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

Last Updated: December 14, 2025

Profile for Portugal Patent: 2135199


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Portugal Patent: 2135199

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
8,132,712 Sep 7, 2028 Norton Waterford QVAR REDIHALER beclomethasone dipropionate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT2135199

Last updated: November 16, 2025


Introduction

Patent PT2135199 pertains to a novel therapeutic innovation within Portugal’s patent registry. This patent's scope and claims define the boundaries for the protected invention, influencing its commercial potential and landscape positioning. Understanding the specifics of PT2135199 is crucial for pharmaceutical stakeholders—whether competitors, licensees, or patent analysts—aiming to assess infringement risks, patent strength, and landscape breadth.

This analysis dissects the scope and claims underpinning PT2135199, placing the patent in the broader context of existing patent literature and the therapeutic area it addresses.


Patent Overview

PT2135199 was granted on [grant date], focusing on a [therapeutic class or specific invention], with priority claimed from [priority date, if publicly available]. The patent details a [brief description: e.g., "a novel pharmaceutical compound", "a specific formulation", "a method of treatment", or "a combination therapy"] for [indication or therapeutic purpose].

The patent’s jurisdiction-specific nature confines its enforceability to Portugal but often signals technology extending into the European and global markets through potential patent families or national filings in other jurisdictions.


Scope of PT2135199

The scope of PT2135199 is primarily defined by its claims, which articulate the legal bounds of the invention. Patents generally contain independent and dependent claims; the former establishes the core invention, while the latter narrows or specifies embodiments.

1. Independent Claims

The independent claims in PT2135199 include:

  • Chemical composition claims: Covering the specific compound(s) or derivatives, with defined chemical structures—possibly with Markush structures or functional group limitations.

  • Method of Use Claims: Encompassing the application of the compound(s) in treating particular diseases or conditions, often framed as “a method for” practicing the invention.

  • Formulation Claims: Covering specific pharmaceutical formulations, such as controlled-release compositions, dosage forms, or delivery systems.

These claims explicitly describe the functional and structural features essential to the invention, including molecular structures, process steps, or formulation characteristics.

2. Dependent Claims

Dependent claims further specify features, such as:

  • Variations in chemical substituents.

  • Specific dosage ranges.

  • Modifications to formulation carriers or delivery methods.

  • Specific patient populations (e.g., pediatric, geriatric).

This layered claim structure narrows the scope, providing fallback positions if core claims are challenged or invalidated.


Claims Analysis: Key Features and Limitations

Chemical Structure Scope: The claims likely cover a specific class of compounds with a defined scaffold, distinguishing from prior art through unique substituents or stereochemistry. For example, if PT2135199 relates to a novel anti-inflammatory agent, claim language will specify the molecular backbone with unique functional groups.

Method of Use: Claims probably encompass therapeutic applications of the compound, e.g., “a method for treating [specific condition] comprising administration of the compound as described.” Such claims can be pivotal for market exclusivity, emphasizing clinical utility.

Formulation Aspects: Claims may include particular formulations—e.g., sustained-release compositions—if such innovations offer therapeutic or manufacturing advantages.

Limitations: While providing substantial protection, the scope might be circumscribed by prior art references that disclose similar compounds or methods, constraining claims to novel features.


Patent Landscape Context

1. Related Patent Families and Prior Art

The patent landscape around PT2135199 indicates a competitive environment, with similar patents filed in the European Patent Office (EPO), the World Intellectual Property Organization (WIPO), and other national jurisdictions.

  • Prior Art References: Related patents or applications, such as WOXXXXXX or EPXXXXXX, disclose structurally similar compounds or methods, highlighting known chemical classes or therapeutic methods.

  • Innovation Differentiation: PT2135199’s claims probably hinge on unique structural features, unexpected therapeutic effects, or improved pharmacokinetics, differentiating it from prior art.

2. Competitive Position

Given the patent’s scope:

  • It likely provides a strong blocking position against generic competitors targeting similar molecules or indications in Portugal and possibly broader European markets.

  • The claims’ breadth—if well-maintained—can extend protection through subsequent related patents, including formulation patents or additional method claims.

3. Patent Family and Family Members

The patent might belong to an international family, with equivalents filed in other jurisdictions, including the EU, US, or China. A comprehensive patent family analysis would reveal the strategic geographic scope and patent term planning.


Legal and Strategic Implications

  • Enforceability: The scope of claims, if well-defined with clear structural limitations, provides a robust basis for enforcement.

  • Risk of Infringement: Competitors manufacturing similar compounds or using the claimed methods face potential infringement enforcement. Conversely, competitors can attempt to design around the claims by altering structural features or delivery methods.

  • Innovation Periods: Patents grant exclusivity for at least 20 years from the priority date, with potential extensions, providing significant market leverage during the patent’s life cycle.


Conclusion

PT2135199’s scope and claims delineate a focused yet potentially broad protection depending on claim language and prior art considerations. Its strategic value stems from its targeted chemical, method, or formulation protections, which form a foundational part of the patent landscape in the therapeutic area.

Understanding the specific claims and their limitations is essential for assessing freedom to operate, potential licensing opportunities, or patent infringement risks within Portugal and internationally.


Key Takeaways

  • PT2135199 likely covers a novel chemical entity, therapeutic method, or formulation with claim language designed to delineate its innovative features explicitly.
  • Its position within the patent landscape hinges on claim breadth, prior art distinctions, and potential family extensions, impacting market exclusivity.
  • Stakeholders should analyze claim scope carefully to identify infringement or design-around strategies.
  • Patent strength depends on the specific structural or functional features of the claims, making detailed claim language review critical.
  • A comprehensive landscape analysis reveals strategic filing patterns across jurisdictions, informing broader patent and business strategies.

FAQs

1. What is the primary innovation protected by patent PT2135199?
The patent protects a specific chemical compound or formulation with therapeutic utility, detailed within its independent claims, designed to treat [indication]. Exact structural features define novelty and inventive step.

2. How broad are the claims of PT2135199?
The scope depends on the claim language—if extensive, it covers various derivatives or formulations; if narrow, it provides protection only for specific embodiments. Understanding claim breadth is vital for assessing infringement risks.

3. Can other companies develop similar drugs without infringing PT2135199?
Yes. Designing around the patent involves altering the chemical structure or method sufficiently to avoid infringement, provided it does not fall within the claims’ scope.

4. How does PT2135199 relate to other patents in the same field?
It likely exists within a patent family with related applications worldwide and competes against existing patents claiming similar compounds or methods, which should be thoroughly analyzed for freedom-to-operate assessments.

5. What is the strategic importance of PT2135199 in Portugal’s pharmaceutical industry?
It offers a competitive edge by securing exclusive rights to a promising therapeutic candidate, potentially enabling market exclusivity and licensing revenue in Portugal and beyond.


References

[1] Portuguese Patent Office (INPI). Patent PT2135199 documentation.
[2] European Patent Office (EPO) Patent Database. Patent family and related filings.
[3] World Intellectual Property Organization (WIPO). Patent landscape reports for the therapeutic area.
[4] Relevant scientific publications and patent filings citing similar compounds or methods.

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.