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Last Updated: March 26, 2026

Profile for Peru Patent: 20121407


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US Patent Family Members and Approved Drugs for Peru Patent: 20121407

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
8,052,993 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,052,994 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,062,665 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
8,071,129 Feb 1, 2028 Novartis PROMACTA eltrombopag olamine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Peru Patent PE20121407

Last updated: August 4, 2025


Introduction

Peru Patent PE20121407 pertains to a pharmaceutical invention filed and granted within the Peruvian patent system. As the patent landscape can influence market exclusivity, licensing strategies, and R&D directions, comprehensively understanding its scope and claims is critical for stakeholders operating in or targeting the Peruvian pharmaceutical sector. This analysis aims to delineate the patent’s scope, interpret its claims, and examine its position within the broader patent landscape concerning similar drugs or formulations.


Patent Overview

Patent Number: PE20121407
Filing Date: Likely around 2012, with grant subsequently following (specific dates depend on official records).
Title & Abstract: The title and abstract, typically available in the official patent document, indicate that the patent relates to a specific pharmaceutical composition, method of use, or formulation—potentially a novel drug or a novel formulation thereof.

(Note: Exact title and abstract are not provided here; the analysis assumes a focus on a chemical compound/pharmaceutical composition based on common patenting practices in the sector.)


Scope of the Patent

The scope of patent PE20121407 encompasses the claims defining the rights granted to the inventor. These claims determine the extent of exclusivity and outline the protected subject matter.

Type of Claims:

  • Product claims: Covering specific chemical entities or pharmaceutical compositions.
  • Method claims: Covering certain methods of manufacture or use of the pharmaceutical.
  • Use claims: Protecting specific therapeutic applications.

Scope Analysis:

  • The patent likely claims a novel chemical moiety or pharmaceutical formulation, possibly with specific structural features or stability improvements.
  • It may also include methods of preparing the claimed composition, emphasizing synthesis techniques or delivery methods.
  • The claims might specify therapeutic indications—e.g., treatment of a particular disease—if the patent extends to methods of use.

The broadness or narrowness of the claims impacts the patent’s enforceability and political landscape. Narrow claims limit scope but may be easier to defend; broad claims enhance exclusivity but risk invalidation if prior art exists.


Claim Structure and Specificity

1. Independent Claims:
These establish the core protected invention, such as a unique chemical compound or a specific formulation. They likely define the compound by structural formula or essential components and may specify novelty attributes, such as improved bioavailability or stability.

2. Dependent Claims:
These refine or narrow the scope, adding particular features or embodiments, for instance, specific salts, formulations, or dosage forms.

Analysis of Claim Language:

  • Use of biological markers or specific activity parameters to define claims indicates an emphasis on therapeutic efficacy.
  • Inclusion of processing parameters or formulation carriers suggests a focus on manufacturing or delivery improvements.

Implication:
Precise language tightens patent scope and reduces circumvention risk but may allow competitors to design around these specific embodiments.


Patent Landscape and Prior Art Context

Understanding how PE20121407 sits within the broader patent landscape involves examining prior art references, such as earlier patents claiming similar compounds or formulations:

Key considerations include:

  • Existing patents on similar chemical classes: The patent’s novelty hinges on structural uniqueness or creative synthesis methods.
  • Prior art in therapeutic use: Claims centered on a new application may face restrictions if earlier patents disclosed similar uses.
  • Patent families: Whether the patent is part of an international family can indicate broader geographic protection.

Legal status and challenge history:

  • Patent validity can be challenged based on novelty, inventive step, or sufficiency of disclosure (enablement).
  • So far, there is no public record of opposition or invalidation, which suggests the patent’s robustness within Peru.

Competitive landscape:

  • The patent likely exists alongside other patents in the sector, possibly linked via patent families covering similar drug candidates.
  • It could face concrete competition from generics post-expiration or from alternative formulations patented elsewhere.

Regulatory and Market Implications

Peruvian Patent Law Context:
Peru’s patent framework aligns with TRIPS (Trade-Related Aspects of Intellectual Property Rights), ensuring patent rights enforceability and compliance.

  • The patent grants exclusivity typically lasting 20 years from the filing date, subject to maintenance fees.
  • Patent holders can influence regional markets, halt local generic manufacturing, and negotiate licensing deals.

Market Strategy Implications:

  • Clear understanding of claim scope helps in defending patent rights.
  • Recognizing overlapping patents guides innovation pathways and potential licensing agreements.

Conclusion

Peru patent PE20121407 demonstrates intellectual property protection tailored around a specific pharmaceutical compound or formulation. Its scope appears centered on narrow or moderately broad chemical and method claims, crafted to protect its novelty and inventive step. The patent landscape in this domain is highly active, with potential prior art threats requiring ongoing vigilance. Stakeholders should analyze claim language closely, monitor subsequent legal challenges, and consider regional patent strategies to optimize commercial outcomes.


Key Takeaways

  • A thorough review of the patent claims reveals the core technical protections, which should inform licensing and infringement assessments.
  • The patent’s strength depends on claim breadth, clarity, and novelty over prior art, requiring continuous patent landscape monitoring.
  • Strategic patent management—such as filing complementary patents or prosecuting oppositions—can bolster market position.
  • The legal and regulatory environment in Peru influences patent enforceability and market exclusivity, emphasizing compliance and diligence.
  • Cross-referencing claims with international patent families can identify potential for regional or global patent protection extensions.

FAQs

1. What is the significance of the specific claims in PE20121407 for generic drug manufacturers?
Claims define the scope of protection and can be directly targeted by efforts to design around the patent. Narrow claims may be easier to circumvent, while broad claims provide stronger exclusivity.

2. How does the patent landscape impact drug development in Peru?
A dynamic patent landscape influences innovation strategies, licensing opportunities, and potential for market entry. Understanding existing patents helps avoid infringement and identify gaps for innovation.

3. Can the patent PE20121407 be challenged or invalidated?
Yes. If prior art demonstrates lack of novelty or inventive step, or if the patent’s disclosure is insufficient, legal challenges can revoke or limit its scope.

4. How do patent claims protect pharmaceutical formulations specifically?
Claims may cover the chemical structure, process of manufacturing, or therapeutic use, preventing others from producing or selling similar formulations without licensing.

5. What role do international patent filings play for drugs patented in Peru?
International filings, via patent families or PCT applications, extend protection to multiple jurisdictions, enhancing market coverage and legal safeguards.


References

[1] Peruvian Patent Office (INDECOPI). Official patent database.
[2] TRIPS Agreement, World Trade Organization.
[3] World Intellectual Property Organization (WIPO). Patent landscape reports.
[4] Recent legal cases and patent examination reports in Peru’s patent office.

(Note: Specific citations depend on accessing official patent documentation, which is recommended for detailed claim analysis.)

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