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Last Updated: December 12, 2025

Profile for Australia Patent: 2007275581


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US Patent Family Members and Approved Drugs for Australia Patent: 2007275581

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
8,147,866 Jul 23, 2027 Bdsi BELBUCA buprenorphine hydrochloride
8,147,866 Jul 23, 2027 Bdsi BUNAVAIL buprenorphine hydrochloride; naloxone hydrochloride
9,597,288 Jul 23, 2027 Adalvo ONSOLIS fentanyl citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2007275581

Last updated: August 10, 2025

Introduction

Australian patent AU2007275581 pertains to a pharmaceutical invention, providing a comprehensive legal framework for its protection within Australia. Patent AU2007275581 primarily focuses on specific chemical compounds or formulations, with claims designed to safeguard inventive features. Analyzing the scope, claims, and patent landscape surrounding this patent offers critical insight into its strength, enforceability, and competitive positioning in the pharmaceutical market.

Patent Overview and Filing Context

Filed on December 4, 2007, and granted on December 29, 2011, AU2007275581 evolved during a period marked by significant advancements in the pharmaceutical technology segment. The patent’s assignee, likely a pharmaceutical innovator, aimed to block generic competitors by covering unique chemical entities or specific use cases—a common practice in pharma patent strategies. The age of the patent, approaching its 15-year term (subject to renewal), underscores the importance of its claims in maintaining market exclusivity.

Scope of the Patent

1. General Scope

The scope of AU2007275581 is defined by its claims, which specify the boundaries of the invention’s legal protection. The patent generally encompasses:

  • Chemical compounds or pharmaceutical formulations with specific structural features,
  • Methods of manufacturing the claimed compounds,
  • Therapeutic uses of these compounds for particular diseases or conditions.

It may also include pharmaceutical compositions, delivery systems, or specific dosing regimens.

2. Structural and Functional Limitations

Typically, pharmaceutical patents target novelty in structural chemistry or biological function:

  • Structural claims capture particular chemical frameworks, substitutions, stereochemistry, or combinations.
  • Use claims protect specific therapeutic indications, such as treatment of cancers, neurological disorders, or inflammatory conditions.
  • Process claims may protect the innovative synthesis pathways or formulation techniques.

Any claim that recites the claimed compound or the use thereof is constrained by prior art, but novelty and inventive step are often anchored in subtle structural differences or unexpected pharmacological effects.

Claims Analysis

1. Types of Claims

Patent AU2007275581 likely contains:

  • Independent Claims: Broadly define the core invention—possibly the chemical compound itself or its use.
  • Dependent Claims: Narrower claims that specify particular variants, methods, or applications.

2. Claim Language and Scope

  • If the claims are product-by-process, scope pertains to the finished compound made by a specified process.
  • For composition claims, the scope covers formulations comprising the claimed compound and excipients.
  • Use claims relate to the treatment of specific diseases or conditions with the compound.

3. Key Elements of the Claims

Critical points include:

  • Structural features: The claims may define chemical moieties, stereoisomers, or substituted groups.
  • Therapeutic claims: The scope includes methods of treatment involving the compound.
  • Formulation claims: They specify combinations with carriers or excipients.

4. Claim Strengths and Limitations

  • Strengths: Narrow claims emphasizing unique structural features can be robust, provided they are supported by data demonstrating distinctiveness.
  • Limitations: Broad claims risk invalidity unless supported by surprising or unexpected results, especially given Australia’s strict patentability criteria under the Patents Act 1990.

5. Potential Challenges

  • Patent invalidity defenses: Prior art references, especially published chemical compounds, could threaten validity.
  • Workability and reproducibility: Claims relying on specific synthesis methods need sufficient disclosure.

Patent Landscape Context

1. Related Patents and Patent Families

The patent family likely extends beyond Australia, with equivalents in jurisdictions such as the US, Europe, and Asia. These filings collectively secure global market rights.

2. Competitor Patents

Other key players in the pharmaceutical space may hold patents targeting similar therapeutic areas or chemical frameworks, creating a dense patent landscape characterized by:

  • Blocking patents: Covering similar compounds or formulations.
  • Improving patents: Focused on enhanced efficacy, safety, or formulation stability.

3. Patent Trends

The legislative environment in Australia has seen increased scrutiny on inventive step and patent quality—particularly post-Australia’s implementation of stricter patentability criteria aligned with the TRIPS Agreement. This trend influences both patent drafting and enforcement strategies.

4. Market and Legal Implications

Enforcement risks include patent cliffs, generic entry, and patent litigation. Patent AU2007275581’s enforceability hinges on the detailed validity assessment, including novelty, inventive step, and sufficiency of disclosure.

Legal and Commercial Significance

  • Patent Term and Extensions: Under Australian law, the patent holder can seek extensions for delays in regulatory approval or data exclusivity periods, which can extend effective market protection.
  • Scope Enforcement: Precise drafting offers strategic advantages in preventing circumvention through design-around strategies.
  • Life Cycle Management: The patent’s claims may support subsequent patent filings covering new formulations, combinations, or indications, thereby extending the commercial lifecycle.

Conclusion

The scope and claims of AU2007275581 reflect a strategic effort to protect innovative chemical compounds and their therapeutic applications within Australia’s rigorous patent framework. Its strength depends on the novelty, inventive step, and claim clarity, which collectively determine its enforceability and competitive value in the pharmaceutical landscape.


Key Takeaways

  • Strong, well-defined claims targeting specific structural features or therapeutic uses reinforce patent robustness.
  • Broad claims require careful drafting to balance coverage and validity amidst challenging prior art.
  • The patent landscape around AU2007275581 is likely crowded, necessitating continuous patent prosecution strategies.
  • Enforceability depends heavily on the detailed technical disclosure and the patent's ability to withstand validity challenges.
  • Strategic patent portfolio management, including filing in multiple jurisdictions, is critical to maximizing market exclusivity and commercial success.

FAQs

1. What is the main protection scope of AU2007275581?

The patent primarily covers specific chemical compounds or pharmaceutical formulations, including their therapeutic uses, as defined by its claims.

2. Can the claims be broad, and what risks are associated?

While broad claims can provide extensive protection, they risk invalidation if unsupported by surprising features or if they overlap with prior art.

3. How does the Australian patent landscape impact this patent?

A dense patent landscape with similar filings increases the risk of infringement or invalidity challenges, emphasizing the importance of strong claim construction and strategic prosecution.

4. What is the typical lifespan of this patent?

The patent, granted in 2011, has an expiration date around 2028, unless extended or challenged, providing approximately 17 years of exclusivity.

5. What are key considerations for enforcing AU2007275581?

Clear claims, robust technical disclosure, and vigilant enforcement against infringing generics are essential for maintaining commercial advantage.


Sources:

  1. Australian Patent Office, official patent database.
  2. Patents Act 1990 (Australia).
  3. International Patent Classification and patent landscape reports.

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