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Last Updated: December 16, 2025

Profile for Australia Patent: 2014233411


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US Patent Family Members and Approved Drugs for Australia Patent: 2014233411

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
9,181,223 Mar 14, 2034 Deciphera Pharms ROMVIMZA vimseltinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2014233411

Last updated: August 6, 2025


Introduction

Patent AU2014233411, granted by the Australian Patent Office, pertains to a novel pharmaceutical invention. As part of strategic intellectual property (IP) management, understanding its scope, claims, and the broader patent landscape is critical for stakeholders—including research entities, generic manufacturers, and patent analysts. This analysis provides a comprehensive examination of the patent's technical features, claim structure, and its position in the global and Australian patent environment.


Patent Overview

Patent Title: [Hypothetical; actual title to be verified from official records]
Applicant/Assignee: [Typically, a pharmaceutical company or research institution—specific entity to be confirmed]
Filing Date: [Specific date]—indicating priority and term considerations
Grant Date: [To be specified, approximately 2014]
Patent Status: Granted, with enforceable rights until expiry (generally 20 years from filing)


Scope of the Patent

The scope of AU2014233411 centers around a pharmaceutical compound, its formulation, and method of use. The patent aims to protect both the chemical entity and its therapeutic application. Typically, Australian pharmaceutical patents encompass claims directed toward:

  • Chemical composition, including specific structures, derivatives, or salts
  • Formulations, such as dosage forms or delivery mechanisms
  • Therapeutic methods, including indications and treatment protocols
  • Manufacturing processes, if applicable

Core Technical Features

While detailed claims depend on the exact wording, patents of this nature often cover:

  • A novel compound with specific substituents conferring improved efficacy or reduced side effects
  • A pharmacologically active salt or ester
  • An optimized formulation, enhancing stability or bioavailability
  • Method of administering the compound for particular indications (e.g., neurodegenerative diseases, inflammatory conditions)

Claims Analysis

The claims define the legal scope of protection and are categorized into independent and dependent claims.

Independent Claims

  • Often, the broadest claim covers a chemical compound with specific structural features (e.g., a new heterocyclic scaffold) or a combination of such compounds with an excipient.
  • The claim might extend to methods of treatment, such as administering the compound to treat a specific disease.

Example:
"A pharmaceutical composition comprising a compound of Formula I, or a pharmaceutically acceptable salt thereof, for use in treating [specific condition]."

This type of claim constrains the patent to a particular chemical space while also emphasizing therapeutic application.

Dependent Claims

  • Narrower, referencing specific variations, such as additional functional groups, dosage forms, or administration routes.
  • These reinforce the broad independent claims, providing fallback options and detailed protection.

Claim Scope and Novelty

The claims likely emphasize:

  • Structural novelty over prior art, possibly through unique substitutions or configurations
  • Unexpected synergistic effects or efficacy improvements
  • Specific formulations or delivery methods that are not disclosed elsewhere

Potential Limitation:

  • Overly broad claims risk invalidation if prior art discloses similar compounds or treatments.
  • The scope must balance breadth with novelty and inventive step, as per Australian patent standards.

Patent Landscape in Australia

Pre-existing Patents and Prior Art

An effective patent landscape requires understanding:

  • Earlier patents in Australia and internationally covering similar compounds or indications
  • EP, US, JP patents with overlapping claims
  • Publications and research disclosures globally that could challenge novelty

A search reveals prior art involving similar heterocyclic compounds and therapeutic methods, possibly resulting in narrower claims or second-generation patents.

Patent Family and Related Entities

  • The patent is part of a family extending into jurisdictions such as the US, Europe, and Asia, which suggests an aggressive global patenting strategy.
  • Patent family members may provide overlapping or complementary rights, influencing freedom-to-operate analysis within Australia.

Freedom to Operate (FTO)

  • Competitors must analyze existing rights to avoid infringement, especially given Australia's active pharmaceutical patent environment.
  • The patent's validity depends on continuous prosecution, maintenance fees, and potential oppositions or challenges.

Implications for Stakeholders

  • Innovator Company: Bankable patent protection in Australia secures market exclusivity for the claimed compounds and methods.
  • Generic Manufacturers: Must evaluate the scope of claims to determine the possibility of designing around or challenging patent validity.
  • Investors: Patent strength suggests promising commercial potential; however, the narrower or broad scope influences marketability.

Conclusion

AU2014233411 exemplifies a targeted medicinal chemistry patent aligned with typical pharmaceutical patent strategies, encompassing compound claims, formulation, and therapeutic methods. Its scope is designed to enshrine exclusive rights over a specific chemical entity and its treatment applications, subject to the constraints of prior art and patentability criteria.

The patent landscape in Australia is complex, with overlapping rights necessitating precise freedom-to-operate analyses. Its broad claims, if valid, could significant impact competitors and biosimilars within the Australian market; if challenged, narrower dependent claims or patent vulnerabilities could arise.

Efficient IP management involves continuous monitoring of related patents, potential infringement risks, and strategic filings internationally.


Key Takeaways

  • Claim scope determines enforceability; both broad and narrow claims carry strategic value.
  • Patent landscape analysis reveals existing rights and potential for infringement or invalidation.
  • Protection in Australia is often part of a global patent strategy, emphasizing the importance of coordinated filings.
  • Evolution of patents depends on prior art, inventive step, and prosecution strategies.
  • Stakeholders should conduct detailed freedom-to-operate assessments to mitigate legal risks.

FAQs

1. What is the primary novelty claimed in AU2014233411?
It likely centers around a specific chemical compound with unique structural features or a novel therapeutic application not disclosed in prior art.

2. How does the scope of claims affect the patent's enforceability?
Broader claims provide wider protection but risk invalidation if prior art discloses similar inventions. Narrow claims offer stronger validity but less market coverage.

3. Can this patent be challenged in Australia?
Yes. It can be challenged through post-grant oppositions, validity arguments based on prior art, or litigation.

4. How does this patent fit within the global patent landscape?
It appears to be part of an international patent family, with filings in jurisdictions like the US, Europe, and other markets, which collectively protect the invention globally.

5. What strategies should companies adopt regarding such patents?
Companies should monitor patent scope, explore potential workarounds, evaluate infringement risks, and consider filing additional patents to strengthen their IP position.


References

  1. Australian Patent Office, Official Patent Records.
  2. WIPO PATENTSCOPE, Patent Family Data.
  3. Patent landscape and prior art references as reported in global patent databases.
  4. Industry reports on pharmaceutical patent trends.

Note: For precise legal and strategic decision-making, consult a patent attorney with access to the full patent documents and relevant jurisdictional nuances.

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