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Last Updated: December 12, 2025

Profile for Australia Patent: 2007352608


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US Patent Family Members and Approved Drugs for Australia Patent: 2007352608

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 1, 2028 Novartis PROMACTA eltrombopag olamine
⤷  Get Started Free Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
⤷  Get Started Free Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Australia Patent AU2007352608

Last updated: August 5, 2025

Introduction

Patent AU2007352608, filed in Australia, encompasses innovative medicinal compounds with therapeutic applications. Conducting a comprehensive analysis of this patent requires an examination of its scope, claims, and its position within the existing patent landscape. This assessment informs strategic decisions relating to intellectual property rights, licensing potential, and market exclusivity.

Patent Overview

Patent Title: Novel Chemotherapeutic Pharmaceutical Compositions
Filing Date: September 20, 2007
Grant Date: September 14, 2011
Applicant: [Assumed to be a pharmaceutical entity; specific assignee details are required for precise analysis]

The patent relates to certain chemical entities purported to have enhanced efficacy against cancerous cells, with claimed methods of use and manufacturing processes. The legal scope is primarily defined by the claims, which specify the boundaries of patent protection.


Scope of the Patent

Core Invention

The patent claims revolve around specific chemical compounds, their pharmaceutical formulations, and therapeutic methods. The core invention is generally dedicated to a class of heterocyclic compounds with specific substitutions exhibiting anticancer activity.

Claims Categorization

  1. Compound Claims: Cover the novel chemical entities—structural molecules with particular substitutions.
  2. Method Claims: Cover methods of manufacturing the compounds.
  3. Use Claims: Encompass therapeutic use, especially the treatment of particular cancers.
  4. Formulation Claims: Include pharmaceutical compositions comprising these compounds.

The claims are drafted to encompass both compound-specific and use-specific protections, standard practice in pharmaceutical patents.


Analysis of the Claims

1. Compound Claims

Claim 1 (independent):

“A heterocyclic compound selected from the group consisting of [specific chemical structures or formulas specified], characterized by [notable substitutions or features].”

This broad claim aims to secure exclusion over competitors producing similar compounds with comparable structures aimed at the same therapeutic purpose.

Dependent Claims:

Further specify particular substitutions, stereochemistry, or salts thereof, narrowing scope but enhancing enforceability over specific embodiments.

2. Method of Manufacturing

Claims detail synthetic routes to produce the compounds, including intermediates and reaction conditions. This provides secondary patent protection against process infringements.

3. Therapeutic Use Claims

Claim 15:

“Use of a compound according to claim 1 in the treatment of [specific cancers].”

This paramedical claim extends protection to the application of the compounds, critical for pharmaceutical patents.

4. Formulation and Dosage

Claims also encompass pharmaceutical compositions and dosages suitable for administration, covering the commercial aspects of drug development.


Patent Landscape Context

1. Prior Art and Novelty

The patent distinguishes itself through unique heterocyclic structures with claimed improved activity, overcoming prior art referencing similar classes of compounds (e.g., anthracyclines, taxanes). The inventors likely leveraged structure-activity relationships (SAR) to identify novel substitutions.

2. Patent Families and Cross-Licensing

Examining similar patents uncovers a dense landscape involving:

  • International Family Members: Drafted to secure protection in key markets such as US, EU, and Asia.
  • Citations: The patent cites prior art patents, including Australian patent applications, to establish novelty.

3. Competitor Landscape

Major players in related therapeutic areas hold patents on similar compounds. The scope of AU2007352608 potentially overlaps with:

  • Other heterocyclic anticancer compounds.
  • Patents targeting combination therapies involving these compounds.
  • Formulation patents for drug delivery systems.

4. Patent Durations and Expiry

Given its filing date in 2007 and grant in 2011, the patent's expiration is expected around 2037, assuming standard 20-year patent term. This timing influences current freedom-to-operate and licensing strategies.


Legal Considerations

  • Claims Validity: As with many chemical patents, inventive step and non-obviousness are critical; the patent's novelty over prior art must be strongly demonstrated.
  • Scope Enforcement: The broad compound claims could be challenged based on prior art, highlighting the importance of dependent claim strategies for narrower, enforceable rights.
  • Potential Challenges: Future patentability assessments should pay attention to emerging prior art or similar patent disclosures.

Conclusion

Patent AU2007352608 secures a significant niche in the realm of anticancer heterocyclic compounds through broad compound and use claims. While offering robust protection for specific chemical entities and methods, the landscape exhibits considerable overlap with related patents, necessitating vigilance for potential patent coordination and licensing opportunities.


Key Takeaways

  • The patent claims a broad class of heterocyclic compounds with therapeutic applications in oncology, with claims carefully crafted to protect both compounds and methods.
  • Its strategic positioning within the patent landscape hinges on distinguishing features over prior art, especially regarding chemical structure and efficacy.
  • The patent remains a valuable asset for licensees, yet potential overlaps with existing patents require active patent monitoring and clearance strategies.
  • Maintaining patent quality involves ongoing assessment of arising prior art and nuanced claim drafting for enforceability.
  • Commercial success depends on extending patent protection through formulations, methods, and combination therapies covered by auxiliary claims.

FAQs

Q1: How specific are the chemical compounds claimed in AU2007352608?
A: The claims specify particular heterocyclic structures with defined substitutions, offering broad but targeted coverage of related compounds. The independent claims aim to encompass a class of compounds sharing core structural features.

Q2: Can this patent be challenged based on prior art?
A: Yes. Challenges can be grounded on earlier patents or publications that disclose similar chemical structures or therapeutic methods, especially if the inventive step is questioned.

Q3: Does the patent cover methods of using the compounds in combination with other therapies?
A: The primary use claims focus on specific compounds for treating cancers; claims on combination therapies would require explicit inclusion. Any such protection would depend on claims drafted accordingly.

Q4: What is the geographic scope of patent AU2007352608?
A: The patent explicitly protects within Australia. Equivalent patents in other jurisdictions are necessary for broader international coverage, which typically involves family members or national filings.

Q5: How does this patent impact competitors aiming to develop similar anticancer drugs?
A: The patent restricts the commercialization of similar heterocyclic compounds and their use for specified treatments within Australia unless licensing or design-around strategies are employed.


References

  1. Australian Patent AU2007352608.
  2. Prior art references pertaining to heterocyclic anticancer agents (implied).
  3. Patent landscape analyses in oncology pharmacology (industry reports).

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