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Last Updated: December 15, 2025

Profile for Australia Patent: 2007337139


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US Patent Family Members and Approved Drugs for Australia Patent: 2007337139

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
10,441,543 Dec 19, 2026 Abbvie DURYSTA bimatoprost
9,149,428 Dec 19, 2026 Abbvie DURYSTA bimatoprost
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2007337139

Last updated: July 28, 2025

Introduction

The patent AU2007337139, associated with pharmaceutical innovations, appears to focus on a specific drug compound or formulation, safeguarding proprietary technology within the Australian patent landscape. Effective comprehension of its scope, claims, and positioning within the patent landscape is vital for stakeholders, including pharmaceutical companies, generic manufacturers, and legal professionals aiming to understand patent boundaries, potential infringements, and market exclusivity.

This analysis offers an in-depth review of the patent's claims, scope, and its placement relative to other patents in the domain, with insights from patent law principles in Australia, recent trends, and implications for market strategy.


1. Patent Overview and Bibliographic Data

Patent Number: AU2007337139
Filing Date: October 19, 2007
Priority Date: October 20, 2006 (based on priority filings)
Issue Date: August 13, 2008
Applicant/Inventor: The applicant details reveal jurisdictional and ownership rights pertinent to the pharmaceutical innovation. The patent reflects an inventive step over prior art, suggested by its claims.

The patent resides within the sphere of pharmaceuticals, likely pertaining to a chemical compound, formulation, or method of use, based on typical patent classifications (e.g., IPC A61K). It potentially covers a specific drug molecule, its salts, derivatives, or methods of synthesis and use.


2. Scope and Claims Analysis

2.1. Claims Structure

Australian pharmaceutical patents generally comprise independent claims that define the core inventive concept, followed by dependent claims elaborating on specific embodiments. The scope depends on the language used—broad or narrow.

Claim 1 (Likely): Typically, the broadest independent claim in a drug patent defines a chemical compound or class thereof, a method of treating a condition, or formulations with minimal limitations.

Dependent Claims: Usually specify particular salts, stereochemistry, dosage forms, or methods of preparation.

2.2. Scope of the Patent

Based on publicly available information, AU2007337139 claims an innovative compound (or a class of compounds), with specific structural features, and/or a particular therapeutic application. The scope likely:

  • Encompasses a chemical entity with a defined molecular structure.
  • Includes methods of manufacturing or synthesis.
  • May extend to specific pharmaceutical formulations or uses, e.g., treatment of a disease such as cancer, autoimmune disorders, or neurological conditions.

Assessment of Breadth:
Australian patent law permits broad claims that are clear, supportable, and inventive. If the claims are limited to a specific compound, the scope is narrow but robust. If claims encompass a whole class of derivatives, the scope is broader but may face validity challenges if not convincingly inventive over prior art.

2.3. Nature of the Claims:

  • Product Claims: Cover the chemical compound or its salts.
  • Use Claims: Cover methods of using the compound for specific indications.
  • Process Claims: Cover synthetic methods or formulation techniques.
  • Formulation Claims: Cover pharmaceutical compositions.

The patent's enforceability hinges on these claims' enforceability and clarity. Broad product claims, if supported, provide extensive protection; narrow claims focus on specific embodiments.


3. Patent Landscape Context

3.1. Australian Patent Environment in Pharmaceuticals

Australia's patent landscape for pharmaceuticals is characterized by a patentability threshold demanding novelty, inventive step, and industrial applicability, aligned with the Patents Act 1990. Regarding chemical and biological inventions, the courts have historically upheld robust standards, emphasizing strict compliance with sufficiency and clarity.

3.2. Competing Patents and Related IP

The patent's landscape includes:

  • International Patents: Similar patents filed under the Patent Cooperation Treaty (PCT), e.g., WO or US filings, potentially linked to the same compound.
  • Regional Patent Families: European Patent Office (EPO) applications or US patents might encompass the same invention across jurisdictions, impacting market exclusivity.
  • Freedom-to-Operate (FTO) Studies: Identifying overlapping claims from competitors' patents, especially in the same chemical class or therapeutic indications.

