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Last Updated: December 15, 2025

Profile for Portugal Patent: 2736510


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US Patent Family Members and Approved Drugs for Portugal Patent: 2736510

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 Jul 27, 2032 Commave Therap AZSTARYS dexmethylphenidate hydrochloride; serdexmethylphenidate chloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Portugal Patent PT2736510: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Patent PT2736510 represents an essential intellectual property asset within Portugal’s pharmaceutical patent landscape. This patent, granted by the Portuguese Institute of Industrial Property (INPI), likely covers a novel drug compound, formulation, or delivery system. An in-depth assessment of PT2736510’s scope and claims provides insights into its innovation, strategic positioning, and competitive landscape within the national and broader European pharmaceutical markets. This analysis offers a detailed examination of the patent's scope, claims, legal strength, and its context within Portugal’s patent environment.


Scope of Patent PT2736510

The scope of a patent defines the extent of legal protection conferred and indicates the boundaries within which competitors cannot operate without risking infringement. PT2736510’s scope depends primarily on its claims, which establish the boundaries of the invention.

Nature of the Patent

Based on typical pharmaceutical patents filed in Portugal, PT2736510 likely protects:

  • A specific chemical compound or molecule with therapeutic activity.
  • A novel formulation enhancing stability, bioavailability, or shelf life.
  • An innovative method of manufacturing or administering the drug.
  • A combination therapy involving known drugs but with a novel synergistic effect.

Scope Considerations

In Portugal, patent protection for pharmaceuticals can be broad or narrowly tailored:

  • Product Claims: Cover particular chemical entities, their salts, stereoisomers, or derivatives.
  • Formulation Claims: Encompass specific delivery forms like sustained-release tablets, emulsions, or injectables.
  • Process Claims: Include unique synthesis routes or purification steps.
  • Use Claims: Cover specific therapeutic applications.

Assuming PT2736510 claims a chemical compound or a specific formulation, the scope will hinge upon the patent's breadth—whether it claims a broad class of compounds or a very specific molecule.


Claims Analysis

The core of PT2736510’s legal protection resides in its claims. These delineate the scope and are categorized as independent and dependent claims.

Independent Claims

Typically, the independent claims set forth the broadest protection, often covering:

  • A novel chemical compound with a defined molecular structure.
  • A specific pharmaceutical composition, including active ingredients and excipients.
  • A unique method of treatment using the compound or composition.

Example: "A pharmaceutical composition comprising compound X, characterized by its specific chemical structure, for the treatment of disease Y."

The claims are expected to contain:

  • Structural Limitation: Precise chemical structures, usually with R-groups or substituents.
  • Functional Limitation: The intended biological activity or therapeutic effect.
  • Methodology Limitation: Steps for synthesis or administration, if claimed.

Dependent Claims

Dependent claims narrow the scope and specify particular embodiments, such as:

  • Specific salts or stereoisomers of the compound.
  • Variations in formulation excipients.
  • Alternative dosages or delivery methods.
  • Specific patient populations or therapeutic protocols.

Claim Scope and Potential Breadth

The patent's strategic strength lies in whether the claims are broad or narrow. Broad claims increase market exclusivity, but they face higher scrutiny and vulnerability to invalidation during examination or litigation. Narrow claims, whilst safer, limit commercial scope.

Assuming PT2736510's claims are well-drafted, they likely balance breadth with specificity, covering a class of compounds or formulations rather than a single molecule, thus providing meaningful market protection.


Patent Landscape for Portugal and European Context

Portugal's patent environment is harmonized with the European Patent Convention (EPC), allowing similar standards for pharmaceutical patenting as in other EPC member states. The landscape involves:

Major Patent Families

  • International patent filings under the Patent Cooperation Treaty (PCT) expanding protection beyond Portugal.
  • European patents obtained via the European Patent Office (EPO) with validations in Portugal.
  • National patents like PT2736510 that provide direct protection within Portugal.

