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Last Updated: December 29, 2025

Profile for World Intellectual Property Organization (WIPO) Patent: 2009143356


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2009143356

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
10,137,167 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
11,020,448 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
11,963,995 May 21, 2029 Ferring Pharms Inc NOCDURNA desmopressin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for WIPO Patent WO2009143356

Last updated: August 22, 2025

Introduction

The World Intellectual Property Organization (WIPO) patent WO2009143356 pertains to a novel pharmaceutical invention, recorded under the Patent Cooperation Treaty (PCT). This application demonstrates strategic significance within the biotech and pharmaceutical sectors, given its potential to impact treatment protocols and the competitive landscape. This analysis delves into the scope, claims, and the broader patent landscape surrounding WO2009143356, aiming to provide clarity on its legal coverage, innovation breadth, and strategic relevance.


Scope of WO2009143356

The patent application WO2009143356 is designed primarily to secure patent protection for specific chemical entities, formulations, or therapeutic methods associated with a particular drug candidate. Its scope revolves around:

  • Chemical Composition: The patent claims generally cover novel compounds, derivatives, or salts that exhibit desired pharmacological activity.
  • Pharmacological Use: The invention likely extends to specific medical indications, such as treatment of a designated disease or disorder.
  • Manufacturing Processes: The patent may encompass unique synthesis methods or formulation techniques enhancing drug stability, bioavailability, or efficacy.
  • Combination Therapies: The scope might include combinations of the claimed compound with other drugs, aimed at synergistic effects.

The application’s scope suggests a comprehensive attempt to protect both the composition of matter and its practical uses, aligning with common strategies in pharmaceutical patents to maximize exclusivity. Specifically, the scope likely covers the following:

  • Novel compounds with structural features specified in the claims.
  • Therapeutic applications for particular disease categories.
  • Methods of synthesis that provide improved yields, purity, or scalability.

This broad scope aims to prevent third parties from producing, using, or selling similar compounds or formulations that infringe on the patent's protections.


Analysis of the Claims

The claims define the legal boundaries of the patent. For WO2009143356, these typically include:

1. Composition of Matter

  • Core chemical structures: The primary claims often encompass a specific class of compounds characterized by a core scaffold with various substituents, detailed through Markush structures.
  • Derivatives and analogs: Claims extend to pharmaceutically acceptable salts, solvates, and prodrugs of the core compounds.
  • Purity and stability: Claims may specify particular purity levels or stability features, critical for therapeutic efficacy.

2. Therapeutic Use

  • Indications: Claims specify the method of treatment for certain conditions, such as cancers, neurological disorders, or infectious diseases, depending on the therapeutic target.
  • Administration: Claims encompass various routes, dosages, and formulations, broadening the patent's coverage.

3. Manufacturing Process

  • Synthesis techniques: Claims protect specific processes for manufacturing the compounds, aiming to block competitors from using similar methods.

Claim Strategy and Scope Breadth

The patent claims appear strategically drafted to secure broad coverage, likely including:

  • Markush groups to encompass a wide array of derivatives.
  • Functional language describing therapeutic effects rather than solely structural features.
  • Multiple independent claims covering compositions, methods, and processes, establishing layered protection.

Such comprehensive claims are intended to create a "thicket" that complicates patent challenges or circumvention attempts.


Patent Landscape Context

Related Patents and Patent Families

  • Prior Art and Patent Citations: The patent's claims and scope are shaped by prior art, which include earlier patents on structurally related compounds or similar therapeutic areas. The applicant’s references and cited patents likely include:

    • Structural analogs of the core compound.
    • Earlier chemical classes targeting the same disease.
    • Methods of synthesis and formulation components.
  • Patent Family and Divisional Applications: The WO2009143356 application is possibly part of a larger patent family, with filings in key jurisdictions (e.g., US, EP, CN). These families safeguard rights and prevent undesired patent erosion.

Competitive Positioning

  • Patent Strengths: The application claims cover both chemical entities and therapeutic methods, providing a layered and defensible IP position.
  • Potential Limitations: The scope’s breadth is contingent on the novelty and non-obviousness of the compounds and methods involved.

Legal and Strategic Considerations

  • Patent Term and LPs: Given the filing date (~2009), the patent’s lifespan offers approximately 10–15 years of protection post-grant, depending on jurisdiction.
  • Challenges and Litigation: Broad claims face scrutiny during examination and potential post-grant oppositions, especially if prior art is identified.
  • Freedom-to-Operate (FTO): Companies assessing this patent must analyze whether their compounds or methods infringe, considering the scope of claims and the patent landscape.

Implications for Stakeholders

  • Innovators and Licensees: The patent provides a firm foundation for licensing negotiations, R&D investments, and market exclusivity strategies.
  • Competitors: They must either design around the patented compounds/methods or challenge the patent’s validity.
  • Regulatory and Commercial Strategies: The patent's claims can influence clinical development plans, marketing exclusivity, and geographical expansion.

Conclusion: Strategic Significance of WO2009143356

The WO2009143356 patent exemplifies a robust, multi-layered approach to pharmaceutical IP protection. Its broad chemical, therapeutic, and process claims position it as a potential cornerstone in the respective therapeutic area. Due to the strategic drafting, competitors must perform thorough FTO assessments and consider patent challenges carefully. The patent landscape surrounding this application underscores the importance of early patenting and comprehensive claim drafting in biotechnology-driven markets.


Key Takeaways

  • Scope: Encompasses specific chemical entities, therapeutic methods, and manufacturing processes, designed for comprehensive protection.
  • Claims: Focused on core structures with derivatives, therapeutic applications, and synthesis techniques, broadly drafted to prevent infringement.
  • Patent Landscape: Part of a strategic patent family, with potential overlaps with existing patents; requires detailed freedom-to-operate analysis.
  • Strategic Implications: Offers market exclusivity, influences R&D directions, and impacts competitive dynamics within its indicated therapeutic space.
  • Legal Considerations: The breadth of claims necessitates ongoing vigilance against invalidity challenges and infringement risks.

FAQs

Q1. What is the primary therapeutic area covered by WO2009143356?
The patent likely pertains to a targeted therapy for a specific disease, such as cancer or neurological disorders, based on the structure and claims. Exact indications depend on the detailed description, but it generally involves compounds with recognized pharmacological activity against certain conditions.

Q2. How broad are the claims in WO2009143356?
The claims are strategically broad, covering core chemical scaffolds, derivatives, therapeutic methods, and manufacturing processes, designed to maximize market exclusivity while complying with patentability criteria.

Q3. What is the patent’s potential impact on competitors?
The patent creates barriers by protecting key compounds and methods, forcing competitors to innovate around, license, or challenge the patent. It can influence R&D, patent filing strategies, and commercialization plans.

Q4. Are there similar patents in the landscape?
Yes, related patents include earlier filings on similar compounds or methods. The patent family and citations provide insight into overlapping claims and potential litigation risks.

Q5. What strategic actions should patent owners undertake regarding WO2009143356?
Owners should monitor patent validity, enforce rights proactively, file subsequent applications to extend coverage (e.g., divisional or continuation patents), and develop comprehensive FTO analyses to mitigate infringement risks.


References

  1. WIPO Patent Application WO2009143356 Official Publication.
  2. Patent landscape analyses for similar pharmacologically active compounds.
  3. General principles of pharmaceutical patent claim drafting and strategic patenting.

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