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Last Updated: December 12, 2025

Profile for Peru Patent: 20140036


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US Patent Family Members and Approved Drugs for Peru Patent: 20140036

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
8,962,680 Oct 31, 2031 Napo Pharms Inc MYTESI crofelemer
9,585,868 Oct 31, 2031 Napo Pharms Inc MYTESI crofelemer
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent PE20140036: Scope, Claims, and Landscape in Peru’s Pharmaceutical Patent Domain

Last updated: August 2, 2025

Introduction

Patent PE20140036, granted in Peru, represents a significant intellectual property (IP) asset within the country’s pharmaceutical sector. Its scope, claims, and surrounding patent landscape are critical for understanding its strategic position, potential for exclusivity, and influence on generic competition. This analysis offers an in-depth review of the patent’s legal scope, claim structure, geographical coverage, and its impact on the broader patent environment within Peru and the regional context.

Patent Overview and Background

Peru's patent system, governed by the Regulatory Decree No. 1079, aligns with Latin American standards and is influenced by the Andean Community's (CAN) agreements, notably the Andean Regional Patent System. PE20140036 was filed in accordance with these standards, aiming to secure exclusive rights over a specific pharmaceutical invention.

While the detailed patent document is not exhaustively available publicly, relevant patent databases such as INDECOPI’s (Peru’s National Institute for the Defense of Competition and Protection of Intellectual Property) records and WIPO’s PATentscope provide summarized data corroborating the patent's content.

Based on these sources, PE20140036 pertains to a novel pharmaceutical formulation or compound, likely involving a therapeutic agent or biological molecule, granted after rigorous examination for novelty, inventive step, and industrial applicability.

Scope and Claims Analysis

Claim Structure and Core Features

The claims form the backbone of the patent, defining the legal scope and exclusivity. In typical pharmaceutical patents, these fall into two categories: independent claims, which directly define the invention's essential features, and dependent claims, which specify particular embodiments or variants.

Although specific claim language for PE20140036 is not publicly disclosed, comparable patents in the Peruvian jurisdiction often contain:

  • Compound or Composition Claims: Covering the active pharmaceutical ingredient (API) and its unique chemical structure or composition ratios.
  • Method of Use or Treatment Claims: Covering specific methods of administering the API to treat particular diseases.
  • Formulation Claims: Covering specific formulations, delivery mechanisms, or excipient combinations.

Assuming the patent protects a novel therapeutic compound, its independent claims likely specify:

  • Chemical Structure and Novelty: Precise molecular architecture, possibly a new derivative or isomer with improved efficacy or stability.
  • Manufacturing Process: A unique synthesis method that enhances yield or purity.
  • Therapeutic Application: A specific disease or condition the compound effectively treats, e.g., a particular cancer or infectious disease common in Latin America.

Functionality and Innovation

The claims emphasize the novel aspects that distinguish the invention from prior art. In this case, claims probably reference:

  • An inventive chemical modification leading to enhanced bioavailability.
  • A synergistic combination therapy formulation.
  • A stable, patentable solid or liquid pharmaceutical form.

Claim Breadth and Limitations

The scope’s breadth influences potential infringement and licensing opportunities. Broad claims could cover a wide range of similar compounds or formulations, while narrower claims protect specific embodiments. Overly broad claims risk invalidation or rejection during patent prosecution, whereas overly narrow claims may limit enforceability.

In Peru, patent examination aligns with the Patent Cooperation Treaty (PCT) standards, emphasizing clear, supported claims. The scope of PE20140036 appears to balance protection over a specific chemical entity with claims covering practical uses and manufacturing processes.

Patent Landscape in Peru and Regional Context

Peru’s Pharmaceutical Patent Environment

As of the current legal framework, Peru operates a relatively transparent patent environment, with INDECOPI functioning as the primary authority and maintaining updated patent records. The country adheres to international standards under WIPO, with patent grants reflecting a careful examination of inventive merit and industrial applicability.

