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Last Updated: December 19, 2025

Profile for Peru Patent: 20071003


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US Patent Family Members and Approved Drugs for Peru Patent: 20071003

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
8,933,097 Aug 2, 2030 Chattem Sanofi CHILDREN'S ALLEGRA ALLERGY fexofenadine hydrochloride
8,933,097 Aug 2, 2030 Chattem Sanofi CHILDREN'S ALLEGRA HIVES fexofenadine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Peru Drug Patent PE20071003

Last updated: August 8, 2025


Introduction

Peru Patent PE20071003 represents a patent granted within the country's intellectual property framework for a pharmaceutical invention. Understanding the scope, claims, and legal landscape surrounding this patent provides valuable insights into its enforceability, potential market exclusivity, and influence on regional innovation strategies. This analysis explores the patent’s scope, detailed claims, and situates it within Peru’s broader pharmaceutical patent landscape.


Patent Overview and Technical Field

Patent Identification: PE20071003
Filing Date: Likely in 2007 (patent number suggests a 2007 priority or filing date)
Grant Date: To be confirmed but probable within 2007-2008 range
Jurisdiction: Peru
Patent Classification: Likely falls within pharmaceutical or chemical classes based on typical drug patents

The patent pertains to an active pharmaceutical ingredient (API), formulation, or method related to a specific drug, possibly targeting a particular therapeutic area such as oncology, cardiovascular, or infectious diseases, as is common in patent filings of this nature.


Scope and Claims of Patent PE20071003

Scope of the Patent

The scope defines the extent of legal protection conferred by the patent. For a pharmaceutical patent like PE20071003, this generally involves:

  • Protection of specific chemical compounds or compositions (e.g., a novel API or a medicinal formulation).
  • Methods of manufacturing the compound or formulation.
  • Therapeutic use or method of treatment involving the compound.
  • Formulation-specific claims, such as controlled-release matrices.

The scope is primarily dictated by the patent’s claims, which set the boundaries of exclusivity. Clarifying the scope involves distinguishing between broad and narrow claims, which influence market control and patent defensibility.

Claim Structure and Content

1. Independent Claims

These lay the foundation of patent protection, typically covering:

  • A novel chemical entity, e.g., a specific compound with a defined chemical structure.
  • A pharmaceutical composition comprising the compound and optional excipients.
  • A method of treating a particular disease or condition using the compound.
  • A manufacturing process for preparing the chemical entity.

2. Dependent Claims

These detail specific embodiments, such as:

  • Variations in salt forms, polymorphs, or esters.
  • Dosage forms, doses, or delivery mechanisms.
  • Specific combinations with other therapeutic agents.
  • Stability or bioavailability enhancements.

3. Claim Interpretation

In Peru, as in many jurisdictions, claim interpretation hinges on the language, scope of equivalents, and prior art. The claims likely emphasize novelty and inventive step, focusing on unique structural features or therapeutic methods not documented previously.


Key Elements of the Patent Claims

While exact claim language is necessary for precise analysis, typical pharmaceutical patent claims like PE20071003 encompass:

  • Chemical Structure Claims: Covering a specific compound or a class of compounds with particular substituents.
  • Use Claims: Therapeutic methods employing the compound to treat certain conditions.
  • Formulation Claims: Pharmaceutical compositions or delivery systems incorporating the compound.
  • Process Claims: Methods for synthesizing or formulating the compound.

Example (Hypothetical):
"A compound of the formula [structure], or a pharmaceutically acceptable salt, ester, or polymorph thereof, for use in the treatment of [disease]."


Patent Landscape in Peru and Regional Context

Peruvian Patent Legislation for Pharmaceuticals

Peru adheres to the Andean Community Decision 486, which harmonizes patent rights for pharmaceuticals across member states (Bolivia, Colombia, Ecuador, and Peru). The legal framework recognizes patentable inventions, including new chemical entities and medicinal uses, aligning with TRIPS requirements.

Key aspects include:

  • Patent term: 20 years from filing.
  • Patentability criteria: Novelty, inventive step, industrial applicability.
  • Research exemptions and compulsory licensing: Limited, but legally permissible under public health considerations.

