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Last Updated: April 2, 2026

Profile for Mexico Patent: 2013001677


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US Patent Family Members and Approved Drugs for Mexico Patent: 2013001677

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
⤷  Start Trial Feb 11, 2032 Abbvie LINZESS linaclotide
⤷  Start Trial Feb 11, 2032 Abbvie LINZESS linaclotide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent MX2013001677: Scope, Claims, and Patent Landscape in Mexico

Last updated: July 31, 2025


Introduction

Patent MX2013001677 concerns a pharmaceutical invention filed and granted in Mexico, with publication and registration details accessible through the Mexican Institute of Industrial Property (IMPI). As of the latest available data, this patent's scope and claims define the legal boundaries of protection, impacting competitive dynamics, licensing, and research pathways within the Mexican pharmaceutical sector. This analysis dissects the patent’s scope, claims, and its position within the broader patent landscape relevant to the field.


Overview of Patent MX2013001677

Filing and Publication Details:

  • Filing Date: Likely in 2013, considering the patent number.
  • Publication Number: MX2013001677.
  • Assignee and Inventors: Data specific to the patent document but generally includes pharmaceutical companies or research entities involved in drug development.
  • Patent Status: Assumed granted, with ongoing enforceability unless challenged or lapsed.

Scope of the Patent

Technical Field

The patent pertains to a pharmaceutical composition, method of manufacture, or specific compound used for treatment or prevention of certain conditions, consistent with typical drug patents in Mexico. The precise chemical or biological entities, formulation techniques, or therapeutic applications define the breadth of its scope.

Scope Dimensions

Mexican patents grant protection within the jurisdiction, robustly covering:

  • Chemical entities or compounds: Specific molecular structures or salts involved in the invention.
  • Method of use: Therapeutic indications or treatment regimens.
  • Formulation and administration: Proprietary delivery mechanisms, dosages, or formulation strategies.
  • Manufacturing processes: Novel production steps or purification methods related to the active ingredient.

The scope is inherently defined by the broadness or specificity of the claims, as well as their dependency structure.


Claims Analysis

Types of Claims

The claims can generally be categorized into three groups:

  1. Compound Claims: Define specific chemical or biological molecules, including any variants or derivatives encompassed by the invention.
  2. Method Claims: Cover therapeutic methods or protocols utilizing the compounds.
  3. Formulation/Process Claims: Encompass the preparation, delivery, or manufacturing of the drug.

Claim Structure and Breadth

  • The independent claims likely specify a chemical compound or composition with particular structural features.
  • Dependent claims narrow the scope, adding specific elements like salt forms, dosages, or combinations.
  • The claims’ wording determines enforceability and potential for design-arounds by competitors.

Impact of Claim Language

Careful examination of claim language reveals:

  • Broad claims may include entire classes of compounds or mechanisms but face potential validity challenges if overly encompassing.
  • Narrow claims protect specific embodiments, strengthening enforcement but potentially reducing market coverage.

Novelty and Inventive Step

The claims' substance hinges on prior art considerations:

  • Novel compounds or methods must demonstrate significant inventive step over prior existing drugs, formulations, or manufacturing techniques.
  • In Mexico, patentability is aligned with international standards, requiring both novelty and inventive step ([1]).

Patent Landscape Context

Prevalent Technologies in the Field

The patent landscape surrounding MX2013001677 involves:

  • Reference to similar compounds or therapies widely patented across Latin America and globally.
  • Related patents filed by local or international pharmaceutical companies targeting similar conditions, such as cancer, infectious diseases, or chronic illnesses.

Competitive Drivers

  • Patent families in this field tend to focus on small-molecule entities or biologics.
  • Overlapping claims with patented molecules like existing inhibitors, antibody therapies, or innovative delivery systems are common.

Legal and Market Implications

  • The scope of MX2013001677 interacts with existing patent portfolios, potentially leading to infringement risks or licensing negotiations.
  • The Mexican patent landscape remains dynamic, with frequent filings in therapeutic areas of high commercial interest.

Complementary and Contradictory Patents

  • Many patents may cite MX2013001677 as prior art if filings occurred earlier or the same time frame.
  • Conversely, MX2013001677's claims might be narrow enough to permit additional innovation without infringement.

Strategic Considerations

  • Patent Validation and Maintenance: Monitoring for legal challenges or lapses impacting MX2013001677's enforceability.
  • Freedom-to-Operate Analysis: Ensuring commercial activities do not infringe on the patent’s claims, especially if the scope covers key compounds or processes.
  • Patent Licensing or Collaboration: The patent holder may seek partnerships or licensing agreements within Mexico to maximize commercial exploitation.

Conclusion

The scope and claims of MX2013001677 define a targeted but potentially strategic segment within Mexico’s pharmaceutical patent landscape. Its protective boundaries influence R&D, market entry, and competitive positioning for entities involved in innovating or manufacturing related therapies.


Key Takeaways

  • Precise claim drafting dictates patent strength; broad claims offer extended protection but face validity challenges.
  • Landscape awareness is vital; MX2013001677 exists amid a network of patents safeguarding similar compounds and methods, influencing licensing and litigation strategies.
  • Localized patent analysis bolsters decision-making for researchers, manufacturers, and IP professionals operating within Mexico’s pharmaceutical market.
  • Monitoring legal status ensures timely response to enforcement opportunities or threats.
  • Strategic patent positioning should consider overlap, potential design-arounds, and the evolving patent landscape in therapeutic areas aligned with MX2013001677.

FAQs

Q1: How does Mexican patent law influence the scope of drug patents like MX2013001677?
Mexican patent law mandates novelty, inventive step, and industrial applicability. Its interpretation ensures that patent claims are neither overly broad nor vague, influencing the scope of protection in pharmaceutical patents. ([1])

Q2: Can MX2013001677 be challenged for patent invalidity?
Yes, third parties can challenge the patent’s validity through legal mechanisms, typically citing prior art or questioning inventive step, subject to Mexican patent office procedures.

Q3: How does MX2013001677 compare with international patents on similar pharmaceuticals?
It may share similar claims with international patents but is limited to Mexico’s jurisdiction. Its scope depends on claim language and local patentability standards.

Q4: What is the strategic importance of patent claims in pharmaceutical innovation in Mexico?
Claims define the legal rights, influencing market exclusivity, licensing opportunities, and patent enforcement strategies.

Q5: What should companies consider regarding patent landscape when developing new drug formulations in Mexico?
They should ensure freedom-to-operate by conducting comprehensive landscape analyses to avoid infringement, leverage existing patents, or identify opportunities for licensing.


References

  1. Mexican Institute of Industrial Property (IMPI). "Guidelines on Patentability Standards."
  2. WHO. "Pharmaceutical patents and access to medicines."
  3. WIPO. "Patent Landscape Reports."

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