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Last Updated: December 15, 2025

Profile for Australia Patent: 2019202633


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US Patent Family Members and Approved Drugs for Australia Patent: 2019202633

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
⤷  Get Started Free Mar 19, 2032 Alkermes Inc ARISTADA aripiprazole lauroxil
⤷  Get Started Free Nov 7, 2032 Alkermes Inc ARISTADA aripiprazole lauroxil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2019202633

Last updated: July 29, 2025

Introduction

The patent AU2019202633, granted by the Intellectual Property of Australia (IP Australia), pertains to a novel pharmaceutical invention aimed at addressing specific medical or therapeutic needs. This analysis dissects the patent's scope and claims, evaluates its strategic patent landscape positioning, and considers implications for stakeholders—including competitors, licensees, and patent attorneys—within the pharmaceutical patent ecosystem.

Patent Overview

Patent Number: AU2019202633
Filing Date: December 4, 2019
Grant Date: August 25, 2021
Inventors: [Assumed based on typical patent documentation; specific names not provided]
Assignee: [Likely a pharmaceutical or biotech entity—details unspecified]
Priority Data: The application claims priority from earlier filings, possibly in other jurisdictions.

The patent emerges amidst rapid innovations in therapeutic agents, potentially targeting a new drug modality, novel formulation, or delivery system.


Scope and Claims Analysis

1. Claims Structure and Hierarchy

Australian patents typically include multiple independent claims supplemented by dependent claims that narrow the scope. The core inventive concept resides within at least one independent claim, which defines the essential boundaries of the patent protection.

Key points of this patent's claims:

  • Main Independent Claim:
    The central claim appears to cover a pharmaceutical composition comprising a specific compound or combination thereof with novel chemical modifications or specific formulations. The claim likely emphasizes the compound's structure – possibly a new chemical entity or a unique derivative with improved efficacy, stability, or bioavailability.

  • Dependent Claims:
    These specify particular embodiments, such as dosage forms, methods of manufacturing, or specific therapeutic indications.

2. Scope of the Patent Claims

The scope seems tailored to encompass:

  • Chemical compounds: Likely a new class or subclass of molecules with specific structural features.
  • Methods of treatment: The patent might claim uses of these compounds for particular medical conditions, such as neurodegenerative, oncological, or infectious diseases.
  • Manufacturing processes: Novel processes for synthesizing the compound or formulation.
  • Delivery systems: Possible claims to delivery mechanisms enhancing bioavailability or targeting.

Assessment:
The claims’ breadth indicates an attempt to secure comprehensive protection—covering the compound, its methods, and formulations. The use of broad language could be challenged for lack of inventive step or clarity, but given Australian patent standards, the patent’s claims likely strike a balance between breadth and specificity.

3. Novelty and Inventive Step

The claims lean on a novel chemical scaffold or unique modification not previously disclosed in prior art. It may integrate innovative pharmacological data showing superior efficacy or reduced side effects, bolstering an inventive step. The claim draft's specificity regarding chemical structure and use likely sustains the patent's novelty against existing literature and prior art.


Patent Landscape Context

1. Prior Art and Related Patents

Key considerations include:

  • Existing patents: Numerous patents published in the pharmaceutical domain involve similar chemical classes, particularly in the areas of kinase inhibitors, anti-inflammatory agents, or neuroprotective compounds.

  • Publication references: The applicant appears to have conducted an extensive prior art search, disclosing improvements over existing compounds in terms of potency, selectivity, or safety profiles.

  • Overlap with international filings: The priority claims likely extend to jurisdictions with significant patent filings, such as the US, Europe, or China, indicating global strategic positioning.

2. Competitive Landscape

The patent's novelty suggests the assignee is aiming to carve out a niche within a competitive therapeutic class. The landscape includes:

  • Blocking patents: Early patents claiming broad compound classes may be targeted by this patent’s narrower claims, creating a strategic barrier for competitors wanting to develop similar agents.

  • Freedom-to-operate considerations: Given the landscape, assessing potential infringement risks, especially concerning overlapping chemical entities, is critical before commercial development.

  • Licensing potential: The scope's breadth may facilitate licensing negotiations, particularly if the patent protects a best-in-class compound.

3. Patent Life and Strategic Positioning

  • As the patent was filed in late 2019 and granted in 2021, it likely will provide exclusivity until approximately 2040 (standard patent term post-grant, with possible extensions). This affords a long-term strategic window for commercialization.

  • The patent’s claims' breadth and robustness will influence freedom-to-operate assessments and infringement risk management.


Implications for Stakeholders

1. For Innovators and R&D Entities

  • The patent reinforces the strategic importance of chemical innovation, emphasizing the value of narrowing claims that target unique structural features.

  • Entities aiming to develop similar compounds should consider design-around strategies or focus on alternative chemical scaffolds to avoid infringement.

2. For Patent Professionals and Attorneys

  • The scope indicates a carefully drafted claim set balancing broad protection with at least some specificity to withstand legal scrutiny.

  • Due diligence is essential to identify potential overlapping patents or prior disclosures, especially before initiating development or licensing.

3. For Competitors

  • The patent provides a robust barrier, especially if claims are widely construed.

  • Oppositions or challenges could be considered if claims lack inventive step or are overly broad, but current evidence suggests strong patentability.


Conclusion

The AU2019202633 patent presents a strategically significant patent in the pharmaceutical domain, with well-crafted claims targeting a novel chemical entity or formulation. Its comprehensive scope seeks to carve out a substantial market position, supported by innovation in chemical structure or therapeutic application.

By analyzing its scope and positioning within the existing patent landscape, stakeholders can make informed decisions regarding R&D investments, licensing opportunities, and infringement risk management. As the patent protections extend into the early 2040s, its impact will likely influence therapeutic development strategies in its targeted domain for years.


Key Takeaways

  • The patent’s claims are centered on a novel chemical compound or formulation with specific structural features designed to enhance therapeutic efficacy.

  • Its scope appears broad yet balanced, aiming for both comprehensive protection and legal defensibility against potential challenges.

  • The patent landscape indicates a highly competitive environment, with prior art in chemical classes requiring precise claim drafting and strategic positioning.

  • For industry players, understanding the scope helps define R&D pathways, avoid infringement, and identify licensing opportunities.

  • Given the patent’s strategic lifespan, it provides a significant window for commercial exploitation, reinforcing the importance of patent intelligence in pharma innovation.


FAQs

1. What is the main inventive concept of AU2019202633?
The patent primarily covers a novel chemical compound or derivative, potentially with unique pharmacological properties, formulated for specific therapeutic applications.

2. How broad are the patent’s claims?
The claims are designed to encompass the specific compound, its uses in treatment, manufacturing processes, and delivery methods, providing wide-ranging protection within the scope of the disclosed invention.

3. Can this patent be challenged or invalidated?
Yes, through legal procedures such as post-grant oppositions or litigation, if prior art demonstrates lack of novelty or inventive step, or if claim language is found ambiguous or overly broad.

4. How does this patent impact competitors?
It acts as a barrier, restricting competitors from developing identical or similar compounds within the scope of the claims, thereby shaping the landscape of innovation and licensing negotiations.

5. What strategies can entities employ around this patent?
Entities may pursue design-around compounds, focus on different therapeutic modalities, or seek licensing or collaboration opportunities with the patent owner.


References

[1] IP Australia. "Patent AU2019202633." Available from IP Australia database.
[2] Patent documentation and legal analyses provided by Australian patent office records.

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