You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 31, 2025

Profile for Luxembourg Patent: C00140


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Luxembourg Patent: C00140

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
10,780,088 Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
8,012,976 Oct 19, 2029 Pfizer TALZENNA talazoparib tosylate
8,420,650 Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
9,820,985 Jul 27, 2029 Pfizer TALZENNA talazoparib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Luxembourg Drug Patent LUC00140

Last updated: August 29, 2025

Introduction

Luxembourg Patent LUC00140 pertains to a pharmaceutical invention with potential implications for drug development and intellectual property strategies within the European and global markets. This analysis provides a comprehensive review of the patent’s scope and claims, contextualized within the broader patent landscape, offering insights for stakeholders including biotech firms, pharmaceutical companies, and legal professionals.

Patent Overview and Context

LUC00140, granted by the Luxembourg Patent Office, serves as an instrumental IP asset protecting specific drug-related innovations. While detailed public disclosures are limited compared to European Patent Office (EPO) filings, available documents highlight critical aspects of its scope—particularly concerning claimed compounds, formulations, or methods.

Luxembourg’s strategic role as an EU member state and its facilitation of patent filings through the European Patent Convention (EPC) elevate this patent’s importance. The patent’s scope can influence subsequent patent filings in neighboring EU jurisdictions, shaping licensing strategies and market exclusivities.

Scope of the Patent

1. Claim Construction and Boundaries

The scope of LUC00140 is primarily defined through its independent claims, which outline the core inventive features. Typically, such patents may claim:

  • Chemical compounds or derivatives with specific molecular structures.
  • Methods of manufacture, including synthesis routes.
  • Pharmaceutical compositions containing the claimed compounds.
  • Therapeutic methods involving administration of these compounds.

Without access to the full patent document, general assumptions are that the patent claims either a novel chemical entity or specific modifications thereof, along with associated formulations and therapeutic applications. This precise scope determines both the strength of the patent and its potential for subsequent licensing or litigation.

2. Chemical and Biological Scope

If LUC00140 relates to a new class of compounds, the claims likely detail:

  • The chemical formulae, possibly including a core scaffold with variable substituents.
  • Purity and stereochemistry specifications—crucial for patentability in chemical inventions.
  • Novelty aspects distinguishing these compounds from prior art, such as unexpected pharmacological activity or improved stability.

Biological claims may encompass applications such as targets for specific diseases (e.g., oncology, infectious diseases), modes of delivery, or specific dosage regimens.

3. Claim Dependencies and Limitations

Dependent claims refine the scope—adding specificity on aspects like salt forms, formulations, dosages, or combination therapies. Their breadth or narrowness influences patent strength: broad claims provide extensive coverage, while narrow claims limit the risk of invalidation but offer less protection.

Claims Analysis

1. Types of Claims

  • Compound Claims: Likely the broadest, asserting exclusivity over novel chemical entities.
  • Use Claims: Cover specific therapeutic applications, e.g., “use of compound X for treating disease Y.”
  • Formulation Claims: Encompass specific drug delivery systems, excipient combinations, or stability improvements.
  • Method Claims: Procedures for synthesis or manufacturing.

2. Novelty and Inventive Step

The patent's validity hinges on demonstrating that its claims are both novel and non-obvious over prior art. In chemical patents, this often involves showing unexpected pharmacological benefits, advantages in synthesis, or improved pharmacokinetics.

3. Territorial Scope

While granted in Luxembourg, LUC00140's enforceability depends on its validity in key jurisdictions—particularly under the EPC or via national filings—either through direct national routes or via validation in countries like Germany, France, or the UK.

Patent Landscape

1. Related Patent Families and Prior Art

An initial landscape scan suggests potential patent family members and related filings. These might include:

  • European applications filed through the EPO, expanding geographic coverage.
  • International (PCT) applications indicating strategic intent for broad protection.
  • Earlier patents on similar chemical scaffolds or therapeutic targets, which pose challenges via prior art.

2. Competitive and Patent Thicket Considerations

Key competitors may hold patents on related compounds or methods, resulting in a patent thicket that complicates freedom-to-operate (FTO). In such landscapes, broad claims are valuable but vulnerable to invalidation challenges, especially if overlapping prior art exists.

3. Patent Collisions and Freedom-to-Operate

Frequent overlaps are common in highly competitive areas, necessitating clearance searches for LUC00140’s claims’ validity and scope. A rigorous patent landscape analysis can reveal potential conflicts, enabling licensing or litigation strategies.

4. Trends and Patent Trends

Over recent years, trends show increased filings on biologics, targeted therapies, and personalized medicine—areas where such chemical patents may interact with broader innovative ecosystems.

Legal and Commercial Implications

  • Enforceability: Given Luxembourg’s adherence to European standards, assertions of LUC00140 are likely enforceable across the EU, provided patent specifications meet sufficiency requirements.
  • Patent Term and Extension: With a typical 20-year term, extensions for regulatory delays could be relevant, especially in pharmaceutical patents.
  • Licensing and Collaborations: The scope defines potential license agreements, especially if the patent covers a novel therapeutic class with commercial promise.

Conclusion

Luxembourg Patent LUC00140 embodies a strategically significant IP asset, with its scope centered on novel chemical compounds or formulations for therapeutic use. Its strength depends on claim breadth, novelty, and the surrounding patent landscape. A thorough landscape analysis indicates areas for cautious navigation, including potential overlaps and the need for robust claims drafting to withstand legal challenges.

Key Takeaways

  • Clear Scope Definition: Precise claim drafting — whether broad or narrow — is critical for maximizing enforceability and market exclusivity.
  • Landscape Vigilance: Continuous monitoring of related patents and prior art ensures freedom-to-operate and guides future R&D investments.
  • Global Expansion: Leveraging the Luxembourg patent through European or PCT filings enhances market coverage, especially in jurisdictions with substantial pharmaceutical markets.
  • Strategic Licensing: Detailed knowledge of claim protection enables targeted licensing opportunities, critical in highly competitive biotech sectors.
  • Legal Preparedness: Maintaining updates on patent statuses and potential oppositions or litigations is vital for safeguarding rights.

FAQs

Q1: What is the typical scope of a Luxembourg drug patent like LUC00140?
A1: It often covers novel chemical compounds, formulations, manufacturing methods, or therapeutic applications, with scope defined by specific claims that establish legal boundaries.

Q2: How does the patent landscape influence the value of LUC00140?
A2: The surrounding patents determine potential infringement risks, licensing opportunities, and the patent’s enforceability, affecting overall valuation.

Q3: Can LUC00140 be extended beyond 20 years?
A3: Generally, pharmaceutical patents are patent-term limited to 20 years, but extensions might be available if regulatory delays, such as testing or approval periods, occur.

Q4: How do claim dependencies impact patent strength?
A4: Dependents narrow the scope, providing specific protection but potentially weakening the patent’s broad enforceability. Independent claims are key to broad protection.

Q5: What strategies are recommended for navigating the patent landscape around LUC00140?
A5: Conduct comprehensive patent searches, monitor related filings, and consider strategic filings in key jurisdictions to secure and defend market rights.


References

  1. European Patent Office. "EPO Patent Database."
  2. World Intellectual Property Organization. "PCT Application Trends."
  3. Luxembourg Patents Office. "Official Gazette of Patents."
  4. H. Trautmann, "Chemical Patent Strategies," Intellectual Property Law Journal, 2022.
  5. M. Chen, "Global Patent Landscapes in Pharma," Pharmaceutical Patent Review, 2023.

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.