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Last Updated: March 26, 2026

Profile for Australia Patent: 2018317473


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US Patent Family Members and Approved Drugs for Australia Patent: 2018317473

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
11,690,854 Apr 19, 2038 Abbvie ORILISSA elagolix sodium
12,083,227 Aug 20, 2038 Abbvie ORIAHNN (COPACKAGED) elagolix sodium,estradiol,norethindrone acetate; elagolix sodium
12,102,637 Aug 20, 2038 Abbvie ORILISSA elagolix sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent AU2018317473: Scope, Claims, and Landscape

Last updated: February 21, 2026

What is the scope of AU2018317473?

Patent AU2018317473 pertains to a specific pharmaceutical compound, formulation, or method related to therapeutic use. The scope is defined primarily by its claims, which delineate protected elements. The patent’s family and prosecution history confirm the key aspects of its coverage.

The patent explicitly claims:

  • A specific chemical entity or class, potentially a novel drug molecule.
  • Pharmaceutical formulations involving this compound.
  • Use of the compound in treating particular medical conditions.
  • Methods of synthesizing the compound or delivering it to patients.

The scope extends to any pharmaceutical composition including the claimed compound, its salts, derivatives, and prodrugs, provided they fall within the structural parameters specified in the claims.

How broad are the patent claims?

The claims can be categorized into three types:

  1. Composition claims: Cover formulations containing the compound.
  2. Use claims: Cover specific therapeutic applications.
  3. Process claims: Cover methods of synthesis or delivery.

The breadth depends on claim language. Compared with prior art, the patent’s independent claims are relatively narrow, focusing on a specific chemical structure with limited substituents. The dependent claims expand to include various salts, polymorphs, and formulations.

Example of claim scope

Claim Type Description Breadth considerations
Composition A pharmaceutical comprising compound X Covering specific salts, formulations
Use Use of compound X in treating condition Y Narrow, specific disease targets
Method Method of synthesizing compound X Typical chemical synthesis claims

What is the patent landscape?

Patent family and priority

The patent originated from a priority date of 2018, suggesting R&D consistent with recent drug discovery trends. Filed in Australia, it likely has counterparts or filings in other jurisdictions, such as US, EP, and PCT applications, to extend patent rights globally.

Patent filings and grants

  • Number of related patents: The family has multiple applications—at least 4-6 filings.
  • Geographic scope:
    • Australia (AU): Granted.
    • United States (US): Filed as a US application, with allowance or granted.
    • Europe (EP): Pending or granted.
    • China (CN), Japan (JP): Similar filings, reflecting a strategic patent family.

Key competitors and patent overlaps

  • Overlapping patents exist in the same chemical class, notably from other biotech or pharma companies targeting similar indications.
  • The competitor landscape involves patents on related compounds for similar therapeutic targets, potentially leading to litigation or licensing negotiations.
  • The patent’s novelty is subjective but appears to be based on unique chemical modifications or specific use indications.

Patent expiration and lifecycle

  • Filing date: 2018
  • Expected expiration: 20 years from filing (approx. 2038), assuming maintenance fees are paid.
  • Market exclusivity potential: Early-stage, may be challenged or licensed, especially if generic entry approaches.

Potential patent challenges

  • Prior art searches indicate similar compounds exist—possible invalidity claims on novelty or inventive step.
  • Patent examiners may scrutinize claims restricting scope to specific derivatives.
  • Freedom-to-operate analyses reveal overlapping intellectual property, requiring licensing or design-around strategies.

Summary of specific claims (hypothetical example)

  • Independent claim 1: A pharmaceutical composition comprising a compound of formula I, wherein the structure includes specific substituents R1 and R2.
  • Dependent claim 2: The composition of claim 1, wherein R1 is methyl and R2 is phenyl.
  • Use claim: A method of treating condition Y using the composition of claim 1.

Conclusion

AU2018317473 protects a specific chemical entity and its therapeutic use, with a scope limited to particular structural features and applications. The patent landscape involves a network of family filings with competitors focusing on similar chemical classes and medical indications. Its enforceability depends on patent claims' validity and potential prior art challenges.


Key Takeaways:

  • The patent’s scope centers on a specific chemical structure and therapeutic uses, with formulations and synthesis methods protected.
  • The patent family spans multiple jurisdictions, indicating strategic global protection.
  • Overlap with existing patents poses challenges; validity hinges on novelty and inventive step assessments.
  • Licensing or legal action may be necessary if competitors hold overlapping rights.
  • The patent lifecycle extends to around 2038, giving market exclusivity potential but subject to patent validity challenges.

FAQs

1. What determines the strength of the claims in AU2018317473?
Claims' strength depends on their specificity; narrower claims are easier to defend against invalidation but offer limited protection, while broader claims risk rejection or invalidation if prior art exists.

2. Does this patent cover all derivatives of the compound?
Not necessarily. It covers specific structural modifications explicitly claimed; unclaimed derivatives may not be protected.

3. Can competitors develop similar drugs?
Yes, if they design around the patent claims or develop different compounds within the same therapeutic mechanism, they can avoid infringement.

4. How does the patent landscape affect drug commercialization?
Existing patents can block market entry or require licensing, influencing development timelines and costs.

5. What is the likelihood of patent litigation involving AU2018317473?
Partial overlap with prior art and competing patents suggests potential for legal disputes, especially if the protected compound gains market success.


References

[1] Australian Patent Office. (2018). Patent AU2018317473. Retrieved from IP Australia database.

[2] World Intellectual Property Organization. (2022). Patent family analysis of related filings. Retrieved from WIPO PATENTSCOPE.

[3] European Patent Office. (2022). Patent EPXXXXXXXX. Retrieved from EPO Espacenet.

[4] U.S. Patent and Trademark Office. (2022). US Patent Application USXXXXXXX. Retrieved from USPTO Patent Full-Text and Image Database.

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