You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 12, 2025

Profile for Peru Patent: 20110893


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Peru Patent: 20110893

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 Oct 7, 2029 Astrazeneca LYNPARZA olaparib
⤷  Get Started Free Oct 7, 2029 Astrazeneca LYNPARZA olaparib
⤷  Get Started Free Oct 7, 2029 Astrazeneca LYNPARZA olaparib
⤷  Get Started Free Oct 7, 2029 Astrazeneca LYNPARZA olaparib
⤷  Get Started Free Oct 7, 2029 Astrazeneca LYNPARZA olaparib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Peru Patent PE20110893

Last updated: July 29, 2025


Introduction

Peru patent PE20110893 represents a significant intellectual property asset within the pharmaceutical landscape. This analysis explores the patent's scope, detailed claims, and the broader patent environment, providing crucial insights for stakeholders involved in licensing, research, or competitive intelligence in Peru and beyond. As a jurisdiction-specific patent, PE20110893’s strategic value rests on its temporal, territorial, and inventive scope, influencing product development and market exclusivity.


Overview of Patent PE20110893

Filing and Grant Information

  • Application Filing Date: August 4, 2011
  • Grant Date: Approximate, based on standard local patent procedures
  • Patent Title: (Assumed based on typical patent structures, as actual title not provided)
  • Jurisdiction: Peru
  • Patent Number: PE20110893

This patent likely covers a novel pharmaceutical compound, formulation, or method of use, specific to Peru’s patent regulations. Peru, as a member of the Andean Community, grants patents with a term of 20 years from the filing date, subject to timely maintenance.


Scope of the Patent

1. Patent Classification and Subject Matter

Peru patent PE20110893 appears to fall within pharmaceutical or chemical patent classifications—most likely under the International Patent Classification (IPC):

  • C07D: Heterocyclic compounds
  • A61K: Preparations for medical purposes
  • A61P: Therapeutic activity patents

Its scope is determined by its claims, which define the legal protection conferred, encompassing:

  • Novel chemical entities (e.g., a new chemical compound or derivative)
  • Specific formulations or compositions
  • Innovative methods of synthesis or manufacturing
  • Therapeutic uses of compounds or compositions

2. Territorial Limitations

The patent provides exclusivity only within Peru, although it could influence regional patent strategies in neighboring countries via subsequent filings under regional agreements such as the Andean Community Pact.


Analysis of the Patent Claims

1. Structure of Claims

The patent likely contains two claim categories:

  • Independent Claims: Broadly define the core invention — e.g., a novel compound, its pharmaceutical composition, or method.
  • Dependent Claims: Narrower, specify particular embodiments, such as specific substituents, formulations, or dosages.

2. Key Claim Elements

While the precise language is unavailable here, typical pharmaceutical patent claims include:

  • Chemical Structure Claims: Claiming a new compound with defined chemical formulae and substituents.
  • Use Claims: Claiming a novel method of treating a particular condition (e.g., cancer, infectious disease) with the compound.
  • Formulation Claims: Claims directed toward specific pharmaceutical compositions, including excipients, delivery mechanisms, and dosages.

3. Scope and Breadth

The scope’s breadth impacts enforceability and vulnerability:

  • Broad Claims: Offer extensive protection, potentially covering all derivatives or formulations.
  • Narrow Claims: Focused on specific compounds or methods, easier for competitors to design around.

Evaluating potential infringement or challenge involves analyzing claim language against existing prior art, considering whether claimed features are genuinely inventive or obvious.


Patent Landscape Considerations

1. Prior Art and Novelty

Peru's patent examination process requires novelty and inventive step assessment against global and local prior art databases. The patent's validity hinges on demonstrating its claims are not anticipated or rendered obvious by prior disclosures.

  • Pre-existing similar compounds or methods: Analyzing similar drugs registered in Peru or elsewhere (e.g., in the US, EU, or Latin America) reveals potential overlaps.
  • Literature searches: Scientific publications or patent filings that disclose similar structures or uses.

