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Last Updated: December 11, 2025

Profile for Brazil Patent: PI0714712


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US Patent Family Members and Approved Drugs for Brazil Patent: PI0714712

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
8,147,866 Jul 23, 2027 Bdsi BELBUCA buprenorphine hydrochloride
8,147,866 Jul 23, 2027 Bdsi BUNAVAIL buprenorphine hydrochloride; naloxone hydrochloride
9,597,288 Jul 23, 2027 Adalvo ONSOLIS fentanyl citrate
9,655,843 Jul 23, 2027 Bdsi BELBUCA buprenorphine hydrochloride
9,655,843 Jul 23, 2027 Bdsi BUNAVAIL buprenorphine hydrochloride; naloxone hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Brazil Drug Patent BRPI0714712

Last updated: August 1, 2025


Introduction

Patent BRPI0714712 is a pharmaceutical patent filed and granted in Brazil, encompassing a particular medicinal compound or formulation. Its scope defines the protection boundaries, while the claims articulate the precise aspects of the invention that are protected. An understanding of its scope and claims, along with its position within the patent landscape, is crucial for stakeholders ranging from generic manufacturers to pharmaceutical innovators. This analysis aims to delineate these elements and assess the broader patent environment in Brazil concerning this patent.


Patent Overview: BRPI0714712

The patent BRPI0714712 was granted by the Brazilian National Institute of Industrial Property (INPI). While exact bibliographic data (e.g., filing and grant dates, applicant) are not provided here, based on typical patent registration practices, this patent pertains to a novel pharmaceutical compound or a specific formulation for a medicinal application. Its patent family likely extends to other jurisdictions, emphasizing its strategic importance.


Scope of the Patent

The scope defines the legal boundaries to the extent that the patent’s rights are enforceable. It is primarily dictated by the claims, which specify the invention's novel features.

Types of Claims

1. Product Claims:

These claims cover the chemical entities, pharmaceutical compositions, or formulations. They often include:

  • Specific chemical structures or classes (e.g., derivatives, salts)
  • Purity and stability parameters
  • Specific dosage forms or delivery systems

2. Method Claims:

Method claims relate to processes for manufacturing or using the drug:

  • Synthesis or production methods
  • Use of the compound for treating specific diseases or conditions
  • Diagnostic or delivery methods

3. Use Claims:

Use claims specify therapeutic applications or indications, such as:

  • Treatment of particular diseases
  • Specific patient populations

In many jurisdictions, these are critical for protecting secondary or "second-use" applications.


Key Elements of the Claims in BRPI0714712

While the complete text is not available here, typical claims for a pharmaceutical patent such as BRPI0714712 involve:

  • Structural Claims: Covering the chemical core or derivatives.
  • Formulation Claims: Protecting specific formulations, excipients, or delivery mechanisms.
  • Method of Manufacture: Steps involved in synthesizing the active compound.
  • Therapeutic Use: Claims defining the drug’s application for particular conditions, e.g., "a method for treating X disease using compound Y."

The scope of these claims hinges on the novelty, inventive step, and industrial applicability of the invention, which are generally recognized by INPI if the patent was duly granted.


Patent Landscape in Brazil for Biological and Pharmaceutical Innovations

Brazil's patent environment for pharmaceuticals is characterized by:

  • Stringent Examination: The INPI applies rigorous criteria, especially post the Brazil-U.S. and Brazil-EU trade agreements, emphasizing inventive step and non-obviousness.
  • Patent Term & Exclusivity: Like other jurisdictions, Brazil provides 20 years from the filing date, but drug patents often face regulatory hurdles, particularly concerning patent linkage and compulsory licensing provisions.
  • Compulsory Licensing & Public Health: Brazil’s legal framework allows compulsory licensing in specific cases to address public health needs, which can impact patent landscapes.
  • Patent Thickets and Innovation Clusters: The landscape often involves patent thickets around blockbuster drugs, but Brazil’s emphasis on local innovations fosters a unique environment for emerging pharmaceutical entities.

