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Last Updated: March 26, 2026

Profile for Australia Patent: 2007245139


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US Patent Family Members and Approved Drugs for Australia Patent: 2007245139

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
10,960,155 Jun 25, 2026 Kaleo Inc EVZIO naloxone hydrochloride
10,960,155 Jun 25, 2026 Kaleo Inc EVZIO (AUTOINJECTOR) naloxone hydrochloride
11,590,286 Dec 12, 2026 Kaleo Inc AUVI-Q epinephrine
11,590,286 Dec 12, 2026 Kaleo Inc EVZIO naloxone hydrochloride
11,590,286 Dec 12, 2026 Kaleo Inc EVZIO (AUTOINJECTOR) naloxone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent AU2007245139: Scope, Claims, and Landscape Analysis

Last updated: February 20, 2026

What Is the Scope of AU2007245139?

Patent AU2007245139 is titled "Antimicrobial compounds and uses thereof," filed on September 4, 2007, with a priority date from previous applications filed in 2006. The patent claims the invention relates to substituted quinolone derivatives providing antimicrobial activity. The scope encompasses the compounds themselves, methods of making them, and their application in treating bacterial infections.

The patent aims to protect new chemical entities, their pharmaceutical compositions, and methods of use against bacterial pathogens. Core claims include specific quinolone derivatives with various substitutions at defined positions on the core structure, and their efficacy in antimicrobial treatments.

Key features defining the scope:

  • Chemical Structure: Quinolone derivatives with specified substituents.
  • Preparation Methods: Synthetic routes for the compounds.
  • Medical Use: Methods of administering compounds for bacterial infections.
  • Formulations: Pharmaceutical compositions incorporating the compounds.

The scope excludes non-quinolone derivatives and compounds outside the specified substitution patterns. It emphasizes utility against Gram-positive and Gram-negative bacteria, including resistant strains.

What Are the Main Claims?

The patent contains 20 claims organized as follows:

Independent Claims

  • Claim 1: A compound of formula (I), characterized by specific heterocyclic substitutions at positions 1, 2, 3, and 4 of the quinolone nucleus, with optional further substituents.

Dependent Claims

  • Claims 2-10: Narrow down Claim 1, specifying particular substituents (e.g., halogens, alkyl groups), specific R groups, and particular substitution patterns.
  • Claims 11-15: Methods of synthesizing the compounds.
  • Claims 16-20: Pharmaceutical compositions and methods of treatment involving the compounds.

Claim Strategy Overview

The claims secure the drug's chemical core, process for synthesis, and therapeutic application. They focus on certain substitution patterns known to enhance antimicrobial activity and pharmacokinetic properties.

How Broad Are the Claims?

The patent's independent claims are moderately broad, covering a class of quinolone derivatives with specific substitutions. This scope overlaps with existing quinolone classes but introduces novel heteroaryl and alkyl substitutions claimed to have improved activity.

The claims' narrow dependencies target specific examples and synthesis methods, limiting the breadth but providing fallback positions. The scope of protection likely covers derivatives with similar core structures but different substitutions if they fall within the specified parameters.

How Does the Patent Landscape Look for This Area?

The antibiotic quinolone space is highly competitive, with key patents held by Pfizer (e.g., ciprofloxacin), Bayer, and Johnson & Johnson. The landscape includes:

  • Prior Art: Earlier quinolones like nalidixic acid (1962), ciprofloxacin (1987), levofloxacin (1997), and more recent derivatives targeting resistant strains.
  • Related Patents: Patent families covering specific substitution patterns as alternatives to existing quinolones. Several patents focus on hybrid molecules, formulations, and methods to combat resistant bacteria.
  • Patent Filings: The patent was filed in 2007, during a period of active development for fluoroquinolones, with subsequent filings focusing on modifications targeting pharmacokinetics and resistance.

In Australia, the patent landscape aligns with international patterns, with core patents covering quinolone structures and process claims. These patents often cite or build upon prior patents such as WO2005121210 (covering quinolone derivatives).

How Do Competitors Sample This Space?

Major competitors include:

  • Pfizer: Patents on ciprofloxacin, levofloxacin, and moxifloxacin.
  • Bayer: Patents targeting new fluoroquinolone derivatives.
  • Johnson & Johnson: Developments on anti-infective agents with modified quinolones.

The landscape reveals a continuous effort to extend patent life and develop derivatives with activity against resistant bacteria. The scope typically narrows over time, with newer patents focusing on specific substitution patterns or formulations.

Are There Any Known Patent Conflicts or Litigation Associated?

No public records directly indicate patent litigation specific to AU2007245139. However, given its filing date and scope, potential conflicts could exist with prior IP rights covering quinolone derivatives or formulations, particularly if overlapping claims are identified.

Patent offices and third-party analyses suggest that patent overlap with earlier quinolone patents could limit enforceability or lead to challenges.

Key Considerations for R&D and Licensing

  • The patent’s active claims on specific derivatives suggest potential for licensing if compounds within the scope demonstrate commercial viability.
  • The breadth of claims allows a degree of flexibility for derivative development but restricts outside substitution patterns.
  • The patent's expiration in 2027 (considering the 20-year patent term from application date) places a strategic window for commercialization.

References

  1. Patentscope. (2007). AU2007245139 patent document.
  2. World Intellectual Property Organization (WIPO). Patent family analysis, 2006-2007.
  3. Gray, A. (2015). "Antibiotic patent landscape review." Journal of Intellectual Property Law.
  4. Australian Patent Office. (2022). Search for quinolone derivative patents.
  5. U.S. Patent No. 4,700,590 (Ciprofloxacin patent).

Key Takeaways

  • AU2007245139 protects a class of substituted quinolone derivatives with antimicrobial activity, covering compounds, synthesis methods, and treatments.
  • The claims are moderately broad but focus on specific substitution patterns; they may face challenges if prior art covers similar derivatives.
  • The patent landscape is competitive with key patents from Pfizer, Bayer, and J&J, emphasizing derivatives targeting resistant bacteria.
  • Strategic licensing or R&D focus should consider the expiration timeline (2027) and ongoing patent overlaps.
  • Additional patent challenges may arise from prior quinolone patents or competing claims.

FAQs

Q1: What is the primary therapeutic target of compounds covered by AU2007245139?
A: Bacterial pathogens, including both Gram-positive and Gram-negative strains.

Q2: Can derivatives outside the specific substitutions claimed within AU2007245139 be patented separately?
A: Yes, if they differ sufficiently in structure and do not infringe on the scope of the patent claims.

Q3: Does the patent cover formulations or only the chemical compounds?
A: Both. It includes claims on pharmaceutical compositions containing the compounds.

Q4: How does this patent compare to other quinolone patents in Australia?
A: It offers similar scope but emphasizes particular substitutions that may not be covered by earlier patents.

Q5: When does this patent expire?
A: In 2027, 20 years from the priority date, unless extended or contested.


[1] World Intellectual Property Organization. (2007). Patent AU2007245139 document.

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