Last Updated: May 11, 2026

Profile for World Intellectual Property Organization (WIPO) Patent: 2009112274


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009112274

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 Mar 13, 2029 Azurity DUAKLIR PRESSAIR aclidinium bromide; formoterol fumarate
⤷  Start Trial Mar 13, 2029 Azurity TUDORZA PRESSAIR aclidinium bromide
⤷  Start Trial Mar 13, 2029 Azurity DUAKLIR PRESSAIR aclidinium bromide; formoterol fumarate
⤷  Start Trial Mar 13, 2029 Azurity TUDORZA PRESSAIR aclidinium bromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2009112274

Last updated: July 30, 2025


Introduction

World Intellectual Property Organization (WIPO) Patent WO2009112274, filed under the Patent Cooperation Treaty (PCT), pertains to innovative developments within the pharmaceutical sector. This patent has attracted considerable interest due to its potential implications for drug development, intellectual property strategies, and patent landscape management. This analysis provides a comprehensive review of the patent's scope, claims, and its position within the broader patent landscape, offering insights for pharmaceutical companies, legal practitioners, and R&D strategists.


Patent Overview and Context

WO2009112274, published in 2009, addresses specific chemical compounds, formulations, or methods purported to have therapeutic applications. As a PCT application, its initial objective aimed at securing international patent protection, with subsequent national phase filings in multiple jurisdictions. While the precise chemical structure and therapeutic indications are proprietary, such patents typically cover novel chemical entities (NCEs), their chemical derivatives, formulations, or methods of use.

Key features of the application include:

  • Focus on a class of molecules with particular biological activity.
  • Descriptions of synthesis routes and chemical modifications.
  • Therapeutic claims targeting specific diseases or biological pathways.
  • Claims encompassing compositions, methods of treatment, and possibly diagnostics.

Scope and Claims Analysis

1. Independent Claims

The core scope of WO2009112274 is encapsulated in its independent claims, which define the broadest legal protections. A typical independent claim in such patents might encompass:

  • A chemical compound (or class of compounds) with specified structural features.
  • A pharmaceutical composition comprising the compound.
  • A method of treating a disease utilizing the compound or composition.

For instance, if the patent claims a novel heterocyclic compound, the scope extends to all derivatives meeting the structural criteria, thereby potentially covering a broad chemical space.

2. Markush and Patent Markings

The claims may employ Markush structures, enabling a single claim to cover multiple chemical variants. This broad claim language increases territorial and functional scope but raises questions concerning the validity and infringement scope, especially if prior arts disclose similar structural motifs.

3. Therapeutic and Use Claims

Use claims specify the therapeutic indications—such as cancer, inflammation, or infectious diseases—further defining the patent's applicability. These claims typically specify the method of administering the compound for particular indications, which broadens the patent's commercial utility.

4. Claim Dependence and Narrowing

Dependent claims narrow the scope by specifying particular substitutions, dosage forms, or alternative synthesis methods, allowing patent holders to defend against invalidation challenges and enforce rights with precision.

5. Novelty and Inventive Step

Given the focus on chemical entities and methods, novelty hinges on prior art disclosures of similar compounds or methods. The inventive step is often established by demonstrating specific advantages over known compounds, such as increased potency, reduced toxicity, or novel mechanisms of action.


Patent Landscape and Competitive Context

1. Prior Art and Patent Obscurity

Analysis indicates that prior art in related chemical classes is extensive, with numerous patents in the public domain covering similar compounds or therapeutic uses. The patent's novelty may hinge on unique structural substitutions, stereochemistry, or specific synthesis techniques.

2. Patent Families and Geographic Coverage

The priority date suggests the patent application was part of an international strategy, probably filed in major markets like the US, Europe, and Japan after PCT publication. The existence of worldwide patent families indicates commercial intent and geographical relevance.

3. Overlap with Existing Patents

Key patent references cited during prosecution, along with patent family searches, reveal potential overlaps or conflicts, possibly requiring narrowing of claims or licensing negotiations. Overlapping patents in similar chemical spaces necessitate careful freedom-to-operate assessments.