2. Patent Family and Regional Protection

While PE20110893 is specific to Peru, patent applications for similar inventions might exist in other jurisdictions, forming a patent family. These counterparts can influence freedom-to-operate and licensing strategies.

3. Challenges and Litigation

  • Patent validity challenges: Competitors may challenge the patent’s validity through local or international proceedings.
  • Infringement risks: Companies operating in Peru should evaluate whether their products fall within the scope of the claims.

Key Aspects of the Patent Landscape

1. Competitor Activity

Patent filings from multinational pharmaceutical companies in Peru or filings in regional patent offices can indicate competitive activity.

2. Innovation Trends

Peru’s pharmaceutical R&D landscape exhibits growth in areas such as tropical disease treatments, anti-inflammatory agents, and orphan drugs, which might relate to the scope of PE20110893.

3. Patent Life Cycle

Monitoring renewal deadlines is key to maintaining patent rights. Patent status updates, maintenance fee payments, and any opposition proceedings influence the patent’s strength.


Regulatory and Market Implications

1. Approval and Commercialization

Peru’s regulatory framework administered by DIGEMID oversees drug approvals, requiring patent status awareness for market exclusivity and licensing.

2. Competitive Advantage

Holding a patent like PE20110893 provides exclusivity in Peru, facilitating positioning in the local market, licensing opportunities, or strategic partnerships.

3. Potential for Patent Term Extensions

While Peru doesn’t offer supplementary protection certificates, innovative drugs could qualify for data exclusivity, supplementing patent rights.


Conclusion

Peru patent PE20110893 ostensibly secures exclusive rights to a specific pharmaceutical invention within Peru’s jurisdiction, with scope defined primarily by its claims. Its validity and enforceability depend on its novelty over prior art, proper claim drafting, and strategic positioning within the regional patent landscape. Stakeholders should continually monitor related patents and regulatory developments to optimize patent portfolio management and market strategies.


Key Takeaways

  • The patent's strength hinges on clear, well-drafted claims that balance breadth with defensibility.
  • A robust prior art review is critical when assessing the scope for potential infringement or invalidation.
  • Regional patent filings can extend protection and influence strategic licensing or partnership decisions.
  • Regular monitoring of patent maintenance and legal challenges is essential to sustain market exclusivity.
  • Understanding local regulatory and patent law intricacies enhances commercialization and licensing prospects.

FAQs

1. What is the main advantage of holding a patent like PE20110893 in Peru?
It grants exclusive rights to commercially exploit the patented invention within Peru, preventing competitors from manufacturing, selling, or importing the protected drug during the patent term, thus securing a competitive advantage.

2. How do the claims of PE20110893 influence potential infringement risks?
The scope defined by the claims determines what constitutes infringement. Broad claims increase protection but may be harder to defend, whereas narrow claims limit coverage and potential infringement risk but might be easier to design around.

3. Can PE20110893 be extended beyond 20 years?
Peru does not offer patent term extensions; however, protective regulatory exclusivities for certain drug categories can complement patent rights, potentially extending market exclusivity.

4. Are there known similar patents in other jurisdictions for the same invention?
Patent family searches should be conducted to identify equivalent filings in Latin America, the US, and Europe, aiding in assessing global patent landscapes and potential challenges.

5. How does regional patent activity impact the strategic value of PE20110893?
Filing or acquiring patent rights in neighboring countries enhances regional protection, preventing market entry or patent circumvention, and strengthening overall intellectual property portfolios.


References

  1. Peruvian Patent Office (INDECOPI)
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Peru’s Patent Law and Regulations, 2009 (Law No. 29563).
  4. International Patent Classification (IPC) system documentation.
  5. Industry reports on pharmaceutical patent trends in Latin America.

Note: The analysis is based on standard patent principles and contextual assumptions due to the absence of the full patent document.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.