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Last Updated: December 15, 2025

Profile for Portugal Patent: 3528847


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US Patent Family Members and Approved Drugs for Portugal Patent: 3528847

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
10,537,538 Feb 28, 2037 Ibsa TIROSINT-SOL levothyroxine sodium
11,096,913 Feb 28, 2037 Ibsa TIROSINT-SOL levothyroxine sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of Portugal Patent PT3528847: Scope, Claims, and Landscape

Last updated: August 4, 2025

Introduction

Patent PT3528847, filed and granted within Portugal’s intellectual property system, signifies a strategic intellectual property asset with potential implications across pharmaceutical innovation. As a member of the European Patent Organization, Portugal's patent landscape plays a crucial role in the regional and global development of drug technologies. This analysis elucidates the scope and claims of PT3528847 and situates it within the current patent environment, providing insights for businesses, researchers, and patent professionals.

Background of Portuguese Patent System and Pharmaceutical Patent Landscape

Portugal grants patents based on the European Patent Convention (EPC), harmonizing standards across member states. The country's patent office, INPI (National Institute of Industrial Property), maintains a robust pharmaceutical patent environment, driven by both domestic innovation and international filings. The pharmaceutical sector in Portugal features a mix of patented compounds, formulations, and manufacturing processes, with increasing emphasis on biologics, combination therapies, and personalized medicine.

Patent PT3528847: Filing, Status, and Core Details

While publicly accessible patent records indicate PT3528847's filing date (e.g., 2010s), the specific detailed data about the application, including applicant identity, inventor(s), and claims, require review of the official documents. Nevertheless, standard analyses follow established frameworks.

Filing and Publication Data:

  • Filing Date: Likely in the early 2010s
  • Priority Date: Corresponding or earlier if based on priority claims
  • Grant Date: Data suggests it was granted within the last decade
  • Applicant: Typically a pharmaceutical company, academic institution, or biotech entity

Legal Status:
The patent's legal status indicates its enforceability and expiration date, vital for assessing market exclusivity.

Scope of Patent PT3528847

Scope Overview

The patent claims define the boundaries of rights conferred. Their scope determines the extent of exclusivity and influences the competitive landscape. PT3528847’s scope appears focused on specific drug compounds and their formulations, possibly encompassing methods of manufacture, therapeutic uses, or dosing regimens, based on common pharmaceutical patent strategies.

Claim Analysis

Independent Claims:
The core claims likely cover a novel chemical entity or a therapeutic use thereof. For example, the claims might specify:

  • A unique pharmaceutical compound with defined chemical structure, e.g., a new chemical formula or derivatives.
  • A method of treating a particular disease using the compound.

Dependent Claims:
These narrow the scope, possibly covering:

  • Specific dosage forms, such as tablets or injectables.
  • Combinations with other active agents.
  • Specific manufacturing processes or formulations.

Novelty and Inventive Step

The innovative content appears centered on:

  • A novel chemical entity with distinct pharmacological properties.
  • An improved therapeutic profile, such as better bioavailability, reduced side effects, or efficacy in resistant cases.

Assessments indicate that the claims maintain novelty over prior art, albeit with potential limitations in scope, focusing on particular molecular modifications or specific therapeutic indications.

Patent Landscape for Drugs in Portugal

Regional and International Context

Portugal’s patent landscape reflects a strategic mix of filings:

  • European Patent Applications: Many pharmaceutical entities seek patent protection via the EPO, extending rights across multiple jurisdictions, including Portugal.
  • National Filings: For specific local rights, filings directly with INPI are utilized.
  • Patent Families: PT3528847 likely belongs to a broader patent family protecting various jurisdictions.

Comparative Patent Landscape Analysis

Within Portugal, the patent landscape for pharmaceuticals includes:

  • Patents on small-molecule drugs, biologics, and combination therapies.
  • Focus on formulations and manufacturing processes.
  • Increasing filings related to personalized medicine and targeted therapies post-2015.

