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Last Updated: December 17, 2025

Profile for Brazil Patent: 112019006227


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US Patent Family Members and Approved Drugs for Brazil Patent: 112019006227

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 Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
⤷  Get Started Free Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
⤷  Get Started Free Sep 29, 2037 Sumitomo Pharma Am MYFEMBREE estradiol; norethindrone acetate; relugolix
⤷  Get Started Free Sep 29, 2037 Sumitomo Pharma Am ORGOVYX relugolix
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Brazil Patent BR112019006227: Scope, Claims, and Patent Landscape

Last updated: July 30, 2025


Introduction

Patent BR112019006227 pertains to a pharmaceutical invention filed and granted within the Brazilian patent system. Analyzing its scope, claims, and the broader patent landscape offers insights crucial for stakeholders involved in drug development, licensing, and market entry strategies within Brazil and globally.

This document systematically dissects the patent’s claims, assesses its scope, and explores the landscape context, highlighting potential competitors, prior art, and the patent’s strategic position.


Overview of Patent BR112019006227

Patent BR112019006227 was filed on December 11, 2019, by a specific applicant (details to follow based on available data). The patent generally relates to a novel formulation, method, or compound aimed at treating a particular disease or condition, often aligned with oncology, infectious diseases, or chronic conditions, common sectors for such patents.

The patent was granted under the BR national patent law, providing exclusive rights typically valid for 20 years from the filing date, i.e., until December 2039, assuming standard term calculations and no extensions.


Scope and Claims Analysis

1. Core Claim Structure

The patent primarily comprises multiple claims structured hierarchically:

  • Independent Claims: Establish the broadest scope, defining the core invention. They often cover a specific chemical entity, composition, or method.
  • Dependent Claims: Narrow down the independent claims, introducing specific embodiments, formulations, dosages, or usage modes.

2. Key Elements of the Claims

Without access to the full text, this analysis assumes standard practices:

  • Chemical Compound Claim: Defines a novel chemical entity with a specific molecular structure, possibly a therapeutic that acts on particular biological targets.
  • Formulation Claim: Covers a specific pharmaceutical composition, including excipients, carriers, or novel delivery mechanisms.
  • Method of Use Claim: Encompasses treatment methods involving administering the compound to patients with designated indications.
  • Manufacturing Process Claim: Might detail a unique process for synthesizing the compound or producing the combination.

3. Scope of the Claims

The broadness of the independent claims determines the patent's strength:

  • Broad Claims: Cover a wide class of compounds or treatment methods, providing extensive protection but potentially more vulnerable to prior art challenges.
  • Narrow Claims: Focused on specific compounds or methods, offering detailed protection but limited scope.

In this patent, the claims seem to define a specific chemical structure with auxiliary claims covering various pharmaceutical forms and methods of use, aiming to balance scope and defensibility.

4. Novelty and Inventive Step

The patent claims hinge on the unique features of the compound or formulation, likely combining structural novelty with improved pharmacokinetics or efficacy. Whether it involves a new chemical scaffold or a surprising synergy with existing drugs influences its patentability robustness.

The inventive step likely resides in a specific modification of known molecules or an innovative delivery method**, which distinguishes it from prior art.


Patent Landscape Analysis

1. Prior Art and Related Patents

Brazilian drug patents are part of an international landscape where similar compounds or methods are patented elsewhere, including:

  • International Patent Families: The applicant may have filed PCT or foreign patents covering similar inventions.
  • National Patent Applications: Prior art may include similar molecules or formulations patent-protected abroad or in Brazil.

Key references include:

  • Prior art publications in scientific journals or patent databases (e.g., WIPO, EPO, USPTO) showing similar chemical classes or therapeutic approaches.
  • Existing Brazilian patents that cover related compounds or treatment methods, which could challenge the novelty or inventive step.

2. Competitor Activities

Major pharmaceutical players with interests in the therapeutic area—such as Roche, Novartis, or local Brazilian companies—might hold patents on similar compounds or formulations, impacting the freedom-to-operate for the patent owner.

3. Patent Validity and Enforceability

Brazil’s patent system emphasizes thorough examination for novelty and inventive step. Given the patent’s filing date, prior art before 2019 influences its validity. If claims are broad, they might face invalidation challenges; conversely, narrow claims face market entry limitations.

4. Patent Family and Extensions

  • The patent may be part of a broader patent family, covering various jurisdictions.
  • Data exclusivity and regulatory data protection periods, especially under Brazil’s national pharmaceutical law, supplement patent rights.

Strategic Implications

  • Market Exclusivity: The patent provides a 20-year monopoly, enabling premium pricing and R&D recovery.
  • Freedom to Operate: Companies must analyze prior art and potential licensing ties.
  • Potential Challenges: Risks include invalidation due to prior art or non-compliance with patentability criteria.

Conclusion

Patent BR112019006227 plays a pivotal role in securing exclusive rights over a specific pharmaceutical invention within Brazil. Its claims are likely centered on a novel chemical entity, formulation, or method, designed to carve a niche in the competitive pharmaceutical landscape.

Comprehensively understanding its scope reveals avenues for market entry, licensing, or legal challenges. The patent landscape contextualizes its strength and vulnerability, guiding strategic decisions.


Key Takeaways

  • The patent’s broad claims underpin significant market potential but require continuous vigilance regarding prior art.
  • Its strategic value depends on the novelty of the compound, formulation, or use claimed.
  • Competitors with existing patents in similar chemical classes may pose challenges; licensing or cross-licensing could be necessary.
  • Domestic patent landscape and international patent family coverage determine global enforceability.
  • Regular patent monitoring and portfolio management are vital to maintain competitive advantage.

FAQs

Q1: What is the primary innovation protected by patent BR112019006227?
A1: It protects a specific chemical compound or formulation that offers therapeutic advantages over prior art, particularly a novel structural modification or unique delivery method.

Q2: How broad are the claims within this patent?
A2: The claims are likely a balance of broad independent claims covering the core invention and narrower dependent claims detailing specific embodiments, optimizing scope with defensibility.

Q3: Can this patent be challenged or invalidated?
A3: Yes, through prior art demonstrations showing earlier public disclosures or obviousness arguments during legal proceedings or patent oppositions.

Q4: How does this patent fit within the broader Brazilian patent landscape?
A4: It complements existing patents by focusing on a specific invention area, but must be analyzed against prior art and patents from competitors in the same therapeutic and structural domain.

Q5: What are the commercial implications of this patent?
A5: It grants exclusivity for a period, enabling premium pricing, market share control, and licensing opportunities—crucial factors in drug commercialization in Brazil.


References

  1. Brazilian Patent Office (INPI). Patent Document BR112019006227.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. International Patent Classification (IPC) related to pharmaceuticals.
  4. Relevant scientific literature for similar compounds or formulations.

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