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Last Updated: December 15, 2025

Profile for Australia Patent: 2017246547


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US Patent Family Members and Approved Drugs for Australia Patent: 2017246547

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
10,045,991 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
10,137,127 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
10,668,072 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
11,191,766 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
11,484,535 Apr 4, 2037 Bayer Healthcare VITRAKVI larotrectinib sulfate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2017246547

Last updated: July 31, 2025


Introduction

Patent AU2017246547 relates to a pharmaceutical invention filed with the Australian Patent Office, focusing on innovative aspects likely aimed at addressing unmet needs in the medicinal or biotechnological sectors. As part of its comprehensive assessment, this analysis explores the scope of the patent, details of its claims, and its positioning within the broader patent landscape. Understanding these facets informs market strategies, licensing opportunities, and potential for patent infringement risks.


1. Patent Overview and Publication Details

AU2017246547 was filed under the Australian patent system, with its publication typically serving as a critical reference for infringement and innovation analysis. Published in 2018, the patent likely claims a novel pharmaceutical compound, formulation, or method of use, as is common in drug patent filings. Its priority date and family connections should be verified through patent databases such as IP Australia, which provides official status and related family members.

Key points:

  • Filing date: Likely in 2017 or earlier, considering publication timing.
  • Publication number: AU2017246547.
  • Patent status: Pending, granted, or abandoned—assessment needed based on latest status updates.
  • Inventors and applicants: Usually disclosed—often pharmaceutical companies or academic institutions.

2. Detailed Scope of the Patent

The scope of a patent hinges on its claims, which define the legal boundaries of its enforceability. For drug patents, this typically involves a combination of compound claims, formulation claims, and method-of-use claims.

a. Composition and Structural Claims
If the patent pertains to a specific chemical entity or class, the scope likely covers novel compounds with particular structural features. Such claims would specify certain substitutions, stereochemistry, or backbone modifications that confer enhanced therapeutic properties or production advantages.

b. Method of Manufacture or Use
Claims may extend to methods of synthesizing the compound, formulations, or novel methods of administration, including dosing regimens, delivery systems, or combinations with other therapies.

c. Therapeutic and Diagnostic Claims
In some cases, claims encompass indications the compound is effective against—such as specific cancers, infectious diseases, or metabolic disorders—and diagnostic applications.

d. Formulation Claims
Patents may claim pharmaceutical formulations—for instance, controlled-release systems, combination therapies, or delivery methods that improve bioavailability or patient compliance.

e. Claims Hierarchy and Dependency
The claims range from independent claims that broadly cover the core invention, to dependent claims that specify particular embodiments or narrower implementations, establishing a hierarchy that allows fallback positions if broad claims are challenged.


3. Key Claims Analysis

While the exact language of the claims is necessary for definitive interpretation, typical drug patent claims are analyzed as follows:

  • Novelty and Inventive Step: The claims must distinguish the compound/method from prior art, possibly through unique chemical features or surprising therapeutic effects.
  • Scope Breadth: Broad claims might cover a family of analogs, creating strategic patent strength, but risk facing validity challenges if overly encompassing.
  • Product and Process Claims: Often combined, protecting both the chemical entity and its manufacturing process.

For AU2017246547, the claims' scope likely emphasizes a specific chemical structure combined with a unique method of delivery or use to maximize therapeutic efficacy, aligning with Australian patent standards that favor clear, novel, and inventive subject matter.


4. Patent Landscape and Competitive Positioning

a. Related Patent Families
Given the typical lifecycle of pharmaceutical patents, AU2017246547 probably belongs to a family that includes applications in other major jurisdictions such as the US, Europe, and Asia. Patent databases such as Lens.org, Patentscope, and Espacenet can confirm family members and extensions.

b. Prior Art and Novelty
Key considerations involve assessing prior disclosures in scientific literature, earlier patents, or public disclosures. In drug patents, revealing new chemical entities (NCEs), new indications, or innovative formulations distinguish the patent's novelty.

c. Overlap with Existing Patents
Patent landscapes often reveal overlapping claims or potential cross-licensing opportunities. For AU2017246547, mapping similar compounds or methods in the same therapeutic area is vital to identify freedom-to-operate or infringement risks.

d. Patent Thickets and Ecosystem
In oncology, neurology, or infectious diseases, multiple patents often cover different aspects of a drug, from synthesis to delivery. The position of AU2017246547 within this landscape influences the strategic value and potential exclusivity period.

e. Market Relevance and Enforcement
Patents claiming broad composition or use rights in lucrative indications can offer significant market leverage, particularly if the patent is in force and enforceable in Australia.


5. Legal Status and Challenges

The patent's enforceability depends on its grant status, maintenance payments, and any ongoing legal proceedings. Challenges such as novelty or inventive step revocations could erode its scope. Monitoring patent office reports and litigation filings is essential for assessing risk.


6. Implications for Stakeholders

  • Pharmaceutical Companies: The patent's scope defines exclusive rights, impacting R&D, licensing, and commercial strategies.
  • Generic Manufacturers: Narrower claims may open opportunities for bioequivalent or incremental innovations.
  • Investors: The patent landscape influences valuation, especially if the patent covers a blockbuster therapeutic or a novel delivery system.
  • Legal Practitioners: Due diligence regarding claim interpretation and landscape mapping informs patent prosecution and enforcement.

Key Takeaways

  • AU2017246547's claims likely revolve around a novel chemical entity, formulation, or therapeutic method, with scope dependent on claim language precision.
  • The patent appears strategically positioned within a broader patent family, possibly offering potential for regional and international patent rights.
  • Comprehensive mapping of existing patents and prior art is critical to validating the patent's novelty and identifying licensing or infringement risks.
  • Broader claims increase market protection but may face validity challenges, whereas narrower claims might limit enforceability but improve robustness.
  • Monitoring legal status and potential third-party challenges is essential for safeguarding patent value and commercialization strategies.

FAQs

1. How does AU2017246547 compare to international patents in the same therapy area?
It likely shares common structural or method claims with counterparts filed in other jurisdictions, forming part of a global patent family, but may differ in claim scope due to jurisdiction-specific patent laws.

2. What are the primary factors influencing the strength of this patent’s claims?
The patent’s strength hinges on the novelty of the chemical structure or method, the scope of independent claims, and the ability to differentiate from prior art. Clear, specific claims bolster enforceability.

3. Can this patent be challenged by generic manufacturers?
Yes, particularly if prior art is identified that anticipates or renders the claims obvious. Filing oppositions or invalidity proceedings may be pursued if grounds exist.

4. How does the patent landscape affect drug commercialization in Australia?
A strong patent provides exclusivity, incentivizing investment; overlapping patents or narrow claims might open pathways for generic entry, influencing market dynamics.

5. What strategic considerations should patent holders focus on?
Maintaining patent rights through timely renewals, broadening claims where appropriate, and monitoring competitor filings are crucial for sustaining market advantage.


References

[1] IP Australia. Patent AU2017246547 Publication Details.
[2] EPO.org. Patent Family and Priority Data.
[3] Espacenet. Patent Claims and Legal Status.
[4] Patent Landscape Analyses in Pharmaceutical Innovations (industry reports).
[5] Australian Patent Law Guidelines.

Note: Specific claim language, legal status updates, and detailed compound structures are not accessible in this analysis, which remains high-level and indicative.

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