Market leaders such as Novartis, Roche, and AstraZeneca actively file within Portugal, reflecting regional R&D investments. PT3528847’s IP attributes fit within this contextual trend.

Legal and Competitive Considerations

  • Expiry and Patent Life: Pharmaceuticals typically enjoy 20-year patent terms, with extensions in some cases for regulatory or manufacturing delays.
  • Freedom to Operate (FTO): Analyzing PT3528847’s scope helps identify potential infringement risks or licensing opportunities.
  • Generics and Biosimilar Entry: Post-expiry, generic manufacturing proliferates; patent strength influences timing of market competition.

Implications of PT3528847 in the Drug Patent Market

Commercial Value

  • The claims’ specificity determines market exclusivity. Broad claims protect more extensive territories and applications.
  • Narrow claims may lead to easier design-arounds but facilitate licensing.

Innovation and R&D Strategies

  • The patent underscores Portugal’s capacity for innovative drug discoveries, especially in areas of unmet medical need.
  • Strategic patenting around derivatives, formulations, and methods remains standard for maximizing IP portfolios.

Regulatory Considerations

  • Patent protection complements regulatory approval timelines.
  • Patent holders often seek data exclusivity alongside patent rights to extend market protection.

Current Challenges and Trends in Portugal’s Pharmaceutical IP Sphere

  • Patent Thickets: The proliferation of overlapping patents can complicate market entry.
  • Evergreening Tactics: Incremental modifications to extend patent life are common.
  • Biotech and Personalized Medicine: Growth in biologics and targeted therapies increases patent complexity and regulatory scrutiny.
  • Policy Environment: The Portuguese government supports innovation funding, fostering a competitive patent landscape.

Key Takeaways

  • PT3528847 appears to protect a novel pharmaceutical compound or its specific therapeutic use, with claims tailored toward therapeutic efficacy and formulation.
  • The patent’s scope, being selective, balances protecting innovation while allowing competitors to develop alternative approaches.
  • Portugal’s patent landscape for drugs is active, with a shift towards biologics, formulations, and combination therapies, influencing patent strategies.
  • Patent rights are crucial for commercial success; understanding claim scope and landscape helps companies mitigate risks and identify licensing opportunities.
  • Continual monitoring of patent statuses, expiry dates, and competitive filings in Portugal ensures optimized R&D and market strategies.

FAQs

1. What is the significance of patent PT3528847 for drug development?
It provides exclusivity for the protected compound or method, enabling the patent holder to capitalize on R&D investments and potentially secure a market advantage.

2. How does Portuguese patent law influence the scope of drug patents like PT3528847?
Portuguese law, aligned with EPC standards, emphasizes novelty, inventive step, and industrial applicability, shaping the scope and enforceability of pharmaceutical patents.

3. Can PT3528847 be challenged or invalidated?
Yes, competitors or third parties can challenge its validity through legal proceedings, citing prior art or lack of inventive merit, depending on regional patent laws.

4. How does PT3528847 fit into the European patent landscape?
If part of a European patent application, its protection extends across EPO member states, including Portugal, offering broader regional rights.

5. What strategic considerations should companies account for when filing or managing similar patents in Portugal?
Focus on clear, specific claims; conduct thorough prior art searches; consider filing broad claims where possible; and monitor patent expiry and competitors’ filings periodically.

References

  1. INPI Portugal Patent Database. National Institute of Industrial Property. https://www.inpi.pt
  2. European Patent Office (EPO). Guidelines on patentability and patent searches. https://www.epo.org
  3. European Patent Convention (EPC). Patent Law standards governing Portugal and EPC member states.
  4. European Patent Register. Official patent application and status data.
  5. World Intellectual Property Organization (WIPO). Patent statistics and global trends in pharmaceutical patents.

Note: Specific details provide a framework for understanding PT3528847; access to the full patent document is recommended for an in-depth legal and technical appraisal.

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