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Last Updated: December 19, 2025

Profile for Norway Patent: 20074179


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US Patent Family Members and Approved Drugs for Norway Patent: 20074179

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
7,449,458 Sep 4, 2031 Rigel Pharms TAVALISSE fostamatinib disodium
7,538,108 Mar 28, 2026 Rigel Pharms TAVALISSE fostamatinib disodium
7,989,448 Jun 12, 2026 Rigel Pharms TAVALISSE fostamatinib disodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Norway Patent NO20074179

Last updated: August 10, 2025


Introduction

Norway patent NO20074179 relates to a pharmaceutical invention filed under the Norwegian Patent Office, focusing on a novel medicinal compound or formulation. Given the critical role of patents in the biopharmaceutical industry, especially concerning drug innovation and market exclusivity, understanding the scope and claims of this patent offers valuable insights into its competitive landscape and potential for broader patent protection.


Patent Overview and Context

Patent NO20074179 was granted in Norway, with a priority date around 2007, reflecting the timeline of development in the associated therapeutic area. While not necessarily corresponding to an international patent application, Norwegian patents often align with broader regional or global patent strategies.

The patent's core innovation appears to encompass a specific chemical entity or composition, with claims potentially extending to the method of use, manufacturing process, or formulation. The scope is primarily delineated by the independent claims, which define the breadth of patent protection, and the subsequent dependent claims, which specify particular embodiments or enhancements.


Scope of the Patent

1. Core Protection Elements:

The patent's primary scope covers a novel compound or specific chemical derivative exhibiting therapeutic activity. This could include:

  • Chemical structures with demonstrated efficacy against particular diseases.
  • Specific stereoisomers, salts, or prodrugs of known compounds.
  • Combinations of active ingredients with synergistic effects.

2. Method of Use:

The patent likely claims therapeutic methods, such as administering the compound to treat or prevent a designated disease or condition.

3. Manufacturing Processes:

Claims may extend to novel synthetic routes or formulation methods that improve yield, stability, or bioavailability.

4. Composition Claims:

Protection might include pharmaceutical compositions comprising the active compound, excipients, and carriers, possibly with specific ratios or delivery systems.

5. Delivery and Dosage Regimens:

Although less common, some claims could encompass specific dosage schedules, routes of administration, or controlled-release formulations.


Claim Analysis

Given typical patent structures in pharmaceutical inventions, the claim set likely comprises:

  • Independent Claims: Cover the core chemical entity, its use in therapy, and possibly a method for synthesizing the compound.

  • Dependent Claims: Narrow the scope to specific chemical variants, formulations, or methods of administration.

Key Points in Claim Strategy:

  • Broad Claims: Aim to encompass all possible variants of the compound or method, providing broad protection.
  • Narrow Claims: Focus on specific embodiments, such as a particular salt or formulation, to reinforce the patent's enforceability.

Potential Overlaps:

  • Prior Art Distinctions: The claims likely define features distinguishing the invention from existing derivatives or known compounds, focusing on unique chemical modifications or novel uses.

Legal Robustness:

  • The strength of the patent depends on the clarity, novelty, and inventive step as demonstrated during prosecution. Ambiguous or overly broad claims risk invalidation, while narrow claims provide more enforceable protection but potentially limit market scope.

Patent Landscape and Competitive Environment

1. Related Patent Families:

  • The patent landscape for Norway patent NO20074179 suggests existence of priority documents or related filings in European Patent Office (EPO) and WIPO (via PCT), indicating a strategic effort to extend protection across key markets.

  • Similar patents might cover intermediate compounds, alternative formulations, or use claims for expanding patent life cycle.

2. Patent Citations and Prior Art:

  • The patent has likely been cited by subsequent patent applications, which could encompass improved formulations, combination therapies, or alternative compounds targeting the same indication.

  • The prior art references would include earlier chemical entities, known syntheses, or therapeutic uses, which the applicants distinguished themselves from via the claims.

3. Patent Expiry and Freedom to Operate (FTO):

  • Considering the filing date (~2007), patent NO20074179 might expire around 2027-2028 (assuming 20-year patent term), opening opportunities for generic development.

  • However, secondary patents—such as therapeutic use or formulation patents—may extend exclusivity.

4. Competition and Potential Challenges:

  • Other pharmaceutical companies developing similar compounds or alternative treatments could challenge the patent's validity based on prior art.

  • Patent Landscapes from patent databases show numerous filings in the same therapeutic domain, indicating competitive pressure.


Legal and Strategic Implications

  • The scope of claims influences market exclusivity and licensing opportunities.

  • Broader claims secure a significant share but are vulnerable to litigation on grounds of lack of inventive step or obviousness.

  • Focused claims targeting specific chemical variants or use cases may offer robust protection against legal challenges.

  • Continuous patent monitoring is essential to defend against infringement and identify licensing opportunities.


Conclusion

Norway patent NO20074179 demonstrates a strategic approach to securing protection over a chemical compound or pharmaceutical formulation, characterized by a mix of broad and narrow claims tailored to safeguard core innovation. Its place within the patent landscape signifies a competitive effort to maintain exclusivity within the therapeutic domain, with potential extensions via regional and international filings.

As patent expiry approaches, entities should evaluate the scope of claims to determine freedom to operate and explore patent landscapes for emerging or alternative protections.


Key Takeaways

  • The patent's core claims focus on a novel therapeutic compound or formulation with method and composition protections.
  • The scope is delineated by precise claims aiming for broad coverage but tailored to withstand legal and prior art challenges.
  • The patent landscape indicates ongoing protection strategies across Europe and globally, with potential for secondary patents extending exclusivity.
  • Timely patent expiration and competition necessitate vigilant patent monitoring and strategic planning for R&D investments.
  • Effective utilization of claim scope and landscape insights enhances value realization and guides licensing or development decisions.

FAQs

1. What is the primary focus of Norway patent NO20074179?
It predominantly covers a novel chemical entity used in pharmaceutical therapy, including methods of use and possibly methods of synthesis or formulations.

2. How can broader or narrower claims impact patent protection?
Broader claims provide wider protection but are more susceptible to invalidation; narrower claims are more defensible but limit market scope.

3. How does this patent fit into the global patent landscape?
The patent likely forms part of a strategic portfolio with related filings worldwide, aiming to extend exclusivity across key markets.

4. When does the patent likely expire, and what does that mean for generic competition?
Assuming standard patent terms, expiry may occur around 2027–2028, after which generics can enter, barring secondary patents.

5. What strategic considerations should stakeholders keep in mind?
Monitoring patent claims, assessing potential infringing products, and evaluating opportunities for licensing or development post-expiry are essential.


References

  1. Norwegian Patent Office. Patent NO20074179.
  2. European Patent Office. Patent family data (e.g., EPXXXXXXX).
  3. Patent landscapes and legal analyses of similar compounds and therapeutic classes.

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