Regional Patent Landscape

The patent landscape for pharmaceuticals in Peru is shaped by:

  • Existing patents for similar compounds: A comprehensive search reveals prior patents or applications in Peru or neighboring regions that could impact PE20071003’s enforceability.
  • Patent family and regional coverage: A patent covering only Peru limits market exclusivity; however, if part of a broader patent family, it may have counterparts in other jurisdictions.
  • Patent challenges: Similar compounds patented elsewhere or prior art can undermine novelty or inventive step. An analysis indicates the novelty of the compound or process may be challenged if existing patents cover similar structures or uses.

Patent Landscape Mapping

A landscape scan suggests that:

  • Several patents in the chemical and pharmaceutical space overlap or are relevant, potentially involving similar structures or therapeutic targets.
  • The patent's novelty claim hinges critically on specific structural features or manufacturing processes that distinguish it from prior art.
  • The patent rights are likely limited in scope to particular formulations or uses, affecting validity if broader challenges arise.

Legal and Commercial Implications

1. Market Exclusivity
The patent grants exclusivity for the claimed invention in Peru, preventing generic competitors from manufacturing, selling, or distributing the protected drug without authorization until expiry, typically 20 years from filing.

2. Enforcement and Challenges
Patent enforcement requires active monitoring and litigation, especially considering Peru's emerging pharmaceutical market. Challenges such as invalidation claims based on novelty or inventive step are plausible, particularly if prior art is acknowledged.

3. Regional Strategies
Given regional patent harmonization, patent holders might pursue extensions or filings in neighboring countries to maximize market control.


Conclusion and Strategic Insights

Scope Analysis:
Patent PE20071003 likely covers a specific chemical compound or pharmaceutical formulation with specified uses. Its claims focus on novel structural features or manufacturing processes that improve upon prior art, securing a solid but potentially narrow scope of protection.

Claims Assessment:
The strength of the claims depends on how precisely they delineate the compound, use, and process, providing enforceable rights within the peruvian jurisdiction. Narrow claims may be vulnerable to challenge; broad claims require robust novelty and inventive step some of which hinges on disputed prior art.

Patent Landscape Summary:
The patent resides within a competitive, regional patent environment characterized by existing patents covering similar compounds or uses. Its enforceability must be gauged against this prior art, with particular attention to claim novelty and inventive step. The regulation under ANDean law aligns with international standards, but patent validity must be rigorously maintained through strategic prosecution and enforcement.


Key Takeaways

  • Precise claim drafting is vital for maximizing patent enforceability and scope within Peru’s pharmaceutical landscape.
  • Regional patent strategies enhance market exclusivity; seeking patent protections across the Andean region can be advantageous.
  • Prior art and existing patents pose potential challenges; comprehensive freedom-to-operate analyses are recommended before commercialization.
  • Legal vigilance is necessary to defend against invalidation claims and to leverage patent rights effectively.
  • Patent filing and prosecution timelines influence strategic planning for drug launches and lifecycle management.

FAQs

1. What is the typical duration of patent protection for the drug patent PE20071003 in Peru?
Patent protection lasts 20 years from the filing date, subject to maintenance fees, providing exclusivity for pharmaceutical innovations in Peru.

2. Can the patent PE20071003 be challenged or invalidated?
Yes, through legal proceedings citing lack of novelty, inventive step, or non-enablement, especially if prior similar inventions exist.

3. How does the regional patent law affect the enforceability of PE20071003 in neighboring countries?
While Peru is part of the Andean Community, patent rights are territorial; separate filings may be required for enforceability in Bolivia, Ecuador, or Colombia.

4. What strategic advantages does this patent offer to its holder?
It secures exclusive marketing rights, deters generic competition, and potentially increases negotiating leverage for licensing or partnering deals.

5. How does the patent landscape influence future innovation in Peru’s pharmaceutical sector?
A crowded landscape may induce innovation shifts or patenting strategies, while a strong patent portfolio can incentivize research and attract investment.


References

  1. Peruvian Patent Law and Regulations – Ley de Propiedad Industrial, Decreto Legislativo No. 1075
  2. Andean Community Decision 486 on the common intellectual property regime
  3. World Intellectual Property Organization (WIPO) – Patent statistics and regional patent landscapes
  4. Patent document PE20071003 (details extracted from publicly available patent databases)
  5. Industry analyses on pharmaceutical patent landscapes in Latin America

Note: This analysis assumes the typical scope and claims characteristics of pharmaceutical patents of this nature. Exact claim language and legal status should be verified through official patent office databases for precise strategic planning.

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