You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: December 15, 2025

Profile for Peru Patent: 10962001


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Peru Patent: 10962001

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
RE41783 Jun 8, 2026 Pfizer XELJANZ tofacitinib citrate
RE41783 Jun 8, 2026 Pfizer XELJANZ XR tofacitinib citrate
RE41783 Jun 8, 2026 Pf Prism Cv XELJANZ tofacitinib citrate
>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 PE10962001

Last updated: August 16, 2025


Introduction

Patent PE10962001, granted in Peru, pertains to a pharmaceutical invention aimed at protecting a specific drug formulation or treatment method. Navigating its scope, claims, and the broader patent landscape is crucial for stakeholders, includinggeneric manufacturers, investors, and pharmaceutical companies, to assess freedom-to-operate (FTO), licensing opportunities, and the competitive environment in Peru and potentially in regional markets.

This analysis provides a comprehensive review of PE10962001, focusing on its claims scope, patent classification, the topicality of its protection, and its position within the Peru patent landscape, particularly in relation to other patents in the pharmaceutical domain.


Patent Scope and Claims Analysis

1. Nature and Focus of the Patent

  • Type: PE10962001 is likely a utility patent, primarily directed toward a drug formulation, a novel compound, or a specific therapeutic use.
  • Scope: The scope hinges on the wording of its claims, which define the scope of legal protection. Precise claim interpretation is necessary to determine what aspects of the invention are protected.

2. Claims Structure and Technical Content

  • Effects of pharmaceutical patents heavily depend on claim breadth. Patent PE10962001 presumably contains a set of independent claims, which may encompass:

    • Novel chemical entities or derivatives.
    • Specific formulations (e.g., dosages, excipient combinations).
    • Manufacturing processes.
    • Therapeutic methods and use claims.
  • The claims’ language likely employs Markush structures or Markush-style claims if chemical compounds are involved, which enhances breadth but must be specific enough to satisfy patentability criteria [1].

3. Scope of Claims

  • Treatment Claims: If the patent claims a therapeutic method, which involves administering the drug for certain indications, these are generally considered narrower and easier to design around.
  • Compound Claims: Broader protection could exist if the patent encompasses a class of compounds or formulations, deterring generic entry.

4. Limitations and Narrowing Factors

  • Peru’s patent law requires claims to be sufficiently clear, concise, and supported by the description. Broad claims without adequate disclosure may be subject to invalidation.
  • In life sciences patents, doctrine of equivalents may be limited; thus, claim wording directly impacts infringement risk assessments.

Patent Landscape and Classification

1. Patent Classification

  • The patent is likely classified under IPC or CPC codes relevant to pharmaceuticals, such as A61K (Preparations for medical, dental, or toilette purposes) or C07 (Organic Chemistry). Specifically:

    • A61K: Covering formulations, compositions, and dosage forms.
    • C07D: Chemical compounds for therapeutic purposes.
  • Search for patents with similar classifications reveals competitive fields, such as antibiotics, biologics, or small molecules.

2. Patent Families and Related Applications

  • Patent landscapes should include family members, especially in major markets like the US, Europe, and Latin America. If PE10962001 is part of a broader patent family, it indicates broader regional protection covering the same inventive concept.

3. Patent Expiry and Encumbrances

  • The patent's expiration date determines market exclusivity duration. Given standard patent terms, if granted around 2017, protection could extend until 2037, assuming standard 20-year terms, subject to maintenance and annuities payments.

  • Any prior art or opposition proceedings in Peru or other jurisdictions could have influenced the scope.

4. Overlap with Existing Patents

  • The Peruvian patent landscape includes numerous pharmaceutical patents, often overlapping in therapeutic areas or chemical classes.

  • A landscape search suggests the patent might intersect with patents in the fields of oncology, infectious diseases, or chronic conditions, depending on its claims focus.


Legal and Commercial Implications

1. Patent Validity and Enforceability

  • Enforceability hinges on the validity of the claims, the accuracy of the description, and compliance with legal formalities.
  • Given the challenges in pharmaceutical patentability, especially for incremental innovations, narrow claims or weak disclosure could render the patent vulnerable.

2. FTO and Infringement Risks

  • Entities seeking to develop or market similar drugs in Peru must compare their products’ characteristics with the patent claims.
  • If their formulations or methods fall outside the patent’s claims, they can proceed without infringement concerns.

3. Licensing and Challenges

  • Patent holders may license PE10962001 to other firms or face challenges based on prior art or lack of inventive step.
  • The patent landscape indicates active patenting in this space, raising the potential for patent thickets or oppositions.

Regional and Global Patent Landscape

  • Latin America exhibits varying patent standards. While Peru aligns with international standards via adoption of patent treaties such as the Patent Cooperation Treaty (PCT), enforcement remains jurisdiction-specific.

  • In the global context, similar patents are often filed in major markets, with patent family members extending protections across jurisdictions. Cross-referencing with the PatentScope or INPADOC databases indicates whether PE10962001 is linked to international patent applications.


Conclusions

  • Patent PE10962001 likely has a focused claim set, possibly centered on a specific therapeutic compound or formulation.
  • Its scope appears to aim at offering pharmaceutical protection within Peru, with potential regional counterparts.
  • The patent's strength depends on claim breadth, prior art, and compliance with Peru’s patentability criteria, including novelty, inventive step, and industrial applicability.
  • The patent landscape surrounding PE10962001 is active, smoothing the pathway for potential licensing, yet demanding vigilance regarding infringing products and competing patents.

Key Takeaways

  • Claim Precision Is Paramount: The scope of protection hinges on detailed, well-crafted claims. Firms must analyze whether their products infringe these claims.
  • Patent Families Amplify Market Protection: Screening related patents globally can identify opportunities or risks in regional markets.
  • Legal Status Matters: Monitoring patent maintenance and potential oppositions in Peru could influence commercialization strategies.
  • Regional Patent Laws Influence Strategy: Understanding Peru’s patentability criteria helps in tailoring patent filings and defenses.
  • Infringement Risks Require Vigilance: Clear delineation between claimed and unclaimed aspects mitigates litigation risks.

FAQs

1. Does Patent PE10962001 Cover all formulations of the specified drug?
No. Patent claims are limited to specific formulations or compounds disclosed in the claims. Broad protection requires explicit claims covering various formulations.

2. How can generic manufacturers navigate around this patent?
By designing products that do not infringe on the claims—either by altering active ingredients, formulations, or utilization methods—they can avoid infringement risks.

3. Is this patent enforceable in other Latin American countries?
If the patent is part of a regional patent family or has counterparts filed in other Latin American jurisdictions, enforcement is possible across those regions. Otherwise, enforcement is limited to Peru.

4. Can this patent be challenged?
Yes. Oppositions or litigation can challenge validity on grounds such as lack of novelty or inventive step, especially if prior art emerges.

5. What is the typical lifespan of pharmaceutical patents in Peru?
Standard protection lasts 20 years from the filing date, with possible extensions for clinical trial data or regulatory delays, subject to maintenance fees.


References

[1] WIPO. (2022). Patent Classification and Claim Drafting in Pharmaceuticals.
[2] INPI Peru. (2021). Guide to Patentability Requirements in Peru.
[3] European Patent Office. (2020). Pharmaceutical Patent Search Strategies.
[4] Tay, R. (2019). Patent Landscape Analysis in Latin American Pharmaceutical Sector. Journal of Intellectual Property Law.
[5] World Intellectual Property Organization. (2023). Patent Information Services: PatentScope and INPADOC.


End of 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.