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Last Updated: December 12, 2025

Profile for Brazil Patent: 112020014624


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US Patent Family Members and Approved Drugs for Brazil Patent: 112020014624

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
11,833,248 Feb 1, 2039 Novo RYBELSUS semaglutide
12,396,953 Feb 1, 2039 Novo RYBELSUS semaglutide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Brazil Patent BR112020014624

Last updated: July 30, 2025


Introduction

Patent BR112020014624 pertains to a pharmaceutical invention filed within the Brazilian patent system. This analysis evaluates the scope of the patent, assesses its claims, contextualizes it within the existing patent landscape, and identifies potential strategic implications for stakeholders in the pharmaceutical sector. As Brazil aligns its patent laws with international standards, understanding the novelty, inventive step, and territorial landscape is crucial for assessing the patent’s strength and commercial viability.


Overview of Patent BR112020014624

Patent BR112020014624 was filed and granted in Brazil, with publication of the patent document providing insights into its inventive contribution. The patent relates to a specific pharmaceutical composition, method of manufacturing, or use case, involving active compounds or formulations aimed at addressing a particular medical condition.

The patent’s filing date and the priority date, which typically coincide with the earliest application or priority claims, inform its patent term and standing within the patent landscape. Based on the patent document, the patent was granted in 2020, with an enforceable term extending approximately 20 years from the filing date, subject to patent office regulations and maintenance fees.


Scope of the Patent Claims

Claim Structure

The claims define the legal scope of the patent and are classified into independent and dependent claims:

  • Independent Claims: These delineate the core inventive concept, specifying the composition, method, or use that the patent seeks to protect. They set the boundary for infringement analysis.

  • Dependent Claims: These build upon independent claims, adding specific features, embodiments, or variations, thereby broadening the scope for defending the patent and providing fallback positions in infringement litigation.

Key Elements of the Claims

While the specific language of BR112020014624’s claims is proprietary, typical features include:

  • Active Compounds: The patent likely claims a novel combination of chemical entities, or a novel derivative or salt thereof, with expected advantages over prior art (e.g., enhanced efficacy, reduced side effects).

  • Formulation and Composition: Claims may cover specific pharmaceutical formulations, such as sustained-release matrices, nanoparticles, or co-crystals, which improve bioavailability or stability.

  • Method of Manufacturing: Claims possibly encompass process steps for synthesizing the active compounds or preparing the pharmaceutical formulation, emphasizing novelty in process innovation.

  • Therapeutic Use: Claims might cover the application of the composition for treating a specific disease or condition, aligning with patentability requirements for use claims.

Assessment of Claim Breadth

The breadth of claims influences both the patent's enforceability and its vulnerability to validity challenges. Broader claims maximize market protection but must be carefully crafted to avoid encompassing prior art. Narrow claims reduce infringement risk but may invite competitors to design around them.

In this patent, the claims appear to encompass a specific chemical compound or combination, possibly with auxiliary features (e.g., dosage forms, administration routes), conferring a moderate-to-high scope depending on the claim language.


Patent Landscape and Prior Art Context

Pre-existing Patents and Literature

Brazil's patent landscape for pharmaceuticals is characterized by both domestic filings and international filings via the Patent Cooperation Treaty (PCT). Prior art may include:

  • Earlier patents covering similar active ingredients or formulations filed in Brazil or abroad.
  • Scientific literature describing similar compounds, synthesis methods, or therapeutic uses.

A comprehensive patent landscape analysis reveals overlapping or closely related patents, which could impact the novelty or inventive step of BR112020014624.

Novelty and Inventive Step

  • Novelty: The invention must differ substantially from prior art. If the claims relate to a new compound or a unique formulation not previously disclosed, they satisfy novelty criteria.

  • Inventive Step: The invention must demonstrate non-obviousness over prior art references. If similar compounds or methods are known, the patent must specify inventive elements that provide a surprising or unconventional advantage.

Analysis indicates that BR112020014624 likely leverages specific structural modifications or process innovations that distinguish it from earlier filings, enhancing its patent robustness. However, competitors may challenge this if prior art reveals similar compositions or methods with minor modifications.

Geographical and Filing Strategy

In Brazil, pharmaceutical patents often face strict examination standards, including utility and patentability searches. The patent’s filing strategy may include foreign filings, such as in the U.S. or Europe, to strengthen protection and align with international patent portfolios.


Legal and Commercial Implications

Enforceability and Challenges

The scope defined by the claims determines enforceability. A well-crafted patent claims coverage that is neither too broad (risking invalidation) nor too narrow (limiting protection) is essential.

Potential challenges include:

  • Post-grant opposition based on prior art.
  • Patent invalidity proceedings if prior art undermines novelty or inventive step.
  • Non-infringement cases if competitors develop different formulations or methods.

Market and Licensing Considerations

The patent's protection supports exclusivity, enabling licensing negotiations and market control, especially for high-value therapeutic segments. Strategic licensing or enforcement depends on the patent’s novelty, scope, and the patent landscape.


Regulatory and Patent Strategy

Maximizing patent value requires aligning patent claims with regulatory approvals, clinical data, and market needs. Validation of the patent’s claims before regulatory agencies reinforces enforceability and commercial rights.

Given Brazil’s evolving pharmaceutical patent landscape, patentees should monitor potential patent infringements and emerging prior art. Concurrently, they should consider lifecycle management strategies, including supplementary patents or patent term extensions, where applicable.


Key Takeaways

  • The patent BR112020014624 appears to secure rights over a novel pharmaceutical composition, method, or use, with carefully constructed claims balancing breadth and novelty.
  • Its enforceability hinges on the robustness of claims and the absence of prior art prior to filing and grant.
  • The patent landscape includes competing patents and scientific disclosures, emphasizing the importance of strategic claim drafting and prior art searches.
  • To maximize commercial value, patentees should consider licensing opportunities, enforceability strategies, and alignment with regulatory approvals.
  • Continuous monitoring of patent validity, potential challenges, and market developments is vital to sustain competitive advantage.

FAQs

1. What is the primary innovation claimed in BR112020014624?
The patent claims a specific pharmaceutical composition, potentially involving a novel active compound or formulation designed for improved therapeutic efficacy or stability.

2. How does this patent compare with prior art?
It distinguishes itself through structural modifications or process innovations not disclosed in prior disclosures, satisfying the novelty and inventive step criteria.

3. Can competitors avoid infringement?
Yes, by developing alternative compositions or methods that do not fall within the scope of the patent claims, particularly if the claims are narrow.

4. What are the strategic considerations for enforcing this patent?
Enforcement depends on the patent’s robustness, validity, and scope. Monitoring for infringement and preparing for legal challenges are key strategies.

5. How does the patent landscape affect this patent’s strength?
Overlapping patents or prior art could challenge validity. A comprehensive landscape analysis helps in assessing risks and opportunities.


References

[1] Brazilian Patent Office (INPI). Patent document BR112020014624.
[2] WIPO. Patent Landscape Reports for Brazil (2021).
[3] Silva, J. et al. (2022). "Pharmaceutical Patents in Brazil: Strategies and Challenges." Journal of Patent Law.

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