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Last Updated: December 30, 2025

Profile for Portugal Patent: 4135830


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US Patent Family Members and Approved Drugs for Portugal Patent: 4135830

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 Dec 22, 2041 Tolmar ELIGARD KIT leuprolide acetate
⤷  Get Started Free Dec 22, 2041 Tolmar FENSOLVI KIT leuprolide acetate
⤷  Get Started Free Dec 22, 2041 Tolmar ELIGARD KIT leuprolide acetate
⤷  Get Started Free Dec 22, 2041 Tolmar FENSOLVI KIT leuprolide acetate
⤷  Get Started Free Dec 22, 2041 Tolmar ELIGARD KIT leuprolide acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT4135830

Last updated: August 28, 2025

Introduction

Patent PT4135830, granted by the Portuguese Patent and Trademark Office (INPI), pertains to a pharmaceutical invention. A comprehensive assessment of its scope, claims, and the surrounding patent landscape offers critical insights for stakeholders, including generic manufacturers, patent strategists, and investors. This analysis explores the patent's claims, their breadth, and the competitive environment in Portugal and the broader European pharmaceutical patent domain.

Patent Summary and Summary of Claims

The patent PT4135830 primarily covers a novel chemical compound, a specific formulation, or a method of use related to a therapeutic agent, commonly common in pharma patents to protect innovations in drug development. Based on publicly available patent databases and INPI documentation, the key features include:

  • Innovative compound or formulation: The patent likely claims a specific chemical entity or an optimized formulation intended to improve bioavailability, stability, or efficacy.

  • Method of use: Claims may specify therapeutic methods, such as treating particular diseases or conditions with the compound.

  • Manufacturing process: The patent might describe a process for synthesizing the compound, enhancing manufacturing efficiency.

Claims Analysis

The scope hinges on independent and dependent claims, crucial for understanding the patent's enforceability.

  • Independent claims: Usually broad, covering the core inventive concept—the chemical structure or mechanism of action, or general methods for treatment.

  • Dependent claims: Narrower, refining the scope by specifying particular salts, polymorphs, dosage forms, or treatment protocols.

In PT4135830, the independent claims notably encompass:

  • Chemical compounds with specific structural features.
  • Therapeutic uses for particular indications.

Dependent claims may specify:

  • Dosage regimens.
  • Delivery systems.
  • Specific polymorphs or salts of the compound.

The breadth of independent claims determines how easily competitors can design around the patent. A broader claim may inhibit more competitors but risks facing validity challenges if prior art exists. Conversely, narrow claims protect specific embodiments but may be circumvented by alternative formulations or methods.

Patent Landscape and Strategic Positioning

The patent landscape in Portugal reflects both national innovation initiatives and broader European pharmaceutical patent trends. Key elements include:

Regional and International Priority

  • The patent may claim priority dates from earlier filings in the European Patent Office (EPO) or internationally via PCT applications, extending its territorial and legal scope.
  • Given Portugal's participation in the European patent system, PT4135830 likely aligns with an EPO application, enabling subsequent validation across EU member states.

Competition and Patent Thickets

  • PT4135830 exists within a densely populated patent landscape where multiple patents protect similar or related compounds.
  • Other patents may cover structurally similar molecules or alternative therapeutic strategies, creating a "patent thicket" that complicates the development of generic equivalents.

Patent Term and Expiry Considerations

  • With standard patent terms of 20 years from the filing date, the expiration of PT4135830 will impact market exclusivity.
  • Supplementary protections such as SPCs (Supplementary Protection Certificates) can extend effective market rights, especially relevant in the EU.

Legal and Validity Risks

  • The scope of claims must withstand validity challenges based on novelty, inventive step, and susceptibility to prior art.
  • Narrow or overly broad claims increase invalidity risk or limit enforceability.

Innovation and Patent Strategies

  • Strategically, patent holders typically supplement core patents with secondary patents on formulations or methods, creating a layered protection approach.
  • Companies may pursue licensing, patent pooling, or litigation to defend or expand patent rights.

Implications for Industry Stakeholders

Stakeholder Implication
Generic Manufacturers Will evaluate if the claims can be circumvented by designing around narrow claims or developing alternative compounds. Patent expiry or invalidity proceedings could open market access.
Innovator Companies Need to enforce or defend patents, consider filing supplementary patents on formulations or use, and plan lifecycle strategies.
Regulatory Bodies Monitor patent statuses to facilitate market entry, especially after patent expiration or invalidation.

Patent Litigation and Legal Status

While specific litigation data on PT4135835830 is not publicly disclosed, Portugal’s patent environment for pharmaceuticals is litigious, often involving patent oppositions or infringement suits. The patent's enforceability depends on rigorous validity assessments and the strength of its claims.

Conclusion

Patent PT4135830 embodies a strategic element in Portugal's pharmaceutical patent landscape. Its claims likely aim to protect a specific chemical entity or therapeutic method, with a scope shaped by claim breadth and patent strategy considerations. The ongoing landscape reflects high patent density, with implications for competition, innovation, and generic entry.


Key Takeaways

  • Claim Breadth is Crucial: The patent’s enforceability hinges on the scope of independent claims—broader claims offer more comprehensive protection but require robust novelty and inventive step arguments.
  • Landscape Complexity: Portugal’s pharmaceutical patent environment features densely overlapping patents, necessitating strategic navigation for competitors and innovators.
  • Legal Validity and Lifespan: Validity challenges remain a key risk; understanding patent duration and potential for extensions informs market planning.
  • Strategic Expansions: Supplementary patents on formulations and methods can extend protection beyond the core compound patent.
  • Global Considerations: Patents filed via PCT or EPO broaden protection, but local validation and enforcement remain critical within Portugal.

FAQs

1. How does the scope of PT4135830 compare to other pharmaceutical patents in Portugal?
The scope of PT4135830 depends on claim breadth, typically aligning with similar innovation patents. Broader claims provide wider coverage but face higher invalidity risks, comparable to other high-value pharma patents.

2. Can a generic company challenge the validity of PT4135830?
Yes. Generic firms can initiate patent oppositions or validity challenges based on prior art, lack of inventive step, or insufficient novelty.

3. What strategies can patent holders use to expand protection for PT4135830?
Filing secondary patents on formulations, methods of use, or specific polymorphs enhances protection layers and extends market exclusivity.

4. How does Portugal's patent system handle patent term extensions for pharmaceuticals?
Patent terms are generally 20 years from filing, with possible extensions via SPCs (Supplementary Protection Certificates) in the EU, including Portugal.

5. Is PT4135835830 enforceable outside Portugal?
If filed via PCT or EPO, the patent can be validated in multiple jurisdictions, but enforcement depends on each jurisdiction's legal proceedings and patent validity.


Sources:

  1. INPI Portugal Patent Database (https://inpi.justica.gov.pt/)
  2. European Patent Office (EPO) Public Patent Data (https://espacenet.com/)
  3. European Patent Convention and Regulations
  4. Portuguese Patent Law (Lei n.º 2/2007)
  5. WIPO Patent Laws and Practice

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