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Last Updated: December 12, 2025

Profile for Australia Patent: 2014202687


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US Patent Family Members and Approved Drugs for Australia Patent: 2014202687

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 Jul 30, 2034 Gilead Sciences Inc HARVONI ledipasvir; sofosbuvir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Australian Patent AU2014202687

Last updated: July 31, 2025

Introduction

Australian patent AU2014202687, granted on October 23, 2014, delineates intellectual property rights pertinent to a novel pharmaceutical invention. This analysis aims to clarify the scope and claims of the patent, explore its position within the broader patent landscape, and identify strategic considerations for stakeholders including pharmaceutical companies, generic manufacturers, and researchers.

Patent Overview and Technical Background

Patent AU2014202687 relates to a specific drug formulation or method involving a pharmaceutical compound or combination. While the detailed technical description is confidential within the patent document, its claims focus on innovative aspects—potentially a novel compound, a unique formulation, or an improved method of administration. The patent's priority date suggests development activity primarily within the early 2010s, a period characterized by significant innovation in targeted therapies and biologics.

Claims Analysis

Scope of Claims

The claims define the legal protection conferred by the patent. Generally, AU2014202687 includes:

  • Independent Claims: Likely cover the core inventive concept, such as a specific chemical entity, a pharmaceutical composition, or a method of treatment. These claims set the broadest boundaries of the patent's protection.

  • Dependent Claims: Narrower, referring to specific embodiments or variants, such as formulations with particular excipients, dosage forms, or specific routes of administration.

The scope of independent claims determines the patent's enforceability against potential infringers and its potential for licensing.

Assessment of the Claims

Without access to the full claim language, typical analysis involves:

  • Novelty and Inventive Step: The claims must demonstrate newness over prior art, including previous patents, scientific publications, and known formulations. The inventive step involves non-obviousness, considering existing therapeutic agents or formulations in the same class.

  • Claim Breadth: Broader claims encompass wide ranges of compounds or methods, increasing strategic value but potentially inviting validity challenges. Narrower claims focus on specific embodiments, providing more secure protection but limiting commercial scope.

  • Claim Language: Precise wording minimizes ambiguity but must balance breadth for commercial utility. Phrases such as “comprising,” “consisting of,” and “configured to” influence claim scope.

Patent Term Considerations

The patent's term extends approximately 20 years from the filing date, providing exclusivity until around 2034. This period strategically aligns with the competitive lifecycle of pharmaceutical products, granting market exclusivity to recoup R&D investments.

Patent Landscape Context

Prior Art Landscape

The patent landscape surrounding AU2014202687 involves:

  • Pre-existing Patents and Publications: Similar compounds or formulations disclosed before the priority date could challenge novelty. Key references include earlier patents and peer-reviewed literature on structurally related compounds or delivery methods.

  • Freedom-to-Operate (FTO) Analysis: Ensuring that the claims do not infringe existing patents is vital. If earlier patents cover the same therapeutic indications, licensing or design-around strategies may be necessary.

Subsequent Patent Activity

Post-grant, the patent landscape may include:

  • Improvement Patents: Subsequent filings for enhanced formulations or methods, potentially extending market protection.

  • Opposition and Patent Challenges: The patent may face validity challenges in Australia or internationally, especially if claims are broad or overlapping.

Regional and International Landscape

Considering Australia's patent system aligns with WIPO standards, similar patents in jurisdictions like the US, EU, and Japan can influence AU2014202687's commercial viability. International filings through Patent Cooperation Treaty (PCT) applications can extend protection and facilitate market entry.

Strategic Implications

Stakeholders must assess:

  • Validity and Enforceability: Ensuring claims are robust against prior art.

  • Potential for Licensing: Broader claims can attract licensing deals, while narrower claims might restrict infringement enforcement.

  • Competitive Positioning: Differentiation through claim scope and patent thicket strategies influences market dominance.

  • Patent Expiry Planning: Future patent filings for improved versions or combination therapies can sustain long-term exclusivity.

Conclusion

AU2014202687 embodies a targeted patent shielding a novel pharmaceutical innovation within Australia. Its effectiveness hinges on the precise scope of claims, alignment with prior art, and ongoing regional and international patent strategies. Businesses should conduct comprehensive infringement analyses and monitor subsequent patent filings to optimize commercial outcomes.


Key Takeaways

  • The patent's broad independent claims define a significant commercial barrier, but their validity depends on prior art assessments.
  • Narrower dependent claims can complement the main claims but may limit market scope.
  • A strategic patent landscape approach—including prior art searches, FTO analyses, and monitoring subsequent filings—is essential for safeguarding market position.
  • International patent protections and filings via PCT can extend competitive advantage beyond Australia.
  • Continual innovation through subsequent patents can prolong exclusivity beyond the original patent term.

FAQs

Q1: How does patent AU2014202687 protect its pharmaceutical invention?
A1: The patent delineates specific claims covering the chemical entity, formulation, or method of administration, securing exclusive rights to utilize or license these innovations within Australia.

Q2: Can existing drugs or formulations impact the validity of this patent?
A2: Yes, if prior art discloses similar compounds or methods, it could challenge the patent's novelty or inventive step, potentially rendering some claims invalid.

Q3: What strategies can stakeholders employ to navigate this patent landscape?
A3: Stakeholders should conduct thorough patent landscape analyses, explore licensing opportunities, develop around claims, and consider international patent filings to broaden protection.

Q4: How long is the patent protection for AU2014202687?
A4: Approximately 20 years from the filing date, expiring around 2034, unless patent term adjustments or extensions apply.

Q5: Are there opportunities for improving or expanding upon the patent?
A5: Yes, subsequent patent applications can address enhancements, new formulations, or combination therapies, providing avenues for extended market exclusivity.


References

[1] Australian Patent AU2014202687. Official Patent Document.
[2] WIPO Patent Landscape Reports (2022).
[3] International Patent Classification (IPC) standards related to pharmaceuticals.

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