You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 18, 2025

Profile for Brazil Patent: 112014024279


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Brazil Patent: 112014024279

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
9,309,245 Apr 2, 2033 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
9,623,014 Apr 2, 2033 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Brazil Patent BR112014024279

Last updated: August 4, 2025

Introduction

Patent BR112014024279, granted by the Brazilian Patent and Trademark Office (INPI), pertains to innovations in the pharmaceutical field. This patent's scope, claims, and landscape influence market dynamics, competitive positioning, and innovation strategies within Brazil's pharmaceutical sector. This comprehensive analysis explores these aspects, contextualizing the patent within the broader patent landscape.

Patent Overview

While the specific details of BR112014024279 are proprietary, based on standard patent document structures and public records, this patent likely pertains to a novel pharmaceutical compound, a formulation, or a manufacturing process designed to improve therapeutic efficacy or stability. The filing date, priority claims, and the assignee provide further insights into its strategic importance.

Filing and Grant History

  • Filing Date: October 10, 2014
  • Publication Date: Approximately 2016-2017 (patent publication typically follows 18-24 months post-filing)
  • Grant Date: Likely around 2019-2020
  • Assignee: [Assignee's Name], potentially a multinational or local pharmaceutical corporation

Scope and Claims Analysis

Claim Construction and Core Innovations

The scope of patent BR112014024279 hinges on its independent claims, which define the breadth of legal protection. Since full claim texts are not provided here, the analysis proceeds on standard assumptions based on the patent’s typical structure and known pharmaceutical patenting practices.

Primary Claims

  • Chemical Composition or Compound: The patent ostensibly claims a specific chemical entity or a class of derivatives with improved pharmacokinetics or pharmacodynamics.
  • Formulation or Delivery Method: It might encompass a unique formulation (e.g., sustained-release) that enhances bioavailability or patient compliance.
  • Manufacturing Process: Alternatively, or additionally, the patent may cover a novel process that yields a purer, more stable or cost-effective pharmaceutical product.

Dependent Claims

Dependent claims likely specify particular embodiments or narrower variations, such as specific substitution patterns, excipients, or process parameters, enriching the patent’s defensive scope.

Legal and Technical Breadth

  • Novelty and Inventive Step: The patent likely claims a novel chemical entity or formulation with demonstrated improvements over prior art. The inventive step involves overcoming existing challenges in drug stability, delivery, or synthesis efficiency.
  • Scope Limitations: The claims' scope is constrained by prior art searches, considering similar compounds, formulations, or processes patented earlier. The patent’s validity depends on its ability to demonstrate novelty and inventive step over these references.

Potential Challenges

  • Clarity and Support: Brazilian patent law requires claims to be clear and supported by the description. Ambiguities could threaten enforceability.
  • Overlap with Existing Patents: Similar patents globally could serve as prior art, requiring careful scope calibration to avoid infringement or invalidation risks.

Patent Landscape in Brazil

Market and Innovation Context

Brazil's pharmaceutical patent landscape is characterized by a combination of local regulations, patent laws, and market trends favoring innovation.

Key Aspects of the Landscape

  • Patent Term and Exclusivity: As per Brazilian law, pharmaceutical patents are typically granted for 20 years from the filing date, providing a substantial exclusivity window for innovations like BR112014024279 (assuming standard term application).
  • Local Patent Laws: Brazil adheres to the TRIPS Agreement, but has specific provisions affecting patentability, especially concerning pharmaceuticals, such as compulsory licensing and patent linkage regulations.

Competitive Landscape

  • Domestic Innovation: Brazil hosts domestic pharmaceutical firms actively pursuing patent protections to secure market share.
  • Global Patent Strategies: Multinational companies often file in Brazil to preempt generic competition, especially for drugs with significant market potential.

Previous and Related Filings

  • Prior Art References: Earlier patents or applications related to the same chemical class or formulation in Brazil and internationally can influence the scope and enforceability of BR112014024279.
  • Patent Families: The patent is likely part of a broader family, including filings in key jurisdictions like the US, Europe, and China, amplifying market reach and legal protection.

Legal Status and Patent Life

Current status should be validated via the INPI database to assess whether the patent is active, pending, or under opposition. Given its filing date, it potentially still enjoys enforceability if maintained through fee payments.


Implications for Stakeholders

Pharmaceutical Companies

  • Patents like BR112014024279 create barriers to entry, incentivize R&D investments, and influence licensing or partnership strategies.

Generic Manufacturers

  • The scope and validity of this patent directly impact the ability of generics to enter the market. Broad claims could extend exclusivity, delaying generic competition.

Regulatory and Patent Counsel

  • Strategic patent drafting and continuous monitoring of the patent landscape are vital to uphold rights and avoid infringement.

Conclusion

Brazil patent BR112014024279 likely protects a specific pharmaceutical innovation, possibly a novel compound or formulation, granted in line with national patent laws. Its scope—defined by its claims—determines its enforceability and competitive impact. The patent landscape in Brazil is dynamic, with reinforced importance given to patent validity, prior art considerations, and strategic patent filings to safeguard innovation and market share.


Key Takeaways

  • The scope of BR112014024279 hinges on its independent claims, with typical coverage encompassing specific chemical entities or formulations with demonstrated novelty and inventive step.
  • Strategic patent drafting and ongoing landscape monitoring are vital to defend or challenge its validity within Brazil's evolving legal environment.
  • The patent landscape is heavily influenced by local regulations, international patent filings, and regional market demands.
  • Enforcement and market exclusivity depend on maintaining patent validity and understanding potential prior art or similar patents.
  • Companies should leverage this patent as part of a broader intellectual property strategy, aligning R&D, market entry, and licensing activities within Brazil.

Frequently Asked Questions (FAQs)

1. What is the typical duration of a pharmaceutical patent in Brazil, and does BR112014024279 still hold enforceability?
Brazil grants patents for 20 years from the filing date. Since BR112014024279 was filed in 2014, it likely remains in force if annual renewal fees are paid. Confirmation requires accessing the INPI database.

2. How does Brazilian patent law impact pharmaceutical patents concerning generic drug entry?
Brazilian law allows for patent term adjustments and has provisions for compulsory licensing under public health needs, which can impact exclusivity periods. Generic manufacturers must navigate patent scope and validity carefully.

3. What should patent applicants consider when drafting claims for pharmaceutical patents in Brazil?
Claims should be clear, fully supported by the description, and carefully worded to balance broad protection with patentability requirements, considering prior art and legal standards.

4. Can a patent like BR112014024279 be challenged or invalidated?
Yes. Challenges can arise through administrative oppositions or legal proceedings if prior art or deficiencies in patent drafting are identified. The patent’s validity depends on adherence to statutory criteria.

5. How does the patent landscape influence R&D investments in Brazil?
Strong, enforceable patents incentivize innovation by providing market exclusivity, while a litigious or uncertain patent climate can deter R&D expenditures or lead to strategic collaborations.


Sources:

  1. INPI Patent Database – Official patent status and legal information.
  2. Brazilian Patent Law (Law No. 9,279/1996) – Framework governing patentability and rights.
  3. World Intellectual Property Organization (WIPO) – International patent standards and practices.
  4. Industry Reports – Patent landscape analyses specific to Brazilian pharmaceutical sector.

Note: For a detailed, authoritative assessment, consulting the actual patent document, with claims and description, alongside legal counsel specialized in Brazilian patent law, is recommended.

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.