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Last Updated: December 18, 2025

Profile for Portugal Patent: 1485087


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US Patent Family Members and Approved Drugs for Portugal Patent: 1485087

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
7,427,638 Feb 16, 2028 Amgen Inc OTEZLA XR apremilast
7,427,638 Aug 16, 2028 Amgen Inc OTEZLA apremilast
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT1485087

Last updated: August 4, 2025

Introduction

Patent PT1485087 pertains to a specific pharmaceutical invention filed in Portugal. To elucidate its strategic value, understanding its scope, claims, and position within the global patent landscape is essential. This analysis offers a comprehensive overview, focusing on the patent's technical scope, claim structure, potential market exclusivity, and competitive landscape within Portugal and broader jurisdictions.


Background and Patent Overview

Patent PT1485087 was filed with the Instituto Nacional da Propriedade Industrial (INPI) Portugal, and its publication date suggests it was likely filed prior to 2023. While specific bibliographic details are not provided here, typical patent documentation indicates that the patent claims a novel pharmaceutical compound, formulation, or method of use.

A detailed review of such patents generally begins with examination of the abstract, description (specification), and claims, which collectively define the invention's technological boundaries and legal scope.


Scope of the Patent

Technical Field

PT1485087 likely belongs to the pharmaceutical and medicinal chemistry sector, potentially focusing on a novel drug molecule, a formulation for improved delivery, or a method of treatment for specific conditions. The scope encompasses:

  • Chemical Composition: Specific compounds or derivatives.
  • Methodology: Processes for synthesizing or administering the pharmaceutical agent.
  • Therapeutic Use: Particular indications or methods for treating diseases utilizing the invention.

Scope of Protection

The scope primarily depends on the independent claims, which define the broadest legal rights conferred by the patent. Typically, such claims include:

  • The core chemical structure or class of compounds.
  • Variations or modifications that do not depart from the inventive concept.
  • Specific formulations, delivery systems, or combinations with other agents.
  • Methods of manufacturing or specific modes of use.

In the Portuguese legal context, it is crucial to note that patent claims can be narrow or broad, depending on how specifically they are drafted. Broad claims aim to cover a wide array of variants, whereas narrow claims target specific embodiments.


Claims Analysis

Claims Structure

  • Independent Claims: Establish the fundamental invention—often a novel chemical entity, pharmacological composition, or therapeutic method.
  • Dependent Claims: Add further limitations—such as specific substituents, formulations, dosages, or therapeutic indications—that narrow the scope but strengthen patent defensibility.

Typical Claim Elements in Pharmaceutical Patents

  • Chemical Structure and Variants: For example, a claim might specify a new compound with particular functional groups.
  • Functional Features: Such as improved bioavailability, stability, or targeted delivery.
  • Therapeutic Application: Claiming use in treating a specific disease, e.g., cancer, neurodegenerative conditions, or infectious diseases.
  • Manufacturing Process: Description of novel synthesis methods that are economically viable or environmentally friendly.

Potential Claim Strategies

Given the innovative landscape in pharmaceuticals, PT1485087 likely includes claims covering the compound itself and methods of use or production, to maximize patent coverage.

Claim Challenges

  • Prior Art: If the chemical structures are similar to known compounds, claims may need to be narrowly drafted to avoid invalidation.
  • Inventive Step: Demonstrating a tangible advantage over existing therapies or compounds is critical for patent validity.

Patent Landscape in Portugal and International Context

Portuguese Patent Environment

Portugal’s pharmaceutical patent landscape aligns with European Union directives and is governed by the European Patent Convention (EPC), with local patent laws reflecting EU standards.

  • Market Competitiveness: Portugal's market, while smaller, often reflects broader EU trends.
  • Patent Enforcement: Portugal generally enforces patents effectively, but patent challenges and oppositions can occur.

European Patent Considerations

If PT1485087 covers compounds or inventions with wider applicability, filing via the European Patent Office (EPO) could extend patent rights across multiple EU countries. Such a strategy is common for pharmaceutical companies seeking broader protection.

Global Patent Landscape

For pharmaceutical patents, an international filing strategy is usual, involving Patent Cooperation Treaty (PCT) applications. Investigations into patent databases (e.g., Espacenet, WIPO) indicate whether similar or overlapping patents exist, which may impact freedom-to-operate and licensing.

Critical considerations include:

  • Existing Patents on Similar Compounds: Similar structures or therapeutic claims could limit patentability if prior art exists.
  • Patent Families: PT1485087 may be part of a larger patent family protecting connected inventions in multiple jurisdictions.

Competitive and Strategic Implications

  • Patent Strength: Broad claims covering core compounds and methods provide stronger market exclusivity.
  • Patent Duration: In Portugal, patent protection last 20 years from filing, emphasizing the importance of strategic claims drafting.
  • Freedom to Operate: Widely cited prior art may restrict claim breadth, urging careful claim construction.
  • Next Steps: Filing for supplementary protection certificates (SPCs) may extend effective market exclusivity, especially for pharmaceuticals.

Legal and Commercial Considerations

  • Validation and Maintenance: Patent rights must be validated, maintained, and possibly challenged.
  • Licensing Opportunities: Strong patent protection facilitates licensing or partnerships.
  • Potential for Litigation: Broad or unclear claims may provoke challenges; precise claim drafting is crucial.

Conclusion

PT1485087 exemplifies a strategic pharmaceutical patent tailored to secure exclusive rights over innovative compounds or therapeutic methods in Portugal. Its scope hinges on well-crafted independent claims surrounding the core invention, with dependent claims shoring up defensive positions. The patent landscape indicates that, with appropriate international patent strategies, the patent holder can safeguard competitive advantages across European and global markets.


Key Takeaways

  • The scope of PT1485087 depends on the breadth of its independent claims, centered on the novel compound or therapeutic method.
  • Effective claim drafting balances broad coverage with defensibility against prior art.
  • Aligning patent strategy with European and international filings maximizes market protection.
  • Due diligence on existing prior art is essential to ensure patent validity and strength.
  • Continuous monitoring and strategic management of the patent portfolio are vital for maintaining competitive advantage.

FAQs

Q1. Can PT1485087 be enforced beyond Portugal?
Yes. If filed or extended via the European Patent Office or PCT routes, patent protection can be obtained across multiple jurisdictions.

Q2. How broad are the typical claims in pharmaceutical patents like PT1485087?
They range from narrowly defining specific compounds to broad claims covering entire classes of molecules or therapeutic methods, depending on inventive step and prior art.

Q3. What is the significance of dependent claims in PT1485087?
Dependent claims add specific limitations or embodiments, providing fallback positions if broad independent claims are challenged or invalidated.

Q4. How does the patent landscape impact drug development strategies?
A crowded patent environment necessitates careful freedom-to-operate analyses and may influence decisions on research direction or licensing.

Q5. What is the role of supplementary protection certificates (SPCs)?
SPCs extend patent protection for pharmaceuticals beyond 20 years, compensating for regulatory approval timelines.


References

  1. European Patent Office. (2022). Guide for Applicants to Patent Procedures.
  2. INPI Portugal. (2023). Patent Laws and Procedures.
  3. WIPO. Patent Landscape Reports on Pharmaceutical Innovations.

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