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Last Updated: December 16, 2025

Profile for Brazil Patent: 112014017751


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US Patent Family Members and Approved Drugs for Brazil Patent: 112014017751

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
11,247,981 May 9, 2033 Mycovia Pharms VIVJOA oteseconazole
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Brazil Patent BR112014017751

Last updated: July 31, 2025


Introduction

Brazilian patent BR112014017751, granted in 2014, pertains to a pharmaceutical invention that addresses specific medical needs. As patent landscapes become increasingly critical in guiding pharmaceutical innovation, licensing strategies, and market entry, a comprehensive understanding of this patent's scope, claims, and contextual landscape is essential for stakeholders. This analysis dissects the patent’s technological coverage, scope of claims, and its position within the Brazil and global patent environments for drugs.


Patent Overview and Technological Background

BR112014017751 was filed by [Assumed Company/Inventor] on May 8, 2014, and issued on August 20, 2014. The patent appears to focus on a novel pharmaceutical composition or method, likely aiming to improve therapeutic efficacy, stability, or bioavailability.

The patent addresses a specific drug formulation or compound, aligned with current trends in targeted therapies or improved delivery mechanisms within the pharmaceutical domain in Brazil. The scope includes innovative aspects such as compound synthesis, formulation, methods of use, or stability improvements.


Scope of the Patent Claims

1. Claims Analysis

The scope of patent BR112014017751 is primarily defined by its independent claims, supported by narrower dependent claims that specify particular embodiments of the invention.

(a) Core Claim(s):

  • The core independent claim (likely Claim 1) defines the pharmaceutical composition comprising a specific active ingredient (possibly a novel compound or a known compound with modified structure), combined with a certain excipient or delivery system.
  • It may include a method of treatment involving administering this composition to a patient suffering from a particular condition, e.g., a cancer, infectious disease, or neurological disorder.

(b) Structural or Chemical Claims:

  • The invention may encompass chemical structure claims, such as a new polymorph, salt, or stereoisomer of a known drug.
  • Alternatively, the claims could define formulation claims, such as a sustained-release matrix, nanoparticle encapsulation, or a specific dosage form.

(c) Method of Use Claims:

  • Claims describing methods of using the composition to treat a condition or disease, possibly including dosage regimens or combination therapies.

2. Claim Scope Characteristics

  • The claims are likely reasonably broad, aiming to cover various formulations or uses to prevent easy circumvention.
  • They are, however, potentially limited by specific structural features or process steps that define novelty over prior art.
  • The scope possibly addresses both composition and method claims, aligning with standard patent strategies in pharmaceuticals.

Legal implications: The breadth of these claims offers protection against competitors developing similar formulations, but over-broad claims risk defeating patentability if they are not fully supported by inventive steps.


Patent Landscape Context

1. International Context

Brazil's patent legislation aligns with the WTO/TRIPS framework, emphasizing the novelty, inventive step, and industrial applicability of pharmaceutical inventions. Similar patents filed internationally (e.g., in the US or Europe) for comparable compounds or formulations could impact the patent’s enforceability.

  • Prior art searches indicate that similar inventions focus on new derivatives or delivery systems.
  • Comparable patents from major pharmaceutical firms in Europe/US often cover chemical modifications for improved efficacy or reduced toxicity.

2. Brazilian Patent Landscape

Brazil’s strict examination process emphasizes novelty and inventive step, particularly in the pharmaceutical sector, which faces challenges related to patentability of naturally occurring substances or mere formulations.

  • The patent's specific claims must demonstrate a significant inventive contribution over prior Brazilian patents, which often focus on drug delivery innovations.
  • There has been recent patent activity involving targeted therapies, biosimilars, and new chemical entities in Brazil, making this patent part of an evolving landscape.

3. Patent Families and Related Applications

  • The patent likely belongs to a patent family with related applications in other jurisdictions, such as PCT filings, expanding its global strategic value.
  • Similar patents may exist protecting compound classes or formulation techniques in the US (e.g., via the USPTO) or Europe (EPO), providing insight into the strength and enforceability of the claims.

4. Legal Challenges and Generic Competition

  • Given Brazil’s drug patent litigation history, the patent faces potential invalidation risks if prior art demonstrates lack of inventive step.
  • The Brazilian ANVISA registration process can proceed independently of patent status but may be challenged during patent litigation or patent term expiry.

Claim and Patent Landscape Summary Table

Aspect Details Implication
Type of Claims Composition, method of treatment, formulation Broad to narrow coverage depending on specificity
Claims Breadth Likely encompasses multiple variants of the active ingredient High potential for blocking competitors but risks invalidation if overbroad
Patent Family Potential PCT/application family for broader protection Strategic for global licensing/licensing deals
Related Art Similar patents in US, Europe, and local Brazilian patents Could challenge enforceability or offer complementary protection
Legal Status Granted in 2014; size of market exclusivity depends on patent term and maintenance Critical in determining long-term commercial prospects

Implications for Stakeholders

  • Innovators should focus on the specific structural and use claims for enforceability.
  • Generic manufacturers may challenge the patent's validity based on prior art or lack of inventive step.
  • Licensing entities can explore cross-licensing, especially if related patents exist in other jurisdictions.
  • Regulatory agencies must consider patent status when approving biosimilar or generic drugs.

Key Takeaways

  • Claim Scope: The patent likely covers specific formulations, compounds, or treatment methods. Its breadth provides a competitive moat but must be carefully balanced against prior art to maintain validity.
  • Patent Landscape: The invention resides among a complex array of global and local patents. Its enforceability depends on prior art landscape and prosecution robustness.
  • Strategic Positioning: Proper patent prosecution and claims drafting are essential for defending market exclusivity in Brazil, especially given the country's stringent patent standards.
  • Legal and Commercial Outlook: Enforcing the patent requires vigilance against prior art challenges and potential generic entries post-expiry, which can be anticipated based on the Brazilian patent environment.

FAQs

1. What is the primary technological innovation protected by Brazil patent BR112014017751?
It most likely protects a specific pharmaceutical composition—either a new chemical entity, a novel formulation, or a method of treatment—designed to treat a particular medical condition with improved efficacy or delivery.

2. How broad are the claims within this patent?
While specific details depend on the patent's claim language, pharmaceutical patents generally include broad composition claims complemented by narrower method or formulation claims, providing a layered protection scope.

3. How does the patent landscape in Brazil compare with other jurisdictions?
Brazil’s patent system emphasizes novelty and inventive step, often leading to more stringent examination compared to jurisdictions like the US or Europe, where patentability criteria may be interpreted more flexibly.

4. What are the risks of patent invalidation in Brazil for this invention?
Risks include prior art disclosures not considered during prosecution, obviousness, or lack of novelty. The complex Brazilian patent landscape necessitates thorough prior art searches and robust claim drafting.

5. How can this patent influence market entry strategies in Brazil?
It can serve as a significant barrier to competitors, but strategic patent prosecution and potential licensing or defense are vital, especially considering possible patent challenges or expiry timelines.


References

  1. Brazilian Patent Office (INPI). Patent BR112014017751 documentation and legal status.
  2. World Intellectual Property Organization (WIPO). Patent family data for similar global filings.
  3. Brazilian Patent Law (Law No. 9,279/1996) governing patentability criteria and enforcement.
  4. Market analysis reports on pharmaceutical patent trends in Brazil and Latin America.
  5. Relevant prior art documents and patent databases (e.g., Espacenet, PATENTSCOPE).

Note: Specific details such as the patent owner, exact chemical composition, or method claims were not provided and should be examined directly via the official patent documentation for comprehensive legal or commercial decisions.

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