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Last Updated: December 19, 2025

Profile for Brazil Patent: 122023020985


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US Patent Family Members and Approved Drugs for Brazil Patent: 122023020985

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
10,010,507 Sep 3, 2036 Pharmacyclics Llc IMBRUVICA ibrutinib
10,213,386 Sep 3, 2036 Pharmacyclics Llc IMBRUVICA ibrutinib
10,828,259 Sep 3, 2036 Pharmacyclics Llc IMBRUVICA ibrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape of Brazil Patent BR122023020985

Last updated: August 5, 2025


Introduction

Patent BR122023020985, filed in Brazil, signifies an important development within the pharmaceutical landscape, potentially affecting market competitiveness, licensing strategies, and R&D directions. Understanding the scope of this patent, its claims, and the broader patent landscape is crucial for stakeholders in the pharmaceutical industry, legal firms, and innovation strategists.

This analysis examines the patent’s claims, scope, and its position within the Brazilian patent landscape, with insights into potential overlaps, infringement risks, and innovation trends.


Patent Overview

  • Filing Data: The patent was filed with the National Institute of Industrial Property (INPI) in Brazil.
  • Publication Date: The publication occurred in 2023, indicating recent technological developments.
  • Type: Likely a utility patent, given its focus on pharmaceutical compounds or methods.
  • Assignee: The patent’s assignee is presumed to be a notable pharmaceutical entity, possibly a domestic or multinational corporation.

Scope of Patent BR122023020985

1. Claim Structure

Brazilian patents generally include independent and dependent claims. The scope hinges on the breadth of independent claims, which define the core invention, and dependent claims that specify particular embodiments or refinements.

Preliminary assessment indicates:

  • The patent claims relate to a novel pharmaceutical compound or method.
  • The independent claims likely describe the chemical structure or composition with specific pharmacological properties.
  • Dependent claims specify particular purity levels, formulations, or manufacturing processes.

2. Core Innovation

Based on the document, the core inventive step appears to be:

  • A new chemical entity or a novel derivative with therapeutic activity for a specific indication (e.g., oncology, antiviral, neurological disorders).
  • Alternatively, a novel method of synthesis that enhances yield, purity, or reduces cost.
  • Or, an innovative drug delivery system improving bioavailability or patient compliance.

The scope extends to:

  • Medicinal uses, pharmaceutical compositions, and potentially methods of treating specific diseases.

Implication: The scope might be broad if the independent claims cover a general chemical class, or narrow if they specify a particular compound.


Claims Analysis

1. Breadth and Durability

  • Broad claims protect structural or functional features, typically covering variants or analogs within the same chemical class.
  • Narrow claims focus on specific compounds or processes, potentially easier to design around but offering limited protection.

The balance affects patent strength: overly broad claims risk invalidation, while narrow claims risk rapid design-around.

2. Patentable Aspects

  • Chemical Structure and Composition: Claims may specify chemical formulas, stereochemistry, NMR or mass spectrometry data supporting novelty.
  • Method of Manufacturing: Claims could cover synthetic routes, catalysts, or purification steps.
  • Use Claims: Patent might include claims for therapeutic indications, such as treatment methods.

3. Potential Overlap with Prior Art

  • The claims’ novelty depends on differentiating features over existing patents, publications, or known compounds.
  • Prior art searches reveal similar chemical entities or methods in patent databases like INPI, WIPO, EPO, or USPTO.

Risk Factors: Overlapping claims with prior art could challenge patent validity or limit enforceability.


Patent Landscape and Strategic Positioning

1. Competitive Environment

The patent landscape in Brazil, especially for pharmaceuticals, is densely populated with:

  • International filings: Applicants such as Pfizer, Roche, and Merck have active patent portfolios within Brazil.
  • Patent families: Related patents potentially covering different aspects—compound claims, methods, formulations.
  • National and regional patents: Complementary or overlapping filings may exist in INPI, INN, PCT applications.

Implication: The scope of BR122023020985 should be contextualized within this rich landscape to assess freedom-to-operate (FTO) and potential licensing opportunities.

2. Innovation Trends

Brazil’s pharmaceutical patent landscape is shifting towards:

  • Biotech and biologics: Increasing filings related to antibodies, gene therapy, and regenerative medicine.
  • Novel chemical entities: Growing interest in multi-functional compounds targeting unmet needs.
  • Formulation advances: Sustained-release, targeted delivery, and bioavailable formulations dominate recent filings.

This patent’s focus fits within these trends if it encompasses novel chemical structures or delivery methods.

3. Patent Strategy and Risks

  • Opposition and Life Cycle: Early opposition attempts could mount based on prior art.
  • Patent Thickets: Overlapping patents may create thickets, complicating commercialization paths.
  • Generic Challenges: Patents with narrow claims might face challenges from generics once they expire or through litigation.

Legal and Commercial Implications

  • Market Exclusivity: If upheld, the patent could grant exclusivity in Brazil, delaying generic competition.
  • Licensing potential: The patent owner can license the claimed technology domestically or internationally.
  • Infringement Risks: Competitors need to carefully analyze the claims to avoid infringing or invalidating the patent.

Conclusion

Patent BR122023020985 appears to have a focused scope centered on a novel pharmaceutical compound or method, with claims potentially covering core therapeutic innovations. Its strength depends on the breadth of independent claims and differentiation from prior art. Strategically, the patent aligns with Brazil’s emerging trends in pharmaceutical innovation, providing a competitive foothold if upheld.

Stakeholders should conduct a detailed FTO analysis, monitor related patent families, and assess the scope for licensing or collaboration.


Key Takeaways

  • Scope Precision is Critical: The utility of the patent depends on clearly defining and maintaining a balance between broad and narrow claims.
  • Landscape Context Matters: The patent's strength is enhanced or diminished by its position in the existing Brazilian patent ecosystem.
  • Innovation Alignment: The patent aligns with Brazil's emerging biotech and pharmaceutical innovation trends, offering commercial potential.
  • Legal Vigilance: Regular monitoring for potential oppositions or challenges can protect the patent's enforceability.
  • Strategic Use: Maximizing licensing or collaboration opportunities will require careful claim interpretation and landscape analysis.

FAQs

1. How broad are the claims typically in a patent like BR122023020985?
The breadth depends on the independent claims. If they cover a general chemical class, scope is broad; if they specify a single compound, scope is narrower.

2. What are the main risks to patent validity in Brazil?
Prevailing risks include prior art disclosures, obviousness, or insufficient disclosure. Overbroad claims may also be challenged.

3. How does Brazilian patent law affect pharmaceutical patent enforcement?
Brazilian law emphasizes public health and ensures the patentability of pharmaceuticals, but it also permits compulsory licensing under certain circumstances, impacting enforcement.

4. Can this patent hinder generic drug entry in Brazil?
Yes, if the patent remains valid, it can delay generic approval until its expiry, affecting market competition.

5. How should a company assess freedom-to-operate concerning BR122023020985?
Conduct comprehensive searches of related patent families, analyze claim overlaps, and consult local patent attorneys to identify potential infringement risks.


References

[1] INPI Patent Database. Official records of patent applications in Brazil.
[2] World Intellectual Property Organization (WIPO). Patent landscape reports.
[3] Brazilian Industrial Property Law No. 9,279/1996.
[4] Patent claim analysis methodologies. Patent Law Journal, 2022.
[5] Trends in Brazilian pharmaceutical patent filings. Pharma Intelligence, 2022.

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