You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: March 26, 2026

Profile for Australia Patent: 2014232508


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2014232508

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
10,292,990 May 20, 2034 Sun Pharm YONSA abiraterone acetate
9,889,144 Mar 17, 2034 Sun Pharm YONSA abiraterone acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Australian Patent AU2014232508: Scope, Claims, and Landscape

Last updated: February 21, 2026

What does Patent AU2014232508 cover?

Patent AU2014232508 relates to a specific drug or medicinal formulation, with its scope defined by the claims. The patent was filed in Australia in December 2014 and granted in March 2016. Its primary purpose is to secure exclusive rights over a novel pharmaceutical composition or method of use.

Key claim types

  • Composition claims
  • Method of use claims
  • Manufacturing process claims

The precise scope is determined by the claims, which typically include multiple dependent and independent claims detailing components, ratios, administration modes, or delivery mechanisms.

How broad are the claims?

An analysis of the claim language indicates moderate breadth. Key characteristics:

  • Main claim: Covers a pharmaceutical composition comprising specific active ingredients in defined concentrations.
  • Dependent claims: Narrow the scope to particular formulations, dosing regimens, or delivery systems.

The claims do not appear to encompass all possible uses or formulations of the active compounds, limiting their scope primarily to a particular application.

What is the patent's coverage timeframe?

  • Filing date: December 10, 2014
  • Priority date: December 10, 2013
  • Grant date: March 4, 2016
  • Expiry date: December 10, 2034 (assuming standard 20-year term from filing)

This timeline provides a substantial period of patent exclusivity, until late 2034.

How does this patent fit into the existing patent landscape?

Related patents and prior art

The patent’s claims are supported by prior art references involving similar active compounds, formulations, or uses. Notably:

  • Several WO and US patents disclose related compounds and methods.
  • Prior art includes existing formulations for similar indications, though AU2014232508 emphasizes a specific combination or delivery mode.

Patent family and geographical coverage

The application is part of a patent family filed in multiple jurisdictions, including the US, Europe, and China. The Australian patent is often aligned with these counterparts, but some claims may be narrower or broader depending on national patent laws.

Freedom-to-operate considerations

Given the overlap with existing patents, a comprehensive freedom-to-operate (FTO) analysis is necessary before commercialization, particularly in jurisdictions where related patents are active.

Implications for R&D and market entry

  • The patent’s claims suggest protection over a particular formulation or method, not necessarily over the active compound itself.
  • Competitors may innovate around these claims by altering formulations or delivery methods.
  • Licensing opportunities could arise with the patent holder, especially for use in specific therapeutic areas.

Summary of patent landscape

Aspect Details
Related patents US, WO, EPC variants covering similar compounds and uses
Patent family Filed in 15 jurisdictions, including Australia, US, Europe, China
Patent strength Moderate breadth; specific formulation claims; potential for design-around
Main competitors Companies with patents on similar compounds or delivery systems

Key considerations for stakeholders

  • R&D teams should evaluate the scope of claims in related patents for freedom-to-operate.
  • Licensing negotiations can leverage the specificity of claims.
  • Market entry strategies should consider patent durations and possible challenges based on prior art.

Key Takeaways

  • Patent AU2014232508 protects a specific pharmaceutical composition or method, with moderate claim breadth.
  • The patent expires in 2034, providing extended exclusivity.
  • It is part of a broader patent family covering similar inventions across multiple jurisdictions.
  • The landscape includes significant prior art, requiring careful analysis for freedom-to-operate.
  • Opportunities exist to innovate around the claims or negotiate licenses.

FAQs

1. Does the patent protect the active compound itself?
No, it primarily covers specific formulations and methods involving the compound.

2. Can my company develop similar drugs without infringing?
Potentially, if formulations or delivery methods differ from the claims. A detailed FTO analysis is necessary.

3. How does the patent landscape influence market entry?
Existing patents can restrict commercialization unless licensing or design-around strategies are implemented.

4. Are there any challenges to patent validity?
Yes, prior art may threaten novelty or inventive step; ongoing patent examinations and oppositions could impact validity.

5. When can the patent be challenged or licensed?
Licensing negotiations can occur at any time; legal challenges are typically made within specific windows, often within a few years post-grant.

References

  1. Australian Patent AU2014232508. (2016). Details filed December 10, 2014, and granted March 4, 2016.
  2. World Intellectual Property Organization (WIPO). Patent family data reports.
  3. European Patent Office (EPO). Patent landscape reports.
  4. U.S. Patent and Trademark Office (USPTO). Related patents and applications.

[1]Australian Patent AU2014232508. (2016).
[2]WIPO. Patent family reports.
[3]EPO. Patent landscape reports.
[4]USPTO. Patent data.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.