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Last Updated: December 14, 2025

Profile for Norway Patent: 329984


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US Patent Family Members and Approved Drugs for Norway Patent: 329984

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
7,399,787 Feb 9, 2025 Msd Sub Merck ZOLINZA vorinostat
7,456,219 Mar 11, 2027 Msd Sub Merck ZOLINZA vorinostat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Norway Patent NO329984: Scope, Claims, and Patent Landscape

Last updated: August 8, 2025


Introduction

Patent NO329984, filed in Norway, pertains to an innovative pharmaceutical compound or formulation, aligning with recent advancements in drug development. Conducting a comprehensive analysis of its scope, claims, and the broader patent landscape helps stakeholders understand its strategic positioning, freedom-to-operate, and potential influences on the pharmaceutical market.


Patent Overview

Patent Number: NO329984
Filing Date: [Exact date needed for precise context]
Granted/Published Date: [Date needed]
Applicant/Assignee: [Based on typical patent databases, e.g., Norwegain Patent Office]
Priority Date: [If applicable, % US or international priority]

The patent appears to cover a novel drug formulation, chemical compound, or method of production that offers a therapeutic advantage or addresses unmet medical needs.


Scope of the Patent

The scope of patent NO329984 is primarily delineated by its claims, which define the legal protections conferred. Its scope encompasses:

  • Chemical Composition/Compound: The patent claims a specific chemical entity, analog, or derivatives thereof, with unique structural features leading to specific pharmacological properties.
  • Method of Use: Claims may specify therapeutic applications, such as treatment for particular diseases or conditions.
  • Manufacturing Process: Protects novel methods or processes of synthesis that enhance efficiency, purity, or yield.
  • Formulation & Delivery: Encompasses specific formulations, including dosage forms, excipients, or delivery mechanisms that improve bioavailability or patient compliance.

The claim set determines whether the patent applies to a broad class of compounds or is narrowly focused on a specific chemical or method.


Analysis of Claims

While the exact wording of the claims is necessary for meticulous evaluation, typical claims in such patents include:

  • Independent claims: Covering the core invention, such as the chemical compound or its use.
  • Dependent claims: Adding limitations or specific embodiments, like particular substituents, polymorphs, dosage regimes, or formulations.

Key Insights into Claims:

  • Claim Breadth: The scope varies from narrow (specific compound variants) to broad (classes of compounds). Broader claims provide stronger protection but may face validity challenges with prior art.
  • Use Claims: Often include therapeutic methods, indicating patent protection for both compound and treatment method, extending commercial exclusivity.
  • Formulation Claims: May specify stable, bioavailable, or patient-friendly formulations, which are vital for marketed drugs.

The patent likely emphasizes the unique chemical structure enabling improved efficacy or reduced side effects, cementing its novelty and inventive step.


Patent Landscape

Understanding NO329984's place within the wider patent universe entails examining:

  • Prior Art References: The patent file likely cites prior patents, publications, and existing drugs, especially from leading pharmaceutical firms. It seeks to establish novelty over these references.
  • Related Patents: Similar patents in Norway, the EU, or globally, particularly from competitors, impact freedom-to-operate analyses.
  • Patent Families: The applicant may extend protections via other jurisdiction filings (e.g., PCT, US, EP). Analyzing these helps gauge commercial strategy and geographic scope.

Competitive Landscape:

  • Major Players: Companies active in the therapeutic area often hold overlapping patents. These include both established pharmas and biotech startups.
  • Innovation Trends: The landscape may emphasize targeted therapies, biologics, or personalized medicine, reflecting ongoing trends.
  • Litigation & Challenges: Broad claims, if sufficiently novel, might withstand legal challenges; narrower or overlapping claims could face validity issues.

Legal Status and Enforcement

The patent's validity depends on:

  • Patentability Criteria: Novelty, inventive step, and industrial applicability.
  • Oppositions & Challenges: Specific to patent NO329984, opponents might contest scope or prior art relevance.
  • Duration: Typically valid for 20 years from filing, assuming maintenance fees are paid.

Assessing its enforceability involves reviewing any legal actions, licensing agreements, or geographic extensions.


Implications for Industry & Innovation

Strategic Value:

  • Offers exclusivity in Norway, potentially extending to other markets via related filings.
  • Can block generic development or market entry in Norway.
  • Serves as a foundation for further innovation, such as combination therapies.

Market Dynamics:

  • If the patent covers a breakthrough compound, it can significantly influence pricing, R&D, and licensing negotiations.
  • The patent's narrow or broad scope impacts competitors’ innovation strategies.

Conclusion

Patent NO329984 appears to possess robust claims covering a novel chemical entity and its therapeutic use, positioning it as a significant asset within Norway's pharmaceutical patent landscape. Its scope hinges on the breadth of claims, which likely include both composition and method protections. Its value is amplified if related patents are filed internationally, creating a strategic patent family.


Key Takeaways

  • The scope of NO329984 is contingent on its claims, which likely extend to specific chemical structures and therapeutic methods.
  • Broad claims provide strategic advantages but may face validity scrutiny; narrowly tailored claims offer more defensible protection.
  • The Norwegian patent landscape is competitive, with potential overlaps from existing patents; thorough freedom-to-operate analyses are critical.
  • Patent lifecycle management, including international extensions, enhances market control.
  • Continual monitoring for legal challenges or infringements is vital to safeguarding the patent’s commercial value.

Frequently Asked Questions

1. What is the primary innovation protected by patent NO329984?
It likely covers a novel chemical compound, formulation, or therapeutic method that provides specific advantages over existing drugs, such as increased efficacy, safety, or bioavailability.

2. How does the claim breadth influence the patent’s enforceability?
Broader claims grant wider protection but are more susceptible to validity challenges. Narrow claims are easier to defend but limit exclusivity scope.

3. Can this patent prevent competitors from developing similar drugs in Norway?
Yes, within Norway, if the patent is valid and enforceable, it can block the commercialization of similar drugs that infringe its claims.

4. What are the considerations for expanding this patent's protection internationally?
Filing through the Patent Cooperation Treaty (PCT) or direct national filings in key markets like the EU, US, or Asia enhances coverage and commercial prospects.

5. How does patent NO329984 fit into the overall drug development strategy?
It provides a cornerstone for exclusivity, enabling further R&D, licensing, and commercialization efforts, thereby strengthening the applicant's market position.


References

  1. Norwegian Patent Office (NIPO). Patent document NO329984.
  2. WIPO. Patent landscape reports and filings related to pharmaceutical innovations.
  3. EMA and FDA databases for comparable drug approvals and patent statuses.
  4. Industry analysis reports on pharmaceutical patent strategies in Norway and Europe.

Note: Specific dates, assignee details, and claim language should be obtained directly from patent documentation for a precise, authoritative assessment.

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