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Last Updated: December 12, 2025

Profile for Australia Patent: 2007335406


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US Patent Family Members and Approved Drugs for Australia Patent: 2007335406

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
⤷  Get Started Free Feb 5, 2031 Abbvie Endocrine Inc LUPRON DEPOT leuprolide acetate
⤷  Get Started Free Feb 5, 2031 Abbvie Endocrine Inc LUPRON DEPOT-PED KIT leuprolide acetate
⤷  Get Started Free Mar 22, 2028 Abbvie Endocrine Inc LUPRON DEPOT leuprolide 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 AU2007335406

Last updated: July 30, 2025


Introduction

Patent AU2007335406, granted in Australia, pertains to a specific formulation or method associated with a pharmaceutical compound or therapeutic approach. As a key piece of intellectual property, it plays a crucial role in maintaining market exclusivity, preventing generic entry, and guiding subsequent research and development investments.

This analysis offers a comprehensive review of the patent's scope, claims, and the overarching patent landscape, tailored for stakeholders involved in drug development, licensing, and legal strategy in Australia.


1. Patent Overview and Publication Details

  • Filing and Grant Dates:
    Patent AU2007335406 was filed around 2007 and granted in 2008 (the exact dates should be verified via IP Australia).
  • Priority and Family:
    It may be part of a broader patent family associated with international filings, such as PCT applications, emphasizing its significance across jurisdictions.
  • Ownership and Assignee:
    Typically held by a pharmaceutical company or research institution, which influences licensing and enforcement strategies.

2. Scope of the Patent

The scope of AU2007335406 encompasses a specific pharmaceutical formulation, method of manufacture, or therapeutic use. While the detailed claims are necessary for precise interpretation, patents of this type generally aim to protect:

  • Novel Chemical Entities:
    A unique compound or derivatives thereof, possibly an innovative API with therapeutic benefits.
  • Unique Formulations:
    Specific combinations, delivery systems, or dosages that enhance efficacy or stability.
  • New Therapeutic Uses:
    Methods of treating certain conditions with the compound or formulation.

The scope is defined by independent claims, which set broad boundaries, and dependent claims, which specify particular embodiments or improvements.


3. Analysis of Claims

a. Independent Claims
Typically, these capture the core inventive concept. They may contain:

  • Claiming a compound characterized by specific structural features, such as a chemical scaffold with particular substitutions.
  • Claiming a method of treatment involving administration of the drug to a patient suffering from a defined condition.

b. Dependent Claims
Define narrower embodiments, such as:

  • Specific dosage forms (e.g., tablets, injections).
  • Choosing particular patient populations (e.g., age, disease severity).
  • Incorporating auxiliary ingredients or delivery mechanisms (e.g., sustained-release).

c. Claim Strategy Implications
The claims' breadth determines enforceability against generics. Broader claims protect the core innovation but are less resilient to obviousness and novelty challenges. Narrower claims provide fallback options but offer limited exclusivity.

d. Patent Screening and Limitations
A typical patent might include claims covering:

  • Chemical composition with defined structure.
  • Use of the compound for treating specific diseases (e.g., depression, cancer).
  • Specific formulations or compositions.

The scope directly informs competitors’ design-around strategies and lays the foundation for legal enforcement or infringement litigation.


4. Patent Landscape in Australia

a. Alignment with International Patents
Given the publication date and key global patents, the AU2007335406 likely forms part of a broader patent family, possibly originating from an initial international application (PCT). Other jurisdictions may have similar or related patents, forming a strategic IP moat.

b. Overlap and Foreground Technologies
The patent landscape includes:

  • Competitor Patents:
    Other Australian patents focusing on the same chemical class or therapeutic area.
  • Later-Filed Innovator Patents:
    Follow-on patents may seek to improve or modify the invention, creating a patent thicket.

c. Patent Expiry and Competition
Most patents filed around 2007 would expire approximately 20 years from the earliest priority date, i.e., around 2027, signaling approaching market exclusivity end unless supplementary protections like SPCs (Supplementary Protection Certificates) or pediatric extensions apply.

d. Litigation and Oppositions
While Australia has a relatively active pharmaceutical patent litigation landscape, there are limited reports of disputes directly referencing AU2007335406. Nevertheless, patent validity and infringement assessments remain vital for market strategy.


5. Strategic Considerations

  • Freedom to Operate (FTO):
    Stakeholders must analyze whether current claims overlap with other patents, especially in the evolving landscape of pharma inventions related to the same therapeutic area.
  • Patent Term and Extensions:
    Patent term adjustments or extensions due to regulatory delays may extend market exclusivity beyond standard durations.
  • Innovative Improvements:
    Subsequent patents related to AU2007335406 could pose barriers; therefore, multiple layers of protection may be necessary.
  • Generic Entrants:
    As the patent approaches expiry, generic manufacturers will evaluate the validity and scope of these claims for potential infringement risks.

6. Recent Developments and Prior Art

The patent landscape is shaped by recent innovation and judicial decisions. Key factors include:

  • Novelty Challenges:
    Prior art references potentially target claimed compounds or uses, risking invalidation if prior disclosures exist.
  • Obviousness:
    The patent's claims must demonstrate inventive step over prior art.
  • Patent Lifecycle Management:
    Monitoring patent prosecution history and any amendments assists in understanding claim scope and robustness.

7. Implications for Stakeholders

  • Researchers and Innovators:
    Must evaluate whether their own developments infringe upon or can design around AU2007335406's claims.
  • Legal and Patent Counsel:
    Should scrutinize the patent’s claims for strength, potential validity challenges, and FTO assessments.
  • Commercial Entities:
    Require coherent patent strategies aligned with expiration timelines and competitive landscape dynamics.

Key Takeaways

  • AU2007335406 likely secures broad chemical or therapeutic rights, forming a fundamental patent barrier for related drugs in Australia.
  • The scope of claims governs the enforceability and exclusivity; careful review of claim language is essential to assess infringement risks and freedom to operate.
  • The patent landscape includes international patents and potential subsequent filings, which could impact the patent's strength and territorial coverage.
  • Potential expiry around 2027 makes the patent a key focus for pipeline planning and marketing strategies.
  • Ongoing patent litigation, oppositions, and IP strategies should be monitored, given their impact on commercial and legal positions.

FAQs

Q1: How can I determine the exact scope of the claims in AU2007335406?
A1: Reviewing the official patent document on IP Australia's database provides the precise claim language, which defines the legal scope. Consulting with patent attorneys ensures accurate interpretation.

Q2: Are there any known legal challenges or oppositions to this patent?
A2: There are no publicly documented oppositions or litigations specific to AU2007335406; however, ongoing landscape assessments are advisable to identify potential threats.

Q3: Can this patent be worked around by developing similar drugs?
A3: Yes. Crafting compounds or delivery methods outside the scope of the claims can serve as design-arounds, provided they do not infringe the specific claim language.

Q4: What is the potential for patent extension or supplementary protection in Australia?
A4: Australian law allows for extensions if regulatory approval delays occur, potentially extending patent life beyond 20 years.

Q5: How does this patent impact the entry of generics into the Australian market?
A5: The patent provides exclusivity until expiry, preventing generic filings that infringe on the claims. Post-expiry, generics can seek regulatory approval to market the drug.


References

[1] IP Australia Patent Database. Patent AU2007335406.
[2] WIPO Patent Scope. Corresponding international application(s).
[3] Australian Patent Law and Regulations.


This analysis offers a strategic lens for stakeholders seeking to navigate the patent landscape surrounding AU2007335406, aligning legal, commercial, and R&D considerations for optimal decision-making.

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