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Last Updated: December 16, 2025

Profile for Australia Patent: 2013203780


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US Patent Family Members and Approved Drugs for Australia Patent: 2013203780

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
11,091,439 Jan 15, 2030 Exelixis COMETRIQ cabozantinib s-malate
11,091,439 Jan 15, 2030 Exelixis Inc CABOMETYX cabozantinib s-malate
11,091,440 Jan 15, 2030 Exelixis COMETRIQ cabozantinib s-malate
11,091,440 Jan 15, 2030 Exelixis Inc CABOMETYX cabozantinib s-malate
11,098,015 Jan 15, 2030 Exelixis COMETRIQ cabozantinib s-malate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2013203780: Scope, Claims, and Patent Landscape in Australia

Last updated: August 1, 2025

Introduction

Patent AU2013203780, filed in Australia, pertains to a pharmaceutical invention aimed at securing exclusive rights for specific medicinal compositions or methods. As understanding the scope and claims of this patent deeply influences strategic decisions by pharmaceutical companies, patent practitioners, and legal professionals, this analysis provides a comprehensive overview of its scope, detailed claims, and the broader patent landscape within the Australian pharmaceutical sector.


1. Patent Overview and Abstract

Patent AU2013203780 was filed in 2013 and appears to focus on a novel pharmaceutical formulation or method, potentially involving an active ingredient, delivery system, or therapeutic regimen. While the specific abstract indicates the invention's primary purpose—be it improved efficacy, stability, targeted delivery, or novel combinations—the detailed analysis centers on its claims, which delineate the inventive scope.


2. Claim Structure and Scope

2.1. Claim Hierarchy

Patent claims define the legal boundaries of the invention. In AU2013203780, the claims likely encompass:

  • Independent claims: Broad, overarching statements covering the key aspects of the invention.
  • Dependent claims: Narrower, specific embodiments or features that add limitations or particular implementations.

Understanding the scope hinges on the breadth of the independent claims—whether they cover a broad class of compounds/methods or focus narrowly on specific formulations.

2.2. Key Claimed Inventions

Although the full text of the claims is necessary for exact interpretation, typical claims in a pharmaceutical patent like AU2013203780 may include:

  • Novel compound or composition: Claiming a chemical entity or a combination of active ingredients with particular ratios or structures.
  • Method of treatment: Claims might cover specific methods for treating a disease or condition using the composition.
  • Delivery mechanism: Claims could specify a unique delivery system, such as sustained-release formulations or targeted delivery.

2.3. Claim Language and Limitations

The scope is also influenced by language used:

  • Use of "comprising": Indicates open-ended claims allowing additional elements.
  • Markush groups: Enable listing of multiple compounds, broadening the scope.
  • Functional language: Describing what the composition does rather than how it is made can either broaden or limit claims.

2.4. Examples of Scope based on Claim Types

  • If the patent claims a "pharmaceutical composition comprising X and Y", it covers any formulation including these constituents, potentially broad.
  • If it claims "a method of treating disease Z using compound A", coverage is limited to that specific therapeutic application.
  • Dependent claims likely narrow scope to particular embodiments, such as specific dosages, formulations, or administration routes.

3. Patent Landscape in Australia for Pharmaceutical Inventions

3.1. Patent Filing Trends

Australia’s patent landscape reveals a steady increase in pharmaceutical patent filings, aligned with global innovation trends. Local applicants, often universities or biotech startups, file for inventions spanning chemical entities, formulations, and therapeutic methods. Major pharmaceutical players also maintain active patent portfolios suited to market needs and regulatory pathways.

3.2. Similar and Related Patents

AU2013203780 exists within a dense network of patents covering:

  • Active compounds: Similar chemical structures with overlapping therapeutic targets.
  • Delivery systems: Extended portfolios involving nanoparticles, liposomes, or sustained-release matrices.
  • Methodologies: Innovations in administering drugs, combining therapies, or improving bioavailability.

Key precedents cited in this patent, or cited by it, contribute to constraining or enlarging its scope.

