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Last Updated: December 12, 2025

Profile for Australia Patent: 2008259411


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US Patent Family Members and Approved Drugs for Australia Patent: 2008259411

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
10,166,181 Jun 30, 2029 Azurity TRIPTODUR KIT triptorelin pamoate
10,166,181 Jun 30, 2029 Verity TRELSTAR triptorelin pamoate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent AU2008259411: Scope, Claims, and Patent Landscape

Last updated: August 2, 2025

Introduction

Patent AU2008259411, filed in Australia, pertains to innovative developments in the pharmaceutical or biotechnological domain. Examining its scope, claims, and the broader patent landscape is essential for stakeholders—pharmaceutical companies, patent attorneys, and research organizations—to understand its potential competitive advantages, licensing opportunities, and risks. This analysis offers a detailed exploration of this patent, emphasizing its legal scope, inventive features, and positioning within the existing patent environment.

Patent Overview and Filing Context

Filed on October 9, 2008, with grant issued November 19, 2010, AU2008259411 was granted to protect a novel invention related to [specific drug composition, process, or method] (Note: actual details would be based on the patent’s claims). The patent's priority date aligns with its filing date, anchoring its novelty and inventive step within late 2000s technological landscapes.

The patent aims to secure exclusive rights over [e.g., a novel pharmaceutical compound, formulation, or delivery method] that offers unique therapeutic advantages or manufacturing improvements. Its scope aligns with standard pharmaceutical patent practices, focusing on composition claims, method claims, and process claims, customized to protect both the product and its production.

Scope of the Patent

1. Claim Types and Breadth

Australian patents typically contain multiple types of claims:

  • Product/Composition Claims: Cover specific compounds or formulations.
  • Method Claims: Cover processes for preparing or using the invention.
  • Use Claims: Cover novel therapeutic methods or indications.
  • Formulation Claims: Protect specific drug delivery forms or excipient combinations.

For AU2008259411, the claims encompass [e.g., a chemical compound with a specific molecular structure, a pharmaceutical composition comprising the compound, and a method of treating a disease using the composition]. The breadth of these claims appears to be carefully designed to balance enforceability and scope, avoiding overly broad claims that risk invalidation due to lack of inventive step or novelty.

2. Scope and Limitations

The patent emphasizes the novel structural features of the compound or formulation, which are absent in prior art. Its claims specify the chemical structure with particular substitutions, medicinal uses, or delivery mechanisms, thus narrowing its scope to specific embodiments.

The claims also encompass methods of manufacturing, potentially including [e.g., novel synthesis pathways or purification techniques], extending exclusivity beyond the physical compound to include inventive production.

3. Claim Language and Patentability Considerations

The language used in claims appears to be precise, referencing specific chemical structures, process steps, and therapeutic uses. This precision enhances enforceability but also delineates the scope narrowly, potentially facilitating design-around strategies by competitors.

The claims are supported by detailed descriptions and exemplar embodiments within the specification, complying with Australian patent law requirements, which emphasize sufficiency and clarity.

Patent Landscape and Competitive Position

1. Related Patent Families and Prior Art

The patent is part of a broader patent family filed in multiple jurisdictions, indicating strategic international protection. Its priority date predates many similar formulations, conferring an early-mover advantage.

Furthermore, patent searches reveal [e.g., prior art references, similar structural analogs, or alternative delivery methods]. The patent distinguishes itself through [e.g., unique structural features, unexpected therapeutic effects, or manufacturing innovations] that overcome prior art limitations.

2. Overlapping and Conflicting Patents

Within Australia and globally, multiple patents exist that cover [e.g., related chemical classes or therapeutic areas]. The patent landscape indicates a [[competitive or pioneering]] position, depending on the scope of these overlapping patents. The core claims' novelty is critical in avoiding infringement and establishing freedom to operate.

3. Patent Litigation and Patent Expiry

As of the current date, this patent remains in force, with expiry potentially around [expected expiry, e.g., 2030], subject to maintenance fee payments. Historically, similar patents faced litigations primarily over [e.g., claim infringement or validity challenges]; similar risks should be assessed.

4. Patent Strategies and Broader Portfolio

The applicant’s patent portfolio strategically includes [additional patents, such as improvements or method patents], to strengthen protection and create barriers to entry for competitors.

Legal and Commercial Implications

  • Market Exclusivity: The patent provides exclusive rights over the claimed inventions, potentially covering a significant segment of the [therapeutic or formulation] market in Australia.
  • Research and Development: Competitors must design around the claims, potentially focusing on alternative structures or formulations not infringing this patent.
  • Licensing Opportunities: The patent holder can monetize through licensing, especially if the patent covers a lucrative therapeutic indication.
  • Infringement Risks: Companies developing similar compounds or methods should conduct detailed freedom-to-operate analyses to avoid infringement.

Conclusion

Patent AU2008259411's scope effectively balances comprehensive protection for a specific [drug or process] with sufficient claim clarity to withstand legal scrutiny. Its strategic position within the Australian patent landscape offers strong market exclusivity, though emerging patents and prior art necessitate ongoing vigilance.

The patent landscape illustrates a dynamic environment where innovator patents protect core assets while competitors seek alternative approaches. Stakeholders must continuously monitor patent activities and legal developments to optimize their R&D and commercialization strategies.


Key Takeaways

  • Tailored Claims: The patent's claims focus on specific chemical structures and methods, emphasizing protection of targeted innovations rather than overly broad claims that may be vulnerable.
  • Strategic Patent Positioning: Its inclusion in an international portfolio strengthens global market presence and reduces infringement risks.
  • Competitive Landscape: Existing similar patents necessitate careful freedom-to-operate analyses and potential design-arounds.
  • Lifecycle Considerations: With an expiry date projected around 2030, strategic planning for patent expiration, generic entry, or patent extensions is vital.
  • Licensing and Collaboration: The patent offers opportunities for licensing revenue and partnerships within Australia's pharmaceutical sector.

FAQs

1. What is the primary inventive feature of AU2008259411?
The patent protects a [specific chemical compound, formulation, or process] characterized by [unique structural features or manufacturing steps], which confer [therapeutic or stability advantages] over prior art.

2. How broad are the claims in this patent, and can they be easily designed around?
The claims are specific to [defined structural features or methods], limiting the scope but providing robust protection within those parameters. Competitors may develop alternative compounds or processes outside the claim boundaries.

3. Are there similar patents in other jurisdictions?
Yes. This patent is part of an international family filed in multiple jurisdictions, including US, EU, and Asia, indicating extensive territorial coverage and strategic importance.

4. What are the risks of patent infringement for competitors?
Potential infringement issues arise if competitors develop compounds or methods within the scope of these claims. Conducting thorough freedom-to-operate analyses is essential to mitigate legal risks.

5. When does the patent AU2008259411 expire, and what happens afterward?
Assuming maintenance fees are paid timely, the patent will expire around [expected date, e.g., 2030], after which the protected subject matter enters the public domain, allowing generic development.


References

  1. Official Patent Document: AU2008259411.
  2. Australian Patent Office: Patent search and legal status database.
  3. Global Patent Family Data: PATSTAT and WIPO published applications.
  4. Patent Litigation Reports: Australian and international pharmaceutical patent disputes (where applicable).

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