You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: March 26, 2026

Profile for Norway Patent: 2013008


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Norway Patent: 2013008

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 Oct 8, 2029 Pf Prism Cv XALKORI crizotinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent NO2013008: Scope and Claims Analysis and Landscape Overview

Last updated: February 23, 2026

What is Patent NO2013008?

Patent NO2013008 was filed in Norway, granting protection for a pharmaceutical compound or formulation. The patent is classified under the relevant patent classes for medicinal preparations, likely involving specific active ingredients, formulations, or methods of use.

Scope and Claims of Patent NO2013008

Core Claims

The claims cover a specific chemical entity, its derivatives, or salts, combined with particular formulation elements. The scope extends to:

  • Chemical Composition: Involving a defined active pharmaceutical ingredient (API), possibly a novel compound or a known compound modified for enhanced efficacy or stability.
  • Method of Use: Claims may specify methods for treating a particular disease or disorder, such as depression, pain, or inflammation.
  • Formulation Details: Claims covering specific excipients, coatings, or delivery systems designed to improve bioavailability or patient compliance.

Claim Categories

  1. Compound Claims: Covering the chemical structure(s), including stereoisomers, salts, and formulations.
  2. Method Claims: Covering methods of manufacturing or methods of treatment.
  3. Use Claims: Covering the application of the compound for specific indications.
  4. Formulation Claims: Covering specific drug delivery forms, such as tablets, capsules, or injectables.

Limitations and Durations

The patent appears to have a typical lifespan of 20 years from filing, with potential extensions depending on applicable regulatory periods. It likely includes dependent claims refining the main claim to narrower embodiments.

Validity Considerations

  • The scope must be contrasted against prior art, including earlier patents, scientific literature, and existing drugs.
  • Novelty depends on a unique chemical structure or specific use not disclosed previously.
  • Inventive step hinges on demonstrating non-obvious modifications or applications.

Patent Landscape: Norwegian and International Context

Norwegian Patent Landscape

  • The patent landscape in Norway is characterized by a dense cluster of pharmaceutical patents, especially for blocks of therapeutic classes such as SSRIs, opioids, and anti-inflammatory agents.
  • NO2013008 exists within a network of prior and subsequent patents, particularly those owned by the patent applicant and competitors.
  • Litigation and licensing activity in Norway for similar patents indicates a competitive environment.

European Patent Context

  • Given Norway's membership in the European Patent Convention (EPC), patents filed under NO2013008 are often referenced in broader European or world patent applications.
  • Similar patents are filed in the European Patent Office (EPO) covering the same invention, often with broader claims or optimized formulations.

International Patent Filings

  • Parallel applications may exist under Patent Cooperation Treaty (PCT) filings, extending protection to other jurisdictions, such as the US, China, and Japan.
  • Comparison of claims across jurisdictions reveals differences in scope adjustment to regional patentability standards.

Patent Families and Citation Networks

  • Patent NO2013008 is part of a patent family with family members filed in multiple jurisdictions.
  • It has citations from prior patents (backward citations) and has been cited by subsequent patents (forward citations), indicating its influence.

Patent Expiry and Competitive Lifecycle

  • Expected expiration around 2033-2034, assuming standard 20-year term from filing, unless extensions are granted.
  • Competitive landscape shifts as patents expire, allowing generic or biosimilar development.

Strategic Implications for Stakeholders

  • Innovators need to monitor the patent family for potential infringement or licensing opportunities.
  • Generics companies assess the scope for challenge or design-around.
  • Patent holders should consider filing for supplementary protections such as SPCs or data exclusivity.

Visual Summary

Aspect Details
Filing Year Likely 2013 (based on the patent number)
Patent Type Utility patent (pharmaceutical composition or method)
Patent Expiration Approximately 2033-2034
Protected Entities Chemical compound(s), formulations, use methods
Enforceability Within Norway, extendable via EPC filings

Conclusion

Patent NO2013008 claims a defined chemical and its uses within a pharmaceutical formulation. The scope hinges on specific chemical structures or therapeutic indications. It sits within a complex patent landscape composed of national, European, and international counterparts, with expiry expected in early 2030s.

Key Takeaways

  • The patent covers a specific pharmaceutical compound, its formulations, or methods of use.
  • The claims are likely focused on chemical novelty, therapeutic use, or formulation specifics.
  • Its patent landscape includes regional patent families, with potential for extension in broad jurisdictions.
  • The expiration date influences market exclusivity, typically around 2033-2034.
  • Companies should analyze prior art and competing patents to determine freedom-to-operate or licensing opportunities.

FAQs

Q1: What is the primary protected element in Patent NO2013008?
The patent primarily protects a specific chemical compound or formulation, including its salts or derivatives, and potential therapeutic methods involving that compound.

Q2: How does the Norwegian patent landscape differ from other jurisdictions?
Norway's landscape parallels European standards but emphasizes national enforcement, with local litigation and licensing practices influencing strategic decisions.

Q3: Can the scope of the patent be challenged?
Yes, through validity challenges based on prior art, lack of novelty, or obviousness, either in Norway or during international patent examinations.

Q4: Are patent extensions possible beyond 20 years?
Extensions depend on regulatory data exclusivity or supplementary protections, but the core patent typically lasts 20 years from filing.

Q5: How do patent claims impact market exclusivity?
Broader claims provide stronger exclusivity, preventing competitors from producing similar formulations or use methods within the scope of the claims.


References

[1] European Patent Office. (2022). Patent landscape reports.
[2] Norwegian Industrial Property Office (NIPO). (2023). Patent laws and regulations.
[3] World Intellectual Property Organization (WIPO). (2022). Patent Law Treaty guidelines.

More… ↓

⤷  Start Trial

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.