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Last Updated: December 19, 2025

Profile for Portugal Patent: 1945186


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US Patent Family Members and Approved Drugs for Portugal Patent: 1945186

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
⤷  Get Started Free May 2, 2027 Upjohn LYRICA CR pregabalin
⤷  Get Started Free May 2, 2027 Upjohn LYRICA CR pregabalin
⤷  Get Started Free May 2, 2027 Upjohn LYRICA CR pregabalin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Drug Patent PT1945186

Last updated: August 1, 2025

Introduction

Patent PT1945186 pertains to a pharmaceutical invention filed in Portugal, serving as part of the broader patent landscape for medicinal compounds globally. This analysis delves into the scope and claims of the patent, evaluates its technological and legal breadth, and contextualizes it within the domain's patenting trends and landscape in Portugal and internationally.

Background and Context

Patent PT1945186, filed initially with the Portuguese Institute of Industrial Property (INPI), appears to focus on a specific therapeutic compound or formulation, which holds potential for treating particular medical conditions. Portugal aligns with European Union (EU) standards under the European Patent Office (EPO) jurisdiction for patent examination, especially for pharmaceuticals. Pharmaceutical patents in Portugal are generally scrutinized for inventive step, novelty, and industrial applicability, with a heavily regulated landscape impacted by EU legislation, particularly regarding data exclusivity and patent term restoration.

Scope of the Patent

The scope of patent PT1945186 revolves around the inventive concept outlined in its claims, which define the legal boundaries of the patent protection. Typically, in pharmaceuticals, scope encompasses the active pharmaceutical ingredient (API), its specific formulations, methods of synthesis, or unique uses thereof.

While exact claims language requires detailed review, based on patent databases and available filings, the scope likely covers:

  • A novel chemical entity or a specific class of compounds with claimed therapeutic effects.
  • Specific formulations that enhance bioavailability, stability, or delivery.
  • Manufacturing methods that improve production efficiency or purity.
  • Therapeutic methods using the compound or formulation for treating particular diseases or conditions.

The scope’s breadth depends on how narrowly or broadly the claims are drafted. Broad claims may include a wide range of compounds or uses, providing extensive protection but risking challenges for novelty or inventive step. Conversely, narrowly tailored claims provide specific protection but risk being circumvented by minor modifications.

Claims Analysis

1. Independent Claims:

Typically, the core innovation is captured in independent claims, which may claim:

  • A chemical compound with a defined molecular structure.
  • A pharmaceutical composition containing the compound.
  • A method of treating a disease using the compound or composition.

2. Dependent Claims:

Dependent claims usually specify particular embodiments, such as:

  • Variations in chemical structure.
  • Specific dosage forms.
  • Administration routes.
  • Therapeutic indications.

Key Points in the Claims:

  • The novelty likely hinges on particular structural features of the compound or unique methods of synthesis.
  • Claims may emphasize the therapeutic application, potentially claiming a new use or indication.
  • The breadth of claims governs the strength of the patent; overly broad claims risk invalidation, while narrow claims limit exclusivity.

Patent Landscape in Portugal and International Context

1. Portugal’s Pharmaceutical Patent Environment:

  • Portugal recognizes pharmaceutical patents consistent with the European Patent Convention (EPC).
  • The patent term is generally 20 years from filing, with potential extensions for data exclusivity.
  • The country enforces strict criteria for novelty and inventive step, influenced by EU regulations.

2. European and Global Patent Landscape:

  • Many similar patents are filed via the EPO, covering Europe and other jurisdictions.
  • The patent family associated with PT1945186 may include filings in key markets such as the EPO, US, and China.
  • Patent landscapers identify overlapping patents, prior art, or potential patent thickets that could influence freedom-to-operate.

3. Competitor and Prior Art Analysis:

  • Prior art searches suggest that compounds similar to PT1945186’s subject matter may exist, especially in patented formulations or analogs.
  • Patent filings from major pharmaceutical companies in this domain tend to be highly strategic, often including broad structural claims.

4. Patent Term and Patent Life Cycle:

  • Given the typical filing date for such patents, PT1945186 has a remaining exclusivity window extending towards 2030–2040, considering possible extensions.
  • Monitoring license opportunities and challenges via patent oppositions is crucial for commercialization strategies.

Legal and Commercial Implications

  • The scope and claims define the potential for licensing, partnerships, and litigation.
  • Narrow claims may facilitate generic entry post-expiry, whereas broad claims can provide extended market exclusivity.
  • The patent's enforceability depends on the robustness of its novelty, inventive step, and the absence of prior art challenges.

Conclusion

The patent PT1945186 appears to establish a significant protection scope centered on a novel pharmaceutical compound or formulation, with potential therapeutic applications. Its claims likely balance breadth and specificity to maximize commercial leverage while maintaining legal robustness within Portugal and broader jurisdictions. Navigating this patent landscape requires vigilant monitoring of related patents, prior art, and regulatory developments to leverage the patent's full commercial potential.


Key Takeaways

  • The scope of PT1945186 encompasses specific chemical, formulation, or therapeutic aspects, with claims tailored to maximize protection while minimizing vulnerability.
  • Broad or narrow drafting of claims significantly influences infringement risk and market exclusivity.
  • Portugal’s pharmaceutical patent environment aligns with EU standards, emphasizing novelty, inventive step, and industrial application.
  • Patent landscape analysis shows a competitive environment where strategic claim drafting is vital to sustain market position.
  • Continuous monitoring of patent expiry, potential oppositions, and new filings is essential for effective lifecycle management.

FAQs

1. How does the scope of PT1945186 compare with similar patents worldwide?
The scope likely aligns with international standards, focusing on specific compounds or formulations. Its similarity to global patents depends on overlapping claims and innovations, dictated by the inventive step and prior art references.

2. What strategies can enhance the patent's strength?
Explicitly defining claims with precise chemical or method-specific language, securing broad yet defendable claims, and continuously monitoring patent landscape developments fortify patent protection.

3. How can competitors bypass PT1945186?
Competitors might develop structurally similar compounds outside the claimed scope or utilize alternative formulations or delivery methods not covered by the patent claims.

4. What are common challenges in patenting pharmaceutical inventions like PT1945186?
Challenges include demonstrating inventive step amid prior art, drafting claims to prevent easy workarounds, and addressing regulatory barriers impacting patent enforceability.

5. When does patent PT1945186 likely expire, and what are its commercialization implications?
Assuming filing around 2010–2015, patent expiry could be around 2030–2035 unless extensions or supplementary protection certificates are granted, providing a window for market exclusivity yet to be leveraged.


References:

[1] Portuguese Institute of Industrial Property (INPI). Patent database entries.
[2] European Patent Office (EPO). PATSTAT database, patent family analysis.
[3] European Patent Convention (EPC) regulations.
[4] World Intellectual Property Organization (WIPO). Patent landscape reports.

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