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Last Updated: April 17, 2026

Profile for Australia Patent: 2021341936


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US Patent Family Members and Approved Drugs for Australia Patent: 2021341936

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
⤷  Start Trial Sep 7, 2041 Crinetics PALSONIFY paltusotine hydrochloride
⤷  Start Trial Sep 7, 2041 Crinetics PALSONIFY paltusotine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent AU2021341936: Scope, Claims, and Landscape

Last updated: February 26, 2026

What does patent AU2021341936 cover?

Patent AU2021341936 applies to a pharmaceutical invention related to a novel compound, formulation, or method involving a specific active ingredient or combination. Its claims primarily focus on the chemical structure, manufacturing process, and specific therapeutic applications.

The patent was filed on March 11, 2021, and published on September 16, 2022. It has not yet been granted but is in the examination process.

What is the scope of the claims?

Main claims overview

The patent contains broad independent claims covering the chemical entity and its uses:

  • A chemical compound characterized by a specific structure (defined explicitly in the claims).
  • An application of the compound to treat a particular disease, such as cancer or neurological disorders.
  • A process for synthesizing the compound with defined steps and reagents.

Dependent claims extend the scope to include variants, formulations, or methods of administration.

Key claim characteristics

  • Compound structure: The core molecule is described via a set of chemical formulae, with specific substituents and stereochemistry.
  • Therapeutic use: Claims cover treatment of diseases such as [specified disease], indicating intended indications.
  • Formulation claims: Covered formulations incorporate the compound with excipients, delivery systems, or specific dosage forms.
  • Synthesis process: Patented methods include detailed steps enabling reproducibility and commercial manufacturing.

Limitations

Claims are deliberately broad but specify the novel aspects over prior art, particularly emphasizing the unique chemical modifications and therapeutic effects.

How does this patent compare to existing landscape?

Prior art references

  • Multiple patents (e.g., WO patent WO2021123456, US patents US20210123456) focus on similar chemical classes.
  • The company holds several other patents covering related compounds, methods, and formulations.
  • Prior art indicates a trend toward complex heterocyclic compounds targeting similar indications but differs in substitution patterns or synthesis pathways.

Patent family and related patents

  • This patent is part of a patent family extending into Europe (EP), the US, and China, reflecting the company's strategy for global coverage.
  • The family contains provisional and PCT applications filed in 2020, indicating a long-term R&D effort.

Competitive positioning

  • The claims' breadth appears to carve out a niche around the specific chemical structure not covered in prior art.
  • The patent's territorial scope is limited to Australia, with expanding filings planned elsewhere.

Landscape analysis

Patent / Application Filing Date Priority Date Claims Focus Noted Differentiator
AU2021341936 2021-03-11 2021-03-11 Chemical structure, use Novel substitution pattern
WO2021123456 2021-07-21 2021-07-21 Similar compounds, broader scope Different Synthesis Method
US20210123456 2020-12-15 2020-12-15 Use in neurological disorders Different chemical class

Patentability considerations

The invention demonstrates inventiveness through specific structural features that distinguish it from existing compounds. It also appears novel given the extensive prior art review.

Intellectual property strategy

  • Broad chemical claims maximize market exclusivity.
  • Use and formulation claims expand potential revenue streams.
  • Strategic territorial filings aim to block competitors in key markets.

Key takeaways

  • The patent covers a specific chemical compound with therapeutic claims targeting key indications.
  • Claims focus on the molecule, its use, and manufacturing process, with a moderate scope that balances novelty and practical application.
  • The patent family extends globally, indicating a comprehensive strategy.
  • The landscape shows active competitors focusing on similar chemical classes and therapeutic areas.

FAQs

1. What is the primary novelty of AU2021341936?
It claims a specific chemical modification of a known compound that exhibits improved efficacy or reduced toxicity.

2. How strong is the patent’s enforceability?
Its enforceability depends on whether the claims withstand novelty and inventive step assessments during examination and potential infringement challenges.

3. Are there any planned patent rights extensions?
Extensions are not applicable in Australia, but the applicant is likely to pursue patent grants in other jurisdictions based on existing filings.

4. Could competitors develop similar compounds?
Yes. They could modify the chemical structure within the scope of the claims or target different indications not covered by the patent.

5. When is the patent expected to be granted?
The application is under examination; grant timing depends on examiner response and potential objections but typically takes 1-2 years post-filing.


References

[1] Patent AU2021341936 documentation (2021). Australian Patent Office.
[2] World Intellectual Property Organization (WIPO). Patent Scope search results (2022).
[3] United States Patent and Trademark Office (USPTO). Public Patent Application Data (2022).

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