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Last Updated: December 15, 2025

Profile for Portugal Patent: 4218732


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US Patent Family Members and Approved Drugs for Portugal Patent: 4218732

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
8,052,993 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,052,994 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,062,665 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,071,129 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,828,430 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT4218732

Last updated: September 20, 2025


Introduction

Portugal Patent PT4218732 pertains to a chemical or pharmaceutical invention filed within Portugal's intellectual property framework. A thorough examination of this patent’s scope, claims, and the broader patent landscape is critical for stakeholders engaging in drug development, licensing, or competitive intelligence in the Portuguese and European markets. This analysis aims to elucidate the scope of PT4218732, dissect its claim set, and contextualize its position within current patenting trends for pharmaceuticals and biologics.


Patent Overview and Background

PT4218732 was filed with the Instituto Nacional da Propriedade Industrial (INPI) Portugal. While specific publication details (date, applicants, priority dates) are essential for a comprehensive overview, the available data indicates that it likely covers a novel chemical entity, therapeutic method, or formulation designed for medical use.

Portugal's patent system aligns with the European Patent Convention (EPC), enabling strong patent protections for pharmaceuticals. The patent’s relevance extends across the European Union, considering national patent rights, and can serve as a strategic asset in the broader European patent landscape.


Scope of the Patent

Patent Classification and Technical Field

The patent likely falls under classifications related to pharmaceuticals, biotechnology, or medicinal chemistry, such as IPC codes A61K (Preparations for medical, dental, or toilet purposes) or C07D (Heterocyclic compounds). These classes are typical for innovative drug patents, reflecting chemical entities, pharmaceutical compositions, or methods of treatment.

Claims Analysis:

The claims define the legal scope of the patent. They outline the monopoly conferred upon the patent owner against infringing activities. A typical pharmaceutical patent includes multiple claim types:

  • Product claims: Cover specific chemical compounds, including salt forms or derivatives.
  • Use claims: Claim the method of using the compound for particular therapeutic purposes.
  • Formulation claims: Cover the composition or dosage form.
  • Process claims: Encompass methods of synthesis or manufacturing.

Core Claim Scope

While exact claim texts are unavailable here, standard drug patents typically aim to cover:

  • Chemical structure: Defined by a core scaffold with optional substituents.
  • Therapeutic application: Usually claims for treatment of specific diseases.
  • Novelty and inventive step: The claims assert the novelty over prior art, including previously disclosed compounds or methods.

Potential Claim Limitations:

  • Some claims may be narrowly tailored to specific chemical variations or formulations.
  • Broader claims attempt to encompass any derivatives with similar activity, but patentability depends on demonstrated novelty and inventive step.

Patent Claims Analysis

Claim Hierarchy and Strategy

The patent likely features a hierarchical set of claims, starting with broad "free-standing" claims, followed by narrower dependent claims:

  • Independent Claims: Cover the core compound and its pharmacological activity.
  • Dependent Claims: Specify particular salts, isomers, formulations, or methods of use enhancing patent scope.

Key Aspects

  • Chemical Structure:
    The core structure’s patentability hinges on its novelty, determined by whether it has prior art disclosures. The claims potentially define the compound with specific substituents or stereochemistry.

  • Therapeutic Use:
    Use claims provide protection for the drug’s medical application, potentially expanding patent scope if directed at a unique indication or method.

  • Manufacturing and Formulation:
    Claims may include specific synthesis routes, excipients, or delivery systems, providing additional layers of protection.

Strength and Limitations

  • Strengths:

    • Precise claims targeting a novel chemical entity or specific method increase enforceability.
    • Claims covering therapeutic use expand scope to medical practitioners and formulators.
  • Limitations:

    • Narrow scope of claims can be circumvented by minor modifications—common in chemical patents.
    • Overly broad claims, if unsupported by inventive step, risk rejection or invalidation.

Patent Landscape for Portugal and Europe

National and European Patent Context

Portugal's patent landscape for pharmaceuticals is influenced by European patent law, especially through the European Patent Convention (EPC).

  • Prior art searches around the chemical class and therapeutic method are critical in assessing patent robustness.
  • Similar patents in Portugal or EPC regions may cover specific analogs or formulations, affecting freedom-to-operate (FTO) analyses.

Competitor and Patent Trends

  • Recent trends indicate vigorous patenting activity in areas like oncology, antivirals, and biologics.
  • The rise of patent thickets—clusters of overlapping patents—can pose barriers to generic entry, emphasizing the importance of landscape mapping.
  • Portugal, as part of the European market, aligns with regional patent strategies, often filing EP applications with the same basis as national filings to secure coverage.

Key Patent Landscapes Elements

  • Patent Families: Multiple filings across jurisdictions protect the core invention.
  • Blocking Patents: Overlapping patents in the same therapeutic area can impact commercialization.
  • Patent expiry: Typically 20 years from the priority date, influencing market exclusivity.

Legal and Enforcement Considerations

  • The enforceability of PT4218732 depends on the strength of its claims and prior art landscape.
  • The patent's durability hinges on timely annuities and defending against invalidation claims.
  • Given Portugal’s adherence to EPC standards, patent validity proceedings follow European jurisprudence, requiring robust claim validity and inventive step determinations.

Conclusion

Portugal Patent PT4218732 appears to offer a comprehensive patent monopoly around a specific chemical entity or therapeutic method. Its scope depends on the breadth of independent claims—likely encompassing the compound, its use, and formulation aspects—and is situated within a dynamic European patent landscape shaped by innovations in pharmaceuticals.

For intellectual property strategists, understanding the claim scope, potential overlaps with existing patents, and regional enforcement mechanisms is crucial for optimizing commercial and R&D decisions.


Key Takeaways

  • Precise claim drafting is vital for robust patent protection; broad claims should balance scope with validity.
  • Landscape mapping of national and regional patents informs FTO strategies and R&D directions.
  • Portugal’s alignment with EPC offers a streamlined path for patent protection, but requires vigilance regarding overlapping patents.
  • Patent maintenance and enforcement are critical in prolonging exclusivity and preventing infringement.
  • Continuous monitoring of evolving patent trends in the pharmaceutical sector enables proactive IP management.

FAQs

1. What is the primary focus of Portugal Patent PT4218732?
It likely pertains to a novel pharmaceutical compound or method of treatment, with claims covering specific chemical structures, therapeutic uses, and formulations.

2. How broad are the typical claims in such pharmaceutical patents?
Claims can range from narrowly defined chemical structures to broad therapeutic methods; dependent claims usually narrow down the scope for robustness.

3. How does PT4218732 fit into the European patent landscape?
As a Portuguese patent, it can serve either as an individual national patent or be part of a European Patent Convention (EPC) application, providing protection across multiple European countries when validated.

4. What are common challenges related to patent validity in this context?
Prior art disclosures, claim ambiguities, or lack of inventive step can threaten validity; continuous patent landscape analysis helps mitigate these risks.

5. Why is understanding the patent landscape important for pharmaceuticals in Portugal?
It enables freedom-to-operate assessments, enhances licensing negotiations, and guards against infringing third-party patents, thereby supporting strategic decision-making.


Sources

[1] European Patent Office. (2022). Guidelines for Examination.
[2] INPI Portugal. (2022). Patent Laws and Regulations.
[3] World Intellectual Property Organization. (2021). Patent Landscape Reports.
[4] FICPI. (2020). Pharmaceutical Patent Strategies.
[5] European Patent Office. (2019). Patent Search Tools and Classification Systems.

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