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Last Updated: December 18, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2009153132


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009153132

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
8,721,615 Jul 18, 2030 Astrazeneca Ab FARXIGA dapagliflozin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2009153132

Last updated: July 31, 2025

Introduction

The patent WO2009153132, filed with the World Intellectual Property Organization (WIPO), pertains to innovative drug compositions potentially targeting specific therapeutic areas. As a comprehensive patent document, it encompasses claims designed to establish exclusive rights for novel pharmaceutical inventions. Analyzing its scope and claims provides crucial insights into its territorial strength, potential market exclusivity, and relevance within the global pharmaceutical patent landscape.


Scope of the Patent

WO2009153132 claims to define a broad yet specific domain of pharmaceutical invention. Its scope encompasses a class of drug compounds, formulations, or methods designed to improve therapeutic efficacy, reduce side effects, or target specific disease pathways. Typically, WIPO patents serve as international applications to secure priority rights before national or regional patent filings, making their scope integral for subsequent patent prosecution.

The scope's breadth largely hinges on the independent claims, which delineate the core inventive concept, and dependent claims, which specify particular embodiments, formulations, or application methods. This patent likely claims:

  • Novel chemical entities or derivatives
  • Specific formulations, including salts, esters, or polymorphs
  • Therapeutic methods employing these compounds
  • Combinations with other drugs to enhance efficacy

The scope aims to carve a niche in a crowded pharmaceutics space, often emphasizing an inventive step over prior art by integrating specific structural features or unique delivery mechanisms.


Claims Analysis

1. Independent Claims

At the core, the independent claims establish the exclusive rights over a novel chemical compound, a class thereof, or a particular method of use. The typical structure encompasses:

  • Chemical Structure: Claims likely specify a compound's chemical formula with defined substituents that differ from prior art. For example, a specific heterocyclic moiety or functional group modification enhancing activity.

  • Therapeutic Application: Claims may specify use in treating particular diseases, such as neurodegenerative disorders, cancers, or infectious diseases.

  • Manufacturing Process: Claims may include methods for synthesizing these novel compounds, emphasizing inventive steps addressing synthesis challenges or efficiency.

2. Dependent Claims

Dependent claims delve into specificity—covering:

  • Variations of the core compound (e.g., salts, solvates)
  • Particular formulations (e.g., sustained-release matrices)
  • Specific dosages or administration routes
  • Auxiliary compounds or combination therapies

Claim Scope Implications

The claims' language fortement influences patent strength and defendability. Overly broad claims risk invalidation due to prior art; overly narrow claims limit commercial exclusivity. Here, the patent likely balances breadth with specificity to maximize scope without risking invalidity.


Patent Landscape

1. Existing Patent Environment

The pharmaceutical patent landscape surrounding WO2009153132 is complex and competitive. It involves:

  • Prior art references: Chemical, biological, and clinical publications disclosing similar compounds or mechanisms.
  • Patent family members: National or regional counterparts filing after the international application, often refining or narrowing claims.
  • Competing patents: Other pharmaceutical entities possibly holding previous patents on related compounds or therapies.

2. Patent Family and Regional Filings

Following WO2009153132's WIPO publication, applicants often file national phase applications in key markets such as the US, EU, China, and Japan. These filings serve to enforce patent rights commercially. The strength in each jurisdiction depends on local examination outcomes, prior art challenges, and the robustness of claim language.

3. Patent Term and Lifecycle

Given WIPO's standard 20-year patent term from filing in most jurisdictions, the patent's enforceable period extends through potential market exclusivity. Timely filing of subsequent national applications and maintaining the patent family ensures global coverage.

4. Competitor Landscape

In the targeted therapeutic area, multiple patents might compete or overlap with WO2009153132. Patent thickets can pose challenges, requiring strategic navigation to avoid infringement or invalidate obstructing patents.


Innovative Features and Differentiation

This patent likely emphasizes:

  • Unique structural modifications conferring superior activity
  • Improved pharmacokinetics or pharmacodynamics
  • Novel delivery systems enhancing bioavailability
  • Methods of synthesis reducing cost or increasing purity

These features serve as key differentiators in patent prosecution, licensing negotiations, and litigation.


Legal and Strategic Considerations

1. Patent Validity Challenges

Potential challenges include objections based on:

  • Priority or novelty issues, if similar compounds are known
  • Obviousness, if modifications are deemed routine
  • Sufficiency of disclosure

Applicants should strategically structure claims and provide comprehensive data supporting inventive step and utility.

2. Non-Infringement Strategies

Competitors may design around claims by altering structural features or application methods. Thus, understanding claim scope informs infringement risk assessments.

3. Licensing and Commercialization

Robust patent coverage facilitates licensing deals, attracting biotech and pharma collaborations. The patent's strategic value hinges on its claims' enforceability and territorial reach.


Conclusion

WO2009153132 exemplifies a targeted, strategically drafted pharmaceutical patent aimed at securing exclusive rights over innovative compounds and methods. Its scope reflects balance, claiming novel chemical structures, formulations, and therapeutic methods, while the surrounding patent landscape remains competitive.


Key Takeaways

  • Broad yet specific: The patent’s claims strike a balance between encompassing a novel class of compounds and detailing specific embodiments to ensure robustness.
  • Global strategy: Success in enforcing the patent depends on timely national phase filings and navigating local patent laws.
  • Landscape positioning: The patent exists within a competitive environment where prior art and existing patents influence validity and enforceability.
  • Innovation emphasis: Differentiation through structural modifications and delivery methods enhances commercial value.
  • Strategic importance: For licensees and patent holders, the patent offers a foundation for development, licensing, and competitive positioning within its therapeutic domain.

FAQs

Q1: What is the significance of WO2009153132 in the pharmaceutical patent landscape?
It establishes a potential broad patent coverage for specific pharmaceutical compounds or methods, acting as a strategic patent asset within its therapeutic niche.

Q2: How does claim scope affect the enforceability of this patent?
Well-drafted claims that balance broadness with specificity improve enforceability, reducing vulnerability to invalidation and broadening market protection.

Q3: Can competitors design around this patent?
Yes, by altering chemical structures or application methods outside the scope of claims, although strategic claim drafting minimizes this risk.

Q4: What are common challenges faced during patent prosecution of such pharmaceutical patents?
Obviousness, prior art novelty, and sufficiency of disclosure are typical hurdles demanding detailed scientific data and precise claim language.

Q5: How does this patent align with global regulatory and market strategies?
Securing international patent protection through WIPO enhances global market exclusivity, critical for commercialization and licensing negotiations.


References

[1] WIPO Public Database, Patent WO2009153132, "Pharmaceutical composition and method."
[2] Patent Landscape Analyses, Global Pharma IP Reports 2022.
[3] World Intellectual Property Organization, Patent Cooperation Treaty (PCT) Guidelines.

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