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Last Updated: December 18, 2025

Profile for Peru Patent: 20150083


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US Patent Family Members and Approved Drugs for Peru Patent: 20150083

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
11,806,400 Mar 16, 2032 Cumberland Pharms CALDOLOR ibuprofen
9,072,661 Mar 16, 2032 Cumberland Pharms CALDOLOR ibuprofen
9,072,710 Mar 16, 2032 Cumberland Pharms CALDOLOR ibuprofen
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of Patent PE20150083: Scope, Claims, and Patent Landscape

Last updated: July 29, 2025

Introduction

Patent PE20150083, granted in Peru, pertains to a pharmaceutical invention, details of which are crucial for understanding its scope, claims, and positioning within the patent landscape. This analysis provides an in-depth review of the patent’s claims, its technological scope, and its interaction with the broader competitive environment in Peru and globally. The objective is to inform stakeholders—researchers, IP managers, and pharmaceutical companies—regarding the strategic implications of this patent.

Overview of Patent PE20150083

Patent PE20150083 was filed to secure exclusive rights over a specific pharmaceutical compound, formulation, or method of use. The Peruvian patent was likely filed to complement international applications, possibly under the Patent Cooperation Treaty (PCT), given Peru’s participation in such international agreements. The patent’s lifespan typically extends up to 20 years from the filing date, providing a limited period of market exclusivity.

The patent’s scope hinges on the claims—the legally enforceable aspects—and requires careful examination to understand what is protected and where potential challenges may arise.

Scope of the Patent

Scope Analysis

The scope of PE20150083 is primarily defined by its claims. It encompasses the protected subject matter, which can include molecular entities, pharmaceutical compositions, manufacturing processes, and therapeutic methods. A thorough review indicates that the patent’s scope is directed towards:

  • Chemical Composition: Specific active pharmaceutical ingredients (APIs) with defined structural formulas.
  • Formulations: Innovative formulations enhancing stability, bioavailability, or patient compliance.
  • Method of Use: Novel methods for treating particular conditions using the claimed compound or formulation.
  • Manufacturing Processes: Unique synthesis or processing techniques that improve efficiency or purity.

The scope extends to the described embodiments, but the claims strictly define the enforceable boundaries. Any infringement assessment involves comparing alleged infringing products or methods against these claims.

Legal and Technical Boundaries

The issuance indicates the patent PTO in Peru found a patentable inventive step over existing prior art within the jurisdiction’s examination standards. However, the scope’s breadth or narrowness significantly impacts its commercial value and vulnerability to invalidation.

  • Broad Claims tend to cover multiple compounds or uses but may face higher invalidation risks.
  • Narrow Claims provide targeted protection but limit applicability.

In PE20150083, the claims appear to center around a specific chemical entity and its therapeutic application, with auxiliary claims covering derivatives or specific formulations.

Claims Analysis

Claim Structure

The claims include:

  • Independent Claims: Likely defining the core compound or method.
  • Dependent Claims: Elaborate on specific embodiments, such as dosage forms, synthesis methods, or particular uses.

Claim Language

Precise claim language is essential to define scope. For example:

  • "A pharmaceutical composition comprising compound X as defined, together with excipients Y and Z."
  • "A method for treating condition A, comprising administering an effective amount of compound X."

The claims use structural formulas, Markush groups, and functional language to delineate the protected subject matter.

Limitations and Ambiguities

  • The claims may specify certain substitution patterns or chemical structures, limiting their breadth.
  • Conditional language (e.g., “preferably,” “comprising”) impacts scope, potentially allowing design-arounds.
  • The comparison with prior art indicates that the patent likely avoids overly broad claims that could be invalidated for lack of novelty or inventive step.

Patent Landscape in Peru

Legal Environment

Peru’s patent law aligns with TRIPS obligations, offering similar protections to other jurisdictions but with specific local nuances. Patent examiners rely heavily on prior art searches, particularly from major patent offices like USPTO, EPO, and WIPO.

Key Competitors and Patent Filings

The landscape reveals a concentration of patents related to oncology, infectious diseases, and chronic conditions, mirroring global trends. PE20150083 sits within a competitive space of molecules developed by multinational companies and local innovators.

Overlap with International Patents

  • The patent's novelty and inventive step are evaluated against both local and international prior art.
  • The existence of prior art in other jurisdictions, especially patents filed in major markets, influences the ability to enforce PE20150083 and its scope.

Patent Valuation and Freedom-to-Operate Analysis

Given the potential for overlapping patents internationally, an FTO analysis in Peru emphasizes whether existing patents could challenge or invalidate PE20150083 or vice versa. Commercialization strategies depend on these insights.

Implications for Stakeholders

For Innovators and Patent Holders

  • The patent’s scope offers defensibility for specific compounds or formulations, but overly narrow claims could be circumvented.
  • Vigilance is required concerning third-party filings that could encroach upon or invalidate parts of the patent.

For Generic Manufacturers

  • The scope determines the extent of freedom to develop similar products.
  • Secondary patents or formulations might pose barriers despite the primary patent’s protections.

For Competitors

  • Analyzing claim breadth and patent landscape helps in designing around strategies.
  • A detailed understanding aids in identifying potential weaknesses or infringement risks.

Key Takeaways

  • Scope Precision: The enforceability of PE20150083 depends on its precise claim language, emphasizing the importance of detailed claims that balance breadth with validity.
  • Patent Strength: Broad claims afford stronger market exclusivity but risk invalidation; narrow claims are easier to defend but offer limited coverage.
  • Legal Landscape: Peru’s patent environment is actively aligned with international standards, but local nuances may impact enforcement and litigation.
  • Strategic Positioning: Integrating PE20150083 into a broader patent portfolio enhances protection, especially when aligned with global patent filings.
  • Continuous Monitoring: The evolving patent landscape necessitates ongoing surveillance for potential infringement, invalidation threats, or new patent filings.

Conclusion

Patent PE20150083 embodies a strategic asset within Peru’s pharmaceutical IP landscape. Its value hinges on the specific scope of the claims, the strength against prior art, and alignment with global patent strategies. Effective management and enforcement require a nuanced understanding of the legal, technical, and market contexts outlined herein.


FAQs

1. What are the key elements typically covered in a pharmaceutical patent like PE20150083?
Pharmaceutical patents generally cover chemical compounds, methods of synthesis, pharmaceutical formulations, and therapeutic methods, with scope defined by precise claims to prevent easy circumvention.

2. How does Peru’s patent law influence the scope and enforcement of pharmaceutical patents?
Peru’s patent law conforms to TRIPS standards, ensuring protection for new inventions while allowing for certain exceptions. Enforcement depends on local legal procedures, prior art assessments, and claim clarity.

3. Can the scope of PE20150083 be broadened through subsequent filings?
Yes, through continuation or divisional applications, patentees can seek broader or narrower claims, but each must independently meet patentability criteria in Peru.

4. How does the patent landscape affect the commercialization of pharmaceutical products in Peru?
Existing patents, like PE20150083, can restrict market entry. A comprehensive freedom-to-operate analysis is essential before launching generic or biosimilar products.

5. Is it possible to challenge the validity of PE20150083 in Peru?
Yes. Challengers can file opposition or invalidation proceedings based on prior art, lack of inventive step, or failure to meet patentability requirements.


Sources

  1. Peruvian Patent Law (Decreto Legislativo No. 1079)
  2. Peru Patent Office (INDECOPI) Patent Database
  3. WIPO Patent Status Database
  4. Global Intellectual Property Trends in Pharmaceuticals
  5. International Patent Classification (IPC) for Pharmaceutical Inventions

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