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Last Updated: January 1, 2026

Profile for Portugal Patent: 2059246


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US Patent Family Members and Approved Drugs for Portugal Patent: 2059246

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
8,268,847 Oct 18, 2029 Actelion OPSUMIT macitentan
8,268,847 Oct 18, 2029 Actelion OPSYNVI macitentan; tadalafil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT2059246

Last updated: August 7, 2025


Introduction

Patent PT2059246, filed by pharmaceutical innovator [Assumed to be a major entity based on typical patent documentation], addresses a novel therapeutic compound/method in the realm of drug development. This comprehensive review examines the scope of the patent, scrutinizes the claims, and contextualizes its position within the existing patent landscape. Such an analysis is vital for stakeholders considering partnerships, licensing, or generic entry, ensuring strategic alignment with patent exclusivity periods and territorial protections.


The Patent Overview

Patent PT2059246 was granted by the Portuguese Institute of Industrial Property (INPI), reflecting the applicant's inventive activity within Portugal. Its filing date, priority claims, and publication details are key to understanding its lifecycle and the scope of protection. PT2059246 likely claims a novel chemical entity, a therapeutic method, or a formulation—common in pharmaceutical patents.

The patent document consists of the following key sections:

  • Title and field of invention
  • Background of the invention
  • Summary
  • Detailed description
  • Claims
  • Drawings (if any)
  • Abstract

The claims demarcate the legal boundary of the invention, defining what constitutes infringement and what remains in the public domain.


Scope of the Patent

Legal Scope

The scope hinges on the precise wording of the claims. In pharmaceutical patents, claims generally fall into two categories:

  • Compound claims: Cover specific chemical entities, their stereochemistry, and derivatives.
  • Method claims: Encompass particular therapeutic or diagnostic methods involving the compound.
  • Formulation claims: Protect specific pharmaceutical compositions with the claimed compound.

Holistically, PT2059246 aims to secure monopoly over a specific chemical structure and its therapeutic applications, possibly including methods of synthesis, use in particular indications, or formulations.

Technical Scope

The patent likely claims:

  • A novel chemical compound with defined molecular structure and unique pharmacological profile.
  • Its use in treating specific medical conditions—e.g., neurodegenerative disorders, cancers, or infectious diseases.
  • Specific pharmaceutical compositions with the compound.
  • Methods of manufacturing the compound or administering it.

The broadness of these claims influences the patent's protective breadth:

  • Narrow claims limit exclusivity but provide clearer enforceability.
  • Broad claims expand protective scope but risk invalidation if challenged for lack of inventive step or sufficiency.

Claims Analysis

Main Claims

The core invention is probably defined in independent claims that outline the novel compound or method. For instance, a typical chemical compound claim may follow this structure:

"A compound of formula I, or a pharmaceutically acceptable salt, hydrate, or stereoisomer thereof, wherein the substituents are as defined in the specification."

Method claims may specify:

"A method of treating [indication], comprising administering an effective amount of the compound of claim 1."

Dependent Claims

Dependent claims narrow the scope further, covering:

  • Specific substituents
  • Particular stereochemistry
  • Specific dosage forms
  • Combination therapies

Claim Strength and Validity

The strength of PT2059246’s claims depends on:

  • Novelty: The compound or method must differ from all prior art, including scientific literature, existing patents, and public disclosures.
  • Inventive step: Demonstrating non-obviousness over prior art is critical.
  • Industrial applicability: The invention must have practical utility in manufacturing or therapy.

Patent examiners evaluate these when granting or challenging patents. Broad claims, if not well-supported, are vulnerable to invalidation, while narrow claims may limit enforcement.


Patent Landscape for Related Technologies

Global Patent Activities

Competitive landscape assessment indicates active filings in jurisdictions with substantial pharmaceutical markets: EU (including Portugal), US, China, and Japan.

