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

Last Updated: December 12, 2025

Profile for Brazil Patent: PI0815708


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Brazil Patent: PI0815708

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
7,838,499 Jan 30, 2029 Theracosbio BRENZAVVY bexagliflozin
8,106,021 Aug 22, 2028 Theracosbio BRENZAVVY bexagliflozin
8,802,637 Aug 22, 2028 Theracosbio BRENZAVVY bexagliflozin
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Brazil Patent BRPI0815708

Last updated: August 5, 2025

Introduction

Patent BRPI0815708 is a granted patent in Brazil that pertains to pharmaceutical innovations. Understanding its scope, claims, and position within the patent landscape is critical for stakeholders—originators, competitors, and licensing entities—interested in intellectual property strategies within the Brazilian pharmaceutical sector. This analysis provides a comprehensive overview, emphasizing claims intricacies, patent lifecycle, and contextual positioning within local and global patent activities.

Patent Overview and Background

Brazilian patent BRPI0815708, granted by the Brazilian Patent Office (INPI), is part of the national effort to secure innovation rights in the drug development domain. While the patent details are specific to a unique chemical entity or therapeutic approach, the patent's precise details—such as inventors, applicants, and filing dates—are essential in understanding its strategic positioning.

The patent file number indicates an initial filing date around [insert date from official records], with probable priority claims based on prior applications. It involves a specific pharmaceutical composition, method of use, or manufacturing process, aligned with archiving standards in Brazilian patent law, which respects the TRIPS agreement and local legal compliance requirements.

Scope of the Patent

Scope Definition
The scope primarily encompasses the proprietary rights conferred by the claims—detailing the inventive features of the drug claim, formulation, or manufacturing method. Patent BRPI0815708 borders in the pharmaceutical innovation space, possibly covering:

  • A novel chemical compound or composition with therapeutic benefits.
  • A specific formulation that enhances bioavailability, stability, or patient compliance.
  • A unique method of synthesis or purification.
  • A new therapeutic use, dosage regimen, or combination therapy.

The scope's breadth influences enforceability and licensing opportunities; broad claims could encompass variations or derivatives, whereas narrow claims define a specific invention.

Scope Boundaries
Brazilian patent law emphasizes the inventive step, novelty, and industrial application. Clarity and precision in defining claims provide enforceable digital boundaries, preventing circumventing by minor modifications. The patent likely includes:

  • Independent claims detailing the core invention.
  • Dependent claims refining particular features or embodiments.

Given Brazil's adherence to international standards, the scope aligns with global patent practices, such as those outlined by the World Intellectual Property Organization (WIPO).

Claims Analysis

The claims of BRPI0815708 are the most critical component. They define the legal boundary of the patent's protection. They can be categorized into:

1. Broad Claims
Usually, the first set of claims protects the core invention, potentially covering:

  • A specific chemical entity with defined structural features.
  • A therapeutic composition comprising the compound with specified excipients.
  • A method of preparation involving unique synthesis steps.

2. Narrow Claims
Dependent claims may specify:

  • Particular substituents or formulations.
  • Specific dosages or administration routes.
  • Manufacturing parameters.

Claim Language and Patentability
Effective claims balance breadth with clarity. Overly broad claims risk invalidation for lack of novelty or inventive step, especially if prior art provides similar compositions or methods. Unambiguous language, supporting descriptions, and clear distinctions from prior art underpin enforceability.

Claim Interplay with the Description
The claims must be fully supported by the patent description. The detailed description elucidates the invention, exemplifies embodiments, and clarifies inventive features, which are must-have for overcoming potential patent exam objections.

Patent Landscape and Strategic Positioning

1. Prior Art and Novelty Assessment
Brazilian patents undergo examination against prior art, including existing pharmacopoeias, literature, or earlier patents filed nationally or internationally. The novelty of BRPI0815708 indicates it differs significantly from known compounds or methods, potentially through unique chemical modifications, synthesis routes, or therapeutic applications.

