of Patents in Access to Medicines.

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