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Last Updated: December 31, 2025

Profile for Brazil Patent: PI0908127


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US Patent Family Members and Approved Drugs for Brazil Patent: PI0908127

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
10,695,398 Apr 27, 2032 Ferring FIRMAGON degarelix acetate
10,729,739 Feb 10, 2029 Ferring FIRMAGON degarelix acetate
10,973,870 Feb 10, 2029 Ferring FIRMAGON degarelix acetate
11,766,468 Apr 27, 2032 Ferring FIRMAGON degarelix acetate
11,826,397 Apr 27, 2032 Ferring FIRMAGON degarelix acetate
9,415,085 Apr 27, 2032 Ferring FIRMAGON degarelix acetate
9,579,359 Feb 10, 2029 Ferring FIRMAGON degarelix acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent BRPI0908127: Scope, Claims, and Patent Landscape

Last updated: August 5, 2025


Introduction

Brazilian patent BRPI0908127, filed under the National Institute of Industrial Property (INPI), exemplifies Brazil’s approach to pharmaceutical patenting, balancing innovation protection with public health considerations. This patent pertains to a specific pharmaceutical compound or process, with its claims defining the extent of legal protection. The present analysis examines the patent’s scope and claims, contextualizing them within Brazil's patent landscape for pharmaceuticals, and evaluates strategic implications for stakeholders.


Patent Overview

BRPI0908127 was filed to secure exclusive rights over a particular pharmaceutical invention. The patent’s publication details—typically available through INPI’s public records—indicate the inventors, assignee, filing date, priority date, and the scope of inventive disclosure. While the detailed document adheres to formal patent documentation standards, the core of its enforceability lies in the breadth and specificity of its claims.


Scope of the Patent

1. Patent Term and Priority:
The patent was granted in accordance with Brazil's standard patent term—20 years from the filing date—assuming all maintenance fees are paid. The priority date aligns with the earliest filing, establishing prioritization over subsequent similar applications.

2. Territory:
As a national patent, BRPI0908127 offers exclusive rights solely within Brazil. The applicant may seek protection in multiple jurisdictions via regional treaties, but the patent's enforcement is limited geographically.

3. Subject Matter:
The patent likely covers a chemical compound, pharmaceutical formulation, or process, aligned with common pharmaceutical patent practices. Its claims delineate the exact scope of protection, differentiating it from prior art. The scope depends on whether the patent claims:

  • A specific active pharmaceutical ingredient (API)
  • A particular dosage form or formulation
  • A novel synthesis process
  • A combination therapy

Analysis of Claims

1. Type and Structure of Claims:
Brazilian patents typically feature independent and dependent claims. The independent claims set the broadest legal scope, while dependent claims narrow protection to specific embodiments.

2. Scope of Independent Claims:
Depending on the invention, the independent claims likely encompass:

  • Chemical Identity: A novel compound with defined structural formulae, such as a specific heterocyclic derivative.
  • Method of Synthesis: Steps detailing the preparation process for the active compound.
  • Pharmaceutical Composition: The formulation containing the active ingredient, including excipients and stabilizers.

3. Claim Language and Specificity:
Claims employing broad language may cover a wide range of derivatives or formulations but risk being vulnerable to invalidation if overly broad or not inventive over prior art. Conversely, narrow claims offer robust protection but limit commercial scope.

4. Claim Novelty and Inventiveness:
Brazilian patent law requires the invention to be both new and inventive, i.e., not disclosed publicly before filing and involving an inventive step. Given the patent’s scope, the claims likely carve out a specific niche—e.g., a new crystalline form or a improved synthesis pathway—that distinguishes it from existing prior art.

5. Potential Challenges and Limitations:
Brazil’s patent law introduces safeguards for public health, such as exceptions to patent rights under the Industrial Property Law (Law No. 9,279/1996). Patents claiming pharmaceutical products may face challenges if they are deemed to lack inventive step or are directed at known substances used in known ways, especially if they serve as secondary claims.


Patent Landscape in Brazil for Pharmaceuticals

1. Key Players and Filing Trends:
Brazil’s pharmaceutical patent landscape involves local and international players. Major pharmaceutical companies actively seek patent protection within Brazil, often filing for drugs already patented elsewhere, subject to patent term adjustments.

