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Last Updated: December 15, 2025

Profile for Peru Patent: 20210182


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US Patent Family Members and Approved Drugs for Peru Patent: 20210182

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 Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free Jun 20, 2039 Ipsen BYLVAY odevixibat
⤷  Get Started Free Jun 20, 2039 Ipsen BYLVAY odevixibat
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Peru Patent PE20210182

Last updated: August 8, 2025


Introduction

Peru patent PE20210182 pertains to a novel pharmaceutical invention, offering insights into the country’s intellectual property landscape for innovative drugs. Understanding its scope, claims, and surrounding patent environment is critical for stakeholders involved in drug development, licensing, and competitive strategy. This analysis dissects the patent’s technical scope, elucidates its claims, and contextualizes it within Peru’s pharmaceutical patent landscape.


Overview of Patent PE20210182

Patent Number: PE20210182
Filing Date: [Filing date not specified in the prompt, assumed to be 2021 based on the patent number]
Grant Date: [Not specified]
Status: Granted / Active (assumed based on the patent number)
Applicant/Assignee: [Not provided, typical for drug patents to be held by pharmaceutical companies or research institutions]

This patent is part of Peru’s pharmaceutical patent framework, which complies with the Andean Community’s (CAN) Decision 486—regulating patentability of pharmaceuticals.


Scope of the Patent

Technical Field and Purpose

Patent PE20210182 pertains to a novel therapeutic compound or formulation designed to treat specific medical conditions. The scope covers the chemical composition, methods of manufacturing, and therapeutic use. The patent addresses unmet medical needs—likely a new chemical entity (NCE), a new medical use of known compounds, or an improved formulation.

Claims Overview

The claims define the legal boundaries of patent protection. They can be broadly categorized as:

  • Product Claims: Covering the chemical compound(s) itself, including variants and analogs.
  • Process Claims: Encompassing manufacturing methods.
  • Use Claims: Covering therapeutic applications and methods of treatment.
  • Formulation Claims: Pertaining to specific pharmaceutical formulations, if applicable.

Given standard practices in pharmaceutical patents, the core claims likely include:

  1. Chemical Composition: A structurally defined compound with specific substitutions or configurations, characterized by particular physicochemical properties.
  2. Method of Synthesis: A process describing the steps to produce the compound with high purity and yield.
  3. Therapeutic Use: The use of the compound to treat or prevent a specific disease or condition, such as cancer, viral infections, or inflammatory disorders.
  4. Pharmaceutical Formulation: A specific formulation that enhances bioavailability, stability, or patient compliance.

Claim Limitations and Scope

Peruvian patent law aligns with international standards, emphasizing novelty, inventive step, and industrial applicability. The claims are expected to specify:

  • Novelty: The compound/process is not disclosed publicly before filing.
  • Inventive Step: The invention involves an inventive leap over prior art.
  • Industrial Applicability: The invention can be made or used in industry, specifically medicine.

Claims are tailored narrowly enough to meet patentability criteria but broad enough to prevent easy design-around.


Patent Landscape in Peru

Legal and Regulatory Context

Peru, as a member of the Andean Community, follows Decision 486, harmonizing patent laws among member states. The key elements include:

  • Patent Term: 20 years from filing date.
  • Patentability Criteria: Novelty, inventive step, industrial application.
  • Patentability of Pharmaceuticals: Limited by the “second medical use” provisions and patent exclusions for certain methods or substances, though chemical entities often qualify if they meet criteria.

Market Dynamics and Patent Trends

Peru’s pharmaceutical patent landscape features:

  • Emerging Local and Multinational Players: Active in innovating and protecting new drugs.
  • Focus on Chronic Diseases and Infectious Diseases: Common target areas for recent patent filings.
  • Legal Challenges: Patent oppositions and compulsory licensing provisions are active, aligning with Peru’s commitment to public health and access to medicines.

Patent Family and Innovation Trends

PE20210182 likely exists within a patent family covering key jurisdictions such as the PCT route, the US, Europe, and Latin America. Such a family enhances patent strength and market exclusivity.

Patent filings tend to cluster around compounds with high therapeutic potential—particularly antiviral, anticancer, and anti-inflammatory agents—highlighting Peru’s strategic focus on addressing local health needs through patent protection.


Implications for Stakeholders

For Pharmaceutical Developers

Understanding the patent’s scope informs licensing negotiations, patent infringement risks, and patent expiry strategies. A broad chemical claim can protect extensive analogs, providing leverage for generic development post-expiry.

For Competitors

Analyzing the claims reveals potential workarounds or areas of freedom to operate. Narrow claims might open avenues for designing around, while broad claims could necessitate licensing or patent challenges.

For Policy Makers

The patent landscape underscores the importance of balancing innovation incentives with public health objectives. Peru’s patent laws carefully vet pharmaceutical patents to prevent evergreening and ensure access.


Key Takeaways

  • Patent PE20210182 likely claims a novel chemical entity, its synthesis, therapeutic application, and possibly formulated pharmaceutical compositions.
  • Its scope is constrained by Peru's patent law, which requires demonstrable novelty, inventive step, and industrial application.
  • The patent landscape in Peru is characterized by strategic filings targeting high-demand therapeutic areas, with a legal framework supporting pharmaceutical innovation.
  • Stakeholders should closely analyze this patent's claims to navigate licensing opportunities, freedom-to-operate issues, and potential challenges.
  • Given Peru's cautious stance on pharmaceutical patents for public health reasons, patent validity and enforcement require meticulous legal and technical scrutiny.

FAQs

1. What is the significance of the scope in patent PE20210182?
The scope determines the extent of protection granted—whether it covers a broad class of compounds, specific formulations, or particular therapeutic uses—directly influencing market exclusivity and licensing potential.

2. How does Peru's patent law impact pharmaceutical patent claims?
Peru adheres to Decision 486, requiring patents to meet strict criteria of novelty, inventive step, and industrial application. Patents for new chemical entities generally qualify unless they are obvious or fall under exclusions.

3. Can existing drugs be patented under PE20210182?
Only if significantly new modifications, formulations, or therapeutic applications are demonstrated. Pure second use claims are more challenging under Peru’s patent law.

4. What are the challenges in patenting pharmaceuticals in Peru?
Challenges include strict examination standards, potential opposition proceedings, and balancing patent rights with public health policies, including compulsory licensing provisions.

5. How does the patent landscape affect drug access in Peru?
While patents incentivize innovation, they can also delay generic entry. The Peruvian legal framework seeks a balance, but patent enforcement and patent term limitations impact drug affordability and availability.


References

  1. Peruvian Patent Law (Decision 486). Office of the Peruvian Patent Office (INDECOPI).
  2. Andean Community Decision 486. Harmonized patent regulations in Latin America.
  3. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  4. Peru's Ministry of Health (MINSA). Policies on pharmaceuticals and patent regulations.
  5. Legal analysis of patent claims in pharmaceutical patents, [Published IP journals].

Note: As specific details such as the filing date, inventor, or chemical structure of patent PE20210182 were not provided, this analysis adopts a general technical and legal framework characteristic of pharmaceutical patents in Peru.

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