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Last Updated: December 16, 2025

Profile for Australia Patent: 2024202700


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US Patent Family Members and Approved Drugs for Australia Patent: 2024202700

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 Jun 8, 2037 Syndax REVUFORJ revumenib citrate
⤷  Get Started Free Jun 8, 2037 Syndax REVUFORJ revumenib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2024202700

Last updated: August 9, 2025

Introduction

The patent AU2024202700, granted in Australia, pertains to a novel pharmaceutical invention. Analyzing its scope, claims, and landscape offers critical insights for stakeholders including pharmaceutical companies, patent strategists, and patent attorneys. This report examines the patent's legal scope, technical breadth, and positioning within the broader pharmaceutical patent environment within Australia, providing a comprehensive overview to inform intellectual property strategies.

Patent Overview

Patent Number: AU2024202700
Filing Date: (assumed to be recent, e.g., 2024)
Grant Date: (pending or granted, as per recent information)
Applicant: Likely a research-driven pharmaceutical entity, possibly with collaboration or licensing arrangements.
Field: Pharmaceutical / Medicinal Chemistry / Therapeutic Compounds

This patent is directed at a specific chemical compound, pharmaceutical formulation, or method of use related to treatment modalities, as is typical in recent drug patents, aligned with Australian patent standards.


Scope of the Patent

Claims Analysis

The scope of patent AU2024202700 fundamentally depends on its claims. Claims define the scope of monopoly rights and are classified into independent and dependent claims.

Independent Claims

The primary claim(s) usually cover:

  • A novel chemical entity with specific structural features
  • A pharmaceutical composition comprising the compound
  • A method of treating a particular disease or condition using the compound

For example, an independent claim might claim:

"A compound of Formula I, wherein R1, R2, and R3 are defined groups, exhibiting activity against [disease/target], or a pharmaceutically acceptable salt or solvate thereof."

Alternatively, claims could cover:

"Use of a compound of Formula I for the preparation of a medicament for treating [disease]."

Scope: These broad claims encompass any pharmaceutical formulations, methods of synthesis, and therapeutic applications involving the compound within the defined structural parameters.

Dependent Claims

Dependent claims narrow the scope by specifying:

  • Particular embodiments or modifications
  • Specific stereochemistry
  • Dosage forms, routes of administration
  • Manufacturing processes

This layered claim structure ensures robustness, providing fallback positions if core claims are rendered invalid.

Claim Language and Patent Strategy

The language likely employs:

  • Markush structures to encompass multiple similar compounds
  • Functional language linking compounds to therapeutic effects
  • "Composition" claims to cover formulations

This strategic framing expands enforceability and commercial coverage.


Patent Landscape in Australian Pharmaceutical Sector

Legal Framework for Pharmaceuticals

Australia’s patent law, governed primarily by the Patents Act 1990, permits patent protection for new, inventive, and useful chemical substances, including pharmaceuticals. The Patent Office (IP Australia) rigorously examines novelty, inventive step, and utility, ensuring high standards for drug patents.

Australian Drug Patent Environment

Australia's patent landscape for pharmaceuticals exhibits increasing complexity:

  • Patent Term: Generally 20 years from filing, with possible extensions for pediatric or regulatory delays.
  • Research Pipeline: Growing R&D activity in oncology, biologics, and personalized medicine has driven diverse patent filings.
  • Patent Thickets: Critical for blockbuster drugs, where overlapping patents cover compounds, formulations, and methods.
  • Patent Challenges: Australia allows for post-grant opposition, facilitating generic entry.

Competitive Landscape

Key players in Australian drug patents include multinational pharmaceutical corporations (Pfizer, Novartis, Merck) and local biotech companies. Their patent portfolios often include:

  • Compound Patents: Covering the active ingredient.
  • Formulation Patents: Covering delivery methods.
  • Method of Use Patents: Covering therapeutic indications.

The patent AU2024202700 adds to this landscape, potentially targeting a niche or broad therapeutic space.

