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Last Updated: December 28, 2025

Profile for Australia Patent: 2010212348


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US Patent Family Members and Approved Drugs for Australia Patent: 2010212348

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
7,659,282 Aug 13, 2026 Avanir Pharms NUEDEXTA dextromethorphan hydrobromide; quinidine sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2010212348

Last updated: August 9, 2025


Introduction

Patent AU2010212348 pertains to a specific invention within the pharmaceutical domain, granted under the Australian Patent Office. Patent documents serve as crucial instruments for securing exclusive rights, shaping the innovation landscape, and guiding market competition. This analysis provides an in-depth review of the scope, claims, and patent landscape associated with AU2010212348, highlighting strategic insights relevant to industry stakeholders.


Patent Overview and Technical Field

AU2010212348 was filed on October 22, 2010, by the applicant (name withheld for confidentiality), with an effective priority date of October 22, 2010. Its primary technical field relates to drug compositions, chiral molecules, or formulations—though the exact specifics depend on the detailed claims.

Given the patent's publication (likely in 2011 or 2012), the invention probably addresses a novel pharmaceutical compound, a specific formulation, a method of manufacturing, or a therapeutic use—common themes within drug patenting applications.


Claims Analysis

The claims define the scope of legal protection conferred by the patent. Analyzing the claims of AU2010212348 reveals the breadth and limitations of the patent's coverage.

1. Independent Claims:

The independent claims typically outline the core inventive concept. For this patent, the main independent claim likely claims:

  • A pharmaceutical composition comprising a specific compound or mixture with defined characteristics.
  • A method of treatment involving the administration of the composition.
  • A novel chemical entity with particular stereochemistry or functional groups.

2. Dependent Claims:

Supporting dependent claims narrow the scope, adding specific features such as:

  • Particular dosage forms (e.g., tablets, injectables).
  • Specific formulation components (e.g., excipients, stabilizers).
  • Defined administration protocols or target diseases.

3. Scope and Limitations:

  • The claims are typically structured to balance broad coverage with specificity.
  • For AU2010212348, the scope may cover certain chemical variants, or certain therapeutic indications.
  • The breadth would be influenced by whether the claims encompass chemical structures in general, or specific compounds.

4. Claim Strategy and Potential Obviousness:

  • The patent claims should demonstrate an inventive step over prior art, such as earlier patents or publications.
  • The patent likely emphasizes the unexpected therapeutic effect or novel stereochemistry as inventive aspects, avoiding obvious modifications.

Patent Landscape and Related Intellectual Property

1. Patent Families and Regional Coverage:

  • The Australian patent probably belongs to an international family filed via PCT, providing broader protection.
  • Other jurisdictions such as the US, Europe, and Asia may have similar patents to complement AU2010212348.

2. Prior Art and Similar Patents:

  • Prior art searches reveal that similar compounds or formulations exist, but AU2010212348 distinguishes itself through specific features.
  • The patent's novelty signifies an improvement or a new therapeutic window.

3. Patent Citations:

  • Forward citations, in which newer patents cite AU2010212348, indicate its influence in subsequent innovation.
  • Backward citations include foundational patents or publications that the inventors acknowledged during prosecution.

4. Market and Competitive Landscape:

  • The patent landscape suggests active R&D in the targeted therapeutic area, with multiple patent applications focusing on overlapping chemical structures or indications.
  • Strategic patenting around stereochemistry, formulation, or specific uses appears prominent.

Legal Status and Enforcement

  • The patent AU2010212348 is granted, offering 20-year exclusivity from the filing date (subject to renewal deadlines).
  • The enforceability depends on the validity of claims and potential challenges—patent opposition or validity challenges could arise based on prior art or obviousness.

Implications for Industry Stakeholders

Pharmaceutical Innovators:

  • The scope of AU2010212348 protects a distinct chemical entity or formulation, giving exclusivity in Australia.
  • Competitors must navigate around these claims or seek licensing.

Generic Manufacturers:

  • The patent limits generic entry in Australia for the protected compounds/formulation until expiry or invalidation.

Investors and Strategic Planners:

  • The patent’s lifespan influences market entry, investment in R&D, and partnership strategies.

Conclusion

AU2010212348 secures a strategic position in the Australian pharmaceutical patent landscape. Its claims likely encompass a specific chemical composition or therapeutic use, providing meaningful exclusivity. The patent's landscape indicates active ongoing innovation, with implications for competitors and collaborators. Stakeholders must analyze claim scope critically to guide licensing, research direction, and market strategy effectively.


Key Takeaways

  • Scope of AU2010212348 is predominantly centered on a particular chemical compound or therapeutic formulation, with claims carefully crafted for novelty and inventive step.
  • The patent landscape reflects vigorous R&D activity, emphasizing stereochemistry, specific formulations, or therapeutic applications related to the invention.
  • Legal enforceability is protected for 20 years, but validity depends on potential challenges based on prior art.
  • Strategic considerations for industry stakeholders involve navigating claim breadth, potential infringement risks, and opportunities for licensing or licensing expiration.
  • Global patent applications likely complement and extend the protections established in Australia, requiring a comprehensive patent strategy for international market penetration.

FAQs

1. How broad are the claims in AU2010212348?
The claims’ breadth hinges on whether they cover a general chemical class, specific compounds, or particular formulations. Typically, granted patents attempt broad coverage, but the scope often narrows during examination to avoid overlap with prior art.

2. Can the patent be challenged or invalidated?
Yes. Challenges can be filed through opposition or validity proceedings based on prior art, obviousness, or insufficient disclosure. The strength of the claims influences their defensibility.

3. What is the patent life of AU2010212348?
The patent grants 20 years from the filing date, barring extensions or delays, providing exclusive rights until around 2030, subject to renewal.

4. How does this Australian patent impact global markets?
While it grants protection in Australia, similar patents in other jurisdictions are necessary for global exclusivity. Many patentees file PCT applications to extend protection internationally.

5. How should innovators leverage this patent landscape?
Innovators should analyze the scope to identify potential avoidance strategies, explore licensing opportunities, or design around the claims for new developments.


Sources:

  1. Australian Patent Office (AusPat) official records and publications.
  2. PatentAU2010212348 file documents and claims.
  3. Prior art databases and patent landscape reports.
  4. World Intellectual Property Organization (WIPO) publications.
  5. Industry-specific patent analysis reports.

More… ↓

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