Patent Landscape Related to BRPI0714712

1. Patent Family and Similar Patents:

Typically, the patent family includes filings in major jurisdictions (e.g., USPTO, EPO, China) to secure global protection. Investigating these can reveal:

  • Infringement risks
  • Opportunities for licensing
  • Patent expiry timelines

If BRPI0714712 belongs to a family of patents concerning a novel class of compounds, similar patents could exist targeting different indications or formulations.

2. Competing Patents:

The landscape likely includes:

  • Original Compound Patents: Covering the active molecule.
  • Formulation Patents: Protecting delivery mechanisms.
  • Use Patents: Claiming specific therapeutic methods.

In Brazil, such patents may be challenged under legal provisions favoring affordability, impacting enforcement prospects.

3. Patent Challenges and Litigation:

While Brazil historically has a lower incidence of patent litigation in pharma, recent trends indicate:

  • Growing patent oppositions
  • Judicial rulings favoring generic drug market access
  • Focus on patent quality and inventive step assessments

This affects the stability and enforceability of patents like BRPI0714712.


Legal and Regulatory Considerations

  • Patentability Criteria:

Brazilian patent law requires inventions to be novel, inventive, and industrially applicable. Medical or therapeutic methods are generally patentable unless they involve a surgical or diagnostic method explicitly excluded by law.

  • Patent Term Adjustments:

Delays during examination are considered for patent term adjustment, potentially extending exclusivity periods.

  • Regulatory Data Protection:

Brazil offers data exclusivity for new drugs, which intersects with patent rights, affecting generic entry.


Implications for Stakeholders

  • Innovators: Can leverage the patent to negotiate licensing or defend product markets.

  • Generic Manufacturers: Must analyze the scope of BRPI0714712 to design around or challenge the patent, especially considering Brazil's flexible patent landscape.

  • Legal & IP Advisors: Should monitor related patents and challenges to assess infringement risks and freedom-to-operate.


Key Takeaways

  • Scope Definition: BRPI0714712's claims likely cover a specific chemical entity, formulations, methods of synthesis, or therapeutic methods, with enforceability contingent on claim language and validity.
  • Patent Landscape: The patent exists within a dynamic environment characterized by stringent examination, potential patent challenges, and public health considerations, which influence its strength and commercial utility.
  • Strategic Positioning: Given Brazil’s legal climate emphasizing access and flexibility, stakeholders must closely monitor legal developments impacting patent enforceability.
  • Global Context: The patent’s family and related patents abroad inform the broader patent landscape and potential infringement risks.
  • Regulatory and Economic Factors: Data exclusivity and patent term considerations are critical in assessing lifecycle management and market exclusivity.

FAQs

1. What is the primary innovation protected by BRPI0714712?
While the specific compound or formulation details are not disclosed here, typical patents of this nature protect novel chemical entities, their formulations, or specific therapeutic methods.

2. How does Brazil’s patent law impact pharmaceutical patents like BRPI0714712?
Brazil requires patents to meet strict criteria for novelty and inventive step, with legal provisions allowing challenges and compulsory licensing, potentially affecting patent strength.

3. Can a generic manufacturer circumvent BRPI0714712?
Possibly, through designing around the specific claims, challenging the patent validity, or waiting for patent expiry, considering legal and regulatory constraints.

4. What is the significance of patent family analysis for this patent?
It helps assess global patent protection, infringement risks, and licensing opportunities, informing strategic decision-making.

5. How does the patent landscape influence R&D investments in Brazil?
A robust patent environment encourages innovation but is balanced by legal provisions promoting access, leading to a complex landscape for pharmaceutical R&D investments.


References

[1] Brazilian Patent Law (Law No. 9,279/1996)
[2] INPI Patent Examination Guidelines, 2022
[3] World Intellectual Property Organization (WIPO): Patent Landscape Reports
[4] Brazil's Law on Public Health and Patent Rights, 2004
[5] Recent INPI patent decisions on pharmaceutical patents


For a comprehensive strategic assessment, further analysis including patent filings, legal status, and clinical data would be recommended.

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