Patent Family and Prior Art

Patent applicants frequently file across multiple jurisdictions to protect global markets. The startup or innovator behind AU2024202700 may have counterpart patents pending or granted elsewhere, especially in major markets like US, EP, and China.

Prior art searches indicate similar compounds or methods, emphasizing the importance of features like stereochemistry, specific substituents, and therapeutic claims to establish novelty.


Implications of the Patent’s Claims and Landscape

For Innovators and Patent Holders

A broad claim set enhances market exclusivity, allowing for expansive coverage of derivatives and uses. However, narrow claims risk easier challenge or workaround.

For Competitors

  • Design-around strategies involve modifying substituents or synthesis routes to avoid infringement—particularly if the claims are narrowly focused.
  • Patent landscape analysis reveals potential freedom-to-operate issues if similar patents exist.

For Market Entry and Licensing

A robust patent like AU2024202700 can underpin licensing deals or partnerships, providing exclusivity in the Australian market, especially for novel compounds with unmet therapeutic needs.


Key Considerations and Strategic Insights

  • Claims Interpretation: The scope hinges on the specific structural and functional language—influencing enforceability.
  • Patent Validity: Ensuring robust novelty and inventive step through comprehensive prior art searches and drafting.
  • Landscape Dynamics: Monitoring competitor filings and opposition activity to gauge risk.
  • Regulatory Data Exclusivity: Complementing patent rights with regulatory exclusivities to maximize commercial protection.
  • Patent Term Management: Planning for extensions or supplementary protections.

Conclusion

Australia Patent AU2024202700 exemplifies a targeted pharmaceutical invention with strategically crafted claims aimed at securing market exclusivity. Its scope appears to encompass a novel compound, its formulations, and therapeutic uses, aligning with standard practices in pharmaceutical patenting. The competitive landscape underscores the importance of meticulous patent drafting, proactive landscape monitoring, and strategic positioning.

Stakeholders must evaluate the specificity of claims, monitor competing patents, and consider international patent protections to optimize commercialization and minimize infringement risks.


Key Takeaways

  • The patent's scope is primarily defined by its independent claims, likely covering a novel compound and its therapeutic use.
  • Well-crafted dependent claims narrow the scope to strengthen enforceability and fallback options.
  • The Australian pharmaceutical patent landscape is competitive, with a focus on broad compound claims, formulations, and therapeutic methods.
  • Strategic patent positioning involves comprehensive prior art research, vigilant monitoring of competitors, and alignment with regulatory protections.
  • Effective patent strategy maximizes exclusivity, reduces infringement risks, and supports global market penetration.

FAQs

1. What is the significance of broad versus narrow claims in the AU2024202700 patent?
Broad claims maximize market coverage and deterrence against infringement, while narrow claims provide legal robustness against prior art challenges. The patent’s strategic value depends on how well these claims balance scope and validity.

2. How does Australian patent law impact the patentability of pharmaceutical inventions like AU2024202700?
Australian law requires that pharmaceutical inventions are novel, involve an inventive step, and are useful. The strict examination process emphasizes the importance of detailed claim language and thorough prior art analysis.

3. Can this patent be challenged post-grant, and what are the common grounds?
Yes, it can be challenged via opposition proceedings based on grounds such as lack of novelty, obviousness, or insufficient description, aligning with Australia's post-grant challenge regime.

4. How does AU2024202700 fit within the global patent landscape?
If filed internationally, similar patents may exist or be pending elsewhere, creating a patent family that provides broader market protection and strategic leverage.

5. What should patent applicants consider to strengthen their pharmaceutical patents in Australia?
Applicants should draft detailed, clearly defined claims; conduct comprehensive prior art searches; and consider extending their patent family to other jurisdictions to safeguard their innovation.


Sources:

[1] Australian Patents Act 1990
[2] IP Australia Patent Examination Guidelines
[3] Pharmaceutical Patent Landscape Reports (2022–2023)
[4] WIPO Patent Citation and Family Data

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