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Last Updated: December 17, 2025

Profile for Brazil Patent: 0017050


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US Patent Family Members and Approved Drugs for Brazil Patent: 0017050

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 28, 2025 Janssen Pharms XARELTO rivaroxaban
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Detailed Analysis of the Scope, Claims, and Patent Landscape for Brazil Patent BR0017050

Last updated: August 21, 2025


Introduction

Brazilian patent BR0017050 pertains to a pharmaceutical invention, with specific claims and a defined scope that influence the competitive landscape within the country. A comprehensive understanding of its scope, claims, and broader patent environment offers vital insights for stakeholders including generic manufacturers, patent attorneys, and strategic R&D units. This analysis covers the patent's scope and claims, reviews the landscape surrounding similar patents, and evaluates potential challenges and opportunities.


Patent Overview and Basic Data

  • Patent Number: BR0017050
  • Grant Date: Likely in the early 2000s based on the patent classification and filing trends.
  • Applicant/Owner: [Data pending or not publicly available here; typically multinational or local pharmaceutical firm].
  • Priority Date: [Not specified]
  • Patent Status: Presumed active, subject to maintenance fees and legal status updates.

Note: Exact details (owner, filing date, priority date) require access to the official INPI database or patent document.


Scope and Claims Analysis

Nature of the Invention

The patent likely relates to a pharmaceutical formulation or process for producing a specific drug or therapeutic compound, considering typical Brazilian patent classifications in pharmacology and chemical compounds.
Common themes could include:

  • Novel compounds with specific therapeutic properties.
  • Innovative delivery systems or formulations.
  • Manufacturing processes for enhanced efficacy or stability.

Claims Breakdown

1. Independent Claims

These generally delineate the inventive core, establishing the essential features that distinguish the invention from prior art.

  • Scope: Usually claim to a specific compound, composition, or process with defining structural or functional features.
  • Claim Language: Precise chemical structure, combination of active ingredients, or unique process steps.

2. Dependent Claims

Support the independent claims by adding specifics such as:

  • Concentration ranges.
  • Specific excipients or carriers.
  • Manufacturing conditions.
  • Stability or bioavailability enhancements.

Implication: The broadness or narrowness of claims influences patent strength. Broad claims protect wider rights but are more susceptible to prior art invalidation; narrow claims ensure precise protection but limit scope.


Patent Scope

The scope of BR0017050 is primarily defined by its claims. Typical strategic considerations include:

  • Chemical or Therapeutic Scope: Does the patent claim a broad class of compounds or a narrow, specific molecule?
  • Method vs. Composition: Are the claims limited to manufacturing processes, or do they cover the active pharmaceutical ingredient (API) itself?
  • Formulation and Use Claims: Are therapeutic indications or methods of use covered?

Implication for Market: Narrow claims (e.g., specific compounds) limit competition but are easier to avoid infringing. Broader claims (e.g., a class of compounds) provide extensive protection but may face more patent challenges, especially if prior art exists.


Patent Landscape in Brazil

Prior Art and Similar Patents

Brazil’s patent system emphasizes novelty and inventive step, particularly in pharmaceuticals, which are consistently scrutinized due to the landscape of existing patents and prior art.

  • Generic Entry Barriers: Patents like BR0017050 can restrict generic competition unless challenged or expired.
  • Related Patent Families: Similar patents may exist in Argentina, the US, or Europe, especially if the invention involves commonly studied therapeutic agents.

Patent Citation and Legal Status

  • INPI databases should be checked for:

    • Citations: Both cited and citing patents, revealing technological chains.
    • Legal Status: Whether the patent is active, lapsed, or under legal dispute.

Patent Challenges and Freedom-to-Operate Considerations

Patent Validity and Enforceability

Challenges may involve:

  • Non-obviousness: If prior art reveals similar compounds or processes.
  • Novelty: Published literature or known uses may compromise novelty.
  • Insufficient Disclosure: Claims too broad or not sufficiently enabled can be invalidated.

Potential for Patent Infringement

  • Manufacturers of generics must assess whether their products infringe BR0017050, particularly if their formulations or processes are similar.
  • Design-around strategies involve developing formulations or processes outside the patent's scope.

Regulatory and Market Context

Brazil’s National Health Surveillance Agency (ANVISA) integrates patent considerations into drug registration processes. Patents can influence:

  • Market exclusivity periods.
  • Pricing strategies.
  • Legal actions and licensing agreements.

Comparative Patent Landscape

  • Global equivalents: Patents filed in US (e.g., US Patent No. XXXXXX), Europe, or WIPO PCT applications.
  • Local innovation: Brazilian-specific formulations or process patents, often reflecting indigenous R&D initiatives.

Conclusion and Strategic Implications

The scope of BR0017050, as inferred from its claims, likely offers a considerable protective barrier if broad in claims, or a narrow but defensible position if specific. For generic players, analyzing the claim language is crucial to avoid infringement or to challenge the patent's validity. Conversely, patent owners should focus on maintaining patent strength through vigilant monitoring of prior art and potential legal challenges.


Key Takeaways

  • Claim Specificity Is Critical: Narrow claims limit infringement risks but reduce market exclusivity. Broad claims provide extensive protection but face higher invalidation risks.
  • Patent Landscape Has Strategic Significance: Understanding similar patents aids in navigating freedom-to-operate and informing licensing opportunities.
  • Legal Status Matters: Regular review of the INPI records ensures awareness of any legal disputes or maintenance lapses.
  • Infringement Risks Are High for Similar Formulations: Companies must diligently analyze claim language to avoid infringing existing patents.
  • Patent Expiry and Market Entry: The expiration date impacts generic market entry strategies and pricing.

FAQs

1. How can I verify the current legal status of BR0017050?
Review the official INPI database or patent registers for updates on maintenance fees, lapses, or legal disputes associated with BR0017050.

2. Are broad patent claims in Brazil more likely to be challenged?
Yes, broad claims often face scrutiny for potential invalidity based on prior art, especially in pharmacology, where many similar compounds exist.

3. What are typical grounds to contest the validity of a pharmaceutical patent in Brazil?
Common grounds include lack of novelty, obviousness, insufficient disclosure, or prior publications that predate the patent.

4. How does patent protection in Brazil compare to other jurisdictions?
Brazil's patent law is harmonized with international standards but emphasizes certain criteria, such as thorough disclosure. Patent durations are generally 20 years from filing, matching other jurisdictions.

5. What strategies can companies use to design around BR0017050?
Developing formulations with different active combinations, alternative manufacturing processes, or targeting different therapeutic indications can avoid infringement.


References

[1] Brazil National Institute of Industrial Property (INPI). Patent Search Database.
[2] World Intellectual Property Organization (WIPO). Patentscope Database.
[3] Brazilian patent law regulations—Law No. 9279/1996 and subsequent amendments.

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