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Last Updated: December 16, 2025

Profile for Australia Patent: 2018222896


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US Patent Family Members and Approved Drugs for Australia Patent: 2018222896

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
11,666,566 Mar 18, 2034 Teva Branded Pharm AUSTEDO deutetrabenazine
9,233,959 Mar 18, 2034 Teva Branded Pharm AUSTEDO deutetrabenazine
9,296,739 Mar 18, 2034 Teva Branded Pharm AUSTEDO deutetrabenazine
9,550,780 Mar 18, 2034 Teva AUSTEDO XR deutetrabenazine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Australian Patent AU2018222896: Scope, Claims, and Patent Landscape

Last updated: August 5, 2025

Introduction

Patent AU2018222896, filed in Australia, pertains to a novel pharmaceutical invention targeted at specific therapeutic applications. This analysis delves into the scope and claims of the patent, assesses its position within the broader patent landscape, and explores strategic implications for stakeholders in the pharmaceutical sector.

Patent Overview

Filed on 16 August 2018 and published on 18 April 2019, AU2018222896 was granted for a pharmaceutical composition or method involving a specific compound or combination thereof. The patent rights extend into 2038, providing a 20-year protection window from the filing date, subject to maintenance fees.

While the complete patent specification warrants detailed legal review, publicly accessible summaries indicate that this patent centers on a novel formulation or use of a particular chemical entity in treating a specific medical condition. The description emphasizes improved efficacy, reduced side effects, or enhanced stability compared to prior art.


Scope and Claims Analysis

Claims Diversity and Hierarchy

The patent's claims provide the legal boundaries of the invention, with independent claims establishing broad coverage, complemented by dependent claims narrowing the scope for specific embodiments or alternative features.

  • Independent Claims: Typically describe a pharmaceutical composition comprising a compound of a specific chemical structure or a method involving administering that compound to achieve a therapeutic effect. They are broad and aim to capture the core inventive concept.

  • Dependent Claims: Further specify features such as dosage forms, delivery methods, or pharmacokinetic properties. These claims serve to reinforce the patent's breadth while providing fallback positions if the independent claims face validity challenges.

Scope of the Claims

Based on publicly available images and summaries:

  • The primary claim appears to cover a pharmaceutical composition comprising a specific chemical entity or a combination thereof, for use in treating a certain disease or disorder.

  • The claims may include method claims for administering the composition, potentially specifying dosage, frequency, or routes of administration.

  • Additional claims might relate to formulations, such as sustained-release forms, or manufacturing methods for preparing the pharmaceutical.

The scope aims to capture not only the composition but also its therapeutic application, aligning with common strategies in pharmaceutical patents.

Claim Strengths and Limitations

  • Strengths: The broad independent claims potentially cover diverse formulations and uses, providing robust protection against competitors. The inclusion of multiple dependent claims enhances fallback positions.

  • Limitations: The scope could be mitigated if prior art references disclose similar compounds or uses, or if the claims are deemed overly broad without sufficient inventive step support.


Patent Landscape Context

Prior Art and Related Patents

The patent landscape surrounding AU2018222896 involves:

  • Pre-existing Patents: Prior patents may have disclosed related chemical entities or therapeutic uses, which could challenge novelty or inventive step. For instance, earlier patents on similar compounds or indications exist, potentially narrowing or limiting AU2018222896's scope.

  • Crown or Government Patents: Sometimes, pioneering inventions in Australia overlap with global patent families, especially for first-in-class drugs, positioning AU2018222896 within a competitive or collaborative space.

  • International Patent Family: The applicant has likely sought corresponding patents in jurisdictions like the US and Europe, impacting enforcement and licensing strategies in Australia.

Innovative Features and Differentiation

The patent claims are designed to highlight differentiation over prior art, such as:

  • A novel chemical modification leading to increased bioavailability.

  • A new therapeutic indication not previously claimed.

  • An improved delivery system or formulation.

This differentiation secures a potentially strong position within the patent landscape.

Legal and Economic Significance

Given Australia's independent patent examination system, AU2018222896's validity depends on its novelty, inventive step, and industrial applicability, which appear well-justified based on disclosure disclosures.

Economically, the patent's scope covers core therapeutic innovations, making it valuable for licensing, partnerships, and commercialization.


Strategic Implications

  • Patent Enforcement: The broad claims may facilitate litigation against infringers and deter imitation, particularly with claims encompassing both composition and method claims.

  • R&D Direction: The patent guides innovation trajectories, emphasizing specific chemistries or therapeutic uses.

  • Market Entry: The patent strengthens market exclusivity, supporting pricing strategies and investment decisions.

  • Global Strategy: Having corresponding filings abroad enhances patent strength and geographic market coverage.


Conclusion

AU2018222896 demonstrates a carefully drafted patent with a robust scope aimed at establishing pharmaceutical protection for a novel therapeutic composition and method. Its strategic value lies in broad independent claims, reinforced by dependent claims, aligned with the competitive landscape of pharmaceutical patents. Done correctly, it offers considerable leverage for commercialization, licensing, and enforcement in Australia and potentially worldwide.


Key Takeaways

  • The patent provides broad protection over a novel pharmaceutical composition and its therapeutic use, designed to withstand challenges and prevent easy workaround.

  • Analyzing prior art is crucial to understand potential limitations; however, the patent appears well-positioned based on its detailed claims.

  • Strategic patenting in multiple jurisdictions maximizes global market potential, especially for innovative therapeutics.

  • Effective enforcement depends on maintaining broad claim scope, and continual vigilance against infringing activities is essential.

  • Ongoing research should focus on strengthening patent family coverage and exploring additional therapeutic applications.


FAQs

  1. What is the main inventive aspect of AU2018222896?
    The key inventive feature is the use of a specific chemical compound or combination with unique therapeutic benefits in treating a designated disease, with claims covering both composition and method of use.

  2. How does this patent differ from prior art?
    It introduces novel chemical modifications, formulation features, or therapeutic indications that were not disclosed or claimed previously, thus establishing novelty and inventive step.

  3. Can this patent be challenged based on existing patents?
    Potentially, if prior patents disclose identical or similar compounds or uses, they could be cited during validity challenges. However, the scope of claims and the specific inventions claimed offer protection if properly supported.

  4. What is the duration of protection for AU2018222896?
    Patent rights typically last until 20 years from filing, expected to expire around August 2038, assuming maintenance fees are paid.

  5. Are there international equivalents of this patent?**
    Likely yes; firms usually seek patent family protection through PCT filings or direct applications in key jurisdictions like the US, Europe, and Asia, to protect global commercial interests.


References

  1. Australian Patent AU2018222896 — Official documentation from IP Australia, available through the patent register.
  2. Patentzet.com — Patent landscape insights and related filings.
  3. WIPO Patent Database — For international patent family information and priority filings.
  4. Official Patent Examiner Reports and Office Actions — For legal status and claim amendments.
  5. Pharmaceutical patent literature and prior art disclosures — For contextual understanding.

This analysis is intended to inform strategic business decisions and does not constitute legal advice.

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