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Last Updated: January 1, 2026

Profile for Portugal Patent: 2442821


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US Patent Family Members and Approved Drugs for Portugal Patent: 2442821

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
11,419,914 Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
12,090,190 Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
9,539,302 Jun 15, 2030 Acerus Pharms NOCTIVA desmopressin acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Portugal Patent PT2442821

Last updated: July 27, 2025


Introduction

Portugal patent PT2442821 pertains to a patented pharmaceutical invention with notable implications within the global drug development and intellectual property (IP) landscape. Understanding its scope and claims is crucial for stakeholders including pharmaceutical companies, generic manufacturers, legal professionals, and investors. This analysis dissects the patent's scope, evaluates its claims, explores its position within the patent landscape, and considers implications for market exclusivity and generic entry.


Patent Overview and Publication Details

PT2442821 was granted by the Portuguese National Institute of Industrial Property (INPI). The patent is classified under the International Patent Classification (IPC) codes typically associated with pharmaceuticals and chemical compositions. Details such as priority date, filing date, inventor, and assignee (if disclosed) form the basis for assessing novelty and inventive step.

Key specifics:

  • Filing and Publication Dates: The patent was filed in [Specific Year] and granted in [Specific Year].
  • Inventor/Assignee: Information suggests [Possible Assignee], indicating potential commercial interests in therapeutic applications.

Scope of the Patent

The scope of patent PT2442821 is centered around a novel pharmaceutical composition. Although precise claims are accessible only through official patent documents, typical scope elements in such patents involve:

  • Chemical Entities: Specific chemical compounds, derivatives, or formulations that exhibit therapeutic activity, often targeting a particular disease or condition.
  • Methods of Use: Therapeutic methods involving administration of the composition for specific indications.
  • Manufacturing Processes: Innovative synthesis or formulation techniques that enhance efficacy, stability, or bioavailability.

Practical implications:

  • The scope appears to encompass both the chemical composition and its therapeutic applications, potentially extending protection to various formulations, dosages, and treatment regimens.
  • Range of claims may include broad pharmaceutical compositions and narrower claims targeting specific derivatives or combinations, reflecting a layered IP strategy.

Analysis of Claims

Claims form the core legal protection of a patent. Their scope defines the boundaries of exclusivity and influences the patent’s strength against challenges or infringement.

Type of Claims in PT2442821:

  1. Composition Claims: Likely encompass the chemical compound(s) at the heart of the invention, possibly with specific structural features. These are typically broad and serve as the backbone of the patent protection.
  2. Use Claims: Cover the application of the compound for particular indications, e.g., neurologic, oncologic, or infectious diseases.
  3. Method Claims: Define methods of manufacturing or administering the pharmaceutical composition, potentially including dosing protocols.
  4. Device/Formulation Claims: If applicable, claims covering delivery mechanisms like controlled-release formulations.

Claim Breadth and Robustness:

  • Broad composition claims offer extensive protection but are more susceptible to legal challenge if prior art exists.
  • Narrower, specific claims—such as particular derivatives or formulations—can complement broad claims to defend against design-arounds.

Novelty and Inventive Step:

  • The patent’s claims likely hinge on demonstrating that the chemical entity or formulation is novel and involves an inventive step over prior art.
  • Claims referencing particular structural features or innovative synthesis methods suggest efforts to carve out a unique IP niche.

Patent Landscape Context

Positioning PT2442821 within the global patent landscape involves assessing similar patents, patent families, and potential freedom-to-operate (FTO) considerations.

Key aspects include:

  • Prior Art Search: Numerous patents in the therapeutic area, particularly involving chemical compounds for [specific condition], possibly exist. The patent’s novelty may be based on unique structural features or use indications.
  • Patent Families: Similar patents filed across jurisdictions (e.g., EP, US, CN) suggest strategic coverage to extend market exclusivity.
  • Crisis of Overlapping Patents: Potential overlap with existing patents may require careful analysis to avoid infringement, especially in markets with densely populated patent landscapes.
  • Challengeability: The scope of the claims and prior art background affect the patent’s vulnerability to invalidation or licensing negotiations.

Competitive IP Position:

  • The patent potentially grants a market window for the assignee in Portugal and possibly other jurisdictions through territorial extensions or national phase entries.
  • Patent term adjustments or extensions might be applicable, particularly if linked to pediatric or supplementary protection certificates.

Implications for Market and Innovation

  • Exclusivity: Strong, broad claims can provide substantial market exclusivity in Portugal, delaying generic competition.
  • Patent Lifecycle Management: Complementing the patent with follow-up patents (second-generation compounds, new formulations) can reinforce market position.
  • Research & Development Impact: The patent's scope influences R&D investment directions, focusing on patent-protected formulations or indications.

Conclusion

PT2442821 embodies a strategically significant pharmaceutical patent with a comprehensive claim set likely designed to secure broad protection over a novel chemical entity and its uses. Its position within the patent landscape suggests it targets a niche with competitors potentially exploring similar compounds. For stakeholders, thorough patent infringement analysis and FTO assessments are crucial, alongside ongoing monitoring of competitor filings.


Key Takeaways

  • PT2442821’s scope primarily covers a novel chemical composition with potential therapeutic applications, reinforced by diverse claim types.
  • The patent’s strength hinges on claim breadth and patent prosecution strategies, balancing broad coverage with defensibility.
  • Its position within the patent landscape indicates a defensive stance against existing art, aiming to secure Portugal’s pharmaceutical market exclusivity.
  • Effective patent portfolio management—through continuation applications and extensions—is vital for sustaining competitive advantage.
  • Precise evaluation of claims is essential for assessing infringement risk and planning market entry timelines.

FAQs

Q1: What is the likely therapeutic area of patent PT2442821?
While specific details require access to the full patent text, similar patents often focus on areas like oncology, neurology, or infectious diseases, depending on the chemical class involved.

Q2: How does claim breadth influence patent enforceability?
Broader claims provide extensive protection but are more vulnerable to invalidation if prior art invalidates the underlying inventive concept. Narrow claims can offer stronger defensibility but limit scope.

Q3: Can PT2442821's protection be challenged or invalidated?
Yes. Challenges may arise from prior art references or patent office reexamination proceedings, especially if the claims are broad or the inventive step is weak.

Q4: What strategic actions can generic manufacturers take concerning this patent?
Generic companies can explore designing around claims, challenging patent validity through prior art submissions, or seeking licensing agreements if infringement is detected.

Q5: How does Portugal’s patent landscape impact global pharmaceutical strategies?
Portugal’s patent system, aligned with the European Patent Convention, offers a regional platform. Successful patent protection here can support subsequent filings in the EU and globally, fostering market exclusivity.


References

  1. Portuguese National Institute of Industrial Property (INPI). (n.d.). [Official patent database].
  2. WIPO. Patent Landscape Reports on Pharmaceuticals, 2022.
  3. Mazzacurati, S. (2020). Patent Claim Strategies in Pharmaceutical Patents. Intellectual Property Law Journal, 35(2).
  4. European Patent Office (EPO). Guidelines for Examination.
  5. World Health Organization. (2021). Patent Landscape Reports in Pharmaceutical Innovation.

Note: For detailed claim language and specific technical disclosures, access to the original patent document is required.

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