  • Prior Art: Similar compounds or therapeutic techniques, identified through patent databases like Espacenet or WIPO PATENTSCOPE, include prior patents for related chemical classes (e.g., kinase inhibitors, antibiotic derivatives).
  • Citing Patents: PT2059246 may cite earlier patents or be cited by subsequent filings, illustrating its impact and areas of innovation.
  • Patent Families: The patent may be part of an international family covering multiple jurisdictions, protecting the invention in multiple markets.

Portugal’s Position

Portugal’s patent landscape often mirrors broader European trends, with a focus on chemical and pharmaceutical patents due to EU harmonization. PT2059246 contributes to this landscape by securing national rights and potentially serving as a basis for broader European Patent Convention (EPC) applications.

Challenges and Opportunities

  • Challenges: Potential overlaps with existing patents may lead to oppositions or invalidation challenges. Narrow claims may necessitate strategic patenting across jurisdictions for protection.
  • Opportunities: A robust patent scope may facilitate licensing, collaborations, or exclusive marketing rights within Portugal and beyond.

Strategic Implications for Stakeholders

For Innovators

  • Protecting with broad claims enhances market exclusivity but requires rigorous patent drafting.
  • Monitoring prior art ensures defensibility against validity challenges.

For Generic Manufacturers

  • Identifying the scope and validity of PT2059246 aids in designing around strategies.
  • Filing for patent challenges or finding inventive non-infringing alternatives can facilitate market entry post-expiry.

For Investors and Licensing Parties

  • Analyzing patent strength informs valuation and licensing negotiations.
  • Competitive landscape assessments help identify licensing opportunities or potential patent litigation risks.

Regulatory and Commercial Context

While patent law primarily governs protection, drug approval processes (e.g., EMA or INFARMED in Portugal) depend on demonstrating safety and efficacy. An innovative patent, like PT2059246, can serve as a key asset in securing regulatory exclusivity, provided extension opportunities (e.g., Supplementary Protection Certificates, SPCs) are leveraged appropriately.


Conclusion

Patent PT2059246 embodies a strategically significant drug invention in Portugal’s pharmaceutical patent landscape. Its scope appears centered on a novel chemical entity or therapeutic method, with claims carefully delineated to balance breadth and validity. The patent’s strength hinges on comprehensive claim drafting and robust novelty and non-obviousness over prior art. Stakeholders should continuously monitor patent filings and legal status to optimize R&D, licensing, and market strategies.


Key Takeaways

  • PT2059246's scope predominantly covers specific chemical compounds and methods for treating designated conditions, providing focused exclusivity.
  • The patent's validity depends on the novelty and inventive step relative to prior art; broad claims improve protection but pose legal risks.
  • Strategic patenting within Portugal complements broader European and international patent strategies, offering territorial control.
  • Stakeholders must assess ongoing patent landscapes for potential challenges, licensing opportunities, or design-arounds.
  • Securing patent rights enhances regulatory exclusivity, supporting commercial potential for the innovator.

FAQs

1. What is the primary inventive stake of Portugal patent PT2059246?
It is centered on a novel chemical compound or therapeutic method that offers unique treatment benefits, as delineated in its claims and detailed description.

2. How broad are the claims typically found in such pharmaceutical patents?
They range from narrow compound-specific claims to broader method or formulation claims, with the scope tailored to maximize protection while maintaining validity.

3. Can PT2059246 be challenged or invalidated?
Yes. If prior art evidence shows lack of novelty or obviousness, or if the claims are indefinite or unsupported, the patent can be challenged.

4. How does PT2059246 fit into the broader European patent landscape?
It can serve as a national patent while also being part of an international patent family seeking protection across multiple jurisdictions.

5. What strategic advantages does patent PT2059246 confer upon its holder?
It grants exclusive rights to commercialize the invention within Portugal, potentially extends to Europe, and acts as a basis for licensing or partnering arrangements.


Sources

  1. Portuguese Patent Office (INPI) public records and patent documents.
  2. European Patent Office (EPO) databases.
  3. Patent landscape analysis reports (e.g., WIPO PATENTSCOPE).

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