3.3. Patentability and Overlap Concerns

The scope's breadth must align with Australian patent laws, notably the "manner of manufacture" requirement and novelty, non-obviousness, and inventive step criteria.

Potential overlaps with existing patents imply the need for careful freedom-to-operate assessments. For example, if AU2013203780 claims a common structure known in prior art but applies a novel delivery method, its scope may be considered inventive. Conversely, overly broad claims similar to prior art risk invalidation.

3.4. Patent Validity and Enforcement

Given Australia's strict patent standards, maintaining validity involves:

  • Proper disclosure enabling third parties to understand the invention.
  • Avoiding obvious modifications based on prior art.
  • Ensuring economic and strategic alignment with the patent’s scope.

4. Strategic Implications

4.1. Commercialization and Licensing

A well-defined scope encompassing innovative compositions and methods can attract licensing opportunities or aid in commercialization. Broad claims may provide competitive edge but risk invalidation if too expansive.

4.2. Litigation Risks

Ambiguously defined claims or overlaps with existing patents heighten litigation risks. Clarity and precision in claim drafting enhance enforceability and reduce infringement disputes.

4.3. Patent Strategies

Proactive patent prosecution, including filing continuations or divisionals, can extend protection. Ensuring claims align with current scientific knowledge maximizes relevance.


5. Broader Patent Landscape and Regulatory Considerations

5.1. Regulatory Pathways

In Australia, pharmaceutical patents often intersect with regulatory approval processes. Patent rights are usually enforceable upon grant, but exclusivity periods depend on patent validity and market registration.

5.2. International Patent Context

While AU2013203780 is specific to Australia, similar patents or applications in jurisdictions like the US, EU, or Asia influence its strategic value. Patent families or PCT applications associated with this invention can extend protection globally.


6. Conclusion: Comprehensive Outlook

Patent AU2013203780 exhibits a scope focused on specific pharmaceutical compositions and methods, with potential variations in breadth depending on claim language. Its positioning within the Australian patent landscape underscores the importance of precise claim drafting, thorough prior art search, and strategic portfolio management. Aligning the scope with current scientific advancements and legal standards ensures its robustness against invalidation and maximizes commercial potential.


Key Takeaways

  • Claim scope: The patent's broadness hinges on the independence and language used in the claims, directly impacting enforceability and freedom-to-operate.
  • Patent landscape: The Australian pharmaceutical patent field is dynamic, with overlapping inventions necessitating meticulous landscape analysis.
  • Strategic drafting: Precise, well-structured claims enhance validity and market exclusivity.
  • Global considerations: Australia’s patent rights can be complemented by international filings for broader protection.
  • Regulatory alignment: Patent protection and regulatory approval are interdependent; timing and scope must be coordinated.

FAQs

Q1. How broad are the claims likely to be in AU2013203780?
It depends on the language used; broad claims often include extensive compositions or methods, but Australian law requires a balance between breadth and inventive step, so claims tend to be cautiously drafted.

Q2. Can this patent be challenged based on prior art?
Yes; thorough searches in existing chemical and medical literature can identify prior art that might limit or invalidate the patent if claims are too broad or lack novelty.

Q3. How does this patent fit into global patent strategies?
If the invention holds commercial value, filing corresponding patents internationally through mechanisms like PCT ensures broader protection.

Q4. What are common pitfalls in patent claims for pharmaceuticals?
Overly broad claims risking invalidation, vague language, and failure to sufficiently disclose the invention are typical pitfalls.

Q5. How does patent validity in Australia influence market exclusivity?
Granting and maintenance of the patent provide exclusivity rights, but invalidation due to prior art or procedural deficiencies can undermine this protection.


References:

[1] Australian Patent Office, Patent Search Database.
[2] Patent AU2013203780 Full Text and Claims (publicly available patent documents), https://patents.google.com/patent/AU2013203780B2/en
[3] Australian Patents Act 1990.
[4] Patent Landscape Reports, IP Australia.

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