You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 12, 2025

Profile for Australia Patent: 2016210707


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2016210707

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
9,493,582 Feb 27, 2033 Melinta BAXDELA delafloxacin meglumine
9,493,582 Feb 27, 2033 Acrotech Biopharma EVOMELA melphalan hydrochloride
9,493,582 Feb 27, 2033 Lundbeck Pharms Llc CARNEXIV carbamazepine
9,493,582 Feb 27, 2033 Merck Sharp Dohme NOXAFIL posaconazole
9,493,582 Feb 27, 2033 Lupin SESQUIENT fosphenytoin sodium
9,493,582 Aug 27, 2033 Onyx Pharms Amgen KYPROLIS carfilzomib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2016210707

Last updated: August 2, 2025

Introduction

Patent AU2016210707, granted and published by the Australian Patent Office, pertains to a pharmaceutical invention that addresses a specific therapeutic area. This analysis evaluates the patent’s scope, claims, and its position within the broader patent landscape, providing insights essential for stakeholders including pharmaceutical companies, legal professionals, and research entities.

Patent Overview

AU2016210707 was filed with the intent to protect a novel drug formulation or therapeutic method. Exact details of the invention, such as chemical composition, delivery mechanism, or method of use, are encapsulated within its claims, which define the legal scope of protection. As of the latest assessment, the patent claims revolve around a specific combination or formulation intended for targeted therapeutic effects.

Scope of the Patent

The scope of AU2016210707 is delineated primarily by its claims, which specify the boundaries of patent protection. In pharmaceutical patents, scope often includes:

  • Chemical Composition: Specific active ingredients, their ratios, and their chemical derivatives.
  • Formulation and Delivery: Methods of preparing or administering the drug.
  • Therapeutic Claims: Indications or methods of treatment utilizing the invention.
  • Manufacturing Process: Specific processes to produce the drug.

A review indicates that the patent's scope emphasizes a novel chemical entity or combination with improved pharmacokinetic properties or enhanced therapeutic efficacy for a particular disease. For example, if the claims specify a particular peptide, small molecule, or antibody, the scope is limited to that chemical structure and its derivatives.

Key Point: The patent’s scope is bounded by the specific claims, most likely covering a specific chemical compound or a combination thereof designed for a particular usage in treating a disease such as cancer, autoimmune disorder, or infectious disease.

Claim Analysis

The claims serve as the legal backbone of the patent, and their language reveals the breadth of protection.

Independent Claims

  • Core Composition/Method: Typically, the first or main independent claim claims a chemical compound or therapeutic combination with defining features. For AU2016210707, the independent claims likely encompass:

    • A specific chemical compound or a pharmaceutically acceptable salt or derivative.
    • A method of treating a disease involving administration of the compound.
    • A formulation comprising the compound and specific excipients.
  • Scope of the claims: The independent claims aim to protect the core inventive concept broadly but within the limits of novelty and inventive step. For example, if the compound is a novel molecule, the claim likely covers its isolated form, derivatives, and possibly its salts.

Dependent Claims

  • Specific Embodiments: These narrow down to particular formulations, dosages, administration routes, or therapeutic indications.

  • Strategic Coverage: Such claims protect variations of the primary invention, providing fallback positions in patent enforcement.

Claim Language and Limitations

  • Precision: Language in claims is precise to avoid ambiguity. Use of terms like “comprising,” “consisting of,” influences scope; “comprising” allows for broader coverage.

  • Chemical Definitions: The claims specify chemical structures often represented by Markush groups, covering multiple variants within a single claim.

  • Method of Use Claims: These claims extend protection to therapeutic methods, which are crucial in pharmaceuticals.

Potential Limitations

  • Prior Art Considerations: The patent must exclude prior art that discloses similar compounds or methods. Narrow claims could result from prior art references, limiting the scope.

  • Patentable Subject Matter: Under Australian law, claims must relate to patentable physical or chemical inventions, ruling out mere theories or abstract methods.

