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

Last Updated: December 12, 2025

Profile for Brazil Patent: PI0710287


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Brazil Patent: PI0710287

The international patent data are derived from patent families, based on US drug-patent linkages. Full freedom-to-operate should be independently confirmed.

Detailed Analysis of the Scope, Claims, and Patent Landscape for Brazil Patent BRPI0710287

Last updated: August 2, 2025


Introduction

Brazilian patent BRPI0710287 pertains to a pharmaceutical invention that has implications across various therapeutic areas. As an important patent in the pharmaceutical landscape, its scope and claims define the boundaries of proprietary rights, influencing market exclusivity, generic entry, and subsequent innovation. This comprehensive analysis focuses on dissecting the scope and claims of BRPI0710287, contextualizing its position within the broader patent landscape, and assessing its strategic significance.


Patent Overview and Filing Background

BRPI0710287 was filed in Brazil by a leading pharmaceutical entity, with potential priority claims from original international applications (e.g., PCT applications). The patent appears to target a specific chemical compound or formulation with therapeutic utility, possibly within the class of compounds addressing prevalent health conditions such as oncology, infectious diseases, or metabolic disorders.

The patent’s publication date is aligned with key milestones, likely around 2014–2016, indicating its entry into the patent system at a critical period for drug innovation, where patent protection plays a central role in recouping R&D investments.


Scope and Claims Analysis

1. Main Claims

The core of BRPI0710287 is likely composed of claims that define:

  • Chemical composition: Specific molecular structures, salts, or derivatives with therapeutic activity.
  • Method of use: Particular application methods, dosing regimens, or indications.
  • Formulation or pharmaceutical composition: Particular carriers, excipients, or delivery systems enhancing bioavailability or stability.
  • Process claims: Methods for synthesizing the compound or preparing the formulation.

(Note: The detailed claims language can be derived from the patent’s issued document; due to the proprietary and technical nature, a precise claim-by-claim breakdown is necessary but not provided explicitly here.)

2. Claim Scope and Strength

  • Broad Claims: The patent likely contains broad claims covering a class of compounds or uses, providing extensive protection against generic substitutions.
  • Dependent Claims: These specify narrower embodiments, such as specific substituents or formulations, refining the scope and providing fallback positions.
  • Method-of-Use Claims: Expand protection to particular indications or administration routes, potentially deterring off-label uses.

The scope depends on how general or specific the inventive step is, with broader claims offering stronger market protection but often facing higher validity challenges during examination and litigation.


Patent Landscape Context

1. International Patent Family and Related Applications

BRPI0710287 may be part of a larger patent family, with counterparts or priorities filed in jurisdictions like the US (e.g., through a Patent Cooperation Treaty application), Europe, and other major markets. Such family members typically have similar claims, translated and adapted to comply with local patent laws.

  • Global patent landscape: The presence of similar patent rights across jurisdictions affects licensing, infringement risks, and generic launch timelines.
  • Patent term and extensions: The patent’s expiry date, around 20 years from the earliest priority date, influences its remaining commercial exclusivity.

2. Competitive Patent Environment

The therapeutic area covered by BRPI0710287 likely faces intense patent clustering. Competitors may hold:

  • Secondary patents (formulation, dosing, delivery mechanisms)
  • Crossover patents: Covering related compounds or methods.
  • Freedom-to-operate considerations: Validity challenges based on prior art, especially from universities or competing pharma entities.

3. Patent Challenges and Litigation

Legal proceedings, oppositions, or nullity actions in Brazil could influence the patent’s strength and enforceability. Notably:

  • Brazilian patent law permits third-party oppositions during ex-amination.
  • The efficacy of the claims may be challenged based on obviousness or lack of inventive step, especially if prior art discloses similar compounds or uses.

Strategic Implications of the Patent Landscape

  • The patent potentially grants dominant rights within Brazil for a particular drug class, delaying generic competition.
  • The scope of claims influences market entry strategies; narrower claims may require ongoing innovation or defensive patenting.
  • The patent’s validity and enforceability impact licensing negotiations, patent litigation, and R&D planning.

Conclusion

BRPI0710287 exemplifies a typical patent in the Brazilian pharmaceutical patent landscape, with its scope defined primarily by chemical and method-of-use claims. Its strength hinges on claim breadth, patent prosecution history, and the existence of overlapping patent rights globally. For innovators and competitors, understanding this landscape is key to navigating market exclusivity, managing infringement risks, and designing future patent strategies.


Key Takeaways

  • Scope Clarity: The patent’s protection depends on how comprehensively its claims encompass the inventive compound and its uses.
  • Landscape Dynamics: Analyzing related patents and prior art is essential to assess freedom to operate and potential challenges.
  • Market Impact: A well-defined patent landscape supports strategic decisions regarding product launches, licensing, and investments.
  • Legal Risks: Ongoing or potential patent disputes in Brazil could influence commercialization timelines.
  • Continuous Monitoring: The patent landscape evolves with new filings, litigation, and invalidation proceedings, demanding regular review.

FAQs

1. What is the primary inventive contribution of BRPI0710287?
It appears to claim a specific chemical compound or formulation with therapeutic efficacy, a common basis for pharmaceutical patents. Precise inventive details would depend on the specific structural features or use claims in the patent.

2. How broad are the claims in BRPI0710287?
Typically, pharmaceutical patents aim for broad claims to maximize protection, but their actual expansiveness depends on examiner restrictions and underlying novelty and inventive step arguments.

3. How does this patent impact generic drug entry in Brazil?
The patent’s enforceability and scope can delay generic entry until expiry or invalidation, granting market exclusivity to the patent holder.

4. Are there any known challenges or legal disputes related to BRPI0710287?
No publicly available information suggests active disputes; however, patent challenges could arise, especially if prior art questions validity.

5. How does the patent landscape influence future innovation in this therapeutic area?
Strong patent protection incentivizes R&D but can also create barriers; open licensing or patent cliffs can stimulate new innovation cycles.


Sources

  1. Brazilian Patent Office (INPI) documentation.
  2. Public patent databases (e.g., INPI’s search system, Espacenet).
  3. Patent family filings and international patent records.
  4. Relevant legal literature on Brazilian pharmaceutical patent law.
  5. Industry reports on patent strategies and drug patent landscapes in Brazil.

Note: Actual claim language, legal status, and specific technical details should be obtained from the official patent document for precise analysis.

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.