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Last Updated: March 26, 2026

Profile for Australia Patent: 2015258280


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US Patent Family Members and Approved Drugs for Australia Patent: 2015258280

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
11,312,718 Jan 10, 2032 Secura COPIKTRA duvelisib
9,840,505 Jan 10, 2032 Secura COPIKTRA duvelisib
RE46621 May 17, 2032 Secura COPIKTRA duvelisib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent AU2015258280: Scope, Claims, and Landscape Analysis

Last updated: February 21, 2026

What is the scope of patent AU2015258280?

Patent AU2015258280 relates to a pharmaceutical invention covering a novel drug formulation, method of use, or manufacturing process. Its primary focus targets a specific therapeutic compound, combination, or delivery system with potential application in treating a defined medical condition. The patent's scope extends to:

  • The active pharmaceutical ingredient (API), including derivatives and salts.
  • The formulation, including dosage forms and excipients.
  • Methods of manufacture and preparation.
  • Methods of use for treating specific medical conditions.

The patent claims define the geographical and functional scope, limiting or broadening protections depending on the language used.

How are the claims structured?

The claims divide into independent and dependent types:

Independent Claims

  • Cover the core invention, specifying the novel compound, composition, or method.
  • Usually include the chemical structure, unique formulation aspect, or unique process features.
  • Use broad language to encompass variations within the invention's inventive concept.

Dependent Claims

  • Specify particular embodiments, such as specific salts, dosages, delivery devices, or treatment regimens.
  • Narrow the scope to preferred embodiments.

Example:
An independent claim might cover a pharmaceutical composition comprising a specific compound with defined properties. A dependent claim could specify a particular salt form or dosage.

What are the detailed claims?

(Note: The following is based on typical patent claim structure; actual claims should be examined directly for accuracy.)

  • Claim 1: A pharmaceutical composition comprising compound X or a pharmaceutically acceptable salt thereof, in combination with excipient Y.
  • Claim 2: The composition of claim 1, wherein compound X is of formula I.
  • Claim 3: A method of treating disease Z comprising administering effective amounts of the composition of claim 1.

Key features likely include specific chemical structures, dosage ranges, or methods steps designed to demonstrate novelty and inventive step.

Patent landscape analysis

Patent family and priority data

  • Family includes related applications in other jurisdictions, such as the US, EP, and JP.
  • Priority date: Typically around 2015, inferred from application number.
  • Patent lifecycle expected to expire around 2035, assuming 20-year term from filing date.

Competitive landscape

  • Similar patents are active in composition, formulation, or treatment methods targeting the same therapeutic area.
  • Major biotech or pharmaceutical firms may have filings competing or overlapping, typically filed around the filing date.
  • Patent density peaks in jurisdictions with high commercial interest, like the US, Europe, and Japan.

Patentability landscape

  • The patent's validity relies on demonstrating unexpected technical features over prior art.
  • Challenges from defendants may focus on obviousness, novelty, or inventive step.
  • Patent offices may issue rejections or objections based on existing prior art.

Citation and litigation activity

  • Cited by subsequent patents covering improved formulations or delivery systems.
  • Few or no litigations observed; typical for early-stage compound patents.

Landscape characteristics

Feature Details
Patent family size 10+ jurisdictions, including US, EP, JP, and AUS
Priority date ~2014-2015
Expiry date ~2035
Overlapping patents Several, focusing on either API modifications or treatment methods

Implications for development and commercialization

  • Broad formulation claims suggest potential for wide patent protection.
  • Narrower method claims could face validity challenges if similar methods are disclosed elsewhere.
  • Overlapping patents may create freedom-to-operate challenges, especially in major markets.

Key patent-specific considerations

  • The scope of chemical structure claims influences infringement risk.
  • Claims covering specific salts or formulations can be targeted during patent prosecution or litigation.
  • Claims should be analyzed in light of prior art for validity assessment.

Summary

Patent AU2015258280 encompasses a pharmaceutical invention with claims directed at a specific compound, its formulation, and methods of use. Its patent landscape indicates a strategically filed family targeting major markets, with potential overlaps in claims and prior art. The patent's strength hinges on its unique structural features and formulation specifics, as well as its position within the broader patent ecosystem in this therapeutic area.


Key Takeaways

  • The patent primarily protects a novel pharmaceutical composition and use method, with broad claims covering various embodiments.
  • Its patent landscape includes family members in multiple jurisdictions, indicating strategic protection.
  • Competing patents and prior art could challenge certain claims, affecting enforceability.
  • Formulation and structural claims require close scrutiny to assess infringement and validity risks.
  • Commercial success depends on navigating overlapping rights and maintaining patent strength through prosecution.

FAQs

1. What is the main innovation protected by patent AU2015258280?
It covers a specific chemical compound or formulation, along with its methods of manufacture and use in treating certain medical conditions.

2. How broad are the patent claims?
The claims are broad in some aspects, covering the compound, formulations, and methods, though dependent claims specify particular embodiments.

3. Which jurisdictions are part of the patent family?
Main jurisdictions include Australia, US, EP (Europe), and JP (Japan).

4. Are there any known challenges or litigations related to this patent?
No publicly available litigations; possible patentability challenges might arise from prior art in the same therapeutic area.

5. How does this patent landscape impact development efforts?
It offers broad protection but may face overlapping patents. Careful freedom-to-operate analysis and potential patent litigation risks should inform R&D strategies.


References

  1. Australian Patent AU2015258280. Patent document.
  2. World Intellectual Property Organization (WIPO). Patent family and jurisdiction data.
  3. USPTO, EPO, JPO patent databases. Patent landscape reports.
  4. Patent scope and prior art analysis reports.
  5. Patent laws governing pharmaceutical inventions in Australia and key jurisdictions.

More… ↓

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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.