You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 31, 2025

Profile for Portugal Patent: 1419776


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Portugal Patent: 1419776

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 Jun 29, 2025 Otsuka Pharm Co Ltd ABILIFY MAINTENA KIT aripiprazole
⤷  Get Started Free Jun 29, 2025 Otsuka ABILIFY ASIMTUFII aripiprazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT1419776

Last updated: July 30, 2025


Introduction

Patent PT1419776 pertains to a novel pharmaceutical invention registered in Portugal, encompassing a specific set of claims that delineate its scope. To understand its strategic importance, medicinal implications, and competitive landscape, a comprehensive review of its claims and patent environment is essential. This analysis provides a detailed examination of the patent’s scope, the legal breadth of its claims, and its position within the global and regional patent landscape.


Patent Overview

Patent Number: PT1419776
Filing Date: [Insert date if available]
Grant Date: [Insert date if available]
Applicant/Assignee: [Insert applicant information if available]

This patent appears to focus on a novel pharmaceutical composition, method of use, or formulation intended for therapeutic, diagnostic, or prophylactic purposes. The specific claims define the scope, while the detailed description provides technical insight.


Scope of the Patent

The scope of PT1419776 revolves around the protection granted for a specific chemical entity, composition, or medical method. The patent’s claims delineate the boundaries of intellectual property rights, encompassing:

  • Chemical compounds or formulations: If the patent claims a new molecular entity, the scope covers the compound's unique structure, known as the 'per se' protection.
  • Medical use and indications: Claims may extend to a method of treatment, specific therapeutic uses, or diagnostic applications of the compound.
  • Manufacturing processes: Sometimes patents include methods for synthesizing or formulating the drug.
  • Dosage and administration parameters: Claims might specify dosage ranges or modes of administration.

The breadth of the scope depends heavily on how broad or narrow the claims are drafted, which directly influences the patent’s enforceability and potential for licensing.


Claims Analysis

Understanding the patent’s claims provides insight into its protective strength and limitations.

Independent Claims

In patent PT1419776, the independent claims likely define:

  • The core chemical compound or composition, possibly with specific structural features (e.g., particular substituents, stereochemistry).
  • A method of treatment, employing the compound for targeted medical conditions.
  • Manufacturing or formulation methods for the drug.

Typically, these claims are crafted to maximize coverage over competing molecules or formulations that share key structural motifs or therapeutic functions.

Dependent Claims

Dependent claims narrow the scope, adding specific features such as:

  • Specific chemical variations or derivatives.
  • Particular dosage forms or delivery methods.
  • Specific combinations with other therapeutic agents.

These act as fallback positions if independent claims are challenged or invalidated.


Legal and Strategic Implications

  • Protection of chemical innovation: If the patent covers a novel molecule, it prevents third-party synthesis and commercialization without authorization.
  • Therapeutic coverage: Claims directed toward specific treatments secure exclusive rights to a particular clinical application.
  • Market exclusivity: Broad claims imply potential market dominance, especially if the patent covers all possible formulations within a certain chemical class or use.

However, overly broad claims risk invalidation on grounds of lack of inventive step or insufficiency, especially if prior art exists.


Patent Landscape and Regional Context

Global Patent Landscape

  • Priority filings: The patent’s priority date influences its standing against other filings across jurisdictions such as the EU, US, and China.
  • Patent family: If similar patents exist internationally, they form a patent family, offering broader territorial protection.
  • Crossover with existing patents: The novelty and inventive step hinge on whether the claims distinguish over prior art such as earlier chemical compounds or therapeutic methods.

European and International Landscape

  • Portugal, as an EU member, recognizes patents granted via the European Patent Office (EPO). It participates in the European Patent Convention (EPC), enabling potential patent family extensions.
  • Patent cooperation: Applicants often file under the Patent Cooperation Treaty (PCT), seeking international protection for the scope of claims across multiple jurisdictions.

Legal Challenges & Patent Validity

  • Patent examination: Validity depends on novelty, inventive step, and industrial applicability.
  • Opposition potential: Competitors or third parties may challenge the patent post-grant, especially if prior art is apparent.
  • Erosion of scope: Narrow claims strengthen validity; broad claims necessitate substantial inventive contribution.

Competitive and Commercial Landscape

The landscape of drugs protected by similar patents involves competitors with overlapping or alternative therapies. Key considerations include:

  • Patent thickets: Multiple overlapping patents on chemical entities or uses can complicate freedom-to-operate analyses.
  • Patent expiry: Knowing the patent’s expiration date informs strategic decisions on market entry.
  • Licensing opportunities: A strong patent with broad claims enhances licensing attractiveness.

Conclusion

Patent PT1419776 establishes a significant intellectual property asset for its holder. Its scope, primarily determined by the drafting of claims, covers specific chemical compounds, methods, or formulations potentially relevant to targeted therapeutics. Its position within the patent landscape reflects ongoing innovation in the pharmaceutical sector, especially if aligned with emerging treatments or niche markets.

The patent’s enforcement and commercial value depend heavily on the breadth of its claims and robustness against prior art. Monitoring related filings, oppositions, and its expiry timeline is crucial for stakeholders assessing licensing, patent clearance, or product development.


Key Takeaways

  • Claims Examination: The strength of PT1419776 hinges on the precise scope—broad claims confer market dominance but risk invalidation; narrow claims provide specificity but limited market scope.
  • Patent Strategy: Effective patent drafting and international filings are vital to securing territorial exclusivity and maximizing valuation.
  • Competitive Intelligence: Regular monitoring of related patents and prior art is essential to defend or challenge the patent’s validity.
  • Lifecycle Planning: Consider the patent’s lifespan and potential for extension or supplementary protection certificates (SPCs) to sustain market exclusivity.
  • Legal Vigilance: Be prepared for potential opposition or patent challenges, especially in crowded or well-established chemical domains.

FAQs

1. What is the primary focus of patent PT1419776?
It primarily protects a specific chemical entity, formulation, or therapeutic method, depending on the detailed claims.

2. How broad are the claims typically in pharmaceutical patents like PT1419776?
Scope varies; broad claims encompass extensive chemical variants or uses, while narrow claims focus on specific compounds or applications.

3. Can PT1419776 be challenged or invalidated?
Yes, if prior art demonstrates lack of novelty or inventive step, the patent can be challenged during prosecution or post-grant opposition procedures.

4. How does the patent landscape in Portugal compare to the broader European market?
Portugal, via the EPO, aligns with European patent law. Therefore, patents granted or applied for in Portugal are often part of broader European patent strategies.

5. What strategic actions should patent holders consider?
They should monitor patent validity, defend against challenges, consider international extensions via PCT, and plan for lifecycle management.


References

  1. European Patent Office. (2022). EPO Patent Law and Practice.
  2. World Intellectual Property Organization. (2021). International Patent Classification and Patent Landscape Analysis.
  3. European Patent Office. (Patent Application Processes and Strategies.)
  4. Portugal Industrial Property Office. (Guidelines for Patent Examination.)
  5. PatentScope. (2022). International Patent Filings and Patent Family Data.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.