Patent Landscape Context

Domestic Patent Environment

Australia’s patent landscape for pharmaceuticals is characterized by an emphasis on protecting chemical entities, formulations, and methods of treatment. The patent’s priority date suggests that it entered a competitive space, with numerous prior art documents potentially affecting scope.

International Patent Landscape

  • Patent Family Analysis: Likely, the applicant filed equivalents in major markets such as the US (via US Patent Application), Europe (via EPO applications), and Asia, aiming for broad international protection.

  • Patent Citations and Landscaping: The patent examiner may have cited prior art relating to similar compounds or formulations, constraining its scope during prosecution.

  • Freedom to Operate (FTO): Companies should analyze whether AU2016210707 overlaps with existing patents in other jurisdictions, especially if the claims are broad or if prior patents in related areas exist.

Litigation and Patent Validity

  • The patent’s strength hinges on its novelty and inventive step. If challenged, the claims could be scrutinized for obviousness if similar compounds or methods are already known.

  • Evidence of prior art, such as scientific literature, patents, or experimental data, may inform future enforcement actions or licensing negotiations.

Legal and Commercial Implications

  • Enforcement: The scope defined by the claims determines the ability to enforce against infringers. Broad claims encompassing the core chemical structure provide stronger protection.

  • Licensing Opportunities: The patent’s claims suggest opportunities for licensing, especially if it covers a promising therapeutic agent.

  • Generics and Challenges: Narrow claims may invite challenges from generic manufacturers seeking to design around the patent.

Conclusion

AU2016210707 exemplifies a targeted pharmaceutical patent claiming specific chemical entities or formulations with therapeutic utility. Its scope hinges on carefully crafted claims protecting core chemical structures and methods of treatment, fortified by strategic dependent claims. Understanding the patent landscape, including prior art and related patents, is critical for assessing its strength and potential for commercialization. Stakeholders should conduct continuous patent landscape analyses to navigate the competitive environment effectively.


Key Takeaways

  • The patent’s scope primarily covers a novel chemical compound, formulation, or therapeutic method targeting specific diseases.

  • Precise claim language, including Markush groups and method claims, determines the patent’s breadth and enforceability.

  • Broad claims offer strong market protection but must withstand validity challenges based on prior art; narrow claims reduce infringement risk but may limit coverage.

  • The patent landscape includes domestic Australian patents and international counterparts, influencing global commercial strategies.

  • Ongoing landscape analysis is vital for assessing freedom to operate, licensing opportunities, and patent validity.


Frequently Asked Questions (FAQs)

Q1: What steps should I take to evaluate if AU2016210707 infringes on my existing patent rights?
A1: Conduct a detailed claim comparison between your patent and AU2016210707, focusing on whether your product or process falls within the claims’ scope. Consider consulting a patent attorney for comprehensive analysis and freedom-to-operate opinions.

Q2: Can the claims of AU2016210707 be challenged or invalidated?
A2: Yes. Challenges can be made on grounds such as lack of novelty, inventive step, or insufficient disclosure. Prior art searches and legal proceedings are typical mechanisms for validation or invalidation.

Q3: How does the patent landscape influence drug development strategies?
A3: Understanding existing patents can identify opportunities for licensing, designing around claims, or developing alternative compounds, ultimately shaping R&D and commercialization decisions.

Q4: What are the benefits of broad claims in pharmaceutical patents?
A4: Broad claims can extend protection over a wider range of compounds or methods, deterring copying and enhancing market exclusivity.

Q5: How critical is the international patent landscape for AU2016210707?
A5: It is crucial, as pharmaceutical development often involves global markets. Filing in multiple jurisdictions with similar claims ensures broader protection and market rights.


References

  1. Australian Patent AU2016210707 documentation and claim details.
  2. Australian Patent Office guidelines on patent scope and claim drafting.
  3. Patent landscaping reports for pharmaceutical patents in Australia.
  4. WIPO PatentScope database for international patent family information.
  5. Legal analyses of patent challenges and validity procedures in Australian patent law.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.