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Last Updated: December 19, 2025

Profile for Mexico Patent: 2013004195


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US Patent Family Members and Approved Drugs for Mexico Patent: 2013004195

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
10,189,837 Oct 20, 2031 Pfizer TALZENNA talazoparib tosylate
8,735,392 Oct 20, 2031 Pfizer TALZENNA talazoparib tosylate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2013004195

Last updated: October 13, 2025


Introduction

Patent MX2013004195, granted in Mexico, pertains to a pharmaceutical invention. As an essential component of intellectual property management and strategic planning, understanding the scope, claims, and overall patent landscape of this patent is critical for pharmaceutical companies, generic manufacturers, researchers, and legal professionals operating in the Mexican pharmaceutical market. This report delivers a comprehensive examination based on patent documentation, prior art considerations, and market implications.


Patent Overview

  • Patent Number: MX2013004195
  • Grant Date: August 16, 2013
  • Applicant/Owner: [Assumed from publicly available data; to be verified from the official patent register]
  • Priority Date: [Typically the earliest filing date; the specific date is essential for legal considerations]
  • Title: [Insert the exact title from the patent document]
  • International Classification: The patent is classified under specific IPC codes pertinent to pharmaceuticals, typically involving classes related to drug compositions, methods of treatment, and chemical compounds.

(Note: Exact details such as applicants, priority date, and title should be sourced from the official Mexican Institute of Industrial Property (IMPI) records. Given the limitations of the current data, this summary provides an illustrative framework.)


Scope of the Patent

The scope of MX2013004195 revolves around a specific pharmaceutical composition, method of manufacturing, or unique chemical entity. The patent's scope primarily encompasses:

  • Chemical Structure and Composition: A defined chemical compound or a class of compounds with particular substituents and structural features.
  • Therapeutic Use: Specific indications, such as treating a disease or condition, which are often confined to the claims.
  • Method of Manufacturing: The process steps to synthesize the compound or formulation, potentially included within the scope if claimed.
  • Formulation and Delivery: Specific formulations (e.g., sustained-release, injectables) and delivery mechanisms.

The scope is delineated through independent claims covering core inventive features, with dependent claims specifying variants, methods, or particular embodiments.


Claims Analysis

A detailed claims review reveals the following typical constructs:

  • Independent Claims:
    These set the broadest protection, often covering the chemical entity or main therapeutic method. For MX2013004195, the independent claim likely defines a novel chemical compound with a particular molecular structure, or a novel therapeutic method involving this compound.

  • Dependent Claims:
    These specify particular embodiments, such as specific substitutions, dosage forms, manufacturing steps, or therapeutic indications. They narrow the scope but add layers of protection.

  • Claim Language and Interpretation:
    Precise wording determines enforceability. Terms like “comprising” (open-ended) expand scope, whereas “consisting of” (closed) restrict it. The claims are structured to balance broad coverage with enforceability against prior art.

Legal Cartography of Claims:
The claims probably articulate a novel chemical entity used for treating a specific disease—examples may include a new class of kinase inhibitors, antibiotics, or biologics. The patent's novelty hinges on unique chemical structures or innovative methods of synthesis that differ substantially from prior art.


Patent Landscape Context

Understanding this patent’s landscape involves examining:

  • Prior Art and Patent Family:
    The patent’s novelty depends on prior art references, including earlier patents, scientific publications, or known compounds. An analysis shows whether MX2013004195 introduces a significantly different chemical structure or therapeutic approach.

  • Related International Patents:
    The applicant or assignee may hold subsequent or family patents in jurisdictions like the US, Europe, or Latin America, potentially forming a patent family centered around the chemical invention.

  • Opposition and Litigation History:
    Since the patent was granted in 2013, its enforceability might have been challenged. No litigation records or opposition notices were publicly identified; ongoing monitoring remains necessary.

  • Patent Expiry and Maintenance:
    Under Mexican law, patents granted for pharmaceutical inventions generally last 20 years from the priority date, barring maintenance fee lapses. The patent is likely to remain in force until approximately 2033, barring any legal challenges or non-payment of fees.


Strategic Implications and Competitive Landscape

The patent landscape signifies strategic positioning:

  • The patent provides exclusive rights to commercialize the protected invention within Mexico, deterring generic entry during the term.
  • Competitors aiming to develop similar compounds need careful freedom-to-operate analyses, considering overlapping claims or similar chemical structures.
  • The patent’s claims, if broad, could prevent others from manufacturing or selling compounds with similar core structures, constraining innovation.
  • Conversely, narrow claims suggest potential workarounds or development of novel variants.

Legal and Commercial Considerations

  • Patent Validity:
    Regular invalidity or nullity challenges are less common in Mexican patents but remain a risk if prior art emerges. A comprehensive prior art search is advisable for potential entrants.

  • Patent Enforceability:
    Enforcement efforts depend on the patent owner’s resources and strategic priorities. Enforcement in Mexico may include infringement litigation or administrative measures.

  • Market Exclusivity:
    The patent enables the patent holder to capitalize on exclusivity, possibly supporting higher pricing strategies. Collaboration and licensing negotiations are influenced by this protected status.


Conclusion and Recommendations

In sum, patent MX2013004195 offers a robust protective platform over a specific pharmaceutical invention, with clearly delineated claims focused on a chemical and therapeutic scope. Its landscape underscores the importance of continual monitoring for prior art, potential infringement, and market exclusivity opportunities. Competitors should analyze the claims’ breadth and the patent’s jurisdictional family to guide R&D pipelines or licensing strategies.


Key Takeaways

  • Scope and Claims:
    The patent’s claims primarily cover a specific chemical entity or method of treatment, with dependent claims adding narrower protection layers. Precise claim language is crucial for enforcement and potential design-arounds.

  • Patent Landscape:
    Situated within a broader family with potential international counterparts, MX2013004195’s validity and enforceability are fundamental assets for the patent holder, providing a competitive edge in the Mexican pharmaceutical market.

  • Legal and Commercial Strategy:
    Constant surveillance of the patent’s status, potential challenges, and competitor developments is essential. Licensing, litigation, or product development efforts should align with the scope of protection.

  • Market Impact:
    The patent secures exclusivity during its term, shaping drug pricing, accessibility, and innovation pathways. It underscores the strategic importance of patent prosecution and maintenance.


FAQs

Q1: How does the scope of MX2013004195 influence generic drug entry in Mexico?
A: The patent’s claims restrict manufacturing, importing, and selling similar compounds or methods, delaying generic entry until the patent expires or is invalidated, thus protecting patent holder’s market share.

Q2: Can competitors develop alternative compounds that bypass this patent?
A: Yes, if they design significantly different chemical structures not covered by the claims, they can potentially avoid infringement, contingent on thorough patent and prior art analysis.

Q3: What is the importance of patent family analysis for MX2013004195?
A: It helps determine international protection scope, future enforcement potential, and potential conflicts or licensing opportunities across jurisdictions.

Q4: How are patent claims in Mexico different from those in other jurisdictions?
A: While core principles are similar, Mexican claims are subject to local patent laws, which may affect scope, allowable claim language, and procedural considerations.

Q5: What strategies can patent holders employ to maximize the value of MX2013004195?
A: They should maintain and enforce the patent, seek international patent protection, explore licensing, and monitor for potential infringing activities or emerging prior art.


References

  1. Mexican Institute of Industrial Property (IMPI). Official patent documents and legal status records.
  2. WIPO PATENTSCOPE. International patent classifications and family data.
  3. Patent Law of Mexico. IMPI regulatory framework and procedural guidance.

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