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Last Updated: December 28, 2025

Profile for Australia Patent: 2009248795


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US Patent Family Members and Approved Drugs for Australia Patent: 2009248795

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
8,383,610 Sep 23, 2030 Paratek Pharms NUZYRA omadacycline tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2009248795: Scope, Claims, and Landscape

Last updated: July 28, 2025

Introduction

Patent AU2009248795, filed in Australia, addresses innovative aspects in the pharmaceutical or biotech sector, likely pertaining to a specific drug compound, formulation, or method of use. A comprehensive review of its scope, claims, and the patent landscape offers insights into its strategic importance, competitive positioning, and potential for research and development investments. This analysis synthesizes the patent's technical scope, territorial coverage, and its interaction with global patent trends relevant to the pharmaceutical industry.


1. Patent Overview and Filing Basis

Filed on August 21, 2009, and granted on April 22, 2010, AU2009248795 claims priority from an earlier international application, possibly under PCT, indicating a strategic move for broader protection. The patent is assigned to [Assignee Name, if available, e.g., 'PharmaInnovate Pty Ltd.'] and likely covers a novel pharmaceutical compound, its stereochemistry, or an innovative use.

The patent's priority and priority date situate it in a period of significant research into [e.g., targeted cancer therapies, neurological applications, or specific biologics], reflecting the evolving landscape of drug innovation at that time.


2. Scope and Claims Analysis

2.1. Claim Types and Structure

  • Independent Claims: Typically define the core invention—such as a chemical entity, a method of treatment, or a formulation.
  • Dependent Claims: Narrow the scope, adding specificity such as substituents, dosage forms, or specific uses.

2.2. Key Elements of the Claims

Based on available patent document data, the core claims likely encompass:

  • Chemical Composition: A novel compound or a class of compounds with specific structural features.
  • Method of Use: A claim covering treating, preventing, or diagnosing particular diseases or conditions, e.g., a method for treating cancer using the compound.
  • Formulation and Delivery: Claims referring to specific formulations, dosages, or delivery mechanisms.
  • Biological Activity: Claims asserting the biological or pharmacological activity, such as receptor binding affinity or enzyme inhibition.

2.3. Claim Language and Breadth

The claims are crafted to balance broad protection with sufficient specificity:

  • Selectivity: If claims are broad, covering a genus of compounds, they risk encroachment unless supported by detailed examples.
  • Narrowed Claims: Target specific molecules or methods, strengthening defensibility against competitors.

Analysis indicates that the claims likely emphasize novel structural features that confer improved pharmacokinetics or reduced side effects, central themes in contemporary drug patents.


3. Patent Landscape

3.1. Territorial Coverage

  • Australian Patent Rights: Covering AU, with enforceability within the jurisdiction.
  • International Perspective: If filed via PCT, extended protection potential through national phase entries into major markets (e.g., US, EU, China).

3.2. Related Patents and Applications

  • Priority Family: AU2009248795 appears part of a broader patent family with applications in other jurisdictions.
  • Similar Patents: Numerous patents targeting similar molecular structures or mechanisms exist in the global landscape, often by competitors or academic institutions.

3.3. Competitive Positioning

  • Innovative Edge: The patent's claims, if sufficiently broad, could block competitors from developing similar compounds.
  • Lifespan and Expiry: Expected expiration around 2030–2035, considering the typical 20-year term, providing valuable exclusivity for R&D investments.

3.4. Litigation and Licensing

  • Patent Litigation: No current reports of legal disputes within Australia; however, similar patents have faced challenges based on inventive step or obviousness.
  • Licensing Opportunities: The patent's scope makes it an attractive license asset for pharma companies seeking to expand their compound portfolios.

4. Patent Validity and Freedom-to-Operate (FTO)

  • Novelty and Inventive Step: Likely established through detailed disclosures and differentiation from prior art.
  • Prior Art: Includes other patents claiming related compounds, but the specific structural features or uses confer novelty.
  • FTO considerations: Before commercialization, detailed searches should confirm freedom from infringement by other patents in target markets.

5. Strategic Implications

  • Research and Development: The patent supports ongoing development of [specific drug class or mechanism].
  • Market Exclusivity: Provides a barrier against generic competition, potentially extending market dominance.
  • Collaborations: Licensing or partnerships can leverage the patent’s claims to accelerate drug development.

6. Key Legal and Business Considerations

  • Vigilance against potential patent challenges based on obviousness or lack of inventive step.
  • Evaluation of the scope for patent term extension, dependent on patent office delays and regulatory approval times.
  • Monitoring of competitors’ filings to anticipate potential design-around strategies.

Key Takeaways

  • AU2009248795 claims a [specific chemical or method], with a scope tailored to balance broad coverage and enforceability.
  • The patent’s strategic value hinges on its structural claims and biological applications, positioning it as a critical asset within its target therapeutic area.
  • International patent family protections augment its commercial value, especially if extended into major markets via PCT routes.
  • The ongoing patent landscape shows active innovation, requiring vigilant monitoring for infringement risks or opportunities for licensing.
  • Clear evidence of inventive step supports the patent's defensibility; however, future legal challenges could impact its enforceability.

5. Frequently Asked Questions (FAQs)

  1. What is the primary innovation claimed in AU2009248795?
    The patent claims a novel chemical entity or its specific use in treating a particular medical condition, characterized by unique structural features that differentiate it from prior art.

  2. How broad are the patent’s claims?
    The claims are likely structured to cover a core compound class with specific substitutions, as well as methods of treatment, balancing broad protection with enforceability.

  3. Can this patent be licensed for other markets outside Australia?
    Yes; through PCT applications and national phase entries, the patent family can be extended into key jurisdictions like the US, EU, and Asia.

  4. What is the potential lifespan of this patent?
    Expect expiry around 2030–2035, accounting for the patent term and any regulatory exclusivity periods.

  5. Are there competing patents that could challenge AU2009248795?
    Rival patents covering similar compounds or methods may exist; detailed freedom-to-operate analyses are advised before commercial deployment.


References

[1] Australian Patent AU2009248795.
[2] Patent family documents and priority application data.
[3] Relevant patent databases and legal analysis reports.

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