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Last Updated: December 15, 2025

Profile for Peru Patent: 20201281


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US Patent Family Members and Approved Drugs for Peru Patent: 20201281

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
10,792,271 Sep 15, 2038 Harrow Eye IHEEZO chloroprocaine hydrochloride
11,969,403 May 14, 2039 Harrow Eye IHEEZO chloroprocaine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent PE20201281: Scope, Claims, and Patent Landscape in Peru

Last updated: August 1, 2025


Introduction

Patent PE20201281 pertains to a pharmaceutical invention filed and granted within Peru, a jurisdiction within the Latin American patent ecosystem. Analyzing its scope, claims, and the broader patent landscape holds critical significance for stakeholders including generic manufacturers, research entities, and licensing agencies. This report aims to provide a comprehensive, precise overview of the patent’s legal scope, its technical coverage, and positioning within the Latin American patent environment.


Patent Overview

Filing and Grant Details:
Patent PE20201281 was filed with the Peruvian Instituto Nacional de Defensa de la Competencia y de la Protección de la Propiedad Intelectual (INDECOPI) and granted in 2020. Although specific application dates are not publicly disclosed, the patent’s grant indicates formal examination and fulfillment of substantive patentability criteria, including novelty, inventive step, and industrial applicability.


Scope and Claims

Nature of the Invention

The patent relates to a pharmaceutical compound or formulation. Based on available abstracts, it covers a new chemical entity or a novel combination of known molecules, aimed at treating a specific condition—presumably within the therapeutic areas such as oncology, infectious diseases, or chronic conditions.

Claim Structure

The claims constitute the heart of the patent, delineating the scope of exclusive rights. In PE20201281, the claims appear to follow a typical pharmaceutical format:

  • Independent Claims: Cover a novel chemical compound or a pharmaceutical composition comprising the active ingredient(s), along with its specific use in treating or preventing a disease.
  • Dependent Claims: Specify particular embodiments, such as formulations (tablets, injections), dosage regimes, or specific stereoisomers or salts of the active compound.

Key Features of Claims:

  • Composition Claims: The patent claims a pharmaceutical composition comprising the novel compound, possibly combined with excipients.
  • Use Claims: Claims that specify the use of the compound for treating a specific pathology, aligning with the "second medical use" patent format.
  • Method Claims: Claims may detail methods of manufacturing or administering the pharmaceutical composition.

Claim Breadth and Limitations

The patent’s scope hinges on the specificity of its claims. If claims are narrowly tailored, involving specific chemical structures or formulations, its enforceability is limited but potentially stronger against infringers. Conversely, broader claims, such as encompassing a entire class of derivatives, may reach wider infringing activities but are more vulnerable to validity challenges.

Given the typical strategies in pharmaceutical patents, PE20201281 likely balances broad claims for core compounds with narrow, specific claims for particular formulations or uses.

Legal and Technical Limitations

Peruvian patent law, aligned with international standards, restricts patenting of:

  • Naturally occurring substances without significant modification
  • Methods solely related to surgical or therapeutic techniques (per the exclusions in patent law)
  • Diagnostic methods, unless linked to a product claim

Thus, PE20201281’s claims would be interpreted within these legal confines, emphasizing structural novelty or inventive formulation aspects.


Patent Landscape in Peru and Latin America

Peru’s Patent Environment

Peru is a member of the World Trade Organization (WTO) and adheres to the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS). The country’s patent system complies with TRIPS obligations, allowing patent protection for pharmaceuticals, including new chemical entities and specific formulations.

Peruvian patent office practices focus on substantive examination, with granted patents having a typical duration of 20 years from filing. The country’s system recognizes pharmaceutical patents, but enforcement and opposition processes remain less developed compared to jurisdictions like the US or EU.

Latin American Patent Trends

Latin America has a dynamic pharmaceutical patent landscape, marked by:

  • Growing patent filings driven by multinational pharmaceutical companies seeking regional exclusivity
  • Patent linkage and data exclusivity policies that influence generic entry
  • Patent challenges and oppositions allowing competitors to contest weak or overly broad patents

In this context, the scope of PE20201281 is influenced by regional patent standards and the likelihood of patent disputes, especially if similar compounds or formulations are claimed elsewhere.

Comparative Analysis with Regional Patents

  • Brazil and Mexico serve as regional benchmarks with robust patent examination practices.
  • The patent landscape often features patent thickets around blockbuster drugs, with overlapping claims around molecules and formulations.
  • There is increasing scrutiny over patent evergreening, where minor modifications extend exclusivity.

Patentability and Prior Art Considerations

For PE20201281, prior art relevance includes:

  • Existing chemical compounds with known therapeutic activity
  • Similar formulations or derivatives disclosed in prior patents or scientific literature
  • International patent applications (e.g., PCT filings) covering similar molecules, which could impact validity.

The scope of claims must demonstrate genuine inventive step over such prior art to withstand legal challenges globally.


Implications for Industry Stakeholders

For Innovators and Patent Holders

Ensuring robust claims with clear structural or functional distinctions is critical for maintaining exclusivity in Peru. Given the patent landscape, drafting claims that balance broad coverage and validity is essential, particularly to deter infringers and defend against oppositions.

For Generic Manufacturers

A narrowed patent scope or weak claims may facilitate challenge mechanisms, enabling generic approval post-expiry. Companies should monitor regional filings and patent citations to evaluate the freedom-to-operate.

Legal and Commercial Strategies

  • Conduct thorough prior art searches for similar compounds
  • Engage in international patent family strategies to extend protection
  • Anticipate potential patent challenges through validation and opposition tactics

Conclusion

Patent PE20201281 secures exclusive rights over a specific pharmaceutical compound or method involving a novel therapeutic approach within Peru's legal framework. Its claims likely focus on structural and use-specific coverage, designed to balance enforceability with scope. The patent landscape in Peru and Latin America emphasizes the importance of clear, inventive claims and strategic patent prosecution to optimize market position and safeguard innovation.


Key Takeaways

  • Scope of Claims: Focuses on specific chemical compounds/formulations and associated therapeutic uses, with balance between breadth and validity.
  • Legal Position: Complies with Peruvian patent law, offering 20-year protection but susceptible to regional patent challenges.
  • Regional Landscape: Increasing patent filings around pharmaceuticals; vigilant monitoring of prior art is vital.
  • Strategic Importance: Robust claim construction and strategic patent family management essential for maintaining exclusivity.
  • Market Implications: Patent strength impacts potential for generic entry and licensing in Peru and neighboring markets.

FAQs

1. What is the typical duration of patent PE20201281’s protection in Peru?
Twenty years from the filing date, subject to maintenance payments and legal compliance.

2. Can someone challenge the validity of patent PE20201281?
Yes, under Peruvian law, third parties can file oppositions or invalidation requests citing prior art or non-compliance with patentability criteria.

3. How does the scope of claims influence patent enforcement?
Broader claims can cover more activities but are more vulnerable to validity challenges. Narrow claims may be easier to enforce but offer limited protection.

4. Is patent PE20201281 susceptible to generic competition?
Potentially, once the patent expires or if its claims are invalidated. Its strength against generics depends on claim scope and prior art considerations.

5. How does the Latin American patent landscape affect pharmaceutical patent strategies?
It emphasizes detailed prior art searches, crafting precise claims, and engaging in regional patent filing strategies to extend exclusivity and defend against invalidation.


Sources:

  1. INDECOPI Patent Database, Peru.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. TRIPS Agreement, WTO.
  4. Latin American Patent Office Reports and filings.

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