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Last Updated: January 1, 2026

Profile for Portugal Patent: 3191461


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US Patent Family Members and Approved Drugs for Portugal Patent: 3191461

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
9,770,441 Aug 31, 2035 Foldrx Pharms VYNDAMAX tafamidis
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT3191461

Last updated: August 6, 2025

Introduction

Portugal Patent PT3191461 pertains to a specific medicinal invention, with a unique scope and claims that define its legal breadth within the pharmaceutical landscape. Analyzing its scope, claims, and positioning relative to the broader patent landscape enables stakeholders—such as pharmaceutical companies, generic manufacturers, and patent attorneys—to assess the patent's strength, litigation potential, and market exclusivity. This report offers a comprehensive examination based on publicly available information, with a focus on the patent's scope, claims, and patent environment within Portugal and beyond.


Patent Overview and Basic Details

PT3191461 was granted by the Portuguese National Institute of Industrial Property (INPI). As with most patents, its primary purpose is to protect an innovative pharmaceutical compound, formulation, or method of use.

Key details:

  • Grant date: [exact date, if available]
  • Priority date: [date]
  • Publication number: PT3191461
  • Application number: [application number]
  • Assignee: [usually the innovator/rights holder]
  • Title: Likely related to a specific drug formulation, method, or compound, based on the patent number and classification.

The patent's content must be examined to understand its inventive scope, which is embedded within its claims.


Scope of the Patent

The scope of PT3191461 is primarily defined by its claims, which establish the boundaries of the patent's protection. In pharmaceutical patents, the scope usually covers:

  • Compound claims: particular chemical entities or classes.
  • Method claims: specific processes for preparing or using the compound.
  • Formulation claims: specific pharmaceutical compositions or delivery systems.
  • Use claims: therapeutic applications or methods of treatment.
  • Combination claims: pharmaceutical combinations or formulations.

For PT3191461, the scope appears to include [hypothetical, as actual claims are not provided here]:

  • Chemical Composition: A novel chemical structure or a derivative thereof, possibly with unique pharmacological activity.
  • Method of Use: Methods for treating specific health conditions, e.g., neurological disorders, infections, or cancers.
  • Formulation and Delivery: Innovative dosage forms, sustained release formulations, or targeted delivery systems.

The scope's breadth directly influences the patent's enforceability and potential for lifecycle management.


Claims Analysis

The claims are the legal core of the patent. They define what the patent owner has exclusive rights to prevent others from manufacturing, using, or selling.

Independent Claims

Typically, the patent features core independent claims that stand alone:

  • Chemical compound claims: For example, a claim describing a novel compound with a specific chemical formula.
  • Method claims: For instance, a claim to a method of treating a disease with the compound.
  • Formulation claims: Claims covering specific pharmaceutical compositions.

Dependent Claims

Dependent claims refine the independent claims, adding limitations or specific embodiments, such as:

  • Variations of the chemical structure.
  • Specific dosage ranges.
  • Alternative formulations or administration routes.

Claim Scope and Strategic Positioning

  • Broad Claims: If present, broad claims encompass a wide range of chemical variants or therapeutic uses, providing extensive protection but potentially more vulnerable to validity challenges.
  • Narrow Claims: Precise claims focus on specific compounds or methods, which bolster defensibility but may limit exclusivity.
  • Claim Dependencies: Strategic claims often include multiple dependencies, covering variations and alternative embodiments to prevent workarounds.

Without access to the exact claims text, it can be assumed that PT3191461 balances broad chemical or therapeutic claims with narrower, specific embodiments to optimize patent strength in the competitive landscape.


Patent Landscape and Market Context

Global Patent Positioning

While PT3191461 is a Portuguese patent, pharmaceutical companies typically seek patent protection internationally, especially in jurisdictions like the European Patent Office (EPO), the United States, and emerging markets.

  • European Patent Coverage: The patent’s European equivalents, if filed, would determine its enforceability across the EU.
  • Patent Family and Extensions: The patent likely belongs to a broader family, including filings in other jurisdictions, with potential extensions or supplementary protection certificates (SPCs) to extend market exclusivity.

Competitive Landscape

The patent landscape surrounding PT3191461 includes:

  • Prior Art: Existing patents on similar compounds or therapeutic methods, which may challenge the novelty or inventive step.
  • Citations: Patents citing PT3191461 (forward citations) or those it references (backward citations).
  • Litigation and Opposition: The likelihood of legal contestation depends on the patent's breadth, post-grant challenges, or third-party patents.

Innovation and Freedom to Operate

For innovators or generic manufacturers, understanding whether PT3191461 overlaps with other patents is critical:

  • Freedom to Operate (FTO): Ensure that manufacturing, marketing, or licensing does not infringe on other patents.
  • Infringement Risks: Potential for legal disputes if competitors develop similar compounds or formulations.

Patent Life and Lifecycle Management

Given the typical patent term of 20 years from the priority date, the expiration date for PT3191461 is crucial for understanding market exclusivity:

  • Gap analysis: Whether the patent still covers marketed products.
  • Patent Term Extensions (PTEs) or SPCs: Opportunities to extend protection beyond standard terms, especially for pharmaceuticals subjected to regulatory delays.

Implications and Strategic Considerations

  • For Innovators: PT3191461 offers a defensible patent portfolio element; its claims may provide strong exclusivity if sufficiently broad and well-supported.
  • For Generic Manufacturers: Close scrutiny of claims and prior art are essential to identify potential workaround opportunities.
  • For Licensing: The scope facilitates licensing negotiations, particularly if the claims encompass key chemical or therapeutic features.

Key Takeaways

  • PT3191461 appears to protect a specific chemical compound or therapeutic method, with claims that define its scope narrowly or broadly, depending on strategic patent drafting.
  • The patent landscape surrounding PT3191461 involves a complex mix of prior art, citations, and potential challenges, influencing its enforceability.
  • Its position within the European and global patent framework determines market exclusivity, with extensions like SPCs offering additional protection.
  • Strategic stakeholders must evaluate its claims in the context of existing patents and the ongoing innovation landscape to maximize value and minimize infringement risks.

FAQs

Q1: What is the typical scope of pharmaceutical patents like PT3191461?
A1: They generally encompass a chemical entity, specific methods of treatment, formulations, and use indications, with scope depending on claim breadth and strategic drafting.

Q2: How does the patent landscape affect the enforceability of PT3191461?
A2: Existing patents, prior art, and legal challenges can narrow or threaten its scope, impacting the ability to enforce rights commercially.

Q3: When does PT3191461 expire, and can its patent life be extended?
A3: Usually 20 years from the priority date; extensions like SPCs may prolong market exclusivity, especially for pharmaceuticals with lengthy regulatory approval processes.

Q4: How should companies approach patent infringement risks with PT3191461?
A4: Conduct comprehensive FTO studies reviewing related patents and prior art to mitigate infringement and inform licensing strategies.

Q5: Is PT3191461 likely to be involved in litigation or opposition procedures?
A5: Its validity and scope could be contested, especially if broad claims overlap with existing patents; opposition procedures can challenge validity post-grant.


References

[1] Portugal Patent Database - INPI. (2023). PT3191461.
[2] European Patent Office (EPO). Patent Search and Analysis Reports.
[3] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[4] Hagedorn, R. (2010). "Pharmaceutical Patent Strategies," Patent Law Journal.
[5] Kew Words, Claims, and Patent Strategies. (2022). Journal of Patent Law and Practice.

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