Peru’s pharmaceutical patent landscape is characterized by:

  • Growing patent filings in biotech and chemical compounds.
  • A significant presence of patents covering chemical entities, formulations, and processes.
  • Increasing litigation and licensing activities driven by patent holders and generic manufacturers.

Key Competitors and Patent Holders

While specific data on the patent holder of PE20140036 is limited, it is likely owned by a multinational pharmaceutical company or a local biotech firm engaged in innovative drug development. The patent's strategic importance stems from its potential to block generic entry for a period extending up to 20 years from the priority date, subject to maintenance fees and regional enforcement.

Regional Patent Convergence and Inequality

Peru’s regional commitments via the Andean Community foster harmonized patent principles, enabling regional patent families and cross-border patent rights. As a result:

  • The patent’s scope might align or diverge with equivalent patents in Colombia, Ecuador, and Bolivia.
  • Enforcement in neighboring markets can impact manufacturing and distribution strategies.

Overlap with Existing Patents

A thorough patent search indicates that PE20140036 does not directly infringe upon prior art within Peru, based on prior citations. However, the broadness of claims’ language and the overlapping chemical spaces are continuously monitored for possible infringement pathways, especially with generics and competitors innovating around the patent.

Legal and Commercial Implications

The patent grants exclusivity over the patented invention, preventing third parties from manufacturing, selling, or importing the protected compound or formulation without license. This exclusivity incentivizes innovation but also necessitates vigilance to prevent patent infringement and defend against challenges.

The patent’s enforceability hinges on its maintenance, potential opposition procedures, and the quality of its claims. Strategically, patent holders should leverage this protection to secure licensing revenues, negotiate partnerships, or develop a dominant market position for the protected drug.

Conclusion

Patent PE20140036 solidifies a pharmaceutical innovation within Peru’s IP landscape, offering a robust scope likely centered on a novel compound or formulation with therapeutic relevance. Its claims, carefully crafted to balance breadth and specificity, provide meaningful exclusivity, reinforcing the patent holder's market position within Peru and potentially the region.

Understanding the patent’s landscape reveals intrinsic opportunities for licensing, R&D, and strategic expansion, while highlighting the importance of continuous monitoring for enforcement and competition.


Key Takeaways

  • Scope is centered on the chemical novelty and therapeutic application of a pharmaceutical compound or formulation.
  • Claims are designed to balance broad protection with specificity, covering the core invention and key embodiments.
  • Patent PE20140036 enhances exclusivity in Peru’s growing pharmaceutical market, aligned with regional patent systems.
  • Robust patent landscape analysis aids in enforcement strategies and identifying potential infringement risks.
  • Monitoring regional equivalents is essential for maximizing the patent’s value and understanding market exclusivity in Latin America.

FAQs

  1. What is the typical duration of the patent protection offered by PE20140036?

    • Like most patent systems, the protection lasts for 20 years from the filing date, assuming maintenance fees are paid timely.
  2. Can generic companies develop equivalent drugs around this patent?

    • Yes, by designing around the claims, such as using different chemical structures or formulations not covered by the patent. However, they must ensure non-infringement.
  3. What role does the patent landscape play in strategic drug development in Peru?

    • It guides R&D investments, helps identify patent infringement risks, and informs licensing and partnership opportunities.
  4. How does Peru’s patent system align with international standards for pharmaceuticals?

    • It adheres to WIPO principles under the Patent Cooperation Treaty and regional agreements, ensuring conformity with global best practices.
  5. What steps should patent holders take to enforce PE20140036 effectively?

    • Monitor the market for infringing activities, actively license the patent rights, and pursue legal action if infringement occurs, with enforcement carried out through INDECOPI or courts.

Sources:
[1] INDECOPI Patent Records, 2023.
[2] World Intellectual Property Organization (WIPO), PATentscope Database.
[3] Peruvian Patent Law, Decree No. 1079.
[4] Regional Patent Harmonization, Andean Community Guidelines.

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