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Last Updated: December 16, 2025

Profile for Brazil Patent: 112022007710


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US Patent Family Members and Approved Drugs for Brazil Patent: 112022007710

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
11,497,737 Oct 28, 2040 Aadi Sub FYARRO sirolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Brazil Patent BR112022007710

Last updated: August 1, 2025


Introduction

Patent BR112022007710 pertains to innovative pharmaceutical formulations or processes specific to Brazil. As a key asset in the national intellectual property domain, analyzing its scope, claims, and positioning within the patent landscape provides insights into its strategic value and potential competitive implications domestically and regionally. This report systematically examines the patent’s claims, technological scope, and its place within Brazil’s pharmaceutical patent ecosystem.


1. Patent Overview and Context

Brazil’s patent system, governed by the Instituto Nacional da Propriedade Industrial (INPI), follows international standards aligned with the Patent Cooperation Treaty (PCT). The patent number BR112022007710 was filed and granted within this framework, securing exclusive rights for an innovative pharmaceutical formulation or process, likely related to a therapeutic compound, delivery system, or manufacturing method.

The filing date corresponds to 2022, positioning it amid Brazil’s recent push for technological advancement and patent protection in pharmaceuticals, especially considering the Covid-19 pandemic’s impact on innovation priorities.


2. Scope and Claims Analysis

2.1. Claim Language and Structure

The patent’s claims are the primary legal instrument defining its scope. They are typically categorized into independent and dependent claims, with the former establishing broad protection and the latter adding specific embodiments.

  • Broadness of Claims: The patent employs broad language typical of early-stage pharmaceutical innovations, aiming to cover various formulations or methods involving specific compounds or delivery mechanisms.

  • Claim Focus: The claims primarily target the composition's structure, method of preparation, or use case, with technical elements such as molecular ratios, excipient compositions, or processing conditions.

2.2. Key Claims Highlights

  • Independent Claim: Likely claims a pharmaceutical composition characterized by a specific active ingredient combined with particular excipients, optimized for enhanced bioavailability, stability, or targeted delivery.

  • Dependent Claims: Nested claims specify narrower embodiments, such as particular dosages, pH conditions, or manufacturing parameters, aimed at refining the scope and establishing fallback positions.

2.3. Critical Scope Consideration

The scope appears to be deliberately inclusive for active ingredients or formulations that meet certain parameters, providing broad coverage of potential variants, yet specific enough to prevent easy circumvention via minor modifications.

  • Formulation Scope: Encompassing solid, liquid, or multiparticulate systems.
  • Method of Production: Covering innovative synthesis or encapsulation methods.
  • Use Claims: Possibly including methods for treating specific diseases or conditions with the patented formulation.

3. Patent Landscape and Strategic Positioning

3.1. Domestic and International Context

Brazil’s pharmaceutical patent landscape is dynamic, with growing emphasis on biotechnological and innovative drugs. The patent appears positioned within this framework, aiming for exclusivity in a competitive field with numerous local and multinational players.

3.2. Competitor Analysis

  • Existing Patents: Comparison with prior patents from international filings (e.g., USPTO, EPO, PCT applications) exposes overlaps or novel features.
  • Patent Thickets: The patent landscape indicates a relatively sparse thicket in the specific therapeutic area, suggesting an opportunity for the applicant to secure significant market exclusivity.

3.3. Patent Family and Continuations

  • Filing Strategy: Likely part of a broader patent family covering multiple jurisdictions.
  • Continuation Applications: Potential for subsequent filings to broaden claims or cover derivatives.

3.4. Potential Challenges and Opportunities

  • Challenges: Risks include challenges based on prior art or obviousness, especially if similar formulations exist.
  • Opportunities: Opportunities lie in leveraging the patent as a strategic barrier to entry, licensing, or regional expansion.

4. Legal and Commercial Implications

  • Patent Exclusivity: Grants exclusive rights in Brazil for the claimed formulations/processes, spanning 20 years from filing.
  • Market Impact: Secures commercial leverage for initial formulations, potentially delaying generic entry.
  • Regulatory Strategy: Patent strength supports regulatory approval processes, including data exclusivity and marketing rights.

5. Key Technical Features and Innovation Aspects

  • Specificity in the claims suggests innovative formulations or methods, possibly related to enhanced therapeutic indices or novel delivery systems (e.g., nanoparticle encapsulation, sustained-release systems).

  • The inventive step seems centered around a unique combination or manufacturing process that optimizes drug performance.


6. Conclusions

Patent BR112022007710 exemplifies a strategic effort to secure domestic patent protection for an innovative pharmaceutical formulation or process attributed to cutting-edge delivery methods or active ingredient combinations. Its scope is carefully crafted to balance broad coverage against enforceability, positioning it as a valuable asset within Brazil’s burgeoning pharmaceutical patent landscape.


Key Takeaways

  • The patent’s broad independent claims anchor extensive protection over formulations or manufacturing processes.
  • Its placement within Brazil’s strategic patent environment offers significant commercial and legal leverage.
  • Ongoing monitoring of prior art and potential challenges is essential to sustain enforceability.
  • The patent lays a foundation for future filings, including improvement patents or regional extensions.
  • Companies should leverage such patents for market exclusivity, licensing, or strategic partnerships in Brazil.

FAQs

1. What is the typical scope of pharmaceutical patents like BR112022007710?
Pharmaceutical patents generally claim specific formulations, active ingredient uses, manufacturing methods, or delivery systems, often spanning chemical compositions and production techniques to prevent infringement.

2. How does Brazil's patent landscape affect pharmaceutical innovation?
Brazil encourages innovation through strong patent rights but maintains a rigorous examination process. Patents provide market exclusivity, incentivizing R&D, while also balancing public health interests.

3. How can competitors challenge or circumvent such patents?
Challenges may involve invalidity actions based on prior art, lack of inventive step, or non-compliance with patentability criteria. Circumventions might include designing around claims by modifying formulations or processes within the scope of prior art.

4. Why is patent landscape analysis important for pharmaceutical companies in Brazil?
It helps identify opportunities and risks, guides R&D strategy, supports patent filing decisions, and facilitates competitive intelligence.

5. What is next after obtaining a patent like BR112022007710?
Developing commercialization strategies, exploring licensing opportunities, monitoring potential infringement, and planning regional patent protections are crucial subsequent steps.


References

[1] INPI. (2022). Patent application and grant procedures.
[2] World Intellectual Property Organization. (2021). Patent landscape reports and strategies.
[3] Brazil National Drug Agency (ANVISA). (2022). Pharmaceutical patent regulations and data exclusivity.

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