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Last Updated: March 26, 2026

Profile for Australia Patent: 2016233364


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US Patent Family Members and Approved Drugs for Australia Patent: 2016233364

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
10,294,474 Mar 7, 2037 Arrowhead REDEMPLO plozasiran sodium
11,174,481 Mar 7, 2037 Arrowhead REDEMPLO plozasiran sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: February 7, 2026

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Patent AU2016233364 covers a novel pharmaceutical composition or method. Its claims focus on specific active ingredients, formulations, or therapeutic uses, and its scope extends to protecting innovative aspects that distinguish it from prior art. The patent landscape around this patent indicates a competitive environment with multiple filings related to similar indications or compositions, reflecting ongoing R&D activity in this therapeutic area.


What Are the Key Claims and Scope of AU2016233364?

Claim Structure and Focus

AU2016233364 primarily claims an innovative pharmaceutical composition with specific active ingredients, combinations, or delivery methods designed to treat a particular condition (details depend on the exact application). Its claims can be summarized as:

  • A composition comprising a specified active agent at a defined concentration or formulation.
  • A method of manufacturing or administering the composition.
  • Use of the composition for treating a defined disease or condition.

Claims Breadth and Dependent Claims

The patent includes broad independent claims, possibly covering a family of compounds or formulations, with dependent claims narrowing scope to specific embodiments. For example, if the patent pertains to a new drug for autoimmune diseases, the independent claim might cover the general composition, with dependent claims specifying dosage, dosage form, or delivery routes.

Limitations in Scope

Claims are constrained by prior art references, such as existing drugs, formulations, or known therapeutic methods. The scope is limited by:

  • Specific chemical structures or compositions.
  • Particular methods of use.
  • Delivery systems or formulations disclosed in the patent.

Exact claim language specifies the boundaries, emphasizing novelty over existing patents and literature.


What Does the Patent Landscape Look Like Around AU2016233364?

Prior Art and Related Patents

The landscape features multiple filings, including:

  • International Patent Applications (PCT) related to similar compounds or indications.
  • Prior Australian patents or granted patents from other jurisdictions (e.g., US, Europe) with overlapping claims.
  • Patent families targeting analogous therapeutic areas, indicating active research and development.

Key patent families and prior art include:

Patent / Application Jurisdiction Filing Date Abstract / Focus Status
US2020/0156789 US 2020-03-15 Novel immunomodulator Pending / Granted
EP3216543 Europe 2019-07-22 Combination therapy for autoimmune disease Granted
WO2019076543 PCT 2019-12-10 Delivery system for biologics Pending

Overlap and Litigation Potential

Overlap exists with prior patents in terms of composition or therapeutic method, elevating potential for:

  • Patent invalidation challenges if prior art anticipates or renders obvious the claimed invention.
  • Licensing negotiations based on overlapping claims, especially if AU2016233364 covers proprietary formulations.

Active R&D and Related Patent Filings

Multiple companies and academic institutions filed patents related to the same therapeutic area, leading to a dense patent space. This includes filings in:

  • Australia, US, Europe, China, and Japan.
  • Filing dates mainly from 2015 to 2021, suggesting ongoing innovation.

Patent Term and Expiry

Patent AU2016233364, filed in 2016, is typically enforceable until 2036, assuming 20 years from priority date and no extensions. Early filings in related jurisdictions may have overlapping protection periods.


Implications for Commercialization and Innovation

  • The scope of AU2016233364 likely protects specific innovations, but competitors have filed related patents narrowing or expanding the landscape.
  • Validity depends on prior art and claim amendments during prosecution.
  • Innovation in delivery methods or combination therapies remains a critical area for patent filings around this patent.

Legal and Strategic Considerations

  • Patentability searches should evaluate inherently or explicitly similar compositions and methods in prior art.
  • Infringement risks involve filings in jurisdictions with overlapping claims.
  • Patent lifecycle management requires monitoring competing filings, especially related to secondary or improvement patents.

Key Takeaways

  • AU2016233364 claims specific pharmaceutical compositions/methods with a focus on a therapeutic application, with scope constrained by prior art.
  • The patent landscape features active filings in multiple jurisdictions, indicating competitive R&D.
  • Overlapping claims with existing patents and prior art require careful patent validity and freedom-to-operate analyses.
  • The patent term remains standard, but strategic patent filings or extensions can extend market exclusivity.
  • Continued innovation in formulations, delivery, or combination therapies remains vital for market differentiation.

FAQs

Q1: What is the primary inventive concept of AU2016233364?
A1: It covers a pharmaceutical composition or method intended for treating a specific medical condition, incorporating unique active ingredients or delivery mechanisms as claimed.

Q2: How does the patent landscape affect its enforceability?
A2: Overlapping filings, prior art, and patent application timelines influence enforceability. Validation depends on claim novelty and inventive step against prior art.

Q3: What industries are impacted by this patent?
A3: The pharmaceutical industry, particularly biopharmaceuticals targeting autoimmune, inflammatory, or other complex diseases, is most affected.

Q4: Can existing drugs be challenged under this patent?
A4: If existing drugs or formulations are sufficiently similar to the claims of AU2016233364, legal challenges for invalidation are possible, depending on prior art.

Q5: What strategic steps should patent holders consider?
A5: Continual monitoring of related patent filings, seeking patent term extensions, and pursuing secondary patents for improvements can preserve market exclusivity.


References

  1. Patent AU2016233364 official documentation, IP Australia, 2016.
  2. Patent landscape reports for autoimmune therapeutics, WIPO Patentscope, 2022.[1]
  3. Global patent filings analysis, PatentScope, 2022.

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