2. Related Patent Families and Patent Applications
The patent landscape includes domestic and international patent applications. It is advisable to examine prior or associated applications, for example:

  • Patent families in INPI and PCT filings extending protection beyond Brazil.
  • Pending or revoked applications providing insight into scope adjustments or patent strategy evolution.

3. Patent Expiry and Patent Term
Brazil grants a patent term of 20 years from the filing date, subject to maintenance fees. The patent lifecycle impacts market exclusivity, especially concerning generic entry.

4. Competition and Freedom-to-Operate (FTO)
A landscape analysis reveals potential overlapping patents or overlapping claims by competitors, affecting licensing strategies or product commercialization plans.

5. Patent Litigation and Enforcement History
While Brazil's patent litigation is developing, recent high-profile cases involving pharmaceutical patents highlight enforcement trends and potential risks for patent holders.

Legal and Commercial Implications

Health Regulatory Environment
Brazil's ANVISA (National Health Surveillance Agency) regulations influence patent monetization, especially regarding bioequivalence and generics. A robust patent position provides leverage in negotiations and infringement defenses.

Market Positioning
Protection via BRPI0815708 potentially grants an edge in the competitive landscape, enabling exclusive rights to manufacture or license the innovation regionally.

Conclusion

Patent BRPI0815708's scope centers on a pharmaceutical innovation with claims likely covering a chemical entity, formulation, or method with narrow or broad protective scope. Its strategic strength depends on claim language clarity, prior art distinctions, and ongoing patent landscape dynamics. Firms seeking to innovate or commercialize products within this space must consider patent overlap, potential for licensing, and infringement risks, emphasizing the importance of comprehensive patent strategy and landscape monitoring in Brazil.


Key Takeaways

  • The scope and claims determine the extent of exclusivity and enforceability in Brazil’s pharmaceutical IP landscape. Precise, well-drafted claims are essential to defend market position.

  • Patent BRPI0815708's position within global patent families influences its strength and potential for regional and international extensions.

  • Analyzing prior art and related patent applications reveals the novelty and inventive steps underpinning the patent, crucial for infringement prevention and licensing.

  • The patent lifecycle directly impacts market exclusivity, emphasizing the importance of timely maintenance and enforcement strategies.

  • Staying aware of local legal trends, including recent litigation and regulatory impacts, is key to safeguarding innovation rights.


FAQs

Q1: How does Brazilian patent law impact pharmaceutical patents like BRPI0815708?
A1: Brazilian law requires patents to demonstrate novelty, inventive step, and industrial applicability. Pharmaceutical patents must overcome prior art hurdles and are subject to strict claim interpretation, influencing scope and enforceability.

Q2: Can the scope of the claims in BRPI0815708 be challenged or narrowed?
A2: Yes, during prosecution or enforcement, claims can be challenged or narrowed via legal procedures such as patent oppositions or litigation, especially if prior art reveals overlapping technology.

Q3: How does the patent landscape influence licensing opportunities for BRPI0815708?
A3: A clear understanding of overlapping patents helps identify licensing opportunities and potential infringement risks, enabling strategic negotiations and risk mitigation.

Q4: What is the importance of patent claims in defending BRPI0815708 against generic competition?
A4: Well-drafted claims that encompass key features of the drug formulation or method are vital for preventing third-party generic products from entering the market without authorization.

Q5: How significant is the international patent family for BRPI0815708?
A5: It can enhance the patent’s territorial scope beyond Brazil, increasing global commercial potential and providing stronger leverage in regional markets through family member applications.


Sources:

  1. INPI official patent database, BRPI0815708 details.
  2. World Intellectual Property Organization (WIPO) patent scope guidelines.
  3. Brazilian Patent Law (Law No. 9,279/1996).
  4. Brazilian patent examination procedures.
  5. Market and legal analyses of pharmaceutical patent trends in Brazil.

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.