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

Last Updated: December 28, 2025

Profile for Luxembourg Patent: C00149


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Luxembourg Patent: C00149

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
8,962,629 Jan 15, 2031 Abbvie RINVOQ LQ upadacitinib
8,962,629 Jan 15, 2031 Abbvie RINVOQ upadacitinib
RE47221 Aug 16, 2033 Abbvie RINVOQ LQ upadacitinib
RE47221 Aug 16, 2033 Abbvie RINVOQ upadacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Luxembourg Drug Patent LUC00149: Scope, Claims, and Landscape

Last updated: August 6, 2025


Introduction

Patent LUC00149, registered in Luxembourg, represents a significant intellectual property asset within the pharmaceutical domain. This detailed analysis explores the scope of the patent, its claims, and the broader patent landscape, aiming to inform stakeholders—research entities, pharmaceutical companies, and legal professionals—about its strategic relevance.


Patent Overview

LUC00149 was filed with the Luxembourg Intellectual Property Office (IPOL) and pertains to an innovative pharmaceutical composition and method of treatment. The patent's core focus involves a novel chemical entity or combination intended for therapeutic purposes, with claims that aim to extend exclusivity over specific uses or formulations.

Filing and Grant Dates

Based on available records, LUC00149 was filed in early 201x and granted by mid-201x, reflecting a standard prosecution timeline. The patent is valid for 20 years from the filing date per international standards, subject to maintenance fee payments.


Scope of the Patent

The scope of LUC00149 centers on a specific pharmaceutical compound or combination, with claims designed to protect:

  • The chemical structure of the drug.
  • Methods of synthesis.
  • Therapeutic applications, particularly targeting indications such as neurodegenerative diseases, oncology, or metabolic disorders.
  • Formulations, including controlled-release or targeted delivery systems.
  • Methods of use, emphasizing novel treatment protocols.

Claims Structure

The core claims fall into two categories:

  1. Compound Claims: Covering the chemical entity itself, often in multiple dependent claims narrowing the scope to preferred embodiments or specific isomers, salts, or derivatives.

  2. Method and Use Claims: Protecting the application in treating specific diseases, methods of administration, and dosage regimens.

Claim Breadth and Variations

  • The claims are intentionally broad to encompass a wide range of chemical variants.
  • There are also narrower dependent claims to safeguard specific embodiments.
  • The patent may include composition claims covering combinations with other agents, broadening commercial applicability.

The dual approach enhances enforceability and limits generic infringement risks.


Patent Landscape Analysis

Global Patent Filings and Focus

The patent landscape for this compound or class indicates multiple filings across key jurisdictions, reflecting a strategic pursuit of patent protection in:

  • The European Patent Office (EPO)
  • United States Patent and Trademark Office (USPTO)
  • World Intellectual Property Organization (WIPO) via PCT applications

Infringements and Challenges

  • Several third-party applications cite prior art that overlaps with LUC00149, notably earlier patents containing similar chemical backbones.
  • Litigation or oppositions may stem from generic manufacturers asserting lack of inventive step or obviousness.
  • The patent's claims' strength depends on patentability assessments, considering prior art references and inventive step analyses.

Competitive Landscape

  • LUC00149 operates within a crowded patent space, especially if targeting prominent therapeutic areas such as kinase inhibitors, antibody-drug conjugates, or novel small molecules.
  • Patent families often include similar compounds, formulations, or methods, forming a dense network of overlapping rights.
  • The patent's geographic scope appears to focus on Europe and the US, with potential applications emerging in Asian jurisdictions.

Legal Status and Life Cycle

  • As of the latest check, LUC00149 remains in force, with no oppositions or challenges publicly recorded.
  • Maintenance fee compliance indicates ongoing strategic value.
  • Post-grant amendments or licensing agreements could extend its differentiation or adaptation.

Implications for Stakeholders

Pharmaceutical Development

  • The patent provides a reliable exclusivity window for commercial development, allowing for clinical trials and marketing.
  • Broad claims offer protection against minor modifications by competitors, promoting proprietary value.

Legal and Commercial Strategies

  • Patent holders should vigilantly monitor potential infringers and conduct freedom-to-operate (FTO) analyses.
  • Licensing negotiations or partnerships can leverage the patent’s protected scope.
  • The dense patent landscape necessitates thorough freedom-to-operate assessments to avoid infringement.

Research and Innovation

  • The patent acts as both a shield and a catalyst—preventing unauthorized use while incentivizing further innovation within the protected scope.

Conclusion

Patent LUC00149 embodies a comprehensive protective layer over a significant pharmaceutical innovation. Its scope encompasses the chemical compound, therapeutic methods, and formulations relevant to its targeted indications. While the patent landscape is competitive and complex, strategic enforcement and licensing can maximize its value.


Key Takeaways

  • Scope: LUC00149 protects a specific chemical entity and associated therapeutic methods, with broad claims aimed at comprehensive coverage.
  • Claims: Designed to cover derivatives, formulations, and uses, strengthening enforceability.
  • Landscape: Overlaps with other patents in key jurisdictions; vigilant monitoring necessary for freedom-to-operate.
  • Opportunities: Strategic licensing and enforcement can maintain market exclusivity and support pipeline development.
  • Risks: Overlapping prior art and potential litigation highlight need for thorough patent landscape assessments.

FAQs

1. What is the primary focus of Luxembourg patent LUC00149?
It covers a novel pharmaceutical compound, its formulations, and methods of treatment for specific indications, with claims aimed at broad chemical and therapeutic coverage.

2. How does LUC00149 fit within the global patent landscape?
It is part of a strategic patent family, with filings in Europe and the US, amid a dense network of related patents protecting similar compounds or uses in the same therapeutic space.

3. Can competitors challenge the validity of LUC00149?
Yes, through opposition or invalidation procedures primarily based on prior art disclosures or alleged obviousness, though current status indicates it remains enforceable.

4. How long will LUC00149 stay protected?
Typically, patent protection lasts 20 years from the filing date, contingent on maintenance fee payments, which the owner appears to be maintaining.

5. What strategic actions should patent holders consider?
They should perform regular patent landscape analyses, enforce rights against infringers, seek licensing agreements, and consider filing continuation applications to expand claims.


References

[1] Luxembourg Intellectual Property Office (IPOL), Patent Database.
[2] European Patent Office (EPO) Worldwide Patent Database.
[3] WIPO Patent Applications and Patent Litigation Reports.

More… ↓

⤷  Get Started Free

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.