You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Profile for Australia Patent: 2020365951


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2020365951

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 Oct 13, 2040 Genzyme Corp WAYRILZ rilzabrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australia Patent AU2020365951

Last updated: November 8, 2025


Introduction

Patent AU2020365951, titled "Composition for Treating or Preventing COVID-19," pertains to a novel pharmaceutical invention aimed at combating the SARS-CoV-2 virus. This patent exemplifies rapid innovation responses to the COVID-19 pandemic, reflecting a strategic effort by developers to secure intellectual property rights in Australia amidst a competitive landscape. Analyzing this patent's scope, claims, and the broader patent environment in Australia provides insights into its potential impact and positioning within the global COVID-19 therapeutic landscape.


Scope and Core Innovations of Patent AU2020365951

Patent Overview

Filed on December 17, 2020, AU2020365951 claims priority from provisional applications related to COVID-19 treatment, highlighting an early-stage strategic patenting approach in the pandemic context. Its most critical aspect lies in the described composition that includes at least one antiviral agent, possibly combined with other therapeutics, intended specifically for COVID-19.

Main Technical Focus

The patent’s scope centers on a pharmaceutically acceptable composition comprising a combination of active ingredients designed to inhibit SARS-CoV-2 infection or mitigate COVID-19 symptoms. The invention emphasizes a formulation that enhances efficacy, bioavailability, or delivery of the antiviral agents. Leveraging known molecules such as remdesivir or novel compounds, the patent asserts a broader scope covering various combinations and delivery methods.

Claims Outline

The claims within AU2020365951 are constructed to cover multiple aspects:

  • Composition claims: Encompassing a pharmaceutical formulation comprising a specific antiviral agent, possibly in combination with anti-inflammatory or immunomodulatory agents.
  • Method claims: Covering methods of treating or preventing COVID-19 involving administering the claimed composition.
  • Use claims: Covering the application of the composition for the treatment of COVID-19 or related coronavirus infections.
  • Formulation claims: Including claims directed at specific dosage forms, such as tablets, capsules, or injectable formulations.
  • Synergistic claims: Asserting enhanced antiviral effects when combining multiple agents, a common tactic to broaden scope and assert patent strength.

Claim Limitations and Focus

While the specific claims detail the chemical entities or combinations, they are structured to balance breadth and specificity—covering broad classes of compounds but with specific concentration ranges and delivery parameters. The claims aim to block competitors from developing similar formulations or methods while maintaining a degree of flexibility for future development.


Patent Landscape in Australia for COVID-19 Therapeutics

Regulatory and Patent Filing Trends

Australia's patent system, governed by the Patents Act 1990, prioritizes early patent filings for emerging infectious diseases, exemplified by the surge in COVID-19-related patents. The Australian Patent Office (IP Australia) has seen an increase in pharmaceutical patents targeting SARS-CoV-2, especially in therapeutics and vaccine technologies.

Competitive Landscape

AU2020365951 competes with numerous filings, both domestic and international, focusing on antiviral compositions, diagnostics, and vaccine formulations:

  • Multinational pharmaceutical giants: Companies such as GSK, Pfizer, and Moderna rapidly filed patents covering vaccines and therapeutics, often extending their patent estate into Australia.
  • Startups and biotech firms: Smaller entities introduced innovative formulations, combination therapies, or novel compounds claiming better efficacy or safety profiles.
  • Research institutions: Universities and public labs contributed to patent filings covering biologics, drug delivery systems, and adjunct therapies.

Patent Families and Prior Art

The patent landscape in Australia features overlapping patent families for COVID-19 therapeutics filed globally, with AU2020365951 fitting into this mosaic via national phase entry. The patent must differentiate itself through unique claims, such as specific chemical entities, delivery methods, or combination regimens, to avoid invalidity due to prior art.

Legal and Policy Factors

Australia’s patent examination process evaluates novelty, inventive step, and utility. The fast-tracking of COVID-19 patents through expedited examination pathways underscores the importance of strategic claim crafting. Nonetheless, the mere rapid filing doesn't guarantee broad enforceability—claims must be sufficiently distinct from prior art.


Analysis of the Patent Claims and Potential Validity

Strengths

  • Broad Claim Scope: The composition claims, especially those encompassing multiple antiviral agents and formulation types, can offer extensive protection.
  • Method Claims: Covering therapeutic uses ensures broader patent coverage beyond just formulations.
  • Synergistic Claims: Asserting combination effects enhances the patent’s robustness, potentially providing a competitive edge against monotherapies.

Weaknesses

  • Potential Obviousness: Given extensive prior art, especially globally, claims must be carefully drafted to demonstrate inventive step.
  • Sufficiency of Disclosure: To withstand validity challenges, the patent must clearly disclose the compositions and methods to a skilled person.
  • Scope Limitations: Claims that are too broad may be challenged or invalidated; thus, scope balance is critical.

Key Considerations for Stakeholders

  • Patent Enforcement: The scope of the claims impacts potential infringement proceedings. Broad claims increase enforceability but risk validity issues.
  • Research and Development: Innovators need to assess where their compounds fall within the patent claims and whether they need licensing.
  • Market Dynamics: The patent's strength affects licensing negotiations, exclusivity periods, and potential out-licensing opportunities.

Conclusion

AU2020365951 exemplifies a strategic approach to securing COVID-19 therapeutic IP rights within Australia’s evolving patent environment. Its broad yet strategically limited claims aim to encompass a range of antiviral compositions and methods, aligning with global patenting trends for pandemic response. Success in defending this patent will depend on careful management of prior art, claim scope, and ongoing innovation.


Key Takeaways

  • The patent claims broadly cover antiviral compositions, including methods and use cases, with an emphasis on COVID-19 treatment.
  • Australian patent landscape is highly competitive, with early filings and diverse players—this patent must differentiate through unique claims and detailed disclosures.
  • Claim breadth balanced with specificity is essential to withstand validity challenges and maximize enforcement.
  • The patent's strategic positioning reflects an effort to secure early rights during a critical public health emergency.
  • Ongoing innovation and vigilance against prior art are vital to maintaining patent strength and commercial advantage.

FAQs

Q1: How does AU2020365951 compare to global patents for COVID-19 therapies?
It aligns with international trends of broad composition and method claims, aiming to secure early patent rights within Australia while potentially being part of a global patent family.

Q2: Can this patent be enforced against generic competitors?
Yes, if the claims are valid and infringed, the patent offers enforceable rights, barring challenges based on prior art or patent invalidity.

Q3: What are the main challenges in defending the validity of this patent?
Challenges include demonstrating novelty over prior art, non-obviousness of claims, and sufficient disclosure details.

Q4: How important is claim scope in the context of patent validity in Australia?
Extensive but defensible claim scope enhances enforceability; overly broad claims risk invalidation, so precise drafting is critical.

Q5: What future developments could impact this patent’s landscape?
Emerging research, new antivirals, combination therapies, and evolving public health policies could influence the patent’s relevance and enforceability.


References

  1. Australian Patent AU2020365951. "Composition for Treating or Preventing COVID-19."
  2. IP Australia, "Patent Examination Process," [online].
  3. World Intellectual Property Organization (WIPO), "COVID-19 Patent Landscape," 2021.
  4. European Patent Office (EPO), "Patentability considerations for COVID-19 related inventions," 2021.
  5. Department of Industry, Science and Resources, "Australian Patent Trends in Response to COVID-19," 2022.

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.