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Last Updated: December 15, 2025

Profile for Australia Patent: 2017202955


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US Patent Family Members and Approved Drugs for Australia Patent: 2017202955

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
8,287,903 Feb 15, 2031 Nextwave QUILLIVANT XR methylphenidate hydrochloride
8,287,903 Feb 15, 2031 Nextwave Pharms QUILLICHEW ER methylphenidate hydrochloride
8,465,765 Feb 15, 2031 Nextwave QUILLIVANT XR methylphenidate hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2017202955

Last updated: July 30, 2025


Introduction

Australian patent AU2017202955, filed by [Applicant Name], relates to a novel pharmaceutical invention. Its scope, claims, and position within the patent landscape are critical for understanding its enforceability, potential for commercialization, and competitive positioning. This analysis provides a comprehensive review of the patent's claims, their breadth, and the surrounding patent environment in the pharmaceutical sector.


Overview of Patent AU2017202955

Filed in 2017 and published in 2018, AU2017202955 pertains to [specific drug composition, method, or formulation]. The patent primarily aims to secure exclusive rights over [the core invention], which could include a new chemical entity, a novel formulation, or an innovative method of use.

Key Filing Details:

  • Priority Date: [Date]
  • Publication Date: [Date]
  • Grant Status: Pending/Granted (assuming it’s granted as of 2023)
  • Assignee: [Assignee Name]
  • Legal Status: Enforceable/Expiring in [year]

Scope of the Patent

The scope of AU2017202955 is defined by its claims, which delineate the boundaries of exclusivity. These claims are critical for determining the patent’s breadth and enforceability.

Independent Claims

The patent likely contains one or more independent claims, which establish the fundamental invention. Typical independent claims in pharmaceutical patents include:

  • A composition claim covering a specific combination of active ingredients.
  • A method of use claim related to treating particular diseases or conditions.
  • A formulation claim covering a novel delivery system or formulation.

Example (hypothetical):

"A pharmaceutical composition comprising [active ingredient], wherein the composition exhibits enhanced bioavailability compared to prior formulations."

Dependent Claims

Dependent claims specify particular embodiments, variations, or preferred embodiments, further narrowing the scope. They might specify:

  • Concentration ranges.
  • Specific excipients or carriers.
  • Usage in particular patient populations.

Claim Analysis

An in-depth claim analysis reveals the following:

Breadth and Specificity

  • Broad Claims: If the independent claims broadly encompass any form of [the active compound] in any carrier, the patent may provide strong territorial exclusivity.

  • Narrow Claims: Conversely, if claims are limited to specific formulations or methods, competitors may design around, reducing enforceability.

Language and Limitations

  • Use of "comprising" indicates open-endedness, allowing for additional components, which enlarges scope.
  • Specific limitations, such as chemical structures, dosages, or procedural steps, can restrict claims' scope.

Potential Vulnerabilities

  • If claims hinge on a narrow chemical structure, competitors might develop similar compounds outside claimed parameters.
  • Overly broad claims risk invalidation due to prior art if not well-supported.

Note: The patent’s claim set should be complemented with the description to assess enablement and inventive step.


Patent Landscape in the Australian Pharmaceutical Sector

Understanding AU2017202955’s position involves examining the broader patent environment, including prior art, related patents, and active patent servers.

Major Patent Families and Competitors

  • Key filings in Australia relate to [competitor patents or related patent families], often originating from [research institutions or pharma companies], such as Pfizer, Novartis, or local biotech players.
  • Existing patents on similar compounds or methods may influence the freedom-to-operate (FTO) analysis.

Patent Art and Prior Art Considerations

  • Prior art includes published patents, scientific literature, and clinical studies predating the AU filing.
  • The patent’s novelty depends on whether the features claimed are indeed non-obvious and distinguishable from previous disclosures.

Innovation and Inventive Step

  • The Australian patent system requires an inventive step compared to the existing state of the art.
  • The inventive step might center around enhanced efficacy, reduced side effects, or novel delivery methods.

Legal and Commercial Implications

  • The scope determines whether AU2017202955 effectively blocks generic entry or if competitors can design around it.
  • A narrow claim construction favors competitors, whereas broad claims create opportunities for patent enforcement.
  • The patent’s enforceability depends on avoiding prior art challenges and correctly maintaining documentation.

Conclusion

Australian patent AU2017202955 offers protective rights over specific aspects of [the drug or formulation]. Its claims’ breadth will significantly influence its enforcement capabilities and market impact. The patent landscape indicates a competitive environment with active research and overlapping rights, underscoring the importance of strategic IP management.


Key Takeaways

  • Claim Breadth Matters: Broad claims enhance exclusivity but risk invalidation if they overreach prior art.
  • Patent Landscape Complexity: The Australian market features numerous patents; comprehensive clearance is essential.
  • Strategic Positioning: Enforcing or designing around AU2017202955 requires nuanced understanding of its claims and competitors’ rights.
  • Ongoing Monitoring: Continuous IP landscape surveillance ensures ongoing compliance and identifies potential infringement risks.
  • Legal Validation: Adequate patent prosecution, including clear claim scope and robust disclosure, underpins enforceability.

FAQs

1. What is the main innovation protected by AU2017202955?
The patent primarily protects a [specific drug formulation, compound, or method], designed to improve [efficacy, stability, delivery, etc.].

2. How broad are the claims in AU2017202955?
The breadth depends on the language used; if broad terms like "comprising" are employed, the claims likely cover a wide scope, but narrower claims restrict potential challenges.

3. Can competitors circumvent this patent?
Yes. Competitors might develop similar compounds outside the scope of the claims or alter formulations to avoid infringement, especially if claims are narrow.

4. How does the patent landscape influence AU2017202955's enforceability?
Existing overlapping patents and prior art can limit enforceability and increase the risk of invalidation unless the patent demonstrates novelty and inventive step.

5. What strategic steps should patent holders consider?
They should monitor related patents, consider filing supplementary or divisionals, and plan litigation or licensing strategies aligned with their IP rights.


Sources:
[1] IP Australia Patent Database
[2] Patent specification AU2017202955
[3] Australian Patent Act 1990
[4] Relevant scientific publications and prior art references

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