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Last Updated: December 18, 2025

Profile for Peru Patent: 20141681


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US Patent Family Members and Approved Drugs for Peru Patent: 20141681

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
⤷  Get Started Free Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib
⤷  Get Started Free Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib maleate
⤷  Get Started Free Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib
⤷  Get Started Free Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib maleate
⤷  Get Started Free Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent PE20141681: Scope, Claims, and Patent Landscape in Peru

Last updated: August 14, 2025


Introduction

Patent PE20141681 pertains to an innovative pharmaceutical product registered under Peru’s patent system. Understanding its scope, claims, and positioning within the broader patent landscape is critical for stakeholders—pharmaceutical companies, generic manufacturers, and legal entities—aiming to navigate Peru's intellectual property regulations effectively. This analysis provides a comprehensive evaluation, consolidating technical claims, scope boundaries, and the surrounding patent ecosystem.


Patent Overview

Patent Number: PE20141681
Filing Date: Likely around 2014 (based on the legal suffix)
Grant Date: Approximate, depending on national procedure duration
Applicant/Assignee: Data not specified here; usually, a pharmaceutical or biotech entity
Patent Type: Likely a utility patent, Protecting a drug compound, formulation, or use

While precise bibliographic data (such as inventor name, title, or applicant) are absent, the core focus involves a drug-related invention—common in pharmaceutical patents filed in Peru, which aligns with international standards under the Patent Cooperation Treaty (PCT) or direct national filings.


Scope of the Patent and Claims Analysis

1. Core Content and Likely Invention Focus
Based on typical pharmaceutical patent characteristics in Peru, PE20141681 likely claims:

  • A novel chemical compound or a pharmaceutical formulation
  • A new therapeutic use of known compounds
  • A specific dosage regimen or delivery system
  • A process for preparing the drug

Given Peru’s patentability guidelines, the scope possibly emphasizes inventive steps over mere discovery, focusing on technical advancements.

2. Claims Analysis

The claims define the protection scope. While the full text is unavailable here, such patents conventionally include:

  • Independent Claims:
    Covering the core inventive subject matter—probably a chemical entity with specific structural features or a formulation exhibiting enhanced stability, bioavailability, or activity.

  • Dependent Claims:
    Covering specific embodiments, such as certain salts, esters, polymorphs, methods of preparation, or associated therapeutic uses.

3. Typical Elements of the Claims
Based on common pharmaceutical patent practices:

  • Chemical Structure or Formula:
    The patent might specify a compound with a certain chemical formula, possibly involving novel substitutions that confer improved pharmacological properties.

  • Pharmaceutical Composition:
    Claims may include a combination of the active ingredient with excipients, defining the dosage form (tablet, capsule, injection).

  • Method of Treatment:
    Claims could specify methods for treating particular diseases or conditions, involving the compound or composition.

  • Process Claims:
    Including specific synthetic routes for the compound, emphasizing efficiency, purity, or environmental benefits.

4. Claim Scope and Limitations
In Peruvian practice, patent claims must be clear, concise, and supported by the description. They generally balance inventiveness and industrial applicability. The scope likely excludes prior-art compounds, thus focusing on inventive structural modifications or novel therapeutic applications.


Patent Landscape in Peru for Pharmaceutical Drugs

1. National Patent Environment
Peru adopted the Andean Community’s decision harmonizing pharmaceutical patent law, aligning with TRIPS (Trade-Related Aspects of Intellectual Property Rights), setting a 20-year patent term from the filing date.

2. Patent Filing Trends (2010-2020)
Peru primarily sees filings for innovative drugs, vaccine-related inventions, and bio-therapeutic agents. The patent landscape is characterized by:

  • Emphasis on chemical and pharmaceutical compound patents
  • Increased filings post-permanent TRIPS adherence in 1997
  • Limited number of pharmaceutical patents granted annually, reflecting cautious examination and strict patentability standards

3. Patent Examination and Grant Process
Peru’s Patent Office (Indecopi) conducts substantive examination, verifying novelty, inventive step, and industrial applicability. The process duration averages 3-5 years, with some applications facing objections based on lack of inventive step or prior art.

4. Patent Challenges and Oppositions
Post-grant oppositions are possible within a set period, often used by competitors to contest broad claims or challenge inventive merit.

5. Patent Clusters and Overlaps
Peruvian patents in the pharmaceutical space often interface with regional and international patents—particularly those filed through Andean Community or WIPO pathways—forming a complex landscape with overlaps, especially for compounds with international patent families.


Legal and Commercial Implications

  • Patent Scope:
    A broad claim scope enhances market exclusivity but risks rejection if claims are deemed to cover known compounds or obvious modifications.

  • Patent Strategy:
    Innovators should focus on drafting claims that cover specific structural features, formulations, and methods, considering Peruvian patent standards for clarity and support.

  • Patent Enforcement:
    Enforcement relies on local courts and customs, with regulatory agencies like DIGEMID involved in compliance issues, including patent invalidations or license negotiations.

  • Public Health Considerations:
    Peru’s strict patentability standards are balanced against public health policies, allowing certain exceptions and compulsory licensing under TRIPS flexibilities, especially for essential medicines.


Conclusion

Patent PE20141681 probably claims a specific pharmaceutical compound, formulation, or use with a clear inventive step. Its scope hinges on structural features, process innovations, or therapeutic applications, designed within Peru’s legal framework, which emphasizes novelty, inventive step, and industrial applicability.

The patent landscape in Peru continues to evolve, influenced by regional harmonization efforts and the balance between patent rights and public health considerations. Stakeholders must align patent drafting and enforcement strategies cautiously with Peru’s legal standards to secure and sustain effective patent protection.


Key Takeaways

  • Precise Claim Drafting Is Critical: Focus on structural novelty, specific formulations, or therapeutic methods to ensure broad yet defensible claims within Peru’s patent standards.

  • Monitor Regional Patent Trends: Peru’s pharmaceutical patent landscape often overlaps with regional filings; a comprehensive regional strategy amplifies market protection.

  • Understand Legal Exceptions: Be aware of TRIPS flexibilities and public health policies that may impact patent enforceability or compulsory licensing.

  • Stay Updated on Examination Practice: Peru’s patent office conducts substantive reviews, especially for chemical and pharmaceutical inventions, requiring robust patent specifications.

  • Innovate Beyond Known Compounds: Differentiation through improved efficacy, safety, or delivery mechanisms is essential for patentability in Peru’s competitive environment.


FAQs

Q1: What types of pharmaceutical inventions are patentable in Peru?
A1: Compounds, formulations, methods of manufacturing, and therapeutic uses that demonstrate novelty, inventive step, and industrial applicability.

Q2: How long does it typically take to get a pharmaceutical patent granted in Peru?
A2: Between 3 to 5 years, depending on examination duration and potential objections.

Q3: Can existing patents be challenged or invalidated in Peru?
A3: Yes, through administrative oppositions or civil invalidation proceedings, especially if claims lack novelty or inventive step.

Q4: Is there any regional patent cooperation relevant to Peru?
A4: Yes. Peru is part of the Andean Community Patent System, providing a regional patent approach, alongside WIPO and PCT filings.

Q5: What is the scope of patent PE20141681 in terms of enforcement?
A5: It likely covers specific compounds or formulations; enforcement requires demonstrating infringement within the scope of granted claims and complying with local procedures.


References

[1] Indecopi. (n.d.). Peru Patent Law and Regulations.
[2] World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) System in Peru.
[3] Andean Community. (2020). Common Patent Regulations.
[4] TRIPS Agreement, WTO. (1994). Trade-Related Aspects of Intellectual Property Rights.

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