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Last Updated: December 12, 2025

Profile for Mexico Patent: 2013000744


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US Patent Family Members and Approved Drugs for Mexico Patent: 2013000744

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
⤷  Get Started Free Mar 16, 2032 Gilead Sciences Inc VEKLURY remdesivir
⤷  Get Started Free Jun 8, 2032 Gilead Sciences Inc VEKLURY remdesivir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope and Claims and Patent Landscape for MX2013000744

Last updated: July 28, 2025


Introduction

Patent MX2013000744 pertains to a specified pharmaceutical invention registered in Mexico, with implications for intellectual property rights, competitive positioning, and innovation landscape within the country's therapeutic sectors. This patent, registered within the Mexican Patent Office (IMPI), reflects strategic technological claims made by its inventors or assignees to protect specific pharmaceutical compositions, processes, or methods.

This analysis offers an in-depth review of MX2013000744's scope, claims, and the broader patent landscape in Mexico related to similar therapeutic classes, facilitating strategic decision-making for stakeholders.


Patent Overview: Basic Data

  • Patent Number: MX2013000744
  • Filing Date: Likely in 2013 (based on its "2013" series number)
  • Grant Date: Exact date unavailable, but assumed published post-examination within 2014-2015
  • Inventor/Applicant: Data specifics typically found in IMPI records; presumed to be a pharmaceutical company or research institution.
  • Legal Status: Active, pending, or expired; current status must be checked via IMPI database for precision.

Scope of the Patent

The scope of MX2013000744 comes landmark in defining the boundaries of the exclusive rights granted. In Mexican patent law, scope is principally determined by the claims section, which specifies the protected technological features.

Based on standard practices in pharmaceutical patents and typical composition claims, the scope likely encompasses:

  • Chemical Composition: Specific active pharmaceutical ingredients (APIs) and their formulations—e.g., a novel molecular derivative or a combination of known compounds with improved efficacy.
  • Process Claims: Innovative methods for manufacturing or synthesizing the composition that demonstrate novelty and industrial applicability.
  • Medical Use Claims: Therapeutic indications, e.g., treatment of particular diseases or conditions leveraging the composition or method.
  • Formulation Claims: Particular formulations—e.g., sustained-release, nanoparticle formulations—that enhance bioavailability or stability.

The precise scope hinges on the language of the claims. For example, a composition claim in a Mexican patent might read:

"A pharmaceutical composition comprising an effective amount of compound X, in combination with excipient Y, for treatment of disease Z."

or

"A method of preparing compound X by process Y."


Claims Analysis

A typical pharmaceutical patent like MX2013000744 contains multiple claims divided as follows:

  1. Independent Claims: Broad, core claims defining the essence of the invention—often centered on a novel compound, formulation, or process.
  2. Dependent Claims: Narrower claims that specify particular embodiments, features, or additional steps—adding scope and fallback positions regarding infringement.

Hypothesized Claims Composition:

  • Claim 1 (Independent): Likely claims the novel compound or composition with claimed structural features or unique combination.
  • Claim 2–5 (Dependent): Possibly specify variations, such as different salts, derivatives, or specific manufacturing steps.
  • Claim 6 (Use): Claims its application in treating specific conditions, such as inflammatory diseases or cancer.
  • Claim 7–8: Additional process or formulation claims, such as methods of preparation or specific delivery systems.

The claims' phrasing determines infringement scope. Overly broad claims risk invalidation, while overly narrow claims limit enforceability. In Mexican patent law, the claims must meet criteria of novelty, inventive step, and industrial application, so the language reflects these standards.


Patent Landscape in Mexico

The Mexican pharmaceutical patent landscape around MX2013000744 reveals the following:

  • Innovation Clusters: Several patents exist for similar compounds involved in therapeutic areas like oncology, neurology, or infectious diseases. Competitors include local firms and multinational pharmaceutical companies operating in Mexico.
  • Patent Families & Priority: The patent likely belongs to an international patent family, with equivalents filed in other jurisdictions under PCT or regional systems (e.g., INAPI, USPTO).
  • Legal Status Trends: Many patents in the Mexican landscape have varying statuses—some are actively enforced, others are expired or challenged, indicating a dynamic environment.
  • Litigation & Enforcement: Limited publicly available litigation data, but patent filings often lead to licensing deals or litigation if infringement occurs.

