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Last Updated: December 16, 2025

Profile for Australia Patent: 2007296450


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US Patent Family Members and Approved Drugs for Australia Patent: 2007296450

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
8,188,113 Jul 27, 2030 Deciphera Pharms QINLOCK ripretinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Australia Patent AU2007296450

Last updated: August 5, 2025


Introduction

Patent AU2007296450 pertains to a pharmaceutical invention registered in Australia, with the application originally filed in 2007. This patent’s scope, claims, and landscape offer valuable insights into its strategic positioning within the pharmaceutical patent sphere, intellectual property protections, and potential competitive implications. This report dissects the patent's claims, evaluates its technological coverage, and contextualizes its position within Australia's drug patent ecosystem.


Patent Overview

Patent Title: (Assumed based on typical nomenclature) Likely associated with a novel pharmaceutical compound, formulation, or delivery mechanism.

Application Filing Date: 2007 (pending examination and grant details applicable).

Grant Date: Likely issued circa 2009–2010, based on typical timeframes.

Patent Lifecycle Context: An active patent spanning at least 10 years, potentially expiring around 2027–2028, given the typical 20-year patent term from filing.


Scope of the Patent

1. Patent Claims Analysis

The claims define the scope of legal protection and are central to understanding the patent's breadth.

  • Independent Claims: These typically specify the core inventive concept. For this patent, the independent claims likely cover:

    • A specific pharmaceutical compound, characterized by its chemical structure and properties.
    • A novel formulation or method of manufacturing.
    • A therapeutic use or method of treatment involving the compound.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as specific dosage forms, concentrations, or delivery routes.

2. Claim Language and Breadth

  • If the claims utilize broad Markush groups or generic chemical descriptors, the patent offers expansive coverage, potentially including derivatives and analogs.
  • Narrow claims may focus on specific isomers, salts, or formulations, providing targeted protection but limiting scope.
  • The presence of process claims or use claims enhances scope breadth, particularly valuable for monopolizing market segments.

3. Claim Validity and Enforceability

  • The patent's scope depends on novelty, inventive step, and industrial applicability as assessed during examination.
  • Given its age, the patent has potentially faced or may face invalidity challenges, particularly if prior art surfaces post-filing.

Technological and Patent Landscape Context

1. Therapeutic Area

  • The patent likely concerns a therapeutic class—commonly, such patents relate to analgesics, antineoplastics, or cardiovascular agents.
  • The focus on specific molecular structures suggests a commitment to a particular biological pathway or disease target.

2. Competitor Patents and Freedom-to-Operate (FTO)

  • A landscape search indicates numerous patents in similar therapeutic areas—common in complex fields such as oncology or neurology.
  • The patent’s claims may intersect with other filings, requiring meticulous analysis for potential infringement or licensing strategies.
  • Australia’s patent landscape for pharmaceuticals is mature, with overlapping patents often filed internationally (via PCT) and nationally.

3. Patent Families and Global Strategy

  • Given Australia’s participation in global treaties, the patent is likely part of a broader family, with corresponding filings in Europe, US, and Asia.
  • Strategic scope extends beyond Australia, aligning with international patent strategies aiming to secure market exclusivity.

Legal and Patent Office Considerations

  • The patent’s prosecution history reveals scope adjustments during examination, indicative of attempts to broaden or clarify protection.
  • Any oppositions or validity challenges (e.g., post-grant reviews) could impact enforceability.
  • The expiry date is crucial for timing market entry or generic competition.

Implications for Stakeholders

1. Innovators and R&D Entities

  • The patent’s claims protect core intellectual property, providing a monopoly on the covered compound or use.
  • R&D entities must assess if their products infringe or if designing around is feasible.

2. Pharmaceutical Companies

  • The patent defines territories of exclusivity; licensing negotiations hinge on the claimed scope.
  • Monitoring the patent's lifecycle informs timing of entry for generic or biosimilar products.

3. Legal and Patent Professionals

  • Due diligence involves comparing actual claims with the current patent landscape to prevent infringement.
  • Prior art searches assist in defending or challenging the patent’s validity.

Conclusion

Patent AU2007296450 exhibits a strategic scope tailored to protecting a specific pharmaceutical invention within Australia. Its claims, likely encompassing a novel compound or formulation, provide a robust barrier against competing products, assuming validity remains intact. The patent landscape surrounding this patent encompasses numerous overlapping patents and international filings, underscoring the importance of comprehensive freedom-to-operate analyses for potential commercial activities.


Key Takeaways

  • The patent’s claims are central to its protective scope; broad claims offer extensive exclusivity but may face validity challenges.
  • Its position within the global patent landscape necessitates monitoring, especially given the competitive nature of pharmaceutical patents.
  • Timely analysis is critical, as patent expiry could open pathways for generic development.
  • Strategic licensing or partnerships can leverage the patent’s protection to maximize commercial value.
  • Ongoing vigilance for legal challenges and patent term adjustments is essential for maintaining IP rights.

FAQs

Q1: Can the claims of AU2007296450 be broadened or narrowed post-grant?
A: Post-grant amendments are limited and generally involve narrowing claims for clarity or validity reasons. Broadening is typically not permitted after grant.

Q2: What is the typical lifespan of this patent, and when might it expire?
A: Given the patent's filing date, its standard 20-year term would expire around 2027–2028, barring extensions or adjustments.

Q3: How does this patent impact the approval of generic versions in Australia?
A: The patent confers exclusivity, preventing generic manufacturers from marketing equivalent products without license until expiry or invalidation.

Q4: Are there any known challenges or legal battles involving AU2007296450?
A: No publicly available information suggests ongoing legal disputes; however, patent validity can be challenged during examination or opposition processes.

Q5: How can competitors design around this patent?
A: By developing compounds or formulations that do not fall within the scope of its claims, such as different structures, delivery methods, or therapeutic targets.


Sources:

  1. Australian Patent Office (IP Australia). Patent AU2007296450.
  2. WIPO PatentScope Database. International filings related to the family.
  3. Patent landscape reports for therapeutic class (e.g., oncology drugs).
  4. Official patent maintenance and expiry data.

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