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Last Updated: March 14, 2026

Profile for Portugal Patent: 3523302


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US Patent Family Members and Approved Drugs for Portugal Patent: 3523302

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 Apr 10, 2038 Eli Lilly And Co RETEVMO selpercatinib
⤷  Get Started Free Apr 10, 2038 Eli Lilly And Co RETEVMO selpercatinib
⤷  Get Started Free Apr 10, 2038 Eli Lilly And Co RETEVMO selpercatinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Portugal Patent PT3523302: Scope, Claims, and Landscape Analysis

Last updated: February 27, 2026

What is the scope of patent PT3523302?

Patent PT3523302 covers a specific pharmaceutical composition, method of treatment, or process related to a particular drug or therapeutic application. It is a Portuguese national patent, likely corresponding to an international patent application that has been granted in Portugal. The scope encompasses:

  • The formulation or composition of the drug, including active ingredients, excipients, or delivery mechanisms.
  • The therapeutic method or treatment regimen utilizing the composition.
  • Manufacturing processes associated with the drug.

Since Portugal is a member of the European Patent Convention (EPC), the patent's scope aligns with broader European patent principles, but actual claims are limited to what is granted within Portugal.

What are the claims of patent PT3523302?

The patent's claims define the legal boundaries of the patent protection. These include:

  • Independent claims: Cover broad aspects, such as the composition or method. They outline the essential features of the invention.
  • Dependent claims: Refine or specify particular embodiments, formulations, or process details.

[Note: Exact claim language would require access to the patent document; the following is a typical structure.]

Sample Claim Types

  • A pharmaceutical composition comprising [specific active compounds], in a defined ratio, for use in the treatment of [disease].
  • A method of manufacturing the composition involving [specific steps].
  • Use of a compound or composition for treating a specific condition.

Claim Constraints

  • The claims are often limited in scope to specific chemical entities or methods, with narrower claims aiming to protect particular formulations.
  • Broad claims may be vulnerable to validity challenges if prior art discloses similar compositions or methods.

Patent landscape analysis

International and European Filing Strategy

Assuming the patent originates from an application filed under the Patent Cooperation Treaty (PCT) or via the European Patent Office, the landscape includes:

  • Priority filings: Potential priority from applications in other jurisdictions such as the US, EP, or WO applications.
  • Regional protection: Claims may overlap with European patents or equivalents in key markets (US, China, Japan).

Major competitors and patent owners

  • Pharmaceutical companies: Likely originators of the patent, possibly involved in innovative therapeutics or formulations.
  • Patent clusters: The patent landscape shows multiple filings in Europe, notably in the EPO patent database, often in relation to similar compounds or treatment methods.

Patent lifecycle and status in Portugal

  • PT3523302 has specific filing and grant dates. The typical patent term lasts 20 years from filing, subject to maintenance fees.
  • Maintenance status can be checked through the Portuguese Patent Office (INPI) database. As of 2023, the patent remains active if annual fees are paid.

Patent litigation and freedom-to-operate (FTO)

  • Potential infringement issues depend on similar patents in the same field.
  • The FTO analysis involves examining overlapping claims with third-party patents.

Complementary patent data sources

  • INPI Portugal database
  • European Patent Office (EPO) Espacenet
  • World Intellectual Property Organization (WIPO) PATENTSCOPE

How does PT3523302 compare to similar patents?

  • The scope may be narrower or broader, depending on claim wording.
  • Similar patents in the same therapeutic area may cluster around specific chemical entities, formulations, or delivery techniques.
  • Patent families in multiple jurisdictions provide broader protection and market leverage.

Key considerations for stakeholders

  • Patent validity: Validation depends on local patent laws and prior art.
  • Patent expiry: Evaluate deadlines for renewal and potential design-around opportunities.
  • Licensing and enforcement: Opportunities to license or litigate depend on patent strength and market dynamics.

Key Takeaways

  • PT3523302 covers a specific pharmaceutical composition or therapy within Portugal, with claims likely focusing on active ingredients, formulations, or treatment methods.
  • The patent claims define the scope and are crucial for competitive positioning and legal enforcement.
  • The broader patent landscape includes filings in Europe and other jurisdictions, with active patent families and potential for patent challenges.
  • The patent's strength depends on claim breadth, prior art, and maintenance status.

FAQs

1. How can I determine the validity of PT3523302?

Review the patent claims against prior art, assess the novelty, inventive step, and industrial applicability, and analyze if any prior art disclosures overlap with the claimed invention.

2. What are the main factors that influence patent scope in pharmaceuticals?

Chemical specificity, formulation details, therapeutic methods, and manufacturing processes determine the breadth or narrowness of claims.

3. How does the patent landscape impact market entry?

Strong, broad patents restrict third-party entry; narrow or weak patents open opportunities for competitors or generics.

4. Can PT3523302 be extended beyond Portugal?

Yes. Filing divisional patents or patent families in other jurisdictions (e.g., EPO, US, China) expands regional protection.

5. What are the typical timelines for patent protection in pharmaceuticals?

Patents generally last 20 years from filing date, subject to maintenance payments; development and regulatory approval timelines can impact effective market exclusivity.


References

[1] European Patent Office. (2023). Espacenet patent database. Retrieved from https://worldwide.espacenet.com

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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.