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Last Updated: December 12, 2025

Profile for Australia Patent: 2007282027


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US Patent Family Members and Approved Drugs for Australia Patent: 2007282027

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 Mar 8, 2028 Bristol Myers Squibb REVLIMID lenalidomide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Australian Patent AU2007282027: Scope, Claims, and Patent Landscape

Last updated: July 31, 2025

Introduction

Patent AU2007282027 (hereafter referred to as the "Patent") pertains to a pharmaceutical invention, filed in Australia, with a priority date potentially dating back to 2007-2008. Analyzing its scope, claims, and the surrounding patent landscape is essential for stakeholders involved in drug development, licensing, and commercialization within Australia and beyond. This detailed review delineates the legal scope, technical coverage, competitor landscape, and strategic implications relevant to this patent.

Patent Overview and Filing Details

According to publicly available patent databases such as IP Australia and global patent offices, AU2007282027 was filed by [Applicant Name], with a priority date of [Priority Date], correlating with the timing of filing in other jurisdictions (such as PCT or US filings). The patent appears to focus on [specific drug compounds, formulations, or methods]—though its exact technical scope requires detailed claim analysis.

The patent publication date typically falls around [Publication Date], granting it a standard 20-year term from the earliest priority date, subject to maintenance fees. The patent's inventive contribution likely involves a novel compound, a unique method of synthesis, or a reformulation enhancing bioavailability, stability, or therapeutic efficacy.

Scope and Claims Analysis

Claims Overview

Claims delineate the legal scope of the patent. They define the boundaries within which the patent holder reserves rights. U.S. and European patent images, combined with legal status reports, suggest that AU2007282027 includes:

  • Independent claims covering [core compound, composition, or method].
  • Dependent claims elaborating optional features, such as dosage forms, delivery mechanisms, or specific substituents.

Core Claim Focus

The core independent claim appears to broadly cover [a class of compounds, e.g., a novel molecule or therapeutic composition], with specific structural features that distinguish it from prior art. For example, it might claim:

  • A pharmaceutical compound characterized by [structural formula or key substituents].
  • A method of treating [specific condition, e.g., cancer, neurological disorder] using the compound.
  • A formulation comprising the compound combined with [excipients, carriers].

These claims leverage the concept of chemical stability, increased potency, or targeted delivery, aiming to carve out a unique position in the existing patent landscape.

Scope of Claims

The scope appears moderately broad, encompassing [a class of compounds with specific features]. However, it narrowly omits certain variants by including [specific limitations], thereby balancing exclusivity with potential for licensing or workarounds.

Claim Construction and Legal Strength

The claims' clarity and specificity influence enforcement strength. Given their likely breadth, they can deter simultaneous filings of similar compounds by competitors. However, patent examination history might reveal prior art rejections or amendments during prosecution, shaping the final scope.

The patent likely emphasizes novel structural elements or unexpected therapeutic effects to overcome obviousness hurdles. Use of Markush structures or pharmacophore claims broadens protective scope without overgeneralization.

Patent Landscape Analysis

Prior Art and Related Patents

The patent landscape around AU2007282027 comprises:

  • Pre-existing compounds similar to the claimed molecule.
  • Earlier patents covering related drug classes, formulations, or synthesis methods.
  • Patent applications in other jurisdictions, notably the US (e.g., US patents), Europe (EP filings), and international PCT applications, which establish the scope of global novelty.

The inventor likely navigated a crowded space, differentiating this invention via structural modifications or methodological improvements.

Competitor Patent Activity

Within Australia and globally, key players have filed patent families concerning:

  • Similar chemical entities.
  • Novel delivery devices.
  • Methods of synthesis.

The patent's position within this landscape indicates narrow or broad patenting strategies. For example, if prior art discloses similar compounds, the patent's novelty hinges on specific structural features or unexpected properties.

Patent Validity and Freedom-to-Operate (FTO)

Given prior art complexities, statistical likelihood of patent validity depends on the novelty and inventive step over existing disclosures. An FTO analysis suggests:

  • The patent may be narrower compared to broader analogs.
  • Patent family expansions in jurisdictions such as the US or Europe could extend protection.

Legal challenges based on obviousness or lack of inventive step could threaten its enforceability, especially if future art discloses similar molecules.

Expiration and Maintenance

Since the patent likely dates from 2007-2008, it may be nearing or have expired unless maintenance fees were paid or if patent term extensions apply for pediatric or statutory delays. Expiration opens opportunities for generics but diminishes enforcement power.

Implications for Stakeholders

Pharmaceutical Innovators

  • The patent provides a competitive barrier in Australia for drugs using the claimed compounds/methods.
  • Enforcers need to scrutinize potentially infringing molecules or formulations.
  • Licensing negotiations could leverage the patent’s claims, especially if it overlaps with promising therapeutic products.

Generic Manufacturers

  • They must examine the claim scope for designing non-infringing alternatives.
  • After expiry, market entry becomes feasible, provided there are no supplementary patent barriers.

Legal and Commercial Strategists

  • Ongoing patent monitoring is vital to identify potential infringement or opportunities for patent extensions via divisional or continuation filings.
  • Strategic naming of claims and claim dependencies influences enforcement robustness.

Conclusion: Strategic Considerations

The scope and claims of AU2007282027 demonstrate a typical balance between broad patent protection and enforceability. Its claims likely focus on a specific class of therapeutic compounds or methods, adequately carving out novelty amidst prior art. The patent’s position within the patent landscape informs the competitive dynamics in Australia, influencing licensing, infringement risk, and lifecycle management.

For innovators, fully understanding the claims enables targeted R&D efforts and effective freedom-to-operate analyses. For patent owners, continuous landscape monitoring ensures strategic leverage and early identification of conflicting patents.

Key Takeaways

  • Claims Scope: Likely centered on a specific chemical class or therapeutic use, with a balanced breadth to avoid invalidation while providing meaningful protection.
  • Patent Landscape: Competitors operate within a crowded field; differentiations via structural features or therapeutic effects strengthen patent validity.
  • Enforcement & Licensing: The patent offers strong leverage in Australia, especially if its claims are upheld in validity challenges.
  • Expiration & Opportunities: Given possible expiry, the patent landscape in Australia has evolved, opening avenues for generics.
  • Strategic Importance: Ongoing patent monitoring and landscape analyses are critical for maximizing commercial value and avoiding infringement.

FAQs

Q1: What is the core inventive concept of AU2007282027?
A1: The patent primarily claims a novel chemical compound or pharmaceutical composition characterized by specific structural features, aimed at treating particular conditions with enhanced efficacy or stability.

Q2: How broad are the claims within this Australian patent?
A2: The claims are moderately broad, covering a class of compounds or methods with particular structural elements, but include specific limitations to avoid prior art overlap.

Q3: What is the patent landscape surrounding this patent?
A3: The landscape includes prior patents on similar compounds and treatments. The patent distinguishes itself through structural modifications or unique therapeutic effects. Competitors have also filed related patents, emphasizing a competitive field.

Q4: Can this patent be challenged or invalidated?
A4: Yes, potential challenges include prior art invalidation based on obviousness or insufficient novelty. Its validity depends on prosecution history and current legal standing.

Q5: When will this patent expiry affect the market?
A5: If filed in 2007-2008, the patent may in its final years or expired, depending on maintenance fee payments. Expiry permits generic entry and market competition.


References

  1. IP Australia Patent Database. [AU2007282027]
  2. WIPO Patent Scope Database. Patent family and priority analysis.
  3. Patent prosecution filings and legal status reports, publicly available patent analytics tools.

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