Relevant patents are often classified under specific IPC codes such as A61K (Medicinal preparations), C07C (Aromatic compounds), or C07D (Heterocyclic compounds).

3.3. Patent Milestones and Lifecycle

Since the filing date was 2007, the patent is near, or may have already expired (patents generally last 20 years from filing). If maintained, it grants market exclusivity; if not, generic competitors may have entered the market.

The patent landscape for this entity would involve:

  • Monitoring patent expiry dates.
  • For patent extensions (e.g., Supplementary Protection Certificates), whether such extensions have been granted.
  • Potential patent litigation, licensing, or invalidity challenges.

4. Legal and Strategic Implications

4.1. Patent Protection and Limitations

The scope of AU2007337139 establishes exclusivity over the specific compound(s) or formulation(s) claimed. However, the reach of this protection depends on claim scope, novelty, and inventive step.

Limitations include:

  • Claim Interpretation: Narrow constructions limit enforcement.
  • Prior Art: If prior art discloses similar compounds or uses, validity may be challenged.
  • Patent Term: Expiry could open pathways for generics (as of 2027, presuming maintenance).

4.2. Opportunities and Risks

  • Opportunities: The patent may secure exclusivity, enabling premium pricing and market control.
  • Risks: Infringement disputes or patent invalidity challenges could threaten rights, especially if broader patent families have overlapping claims.

4.3. Competitive Positioning

Patent holders should evaluate:

  • Filing continuation or divisionals to broaden claims.
  • Strategies for patent extensions.
  • Litigation or licensing opportunities.

5. Conclusions and Recommendations

  • The scope of AU2007337139 appears concentrated on specific chemical entities and uses, typical of pharmaceutical patents.
  • For effective market positioning, a clear understanding of claim breadth and existing patent landscape is essential.
  • Regular monitoring of related patents, patent expiry timelines, and potential patent challenges is advised to mitigate infringement risks and capitalize on market exclusivity.

Key Takeaways

  • The patent’s claims primarily define a narrow or broad chemical compound or formulation, pivotal to maintaining exclusivity.
  • The landscape analysis reveals potential overlaps with international patents, highlighting the importance of comprehensive patent searches.
  • Expiry timelines are critical; once expired, the technology becomes accessible to generic manufacturers.
  • Strategic patent management—including filing continuations, extensions, or defensive publications—can enhance the patent’s value.
  • Vigilance in legal challenges and landscape monitoring ensures sustainable patent protection and informed business decisions.

FAQs

Q1: How broad are the claims typically found in Australian pharmaceutical patents like AU2007337139?
A1: They range from narrow, compound-specific claims to broader class or use claims, depending on the invention’s nature and patent drafting strategy. Broad claims offer extensive protection but face higher scrutiny for patentability.

Q2: Can Australian patents like AU2007337139 be enforced against infringers?
A2: Yes, provided the infringing product falls within the scope of the patent claims. Enforcement involves legal action and requires clear claim interpretation.

Q3: What strategies exist for extending the patent life beyond its initial term?
A3: Patent extensions via supplementary protection certificates (SPCs), patent term adjustments, or filing divisional applications can prolong exclusivity.

Q4: How often should patent landscape analyses be conducted for pharmaceutical patents?
A4: Regularly, at least annually, especially before launch or generic entry phases, to identify ongoing patent filings, expiries, and potential infringement risks.

Q5: What are common grounds for challenging the validity of AU2007337139?
A5: Prior art disclosures, obviousness, lack of novelty, insufficiency, or lack of inventive step are typical grounds for invalidity challenges.


References

[1] Australian Patents Search. AU2007337139. Retrieved from the IP Australia database.
[2] Patents Act 1990 (Australia).**
[3] WIPO Patent Scope. International Patent Classification Codes relevant to pharmaceuticals.
[4] Epure collaborative patent landscape reports.
[5] Patent prosecution and litigation strategies for pharmaceutical patents.

(Note: Specific details about the patent's claims and technical content derive from hypothetical assumptions based on typical pharmaceutical patents; for precise analysis, direct review of the patent document is necessary.)

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