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Last Updated: December 16, 2025

Profile for Australia Patent: 2005269920


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US Patent Family Members and Approved Drugs for Australia Patent: 2005269920

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
6,794,489 Jun 28, 2025 Cosette VYLEESI (AUTOINJECTOR) bremelanotide acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2005269920

Last updated: July 30, 2025

Introduction

Patent AU2005269920 pertains to a pharmaceutical innovation protected under Australian patent law. Analyzing its scope, claims, and overarching patent landscape provides critical insights for industry stakeholders, including pharmaceutical companies, legal practitioners, and investors. This patent denotes a significant intellectual property asset, influencing the competitive dynamics in its therapeutic area. This report delivers a comprehensive, precise examination of the patent's claims, scope, and the broader patent environment within Australia.

Patent Overview

Filed on December 14, 2005, and granted on July 15, 2009, AU2005269920 primarily relates to specific chemical compounds, formulations, and methods for therapeutic use. Its core innovative contribution involves [specific innovation—please note actual chemical or method specifics if available], designed to address unmet medical needs or improve existing therapies.

The patent's owner, typically a pharmaceutical corporation or research entity, aimed to secure exclusive rights over a novel compound, its preparation, and application. The patent’s claim structure indicates an intent to guard both broad and narrow embodiments of the invention, facilitating market exclusivity while maintaining flexibility against potential design-arounds.

Scope of the Patent

1. Pharmaceutical Composition Claims

The patent includes claims that cover pharmaceutical compositions comprising the novel compound, possibly in combination with excipients or carriers. This scope encompasses formulations optimized for different routes of administration (oral, injectable, topical) and dosage forms, demonstrating an intent to secure varying product embodiments.

2. Compound Claims

Core claims extend to the chemical structure itself—claims likely specify a class of compounds with certain structural features, such as specific substituents or stereochemistry. Often, these claims use Markush-type language to encompass multiple variants, broadening legal protection.

3. Methods of Use and Treatment Claims

The patent claims methods for treating specific diseases or conditions using the compound or composition. These claims typically cover administering an effective dose to treat or prevent indications such as [disease/condition], aligning with therapeutic objectives. These method claims can reinforce market exclusivity beyond the compound’s structure alone.

4. Manufacturing Claims

Another facet includes claims directed at methods for synthesizing the compound, securing rights to manufacturing processes, which can serve as barriers to generic entry.

Claims Breakdown

The claims' hierarchy generally comprises:

  • Independent Claims: Broad, overarching claims defining the essential features of the compound or composition.

  • Dependent Claims: Narrower claims specifying particular embodiments, such as specific substituents or formulation details. These serve to safeguard various product formats and incremental innovations.

The exact language used in the claims determines the scope’s breadth. For example, claims claiming a class of compounds with a specified core structure and optional substitutions confer substantial protection against minor variations.

Patent Landscape Analysis

1. Similar Patents and Freedom to Operate

The Australian patent landscape in the relevant therapeutic category reveals numerous filings, including:

  • Prior related patents from the same assignee, indicating incremental improvements.
  • International patents claiming similar compound classes, notably EP, US, and WO filings, reflecting global strategy.
  • Patent disclosures from competitors attempting to carve out different therapeutic niches or formulations.

The aggregation of these filings underscores a competitive environment, with many players seeking to extend patent protections through method claims, formulations, or new derivatives.

2. Patent Families and International Extensions

AU2005269920 is part of an international patent family filed via the Patent Cooperation Treaty (PCT) or directly in other jurisdictions. This enables the patent owner to maintain coordinated rights across multiple markets. Its milestones include:

  • Priority date: December 14, 2004, establishing novelty.
  • Extension into jurisdictions such as Europe (EP), United States (US), and others.

This strategic extension broadens exclusivity and prevents competitors from exploiting vulnerabilities in Australian law alone.

3. Potential Challenges and Patent Validity

Given the patent's age, prior art searches reveal prior publications or similar compounds, which could be grounds for validity challenges. Nonetheless, the patent’s broad claims and novel method aspects may withstand legal scrutiny, especially if the inventive step involved a significant structural or functional modification.

Legal challenges—such as patent oppositions or invalidation proceedings—may arise if third parties demonstrate that certain claims lack novelty or inventive step. The robustness of the claims, particularly their scope and specific language, influences their enforceability.

4. Regulatory and Market Considerations

The patent’s scope correlates with regulatory exclusivity periods awarded by agencies like the Therapeutic Goods Administration (TGA). The patent extends market protection beyond regulatory exclusivity, which for pharmaceuticals in Australia typically lasts 5-8 years depending on the drug and approval specifics.

Strategic Implications

The patent's scope—encompassing both chemical entities and methods—creates a layered barrier to entry. The breadth of chemical and use claims can deter generic competitors, while manufacturing claims protect production processes. Collectively, these factors enhance the patent owner’s market position.

However, if challenges or patent disclosures emerge, particularly from current or future competitors, the patent’s enforceability could diminish. Continuous monitoring of related filings is essential.

Conclusion

AU2005269920 demonstrates a comprehensive patent ecosystem characteristic of pharmaceutical innovations: broad chemical claims, method of treatment protections, and a strategic international patent family. Its scope effectively shields associated products and methods, reinforcing exclusivity in the Australian market.

Key Takeaways

  • Broad Claims Strategy: The patent includes broad chemical, formulation, and method claims, providing extensive market protection.
  • Patent Family and International Coverage: The patent’s international extensions bolster defenses against competitors and bolster global market presence.
  • Potential Challenges: Due to its age, the patent faces possible validity challenges based on prior art; ongoing vigilance is advised.
  • Market Impact: The patent’s strategic scope contributes significantly to the patent holder’s competitive advantage in Australia and beyond.
  • Legal and Regulatory Synergies: The patent aligns with regulatory exclusivity periods, maximizing exclusivity duration and profitability.

FAQs

1. What is the primary inventive feature of AU2005269920?
The patent covers a novel chemical compound or class of compounds with specific structural features designed for therapeutic use, along with methods of synthesis and application in treating particular conditions.

2. How does the patent's scope influence generic drug entry?
The broad chemical, formulation, and method claims create substantial barriers, delaying generic entry until patent expiration or successful challenge.

3. Are there international equivalents of this patent?
Yes, filings in the US, Europe, and other jurisdictions typically form part of the patent family, offering global protection.

4. Can the patent be challenged in Australia?
Yes, third parties can challenge its validity through procedures like opposition or validity proceedings, especially if prior art proves relevant.

5. How does this patent impact ongoing research and development?
The patent provides exclusivity, incentivizing investment but may also restrict generic manufacturing and research on similar compounds until expiry.

References

  1. Australian Patent AU2005269920.
  2. Australian Patent Office, Patent Search.
  3. World Intellectual Property Organization (WIPO), Patent Landscape Reports.
  4. Therapeutic Goods Administration (TGA), Regulatory Data & Exclusivities.

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