2. Regulatory & Legal Framework:
Brazil’s Law No. 9,279/1996 aligns with TRIPS provisions. The law emphasizes novelty, inventive step, and industrial applicability. Notably, patent term adjustments for pharmaceutical products—up to five additional years—are standard, compensating for regulatory delays.

3. Patentability Challenges and Public Policy:
Brazil’s patent system balances innovation incentives with public health, especially under the Framework of the Treaty of Patent Law. Challenges such as patent examinations for obviousness or prior art are robust, with frequent oppositions. The nation also has established patent examination guidelines to preempt overly broad claims.

4. Specific to BRPI0908127:
If the patent claims involve a mere new use of an existing drug or a known compound with obvious modifications, it could face validity challenges in Brazil’s courts or patent office. Conversely, claims covering a new chemical entity or a surprising combination can enjoy stronger protection.


Implications for Stakeholders

  • Pharmaceutical Innovators: The scope of BRPI0908127 exemplifies strategic claim drafting—balancing broad claims for market exclusivity against risks of invalidation.
  • Generic Manufacturers: Understanding the scope and claims helps identify potential patent cliffs or opportunities for patent challenges.
  • Legal and Patent Practitioners: Analyzing claim language and prior art landscape informs patent prosecution strategies and dispute resolutions.
  • Policy Makers: The patent landscape underscores the importance of aligning patent policies with public health goals, as seen in Brazil’s exceptions and limitations.

Key Takeaways

  • Scope Precision: The patent’s enforceability hinges on the specificity of its claims; broad claims risk invalidation, while narrow claims may limit market exclusivity.
  • Claims Strategy: Effective claim drafting involves balancing legal breadth with technical specificity, particularly in complex chemical inventions.
  • Landscape Dynamics: Brazil’s robust patent examination process, aligned with TRIPS, makes it a challenging environment for overly broad or obvious pharmaceutical patents.
  • Legal Safeguards: Brazil’s legal framework provides mechanisms (e.g., compulsory licensing, patent opposition) to prevent patents from unduly restricting access to medicines.
  • Market Opportunities: Patents like BRPI0908127 offer competitive advantages, but their longevity depends on ongoing maintenance and legal defenses.

FAQs

1. What is the typical duration of a pharmaceutical patent in Brazil, and how does BRPI0908127 fit within this?
Brazilian patents last 20 years from the filing date, subject to maintenance fees. BRPI0908127, granted within this framework, provides its owner exclusive rights for this period, assuming compliance with procedural requirements.

2. How does Brazilian patent law affect patent claims related to pharmaceutical use or formulations?
Brazil prioritizes inventive step and novelty. Claims covering new compounds or surprising methods are favorably examined, but claims merely covering known uses or formulations may face challenges under Section 4 of the law, especially if they lack inventive merit.

3. Can third parties challenge BRPI0908127’s claims?
Yes. Post-grant opposition, nullity actions, or patent invalidation proceedings allow third parties to challenge patent validity, especially if claims are overly broad or not supported by inventive activity.

4. How does Brazil’s public health policy influence pharmaceutical patent protection?
Brazil’s legal framework permits exceptions such as compulsory licensing, especially for public health emergencies, which can limit patent enforceability regardless of the patent’s scope.

5. Are there international strategies for protecting pharmaceutical patents similar to BRPI0908127 in other jurisdictions?
Yes. Companies often file corresponding patents in major markets like the US, EU, and Latin America to ensure comprehensive protection. Regional Patent Cooperation Treaty (PCT) filings can streamline this process.


References

[1] INPI Patent Records, BRPI0908127.
[2] Brazilian Industrial Property Law (Law No. 9,279/1996).
[3] WIPO Patent Cooperation Treaty (PCT).
[4] World Health Organization, Brazil’s Patent Policies and Public Health.
[5] Brazilian Patent Examination Guidelines, INPI.


Concluding Remarks:
BRPI0908127 exemplifies Brazil’s nuanced approach to pharmaceutical patents—aiming to protect genuine innovation while safeguarding public health interests. Stakeholders must continuously monitor the patent landscape, craft precise claims, and understand legal safeguards to optimize patent strategies within Brazil’s dynamic pharmaceutical environment.

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