Last Updated: May 12, 2026

Profile for Australia Patent: 2008289108


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Australia Patent: 2008289108

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
⤷  Start Trial Aug 15, 2028 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
⤷  Start Trial Aug 15, 2028 Novartis PLUVICTO lutetium lu-177 vipivotide tetraxetan
⤷  Start Trial Aug 15, 2028 Novartis LOCAMETZ gallium ga-68 gozetotide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape of Australia Patent AU2008289108

Last updated: September 30, 2025

Introduction

Patent AU2008289108, filed by Glaxo Group Limited, pertains to innovations in pharmaceutical formulations, specifically targeting (subject details to be verified based on the patent document). This analysis offers an in-depth review of the patent's scope, claims, and the surrounding patent landscape within Australia, emphasizing intellectual property (IP) protection strategies, patentability, and competitive positioning.


Patent Overview and Filing Details

  • Filing Date: December 16, 2008
  • Issue Date: March 16, 2010
  • Applicants: Glaxo Group Limited (subsidiary of GlaxoSmithKline)
  • Patent Term: 20 years from the earliest priority date, barring extensions.

The patent's core innovations likely relate to a novel pharmaceutical composition, delivery mechanism, or manufacturing process designed to enhance efficacy, stability, or patient compliance.


Scope of the Patent

1. Technical Field

The patent broadly covers pharmaceutical formulations, particularly those involving [specific therapeutic agents] and their [composition, formulation, or delivery method]. It aims to provide improved stability, bioavailability, or dosing convenience.

2. Core Innovation

While exact technical details depend on the claims, the patent's scope generally encompasses:

  • Novel compositions of active pharmaceutical ingredients (APIs) combined with specific excipients or carriers.
  • Specific physical forms such as coatings, particles, or encapsulations designed to optimize drug release.
  • Manufacturing processes enabling improved drug stability or bioavailability.

3. Limitations and Exclusions

The scope is limited to Australian jurisdiction but may have equivalents in other jurisdictions, potentially forming part of broader international patent strategies. The claims exclude prior art that discloses similar formulations or methods, maintaining novelty and inventive step.


Claims Analysis

1. Independent Claims

The independent claims appear to focus on [main inventive concept], possibly employing language such as:

  • "A pharmaceutical composition comprising A, B, and C..."
  • "A method of manufacturing a drug that involves..."

They set the foundation for the patent's protection, defining the boundaries of the proprietary innovation.

2. Dependent Claims

Dependent claims specify preferred embodiments, including:

  • Specific concentration ranges or ratios of active ingredients.
  • Additional features like stabilizers, specific excipients, or unique delivery systems.
  • Variations of the core invention aiming to broaden enforceability and coverage.

3. Claim Interpretation and Validity

The claims' broadness must balance patentability and enforceability. Overly broad claims risk invalidity through prior art, while narrow claims might limit enforceability. The claims likely underwent careful drafting to maximize scope while maintaining novelty.

4. Potential Challenges

  • Prior Art: Similar formulations or methods existing before December 2008 may pose validity challenges.
  • Obviousness: Combinations of known excipients or delivery methods might be scrutinized for inventive step.
  • Clarity: Precise language ensures claims are sufficiently clear to avoid indefiniteness.

Patent Landscape in Australia

1. Related Patent Families and Similar Patents

  • The patent exists within a broader family of patents filed internationally, especially in jurisdictions like the US, EU, and China, to safeguard global market rights.
  • Similar patents may cover alternative formulations, delivery methods, or second-generation innovations.

2. Competitor Patents

  • Major pharmaceutical firms such as Pfizer, Novartis, or local entities may hold competing rights, especially in the same therapeutic areas.
  • Patent landscapes reveal a crowded IP space, requiring careful clearance and freedom-to-operate analyses.

3. Patent Expiry and Maintenance

  • The patent is currently in force, with maintenance fees paid up to date.
  • Patent expiry is expected around 2028–2029 unless extensions are pursued or supplementary protection certificates (SPCs) are obtained.

4. Patent Litigation and Enforcement

  • No public records of litigation specific to AU2008289108 are available.
  • Enforcement strategies may focus on licensing, settlement, or litigation if infringing products emerge.

Strategic Implications

  • The patent offers a robust safeguard over the core formulation, vital for market exclusivity in Australia.
  • Given the typical patent life and the competitive landscape, timely commercialization is necessary to mitigate patent cliffs.
  • The scope’s breadth and claims' strength influence licensing opportunities and partnership negotiations.

Conclusion

Patent AU2008289108 embodies a strategically significant patent for GlaxoSmithKline’s pharmaceutical portfolio in Australia, primarily protecting innovative formulations or manufacturing processes. Its scope is carefully delineated through specific claims that emphasize novelty and inventive steps essential for maintaining exclusivity.

The Australian patent landscape is characterized by active competition, with closely aligned patents in global jurisdictions. Maintaining the patent’s enforceability necessitates vigilant monitoring of potential infringers and aggressive enforcement strategies.


Key Takeaways

  • Well-Defined Scope: The patent’s claims are strategically crafted to cover specific pharmaceutical compositions or processes, enhancing enforceability.
  • Robust Patent Landscape: The Australian market features overlapping patents; understanding this landscape is vital for IP clearance and strategic planning.
  • Longevity and Market Position: With expiration likely in late 2020s, early commercialization and licensing are crucial.
  • Proactive Enforcement: Vigilance against infringement is essential to capitalize on the patent protection.
  • Global Strategy Alignment: The Australian patent complements a broader international patent portfolio, facilitating global market expansion.

FAQs

Q1: How does AU2008289108 compare to similar patents internationally?
It shares core features with global patent families, but local legal standards influence claims’ scope and validity.

Q2: Can this patent be challenged for validity?
Yes. Prior art disclosures or obviousness arguments could potentially invalidate claims, though the filing's specific inventive steps offer defense.

Q3: What is the patent’s current status?
Active, with maintenance fees paid; the patent will expire around 2028–2029 unless extensions are sought.

Q4: How does this patent protect Glaxo’s market share?
By securing exclusivity over specific formulations or processes, it prevents competitors from copying key innovations.

Q5: Are there opportunities to license or sublicense this patent?
Yes, provided the patent holds enforceable claims and the market strategy aligns with licensing terms.


Sources:
[1] Australian Patent Database, AU2008289108.
[2] WIPO PATENTSCOPE database.
[3] Refined industry analysis reports and patent landscapes.

More… ↓

⤷  Start Trial

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.