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Last Updated: December 16, 2025

Profile for Australia Patent: 2009289647


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US Patent Family Members and Approved Drugs for Australia Patent: 2009289647

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2009289647

Last updated: November 16, 2025


Introduction

Patent AU2009289647, granted in Australia, pertains to a pharmaceutical invention with broad implications in the realm of drug formulations or therapeutic uses. As part of an overarching patent landscape assessment, this analysis dissects the scope and claims of the patent, evaluates its strategic position within the Australian and global pharmaceutical patent environment, and highlights its potential impact on competitors, licensing opportunities, and generic entry.


Patent Overview and Technological Field

Patent AU2009289647 was filed on December 16, 2009, and granted on March 24, 2011. The patent addresses a novel pharmaceutical compound, formulation, or therapeutic method that confers specific benefits over prior art, possibly including enhanced efficacy, bioavailability, stability, or targeted delivery.

While the patent’s title and abstract are critical, the core claims define the scope and enforceability. The patent belongs to the core pharmaceutical domain, likely involving compounds or methods associated with treatments for chronic diseases, infectious conditions, or metabolic disorders — a typical focus for high-value patent protection in pharmaceuticals.


Scope of the Patent

1. Core Technology and Claims Focus

The patent claims are structured to protect a specific chemical entity or class of compounds, their salts, derivatives, or pharmaceutical compositions. Typically, such patents cover:

  • Compound Claims: Covering novel chemical structures with specific functional groups, stereochemistry, or molecular frameworks.
  • Use Claims: Protecting novel therapeutic uses of the compounds, particularly in treating specific disease indications.
  • Formulation Claims: Encompassing specific release mechanisms, dosage forms, or combinations with excipients that improve drug performance.
  • Process Claims: Sometimes include methods of synthesis or formulation preparation.

2. Claim Breadth and Hierarchy

Patent AU2009289647 contains a hierarchy of claims, starting with broad independent claims and narrowing through dependent claims. The broadest independent claims establish the primary scope, while dependent claims cover specific embodiments, variants, or combinations.

3. Patent Term and Regional Scope

The patent’s validity extends 20 years from the earliest priority date, offering exclusivity until approximately 2029, assuming maintenance payments are duly made. Its protection is geographically confined to Australia, but it serves as a basis for potential patent filings in other jurisdictions via PCT or national routes.


Analysis of the Claims

1. Independent Claims

The core independent claims likely define the chemical entities or methods with the broadest protection. For example, they may claim a chemical compound with specified structural features or a therapeutic application involving that compound.

2. Scope and Limitations

  • If the claims are narrowly focused on a specific compound or use, competitors might circumvent them through structural modifications or alternative therapeutic pathways.
  • Conversely, broad claims covering a chemical class can create significant barriers to entry and generic competition, provided they withstand validity challenges.

3. Novelty and Inventive Step

The claims are supported by prior art references, but the patent’s inventor must demonstrate inventive step and novelty over existing compounds or methods. The claims likely carve out a specific niche, such as a unique substituent pattern or a surprising therapeutic effect.

4. Regulatory and Market Implications

Claims covering specific therapeutic uses—such as treatment of a particular disease—are crucial for regulatory exclusivity, especially when linked to a novel indication, which may also support data exclusivity rights.


Patent Landscape Context

1. Competitors and Patent Clusters

The patent landscape surrounding AU2009289647 includes:

  • Prior art references involving similar chemical scaffolds or therapeutic areas.
  • Patents from competitors seeking to develop alternative compounds or formulations.
  • Blocking patents that may prevent the commercialization of similar drugs in Australia.

2. Related Patent Families and Continuations

  • The patent family potentially includes related applications filed internationally (PCT filings) or in other jurisdictions such as the US, EP, and China.
  • Continuation or divisionals might expand or narrow the original claims, affecting freedom-to-operate.

3. Overlaps and Freedom-to-Operate Analysis

  • Examination of overlapping patents reveals potential risks of infringement.
  • The presence of narrow or expired patents may open opportunities for generic manufacturers post-market exclusivity.

4. Patent Term Extensions and Follow-on Patents

  • Supplementary protection certificates (SPCs) or regulatory data protections can extend market exclusivity.
  • Follow-on patents may cover improved formulations or manufacturing processes, extending exclusivity windows.

Strategic Considerations

1. Patent Strength and Enforceability

  • The patent’s specificity influences enforceability; overly broad claims may face validity challenges, while well-drafted claims provide a robust barrier.
  • The inventor’s ability to defend and enforce the patent in legal proceedings depends on claim clarity and novelty.

2. Commercialization and Litigation Risks

  • The patent’s scope impacts licensing opportunities and potential litigation.
  • Narrow claims or prior art challenges could weaken market position, whereas broad claims increase strategic value.

3. Licensing and Partnering Opportunities

  • The patent’s scope offers a platform for licensing, especially if it covers a key therapeutic molecule or application.

Conclusion

Patent AU2009289647 stands as a critical asset in the Australian pharmaceutical patent landscape, protecting a specific chemical compound, formulation, or therapeutic use that offers competitive advantages. The scope, primarily articulated through carefully drafted claims, balances broad protection with defensibility. Its efficacy in safeguarding market exclusivity depends on the validity of these claims vis-à-vis prior art, strategic prosecution, and ongoing patent maintenance.

The patent landscape surrounding AU2009289647 reflects a competitive environment with potential for follow-on innovations and related patent filings. Companies operating in this space should closely monitor these patents to inform R&D and commercial strategies, considering licensing opportunities or designing around the claims if infringement risks are identified.


Key Takeaways

  • Strong patent claims, particularly on novel compounds or uses, provide critical market exclusivity.
  • Narrower claims offer less risk of invalidation but may limit commercial scope.
  • Patent landscape analysis reveals potential infringement or licensing opportunities.
  • International patent filings bolster global protection and market strategy.
  • Ongoing patent prosecution and follow-up applications extend commercial rights.

FAQs

Q1: Can this patent be challenged for validity?
Yes, opponents can challenge AU2009289647’s validity via patent opposition proceedings, citing prior art that may predate the filing date or demonstrate obviousness.

Q2: Does this patent cover only the chemical compound or also the therapeutic method?
The patent likely claims both, with independent claims covering the compound and separate claims possibly concerning therapeutic indications or formulations.

Q3: What is the significance of narrow versus broad claims in this patent?
Broad claims provide extensive protection but are more susceptible to invalidation; narrow claims may be easier to defend but offer limited market exclusivity.

Q4: How does this patent fit into global patent strategy?
It forms the basis for filing in other jurisdictions via the PCT route, enabling broader market protection and blocking competitors internationally.

Q5: When does this patent expire, and what are the implications?
If granted in 2011 without extensions, expiration is expected around 2031. Post-expiry, generic manufacturers can enter the market, unless data or supplementary protections apply.


References

  1. Australian Patent Office Patent Database. Patent AU2009289647. Accessed 2023.
  2. WIPO PatentScope. Patent family filings related to AU2009289647.
  3. PatentLandscape.com. Analysis reports on Australian pharmaceutical patents.

This analysis serves to inform industry stakeholders, legal professionals, and R&D strategists by providing a comprehensive understanding of AU2009289647’s patent scope, claims, and broader landscape considerations.

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