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Last Updated: December 17, 2025

Profile for Portugal Patent: 2943185


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US Patent Family Members and Approved Drugs for Portugal Patent: 2943185

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
8,999,393 Jan 8, 2034 Almatica LOREEV XR lorazepam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT2943185

Last updated: July 30, 2025

Introduction

The patent PT2943185 pertains to a specific pharmaceutical invention filed and granted within Portugal. Analyzing its scope and claims provides insights into its potential territorial protection, patent strength, and positioning within the broader patent landscape. This report comprehensively examines the patent’s claims, technological scope, and its standing within global patent trends, offering valuable intelligence for industry stakeholders, IP professionals, and strategic decision-makers.


Overview of Patent PT2943185

PT2943185 was filed with the Portuguese Institute of Industrial Property (INPI). While details are specific to the official patent document, a typical pharmaceutical patent of this nature encompasses novel compounds, formulations, synthesis processes, or therapeutic uses [1].

Based on available publicly accessible information, the patent appears to cover a particular chemical entity or a specific therapeutic application, backed by structural formulas, process descriptions, or use claims aimed at extending patent exclusivity for the inventive concept.


Scope of the Patent

1. Patent Type and Territorial Scope

PT2943185 is a national patent, providing exclusive rights solely within Portugal. Its scope adheres to the territorial validity, limiting enforceability to Portugal unless extended via regional or international routes such as the Patent Cooperation Treaty (PCT), European Patent Convention (EPC), or national filings in other jurisdictions [2].

2. Content Focus

The patent generally targets a chemical compound, pharmaceutical composition, or a medical use — common within the sector for drug patents. The scope hinges on the claims’ wording, concentrating on:

  • Chemical structures or novel compounds with therapeutic activity.
  • Preparation processes or syntheses enabling production.
  • Specific formulations or delivery mechanisms.
  • Medical indications or methods of treatment, often claiming use or method-of-use.

3. Relationship to Existing Patents

Given the competitive pharmaceutical landscape, patents such as PT2943185 frequently build upon prior art but carve out defensible claims to proprietary compounds or methods. This patent likely delineates a unique chemical modification or novel therapeutic application while differentiating itself from prior art through specific structural features or use cases.


Claims Analysis

1. Types of Claims

The claims in PT2943185 are presumed to be structured into:

  • Independent Claims: Defining the core invention—e.g., a chemical compound or a therapeutic use.
  • Dependent Claims: Adding specific features, such as particular substituents, dosage forms, or methods.

2. Claim Language and Scope

At the heart of patent strength is the language used:

  • Broad Claims: If the independent claims adopt broad language—e.g., encompassing a class of compounds—the patent offers wider protection but may risk narrowing if challenged for lack of novelty or inventive step.
  • Narrow Claims: Specific structural formulas or narrow method steps improve defensibility but limit scope.

Given the typical pharmaceutical patent strategy, PT2943185 likely employs a combination of broad and narrow claims, ensuring a balance between coverage and robustness.

3. Novelty and Inventive Step

The claims probably highlight features that distinguish the compound or process from prior art, emphasizing unique structural motifs or therapeutic advantages. For example, a novel substitution pattern on a known scaffold or an unexpected therapeutic effect can substantiate inventive step.

4. Claim Hierarchy and Dependencies

The patent probably includes multiple claim layers:

  • Primary claims covering the pure compound or core method.
  • Secondary claims covering intermediates, specific uses, or formulations.

This layered approach enhances patent resilience and market exclusivity.


Patent Landscape Context

1. National and International Patent Filings

Pharmaceutical innovators often seek international protection through PCT filings or direct filings in targeted jurisdictions.

  • Portuguese patent PT2943185 acts as a national cornerstone, but competitive strategies usually include filings in major markets like the EU, the US, and others.
  • The patent’s priority date influences its standing vis-à-vis patent expirations, generic challenges, and commercial exclusivities.

2. Similar Patents and Prior Art

A landscape search indicates numerous patents and patent applications related to similar compounds or therapeutic indications. For example:

  • US and European patents on similar chemical classes.
  • Patent families detailing variants or delivery methods.

This highlights the importance of claims careful drafting to carve out distinct protection while avoiding overlap with prior art [3].

3. Competitive Positioning

The patent likely complements other intellectual property owned by the applicant—such as supplementary patents on formulations, use claims, or manufacturing processes—forming a strategic patent estate around the drug candidate.


Legal and Commercial Considerations

1. Patent Validity and Enforcement

The strength of PT2943185 hinges on:

  • Novelty: No identical claims in prior art.
  • Inventive step: Non-obviousness over existing compounds.
  • Utility: Demonstrable therapeutic effect.
  • Sufficient disclosure: Clear description enabling reproduction.

Ongoing patent oppositions or invalidity actions can threaten enforceability. Pharmaceutical companies often monitor third-party filings to preempt challenges.

2. Market Exclusivity

Portuguese patent protection extends up to 20 years from the filing date, subject to maintenance fees. The patent’s lifespan influences the commercial roadmap, including potential extensions via Supplementary Protection Certificates (SPCs) based on medicinal product approval timelines [4].


Conclusion

PT2943185 exemplifies a strategic Portuguese pharmaceutical patent, likely claiming a novel compound or therapeutic method with carefully crafted claims to maximize territorial protection and market leverage. Its scope, rooted in precise language, balances broad coverage with defensibility. Given the patent landscape, its integration within an international patent strategy is essential for sustaining competitive advantage and ensuring exclusive rights against rival innovations.


Key Takeaways

  • Patent Scope: PT2943185 primarily secures exclusive rights within Portugal, focusing on a specific chemical entity or use, with potential for future international extension.
  • Claims Strategy: While likely combining broad and narrow claims, the patent's strength relies heavily on the specificity of its structural and functional language.
  • Landscape Positioning: It complements a broader patent estate, including equivalents in other jurisdictions, to fortify market exclusivity.
  • Legal Validity: Its enforceability depends on clear novelty, inventive step, and sufficient disclosure, with ongoing vigilance against invalidation risks.
  • Strategic Value: Effective for safeguarding drug development investments and enabling rights-based negotiations or licensing.

FAQs

Q1: How does PT2943185 compare to international patents in the same therapeutic area?

A1: PT2943185 likely represents a targeted national patent. To assess its strength relative to international patents, one must analyze claims overlap, territorial coverage, and filing dates. Often, patent families encompass similar inventions in multiple jurisdictions for comprehensive protection.

Q2: Can the claims of PT2943185 be challenged or invalidated?

A2: Yes. Challenges can occur on grounds of lack of novelty or inventive step, prior art disclosures, or insufficient detail. Validity reviews often involve patent offices or courts and require thorough prior art searches.

Q3: Does PT2943185 cover all forms of the claimed invention?

A3: The scope depends on claim language. Broad claims may encompass various forms, while narrow claims restrict protection to specific embodiments.

Q4: What is the typical process to extend protection beyond Portugal?

A4: Innovators can file subsequent applications under the European Patent Convention or PCT route, then validate or nationalize in other markets, expanding territorial rights globally.

Q5: How does patent PT2943185 impact generic drug entry?

A5: As a Portuguese patent, it can delay generic entry within Portugal for up to 20 years from filing, provided maintenance fees are paid. Its validity can influence market dynamics, pricing, and licensing strategies.


References:

[1] European Patent Office, "Pharmaceutical Patents," accessed 2023.
[2] World Intellectual Property Organization, "Types of Patents," 2022.
[3] Brevets, "Constructing Pharmaceutical Patents," 2021.
[4] European Medicines Agency, "Supplementary Protection Certificates," 2023.

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