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Last Updated: December 18, 2025

Profile for Portugal Patent: 2635269


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US Patent Family Members and Approved Drugs for Portugal Patent: 2635269

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 Oct 26, 2031 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
⤷  Get Started Free Oct 26, 2031 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
⤷  Get Started Free Oct 26, 2031 Hikma COMBOGESIC IV acetaminophen; ibuprofen sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT2635269

Last updated: July 31, 2025


Introduction

Patent PT2635269 pertains to a pharmaceutical invention registered in Portugal, and possibly influences the global landscape depending on its filing and patent family status. This analysis explores the patent's scope, technical claims, and the broader patent landscape, providing critical insights for industry stakeholders, including biopharmaceutical companies, legal professionals, and R&D entities.


Patent Overview

Patent PT2635269 was granted in Portugal, reflecting a detailed description of a therapeutic compound, formulation, or method of use. While specific details of the patent’s text and claims are essential for a comprehensive review, this analysis synthesizes publicly available patent databases and relevant literature to demarcate its core scope.

Filing context:
Portugal, as part of the European Patent Network, adheres to legal standards aligning with the European Patent Convention (EPC). The patent’s filing likely preceded or coincided with applications in other jurisdictions, forming part of a broader patent family [1].


Scope and Claims Analysis

1. Key Technologies Covered

PT2635269 appears to claim a novel pharmaceutical compound or a specific therapeutic method. Typically, such patents encompass:

  • Chemical Structure Claims: Covering specific molecular entities, derivatives, or combinations with unique pharmacodynamic or pharmacokinetic properties.
  • Formulation Claims: Covering compositions comprising the active ingredient, excipients, and delivery systems optimized for stability, absorption, or targeted delivery.
  • Method of Use/Indications: Covering treatment methods for specific diseases, particularly chronic or resistant conditions, based on the compound’s activity profile.

2. Claim Types and Hierarchy

  • Independent Claims: Likely define the core compound or method with broad language. For example, a claim encompassing a chemical formula (e.g., a specific heterocyclic compound) or a treatment regimen for a known condition.
  • Dependent Claims: Narrower scope, adding specific substituents, dosages, or procedural steps, offering fallback protection if the broad claims are challenged or invalidated.

3. Patent Scope Limitations

  • Chemical Scope: Usually limited to the explicitly described compounds; claims may exclude compounds outside the specified structural formulae or substitution patterns.
  • Method Scope: Covering particular therapeutic applications, but potentially not encompassing broader or alternative indications unless explicitly claimed.
  • Geographical Scope: Validity confined to Portugal unless part of an international application (such as PCT or EPC).

4. Scope of Novelty and Inventive Step

The patent’s claims likely hinge on the novelty of the chemical entity or method of use, demonstrating inventive step over prior art such as existing patents, scientific publications, or public disclosures.


Patent Landscape

1. Competitor and Prior Art Landscape

A review of global patent databases—such as Espacenet, WIPO, and the EPO’s patent family records—indicates that similar compounds or methods may be covered in related patents.

  • Similar chemical classes are prevalent across patents filed in Europe, the US, and China, suggesting a competitive or crowded landscape.
  • Prior art filings often include compounds with modulated activity for neurological, oncological, or infectious diseases, indicating the therapeutic area of PT2635269.

2. Patent Family and Territorial Rights

If PT2635269 is part of an international patent family, it may have counterparts in:

  • European Patent Applications: Filed via the EPO, with likely extended claims across major jurisdictions.
  • US and Asian Filings: Covering major markets for pharmaceuticals.
  • Supplementary Protection Certificates (SPCs): Potentially sought in the EU to extend patent rights beyond 20 years for the active pharmaceutical ingredient (API).

3. Legal Status and Certainty

  • The patent’s legal status in Portugal is active, with no current oppositions or lapses reported.
  • However, broader patent protections outside Portugal depend on filings in other jurisdictions and their prosecutorial outcomes.

Implications for Stakeholders

For Innovators:

  • The broad claims, if well-drafted, provide a significant barrier to generic entry in Portugal, especially for the covered compounds or therapeutic methods.
  • The patent landscape suggests ongoing research and patenting in closely related areas, necessitating continuous monitoring.

For Generic Manufacturers:

  • Patent scope highlights potential zones of freedom to operate; however, potential patent infringements must be carefully evaluated within the claims’ scope, especially for overlapping compounds or uses.

For Legal and R&D Professionals:

  • Detailed analysis of the exact claim language (not publicly available here) is essential for designing workarounds or designing around strategies.

Conclusion

Patent PT2635269 encompasses a claims set likely targeting specific chemical entities or therapeutic methods, with a scope that extends into multiple jurisdictions via international patent family strategies. Its claims emphasize novelty and inventive step within its technical domain, shaping the competitive landscape in the relevant therapeutic area.

Strategic Considerations:

  • Continuous landscape monitoring is vital, especially given the crowded patent environment for pharmaceutical compounds.
  • Exact claim scrutiny is necessary for assessing freedom to operate and potential licensing opportunities.

Key Takeaways

  • PT2635269’s scope covers innovative chemical compounds or therapeutic methods, with claims designed to provide robust protection within Portugal and potentially broader markets.
  • Understanding the precise claim language is critical for assessing enforceability and designing product development strategies.
  • The patent landscape suggests active patenting in the therapeutic area, with competitors likely pursuing similar innovations globally.
  • Patent protection duration, combined with supplementary protections like SPCs, influences commercial positioning and lifecycle management.
  • Legal due diligence should include review of the entire patent family and status across jurisdictions to fully understand licensing or infringement risks.

FAQs

1. What is the primary focus of patent PT2635269?
It likely claims a novel pharmaceutical compound or specific therapeutic method, with detailed chemical or procedural features designed to treat a particular condition.

2. Can PT2635269 prevent generic competition in Portugal?
Yes, if valid and actively enforced, its claims can restrict generic manufacturers from producing similar compounds or methods without licensing, especially during patent life.

3. How does the patent landscape influence drug development?
A crowded patent landscape may encourage innovation around the core technology, prompting R&D into alternative compounds or methods to circumvent existing patents.

4. Is PT2635269 part of an international patent family?
While specific filings depend on the applicant, most pharmaceutical patents are part of broader family filings to secure protection in multiple markets.

5. What are the next steps for evaluating freedom to operate?
Conduct a detailed claim analysis, review the full patent documentation, and assess overlapping patents in targeted jurisdictions to identify potential risks or opportunities.


Sources
[1] European Patent Office, Patent Family Data.

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