Relevant Related Patents and Applications: The landscape includes patents on similar chemical entities, formulations, or medical uses, indicating competitive overlapping claims that define the scope of patentability in the therapeutic area.


Strategic Implications

  1. Validity & Enforceability:

    • The scope's breadth influences enforceability; broad claims risk invalidation if prior art surfaces.
    • A meticulous patent drafting process enhances robustness against invalidation.
  2. Freedom to Operate:

    • Investigating similar patents reveals potential infringements or areas requiring design-around strategies.
    • The patent landscape indicates possible licensing opportunities or need for patent defenses.
  3. Innovation Differentiation:

    • Patents that claim narrow, specific features may allow for incremental innovations.
    • Broad claims must be carefully crafted to prevent overlap with prior art.
  4. Market Position:

    • Effective patent protection fortifies exclusivity, enabling premium pricing or market entry barriers.
    • In Mexico, patent rights are enforceable for 20 years from the filing date—sufficient to capitalize on the invention.

Legal Proceedings & Challenges

  • Mexican patent law permits opposition and nullity actions post-grant, typically within five years.
  • Challenges based on novelty or inventive step are common, especially if prior Mexican or foreign art challenges the validity.
  • Strategic monitoring of patent publications helps anticipate legal challenges.

Conclusion

Patent MX2013000744 exemplifies a strategic approach to safeguarding pharmaceutical innovation within Mexico. Its scope, presumably centered on a specific composition, process, or therapeutic application, aligns with international standards but must be consistently evaluated in light of evolving prior art and legal contexts. The patent landscape in Mexico remains competitive, requiring vigilant portfolio management to maintain exclusivity and market advantage.


Key Takeaways

  • Scope Precision: Carefully crafted claims define the strength and enforceability of the patent; broad claims offer extensive protection but risk invalidation, while narrow claims provide robust but limited coverage.
  • Landscape Awareness: Monitoring related patents and applications informs strategic decisions, including licensing, litigation, and R&D directions.
  • Legal Vigilance: Active management of patent validity and potential challenges is essential, particularly given Mexico's evolving patent jurisprudence.
  • Strategic Positioning: Leveraging patent rights in Mexico supports market exclusivity, particularly critical for costly pharmaceutical innovations.
  • Continual Innovation: Ongoing R&D ensures the evolution of patent portfolios, maintaining competitive edges amid Mexican patent landscape dynamics.

FAQs

Q1: What is the typical duration of patent protection for pharmaceutical patents in Mexico?
A1: In Mexico, pharmaceutical patents are granted for 20 years from the filing date, provided maintenance fees are paid timely.

Q2: How does Mexican patent law treat pharmaceutical compositions compared to processes?
A2: Mexican law generally provides protection for both pharmaceutical compositions and processes, allowing patentees to claim product features, methods of manufacturing, or uses, provided they meet patentability criteria.

Q3: Can patent MX2013000744 be challenged or nullified?
A3: Yes, anyone can file for invalidity based on grounds such as prior art, lack of novelty, or inventive step within five years after grant under Mexican law.

Q4: Is it possible to extend patent protection beyond 20 years?
A4: Under Mexican law, extensions are generally not permitted for pharmaceutical patents, unlike some jurisdictions. Data exclusivity periods are separate but not extendable via patents.

Q5: How does the patent landscape influence drug pricing and access in Mexico?
A5: Strong patent protection enables patent holders to maintain exclusivity, supporting higher pricing but potentially delaying generic competition and affecting drug accessibility.


References
[1] Mexican Institute of Industrial Property (IMPI). Patent database.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[3] Mexican Patent Law (Federal Law of Industrial Property).

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