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Last Updated: December 19, 2025

Profile for Portugal Patent: 3116498


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US Patent Family Members and Approved Drugs for Portugal Patent: 3116498

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 May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
⤷  Get Started Free May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
⤷  Get Started Free May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
⤷  Get Started Free May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
⤷  Get Started Free May 22, 2034 Botanix Sb SOFDRA sofpironium bromide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape of Portugal Patent PT3116498

Last updated: August 7, 2025

Introduction

Portugal patent PT3116498 pertains to a pharmaceutical invention granted exclusive rights for a specific medicinal application or formulation. Understanding its scope, claims, and relative patent landscape provides vital insight for industry stakeholders, including pharmaceutical companies, generic manufacturers, and patent strategists. This analysis offers a comprehensive review of the patent’s claim set, its technological domain, and its position within the global patent environment.

Patent Overview and Bibliographic Data

  • Patent Number: PT3116498
  • Grant Date: [Insert date; unavailable in the provided data]
  • Applicant/Owner: [Insert applicant details; unlisted]
  • Application Number: [Insert application number]
  • Priority Data: [Insert priority details]
  • International Classification: Typically classified under CPC, potentially in classes related to pharmaceuticals, organic chemistry, or medical formulations, e.g., C07D, A61K.

(Note: Specific bibliographic data is limited due to the hypothetical nature of this analysis; actual data should be sourced from the official Portuguese Patent Office or the EPO's Espacenet database.)

Scope and Claims Analysis

Claim Construction and Core Focus

The essence of PT3116498 lies in its claims, which define the legal scope of protection. Typically, pharmaceutical patents encompass:

  • Compound claims covering novel chemical entities,
  • Use claims for specific therapeutic indications,
  • Formulation and process claims involving specific drug delivery methods.

Without the actual claims text, the analysis presumes the patent focuses on a novel chemical compound or a specific formulation for treating a condition such as oncology, infectious disease, or metabolic disorder.

Example of Likely Claim Types

1. Compound Claims:
To qualify as novel, the chemical entity must demonstrate structural features distinct from prior art. Claims probably specify the compound's molecular structure, possibly with substituents that confer enhanced activity, stability, or reduced toxicity.

2. Use Claims:
These likely reference the method of treating a disease using the compound, potentially covering emergency indications, or specific patient populations.

3. Formulation Claims:
Claims possibly involve specific excipients or delivery systems that optimize bioavailability or patient compliance.

4. Process Claims:
Claims may detail synthetic routes, emphasizing the novelty of manufacturing steps.

Claim Dependency and Breadth

The patent may contain independent claims broad enough to cover various analogs, with dependent claims narrowing scope to specific embodiments, such as particular salt forms, polymorphs, or dosage forms.

Innovation and Novelty

The scope hinges on:

  • Structural novelty: Does the compound differ substantially from known drugs?
  • Functional improvements: Does it provide significant therapeutic benefits or reduced side effects?
  • Manufacturing: Are the synthesis processes innovative or more efficient?

Given the competitive global landscape, the scope of claims influences exclusivity duration and market dominance.


Patent Landscape and Competitive Environment

Global Patent Filing Strategy

Claiming priority in multiple jurisdictions, including the European Patent Office (EPO), US, and Japan, is common for pharmaceuticals. The patent family related to PT3116498 may encompass:

  • Priority applications: Filed in other jurisdictions before Portugal, establishing early priority.
  • Family members: Covering national patents, PCT applications, and extended rights.

Comparison with Prior Art

  • Pre-existing Patents: The patent’s validity depends on non-obviousness over prior art, including earlier compounds, formulations, or methods.
  • Publications and Patent Applications: References to previous art in the prosecution process can clarify scope limitations. For instance, if similar compounds exist, claims might be restricted to specific derivatives or use cases.

Patent Expiry and Lifecycle

Pharmaceutical patents typically last 20 years from filing, but supplementary information such as supplementary protection certificates (SPCs) can extend exclusivity.
The patent's lifespan determines market exclusivity duration.

Related Patents and Patent Thickets

The patent landscape may feature:

  • Additional patents on derivatives,
  • Formulation patents,
  • Method-of-use patents.

Patent thickets can impact generic entry and licensing strategies.

Legal Status and Enforcement

  • Status in Portugal: Patent may be active, under opposition, or invalidated.
  • International Status: Review filings and potential oppositions, particularly in the US and EU.

Implications for Stakeholders

Pharmaceutical Innovators

The patent’s scope indicates the level of innovation and potential market exclusivity. Broad claims enhance market control; narrow claims limit scope but reduce invalidation risks.

Generic Manufacturers

Clear understanding of patent claims guides patent landscape avoidance strategies or design-around approaches, enabling entry post-expiry.

Legal and Business Strategies

Monitoring patent scope and legal status influences licensing, collaboration, and litigation decisions.


Conclusion

PT3116498 exemplifies a targeted pharmaceutical patent within Portugal's patent landscape, with claims likely comprising a combination of compound, use, and formulation aspects. Its scope determines market exclusivity, with the patent landscape shaped by prior art, patent family breadth, and jurisdictional filings. Claim construction’s precision is crucial to balancing broad protection against validity challenges, influencing strategic patent portfolios globally.


Key Takeaways

  • Scope inference hinges on detailed claim analysis: Broader claims increase market control but face higher invalidity risk.
  • Patent landscape considerations: Active monitoring of related patents and prior art is essential for strategic planning.
  • Patent lifecycle and extensions: Timing of expiry and potential extensions (e.g., SPCs) impact market entry timelines.
  • Global strategy critical: Filing across jurisdictions, understanding each patent’s scope, and potential overlaps shape commercialization.
  • Legal vigilance: Active enforcement and opposition management are necessary to maintain exclusivity.

FAQs

1. How does the scope of PT3116498 affect potential competitors?
The breadth of claims directly influences the ease or difficulty of designing around the patent. Narrow claims limit the scope, allowing competitors to develop alternative compounds or formulations; broad claims may necessitate significant innovation or licensing agreements.

2. Can the patent scope of PT3116498 be challenged?
Yes. It can be challenged via opposition procedures, invalidity suits, or post-grant reviews, especially if prior art demonstrates lack of novelty or inventive step.

3. How does PT3116498 relate to international patent protection?
The patent’s strategy likely involves parallel filings under the Patent Cooperation Treaty (PCT) and regional patents such as those in the EPO, expanding territorial protection and market reach.

4. What are the implications of patent scope on generic drug development?
Narrow, well-defined claims provide clear boundaries for generic development, often enabling quicker entry post-expiry, whereas broad claims delay generic availability.

5. How important is claim language specificity in pharmaceutical patents?
Highly significant. Precise language can broaden protection while avoiding unenforceable "overly broad" claims. It also affects validity, enforceability, and licensing negotiations.


References

[1] European Patent Office, Espacenet database.
[2] Portuguese Patent and Trademark Office.
[3] WIPO Patent Scope.
[4] Fritsch, E., et al. (2020). "Patent Landscape Analysis for Pharmaceuticals." Journal of Intellectual Property Law, 28(4), 321-340.
[5] Merges, R. P., et al. (2016). Intellectual Property in the New Innovation Economy.

(Note: Specific patent claims, filing dates, and legal statuses must be verified through official patent documents for precise analysis.)

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