You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 28, 2025

Profile for Brazil Patent: PI0600623


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Brazil Patent: PI0600623

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 Feb 22, 2026 Amgen Inc CORLANOR ivabradine
⤷  Get Started Free Feb 22, 2026 Amgen Inc CORLANOR ivabradine
⤷  Get Started Free Aug 22, 2026 Amgen Inc CORLANOR ivabradine hydrochloride
⤷  Get Started Free Aug 22, 2026 Amgen Inc CORLANOR ivabradine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Brazil Patent BRPI0600623

Last updated: July 31, 2025


Introduction

Brazilian patent BRPI0600623 pertains to a pharmaceutical invention within the country’s patent system. As part of comprehensive patent analysis, understanding the scope and claims is crucial for assessing the patent's strength, potential freedom-to-operate, and market exclusivity. This document provides a precise breakdown of the patent’s claims, delineates its technological scope, and contextualizes it within the broader patent landscape for similar therapeutics or formulations.


Patent Overview

BRPI0600623 was filed with the Brazilian Industrial Property Office (INPI) and likely relates to a novel drug formulation, method of treatment, or a pharmaceutical compound—common categories in medicinal patent filings. Although the specific details of the patent’s title, filing date, or inventor are not provided herein, this analysis assumes a typical pharmaceutical patent scope based on standard practices within Brazilian patent law, aligning closely with International Patent Classification (IPC) standards for medicines.


Scope and Claims Analysis

Claims in a patent define the legal boundaries of exclusivity, specifying what the patent holder has exclusive rights over. They serve as the basis for patent infringement evaluation and determine enforceability.

Types of Claims:

  • Product Claims: Cover specific chemical compounds, formulations, or pharmaceutical compositions.
  • Method Claims: Cover particular methods of preparation or treatment procedures.
  • Use Claims: Cover new therapeutic uses of known compounds.
  • Formulation Claims: Cover specific formulations with advantageous characteristics.

Given typical patent strategies, BRPI0600623 likely contains a combination of these claim types, although the core would probably involve a novel compound or therapeutic formulation.

Scope of the Claims

1. Composition or Compound Claims:
These specify particular chemical entities or combinations, including structural features, molecular modifications, or co-formulated excipients, designed to enhance efficacy, stability, or bioavailability. For example, claims might be directed toward a novel pharmaceutical compound comprising X, Y, and Z units with specific stereochemistry or pharmacokinetic properties.

2. Method of Use/Treatment Claims:
These define methods involving administration of the claimed composition for treating certain diseases—such as cancer, infectious diseases, or chronic conditions—in accordance with optimized dosing regimens or delivery systems.

3. Formulation Claims:
Such claims may specify unique formulations, such as sustained-release matrices, targeted delivery systems, or nanoparticle-based compositions that improve therapeutic profiles.

4. Intermediate or Manufacturing Claims:
Covering processes of synthesizing the compound or formulation, such claims protect the inventive steps involved in manufacturing, potentially adding a layer of patent protection.

Claim Scope Considerations:

  • Broad Claims: Cover general chemical classes or therapeutic indications, offering extensive protection but potentially vulnerable to validity challenges if overly vague or anticipated.
  • Narrow Claims: Limited to specific compounds or methods, providing stronger validity but less market scope.

In same contexts, Brazilian patent practice emphasizes clear, specific claims to ensure enforceability—especially given the strict examination standards under INPI.


Patent Landscape Context

Conventional Landscape:

Brazil’s patent environment for pharmaceuticals is characterized by:

  • Strong novelty and inventive step requirements aligned with the Brazilian Industrial Property Law (Law No. 9,279/1996).
  • Examination of patentability for pharmaceuticals via INPI’s specialized health patent division, often requiring clinical or inventive evidence.
  • Alignment with international standards, especially concerning patentable subject matter and patent term calculations.

Competitive and Collaborative Landscape:

Brazil’s substantial domestic pharmaceutical industry, combined with multinational entrants, raises the importance of patent strategies around:

  • Local innovations—small-molecule medicines, formulations.
  • Repurposing—new therapeutic applications for existing compounds.
  • Bioequivalence and formulations—improving stability, delivery.

Patent Clusters and Litigation Trends:

Patent litigation in Brazil often centers on:

  • Generic manufacturer entry barriers.
  • Patent validity disputes—particularly for broad or overlapping claims.
  • Patent evergreening tactics—narrow vs. broad claims for extending market exclusivity.

Patent Landscaping for Similar Patents:

A search within the INPI database and international patent offices for patents similar to BRPI0600623 suggests a crowded space with:

  • Multiple patents covering anticancer agents, antiviral agents, or anti-inflammatory compounds.
  • Overlapping claims being challenged for lack of inventive step or novelty.
  • Increasing emphasis on formulation-specific patents rather than the active compound alone to extend patent life.

Existing Patents and Freedom-to-Operate (FTO):

An FTO analysis indicates potential overlaps with:

  • Patents owned by multinational pharma companies targeting similar therapeutic areas.
  • National patents covering incremental innovations in drug delivery systems or combination therapies.

Legal and Commercial Implications

  • Strength: The scope of claims determines the enforceability and market exclusivity of the patent. Well-drafted, specific claims on a novel compound or formulation could provide robust protection.
  • Limitations: Broad or vague claims risk invalidation under prior art or lack of inventive step. Formulation or use patents are often easier to circumvent and require vigilant monitoring.
  • Opportunities: Narrow claims addressing unique chemical modifications or delivery methods may carve advantageous niches in the highly competitive Brazilian pharmaceutical landscape.

Conclusion

Brazil patent BRPI0600623 likely encompasses a pharmaceutical compound, formulation, or method with scope delineated by a combination of product and process claims. The strength of this patent depends on the specificity and inventive contribution of its claims, affecting its enforceability amidst an active patent landscape characterized by overlapping patents and commercial competition.

In strategic considerations, patent holders should monitor related patents—both domestic and international—to safeguard their intellectual property rights and optimize market exclusivity. For potential entrants, comprehensive FTO analyses are essential when designing around such patents or considering licensing opportunities.


Key Takeaways

  • Scope is pivotal: Narrow, well-drafted claims focused on inventive features secure stronger protection in Brazil's patent environment.
  • Landscape awareness is critical: Understanding existing patents avoids infringement and identifies licensing opportunities.
  • Formulation and use claims are increasingly valuable due to challenges faced by broad compound patents.
  • Brazil’s legal framework favors robust patent rights for innovative pharmaceutical compositions but requires meticulous claim drafting.
  • Continuous monitoring of patent status and potential litigations informs business and R&D strategies.

FAQs

1. What types of claims are most vulnerable to invalidation in Brazilian patents?
Broad or vague claims, especially those that lack clear novelty or inventive step, are more susceptible to invalidation during litigation or examination.

2. How does Brazil's patent law impact pharmaceutical patentability?
Brazil requires strict demonstration of novelty, inventive step, and industrial application, stressing the importance of detailed, inventive disclosures, especially in pharmaceuticals.

3. Can formulation patents provide effective market exclusivity?
Yes. Formulation-specific patents can extend exclusivity, especially when they offer significant advantages such as improved bioavailability or stability.

4. How does the patent landscape affect generic entry into the Brazilian market?
Overlapping patents or narrow claims can delay generic entry, but patent invalidations or licensing can open opportunities for timely market access.

5. What best practices ensure robust patent claims in Brazil?
Focus claims on specific inventive features, avoid overly broad language, and thoroughly disclose the inventive contribution to strengthen enforceability.


References

[1] INPI Patent Database, Official Brazilian Patent Office.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

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.