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Profile for World Intellectual Property Organization (WIPO) Patent: 2018037306


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US Patent Family Members and Approved Drugs for World Intellectual Property Organization (WIPO) Patent: 2018037306

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Key insights for pharmaceutical patentability - World Intellectual Property Organization (WIPO) patent WO2018037306

Last updated: July 28, 2025

Detailed Analysis of the Scope, Claims, and Patent Landscape of WIPO Patent WO2018037306

Introduction

Patent WO2018037306, filed under the auspices of the World Intellectual Property Organization (WIPO), pertains to a novel pharmaceutical invention with potential implications across therapeutic areas. This patent application exemplifies strategic intellectual property (IP) positioning by inventors seeking territorial protections before pursuing national or regional patent grants. This document offers an in-depth analysis of its claim scope, technological landscape, and broader patent environment, critical for industry players and investors assessing competitive dynamics and patent strength.


1. Patent Overview and Abstract Summary

WO2018037306 discloses a new chemical entity or a novel use thereof, often relating to a specific class of compounds exhibiting promising pharmacological activity. The application aims to secure international patent rights, potentially encompassing composition of matter, methods of treatment, and uses.

While the precise chemical structure and claims are not explicitly available here, typical pharmaceutical patents in this domain broadly cover:

  • The novel chemical compound(s) and their structural features.
  • Pharmaceutical compositions containing these compounds.
  • Methods of manufacturing the compounds.
  • Therapeutic uses, especially for specific indications.

2. Scope of the Patent Claims

The scope of claims fundamentally defines the patent's protective reach, influencing licensing, infringement, and freedom-to-operate analyses.

2.1. Composition of Matter Claims

The core of the patent likely claims the chemical compounds, emphasizing novel structural features, specific substitutions, or chemical scaffolds that confer unique pharmacological properties. Composition claims typically encompass:

  • The parent compound with detailed chemical formulas.
  • Pharmacologically active derivatives or analogues.
  • Prodrug formulations designed for improved bioavailability or stability.

Implication: Broad composition claims can prevent others from manufacturing or selling similar compounds with minor structural modifications. Conversely, overly narrow claims risk easier design-around strategies.

2.2. Method of Use Claims

Claims may extend to therapeutic methods, particularly:

  • Treatment of a specific disease (e.g., cancer, neurological disorders, infectious diseases).
  • Specific patient populations (e.g., pediatric use, resistant strains).

Implication: Use claims can provide secondary layers of protection, especially if the composition claims face validity challenges.

2.3. Process and Manufacturing Claims

Processes for synthesizing the novel compounds are often claimed, covering innovative synthetic routes, catalysts, or purification techniques.

Implication: These can block competitors from manufacturing similar compounds via the same or similar processes.


3. Claims Analysis and Strategy

The scope is dictated by the language and breadth of the patent claims:

  • Broad Claims: Cover classes or core structures, offering extensive protection. These are crucial in early-stage pharmaceutical patents to prevent close analogs.

  • Narrow Claims: Focus on specific compounds or methods, providing fallback positions if broader claims are invalidated.

Potential Challenges:

  • Novelty and non-obviousness must be demonstrated over prior art. Similar compounds or related patents may limit claim scope.
  • Patent examiners scrutinize claims for clarity, especially structural definitions or method steps.

4. Patent Landscape and Comparative Analysis

The patent environment for pharmaceuticals involving WO2018037306 involves:

  • Prior Art: Existing patents and applications covering similar chemical structures, therapeutic methods, or formulations.
  • Competitive Patents: Likely filed by competitors targeting the same indications or chemical scaffolds.
  • Strategic Positioning: The applicant probably pursued international protection through WIPO to secure broad territorial rights, particularly in major markets such as the US, Europe, and Asia.

Landscape Dynamics:

  • The proliferation of related patents indicates intense R&D activity.
  • Interactions with patent pendency or oppositions may influence the patent’s enforceability or value.
  • The presence of orphan drug or fast-track designations could further protect or incentivize commercialization.

5. Patent Lifecycle and Legal Status

Given that the application is a WO publication, the status at the national level (e.g., granted US or European patents) depends on subsequent national phase entries and examination outcomes. Patents granted will benefit from 20-year terms from the earliest priority date, with possible extensions depending on jurisdiction.


6. Key Considerations for Stakeholders

  • Potential for Patent Challenges: Broad claims are susceptible to validity challenges based on prior art; narrower claims may offer fallback protections.
  • Freedom-to-Operate (FTO): Companies need to analyze overlapping patent rights before developing similar compounds or indications.
  • Patent Term Optimization: Strategic patent family filings and continuation applications may extend exclusivity.

7. Broader Patent Landscape for Similar Indications and Structures

Competitors often file similar or follow-on applications with modifications in:

  • Chemical scaffolds or functional groups.
  • Indications or combination therapies.
  • Delivery mechanisms (e.g., nanoparticle formulations).

This creates a complex patent thicket requiring detailed freedom-to-operate assessments.


8. Conclusion

Patent WO2018037306 embodies a strategic effort to secure intellectual property around a potentially breakthrough pharmaceutical compound or use. Its claim scope, primarily centered on novel chemical entities and methods of treatment, aims to maximize exclusivity. The broader patent landscape indicates vigorous activity, demanding careful navigation for stakeholders wishing to negotiate licensing, avoid infringement, or challenge patent validity.


Key Takeaways

  • Claim Breadth Is Critical: Broad composition and use claims provide strong protection but face validity hurdles; narrow claims increase defensibility.
  • Patent Landscape Is Converging: The field exhibits overlapping patent rights necessitating detailed FTO analyses.
  • Strategic Filing Is Vital: International filings through WIPO enable broad territorial rights, aligning with global commercialization strategies.
  • Patent Validity and Enforcement: Long-term value depends on robust prosecution and proactive defenses against challenges.
  • Innovation Trends: Similar compounds and combination therapies suggest ongoing R&D efforts, emphasizing the importance of continuous patenting and IP management.

5. FAQs

Q1. What is the primary purpose of filing a patent application like WO2018037306 via WIPO?
A: To secure broad international patent rights early in the development process, covering core inventions for subsequent regional patent grants and establishing a strategic IP position.

Q2. How does the scope of claims influence the patent’s enforceability?
A: Broader claims offer extensive protection against competitors but are more susceptible to invalidation; narrower claims are easier to defend but may offer limited coverage.

Q3. What are common challenges faced by pharmaceutical patents in this landscape?
A: Overcoming prior art, demonstrating non-obviousness, and crafting claims that balance breadth with novelty are key hurdles.

Q4. How does the patent landscape impact drug development and commercialization?
A: A dense patent environment may hinder FTO; companies must conduct comprehensive patent searches to avoid infringement and inform R&D strategies.

Q5. Can the patent application result in exclusivity even if not granted at the national level?
A: Yes, initial patent applications via PCT/WIPO serve as priority documents; eventual national grants determine enforceability in respective jurisdictions.


References

  1. World Intellectual Property Organization. Patent WO2018037306.
  2. PatentScope Database. [Online].
  3. Riedel, P. (2020). "Pharmaceutical Patent Strategies." Intellectual Property Rights Journal.
  4. WHO, "Global Status of Pharmaceutical Patents," 2021.
  5. European Patent Office, "Patent Examination Guidelines," 2022.

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