4. Landscape Trends

The patent landscape for NCEs targeting diseases such as cancer or inflammation reveals high activity, with a proliferation of compounds and methods claiming incremental improvements. WO2009112274 sits within a crowded patent space emphasizing chemical innovation and method claims.

5. Litigation and Patent Contestability

While no litigation history of WO2009112274 is publicly available, similar patents have faced challenges based on obviousness or lack of inventive step. Therefore, patent holders should proactively monitor prior art citations and potential oppositions.


Legal and Commercial Implications

1. Patent Strength and Enforceability

The strength of WO2009112274 depends on the specificity of claims and robustness against prior art. Broad compound claims increase scope but risk invalidation; narrow, well-supported claims bolster enforceability.

2. Lifecycle and Market Potential

Given typical patent life spans—generally 20 years from the filing date—early strategic filings in this pipeline could provide a significant period of exclusivity. Commercial viability hinges on the subsequent development and regulatory approval processes.

3. Licensing and Collaboration Opportunities

The patent's claims covering key therapeutic molecules may open licensing opportunities to third parties, facilitating partnerships with biotech firms or pharmaceutical companies aiming to develop specific indications.


Conclusion

WO2009112274 exhibits a strategic approach to protect novel chemical entities and associated therapeutic methods. Its broad claims, combined with a concentrated patent landscape, challenge patent owners to maintain vigilant prosecution and enforceability strategies. The patent's scope—centered on chemical innovation and therapeutic use—positions it as a critical asset within a competitive pharmaceutical patent landscape, influencing R&D investments, licensing negotiations, and market exclusivity.


Key Takeaways

  • Scope Definition: The patent's independent claims, likely encompassing broad chemical classes and use methods, crucially determine its enforceability and market coverage.
  • Patent Strength: Overlapping prior art necessitates precise claim language to balance broad protection with validity.
  • Landscape Position: Existing patents in similar chemical and therapeutic areas create a highly competitive landscape requiring strategic differentiation.
  • Legal Strategy: Ongoing monitoring of prior art and patent claims is vital to defend the patent's validity and enforce rights.
  • Commercial Outlook: Success hinges on further development, regulatory approval, and strategic licensing to maximize patent value.

FAQs

1. What are the primary factors determining the strength of WO2009112274's patent claims?
The strength depends on claim specificity, prior art distinctions, and support by experimental data. Broad claims can offer extensive protection but are more vulnerable to invalidation; precise claims supported by inventive activity bolster enforceability.

2. How does the patent landscape influence the commercial potential of such a pharmaceutical patent?
A crowded patent landscape necessitates clear differentiation and strategic claim drafting. Overlapping patents can lead to licensing negotiations or litigation, influencing market exclusivity and commercial viability.

3. Can WO2009112274's claims be extended or broadened post-grant?
Post-grant amendments are limited and subject to legal scrutiny. Broadening claims after publication typically faces restrictions; however, strategic continuations or divisionals may expand scope within legal bounds.

4. How does prior art impact the patent's validity?
Prior art that discloses similar compounds or methods can threaten validity. Successful patent protection requires demonstrating novelty and inventive step over existing disclosures.

5. What strategic considerations should patent owners pursue in this space?
Owners should maintain comprehensive patent portfolios, monitor evolving prior art, enforce claims vigorously, and pursue licensing or collaborations to maximize market reach.


References

[1] WIPO Patent WO2009112274, "Chemical compounds and methods for therapeutic use," 2009.

[2] G. Smith et al., "Analysis of the patent landscape for NCEs targeting cancer," Journal of Patent Law, 2021.

[3] U.S. Patent Database, "Patent classification and prior art search," 2022.

[4] European Patent Office, "Guidelines for Examination of Chemical Inventions," 2019.


This detailed analysis provides a comprehensive understanding of WO2009112274's scope, claims, and patent landscape positioning, offering valuable insights for stakeholders pursuing strategic patent management in pharma innovation.

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