Competitive Landscape

Portugal’s pharmaceutical patent landscape features:

  • Local Innovators: Portuguese biotech firms focusing on niche therapies.
  • Multinationals: Major pharmaceutical companies filng patents for emerging drugs or formulations.
  • Research Collaborations: University-industry partnerships contributing to innovation pipelines.

Patentability and Novelty Requirements

PT2736510’s novelty and inventive step are critical. The patent examiner would assess:

  • Prior art disclosed in global patent databases (EPO, USPTO, WIPO).
  • Similar molecules or formulations in scientific literature.
  • Whether PT2736510’s claims demonstrate a significant inventive advance.

Assuming PT2736510 was granted, it suggests that the claims overcame prior art rejections, reflecting a suitable balance of novelty and inventive step in Portugal's legal environment.

Legal and Regulatory Framework

  • Data Exclusivity: Protected under EU regulations, with data exclusivity up to 8 years.
  • Supplementary Protection Certificates (SPCs): Potential to extend patent life for patented drugs beyond 20 years, compensating for regulatory approval delays.

Implications for Stakeholders

  • Innovators/Patent Holders: PT2736510 provides a strategic barrier to entry within Portugal, supporting exclusivity and market positioning.
  • Competitors: Must navigate around the claims by developing alternative compounds, formulations, or delivery systems.
  • Legal Enforcers: The claims guide enforcement actions against infringers, emphasizing active ingredients or methods detailed in the patent.
  • Regulators and Marketers: Recognize patent expiration dates, which influence timing of market entry and generic competition.

Future Outlook and Strategic Considerations

  • Patent Maintenance: Regular renewal fees and vigilant monitoring for potential infringements.
  • Potential Challenges: Opposition or invalidation actions based on alleged prior art or non-compliance issues.
  • Patent Extensions: Use of SPCs to extend effective market exclusivity.
  • Global Strategy: Filing similar patents internationally to prevent market leakage beyond Portugal.

Key Takeaways

  • PT2736510 likely claims a novel pharmaceutical compound or formulation with specific structures and use indications.
  • Its scope hinges upon the breadth of its independent claims, balancing broad protection and patentability standards.
  • The patent landscape in Portugal is integrated within the European system, enabling strategic protection through national and regional filings.
  • Maintaining robust patent strategies including potential SPC filings can prolong market exclusivity.
  • Competitors must navigate around the specific claims, emphasizing the importance of thorough patent drafting and monitoring.

FAQs

1. What is the typical scope of pharmaceutical patents like PT2736510 in Portugal?
Pharmaceutical patents generally cover active compounds, formulations, methods of preparation, and therapeutic uses. The scope depends on the claims’ structure—broad claims protect a chemical class, while narrow claims focus on specific compounds.

2. How does Portugal’s patent system influence patent protection for drugs?
Portugal, as part of the EPC, requires patents to meet novelty, inventive step, and industrial applicability standards. The system allows for national patents and European patents validated stateside, with mechanisms like SPCs to extend protection.

3. Can PT2736510 be challenged or invalidated after grant?
Yes. Oppositions or nullity actions can challenge its validity based on prior art, insufficient disclosure, or non-compliance with formalities. Patent enforcement involves monitoring and potentially legal action.

4. How does patent PT2736510 impact generic drug development in Portugal?
The patent grants exclusivity, preventing generics from entering the market for its duration unless the patent is invalidated or expires. Patent duration, including SPCs, determines the timeline for generic entry.

5. What strategic moves should patent holders consider for PT2736510?
Continual portfolio management, potential SPC extensions, monitoring patent infringements, and considering international filings to extend exclusivity are crucial strategic actions.


References

  1. Portuguese Institute of Industrial Property (INPI). Patent Database. [Online].
  2. European Patent Office (EPO). Patent Law and Practice. [Online].
  3. European Commission. Patent protection and data exclusivity rules. [Online].
  4. WIPO. International Patent Filings and Strategies. [Online].

Note: This analysis assumes typical characteristics of pharmaceutical patents in Portugal and general practices based on available information. Specific details of PT2736510 claims and description are available within the official patent documentation for precise scope and legal interpretations.

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