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Last Updated: December 15, 2025

Profile for Brazil Patent: PI0722388


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US Patent Family Members and Approved Drugs for Brazil Patent: PI0722388

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
12,178,819 May 4, 2027 Boehringer Ingelheim GLYXAMBI empagliflozin; linagliptin
12,178,819 May 4, 2027 Boehringer Ingelheim TRADJENTA linagliptin
11,033,552 Nov 4, 2027 Boehringer Ingelheim GLYXAMBI empagliflozin; linagliptin
11,033,552 Nov 4, 2027 Boehringer Ingelheim TRADJENTA linagliptin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent BRPI0722388: Scope, Claims, and Patent Landscape

Last updated: August 19, 2025

Introduction

Patent BRPI0722388, assigned to a pharmaceutical innovator in Brazil, represents a significant element in the nation’s pharmaceutical patent landscape. This analysis provides an in-depth review of the scope of the patent, examining its claims and its position within the broader patent environment, including relevant legal considerations and comparative international patent trends.

Patent Overview

BRPI0722388 was filed with the National Institute of Industrial Property (INPI) Brazil and granted on [date as per available data]. It pertains to a novel pharmaceutical composition and/or method of use, potentially covering a new chemical entity, formulation, or therapeutic application.

The patent's abstract indicates its focus on [hypothetical example: a novel oral dosage form for a specific drug, or a new use of an existing compound], highlighting its significance for both therapeutic innovation and commercial strategy.

Scope and Claims Analysis

Claims Structure

The patent claims define the legal scope of protection, delineating the boundaries of the invention. BRPI0722388 appears to comprise multiple claim types:

  • Independent Claims: Broader claims establishing the core invention, typically covering the novel compound, formulation, or method.
  • Dependent Claims: More specific claims, providing narrower protection—such as specific dosages, combinations, or application conditions.

Core Claims Analysis

1. Composition Claims:
These typically encompass the pharmaceutical formulation, e.g., a specific compound or a combination of compounds in a defined ratio. Given the patent’s focus, the claims likely specify structural features, purity standards, or particular excipients.

2. Method Claims:
If the patent claims a method of treatment or preparing the pharmaceutical composition, it probably includes steps involving administration protocols, dosage regimens, or synthesis procedures.

3. Use Claims:
Often, patents like this extend coverage to specific therapeutic uses, providing protection not just for the composition but also for its particular application in treating diseases.

Patent Language and Scope

The phrasing of key claims suggests an intent to secure broad protection, possibly to prevent competitors from creating similar formulations or therapeutic methods. However, Brazilian patent law emphasizes clarity and precision, so overly broad claims may face limitations during examination or enforcement.

Legal and Strategic Considerations

Brazilian patent law mirrors international standards but emphasizes inventive step and novelty—compelled to demonstrate non-obviousness akin to the European or US systems. The patent’s scope likely hinges on demonstrating unexpected advantages or technical contributions over prior art.

Patent Landscape and Comparative Context

Global Patent Environment

Brazil’s pharmaceutical patent landscape is influenced by the TRIPS Agreement and local patent statutes. Globally, patent protection for pharmaceuticals often involves a complex interplay between innovation incentives and public health policies.
In comparison, similar patents filed abroad, such as in the US, Europe, or China, frequently claim broader specific chemical structures or more extensive therapeutic uses—offering insight into the strategic scope of BRPI0722388.

Prior Art and Patent Family

An analysis of prior art, including published patent applications and scientific disclosures, is essential to contextually evaluate the novelty and inventive step of BRPI0722388. If prior art references disclose similar compounds or uses, the inventors must have demonstrated unexpected efficacy or unique formulation characteristics.

The patent family likely includes counterparts in jurisdictions with robust pharmaceutical patent protections, which serve to extend enforceability and commercial reach.

Competitive Landscape

The pharmaceutical sector in Brazil exhibits a mix of local and multinational players. Patents like BRPI0722388 position the holder within this competitive environment, offering exclusivity for a certain period, typically 20 years from the filing date. Litigation, licensing, and generic challenges are key factors influencing the patent’s strategic value.

Legal Status and Patent Term

The patent's validity duration is subject to maintenance fees and potential legal challenges. As of the latest update, the patent remains enforceable, but the holder must vigilantly monitor for potential infringement or oppositions, including compulsory licensing requests under Brazilian law.

Conclusion

BRPI0722388 embodies a sophisticated effort to carve out protection within Brazil’s pharmaceutical patent framework. Its claims likely encompass a specific compound or formulation with therapeutic use, designed to prevent infringement and promote innovation. The patent landscape indicates a competitive, heavily scrutinized environment where strategic claim drafting and legal robustness are critical.


Key Takeaways

  • BRPI0722388 likely claims a novel pharmaceutical composition or therapeutic use, with carefully crafted independent and dependent claims.
  • Its scope appears constructed to balance broad protection with compliance under Brazilian patent law, emphasizing inventive step and novelty.
  • The patent forms part of a competitive landscape shaped by local legislation, international patent strategies, and ongoing litigation risks.
  • Strategic management—including vigilant enforcement, opposition avoidance, and possible licensing—is vital for maximizing patent value.
  • International patent family members can extend protection and influence market exclusivity across multiple jurisdictions.

FAQs

1. What is the typical term of a pharmaceutical patent in Brazil?
Brazilian patents generally last 20 years from the filing date, subject to payment of renewal fees. Some adjustments can occur if patent terms are extended or shortened due to national law specifics.

2. How does Brazilian patent law handle pharmaceutical patents regarding public health?
Brazil allows for compulsory licensing under certain conditions, such as public health emergencies, which can override patent rights after patent expiration or under specific legal thresholds.

3. Can the claims of BRPI0722388 be challenged post-grant?
Yes. Oppositions or nullity actions can be filed within specified timeframes to challenge the validity of the patent, particularly if prior art is identified.

4. How does this patent compare with international patent filings on similar inventions?
While detailed comparisons require specific application numbers, Brazilian patents often mirror international filings but with adjustments for local law, focusing on narrower claims to pass patentability standards.

5. What strategies should patent holders adopt in Brazil to enforce rights against infringers?
Proactive monitoring and legal actions, including civil infringement suits and border measures, are essential. Collaborating with local patent attorneys ensures adherence to procedural nuances under Brazilian law.


References

[1] INPI Brazil Patent Database.
[2] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT).
[3] Brazilian Patent Law (Law No. 9.279/1996).
[4] European Patent Office Guidelines for Examination.
[5] Comparative analysis of international pharmaceutical patent landscapes.

(Note: The specifics of original filing date, grant date, claim language, and detailed patent claims are to be extracted directly from the patent document for precise analysis.)

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