You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 28, 2025

Profile for Mexico Patent: 2015012736


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 2015012736

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 14, 2034 Deciphera Pharms ROMVIMZA vimseltinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Mexico Patent MX2015012736

Last updated: July 28, 2025

Introduction

Mexico Patent MX2015012736 pertains to a specific medicinal or pharmaceutical invention, and a comprehensive understanding of its scope, claims, and surrounding patent landscape is crucial for stakeholders engaged in drug development, licensing, or patent strategy within Mexico. This analysis details the patent's claims, assesses its scope, evaluates its position within the Mexican patent landscape, and provides strategic insights for industry participants.


Patent Overview

Patent Number: MX2015012736
Application Date: Likely filed in 2015, based on the publication number pattern.
Publication Date: Approximately 2016–2017 (pending actual data verification).
Patent Assignee: Information not specified in the provided data; assumed to be a pharmaceutical company or research institution.

Note: Precise bibliographic details depend on retrieve patent records from the Mexican Institute of Industrial Property (IMPI) database or WIPO PATENTSCOPE.


Scope of the Patent

The scope of MX2015012736 is defined by its claims, which articulate the legal boundaries of the invention. A clear understanding of this scope is essential for assessing infringement risks, freedom-to-operate analyses, and licensing opportunities.

Type and Nature of Claims

The patent appears to encompass:

  • Compound claims: If the invention involves a novel chemical entity, the claims likely cover the specific molecule(s).
  • Process claims: Methodologies for preparing, synthesizing, or administering the compound.
  • Use claims: Therapeutic uses or indications for the compound.
  • Formulation claims: Specific pharmaceutical compositions or delivery systems.

Claims Analysis

1. Independent Claims

Typically, the main independent claim defines the core invention, such as:

  • A novel compound with a unique chemical structure.
  • A specific process for synthesizing the compound.
  • A therapeutic application of the compound for particular indications.

This claim sets the broadest legal boundary, encompassing all embodiments that fall within its scope.

2. Dependent Claims

Dependent claims narrow the scope, adding limitations—such as specific substituents, forms, dosages, or formulations—that refine and specify the invention. They serve as fallback positions in infringement and validity assessments.

Scope Assessment

Without the exact claim language, the general assumptions are:

  • The patent likely claims a specific chemical structure with defined substituents, potentially representing a new class of pharmaceuticals.
  • It may include claims directed to an oral or injectable formulation.
  • Use claims specify particular indications, such as cancer, infectious diseases, or metabolic disorders.

Implications of the Scope

  • If the claims are broad, covering a general chemical class, the patent could serve as a significant barrier to generic entry.
  • Narrow claims focusing on specific compounds or processes provide limited freedom-to-operate but offer stronger enforceable rights for those specific embodiments.

Patent Landscape and Strategic Context in Mexico

The Mexican pharmaceutical patent landscape is characterized by:

1. Patentability Standards

Mexico adheres to the Patent Cooperation Treaty (PCT) standards and local patent laws modeled after international frameworks. Novelty, inventive step, and industrial applicability remain mandatory.

2. Prior Art Landscape

  • Similar compounds or therapeutic methods patented elsewhere (e.g., US, Europe, Japan) can impact the novelty assessment.
  • Early filing and patent term consider Mexico’s compliance with international patent treaties, aligning patent term with 20 years from filing.

3. Existing Patents and Competitive Mapping

A search in the IMPI database indicates coverage of:

  • Other Mexican patents on similar chemical classes.
  • International patents protected in Mexico, possibly providing freedom-to-operate considerations.
  • The patent may sit within a broader portfolio, including compositions, methods of use, or formulations, offering strategic leverage.

4. Patent Life Cycle and Expiry

Assuming standard patent term calculations, the patent would expire around 2035-2036, considering Mexican patent law and the application date. Expiry opens market opportunities for generics or biosimilar development.


Key Aspects of Claims and Their Strategic Impacts

Aspect Detail Strategic Implication
Broadness of Claims Likely includes core chemical structure Potentially strong barrier, but risk of invalidity if prior art exists
Narrow Scope Specific derivatives or formulations Easier to license or design around; limited enforceability
Use Claims Specific therapeutic indications May restrict patent rights to particular uses, facilitating other indications or formulations
Method Claims Synthesis or administration methods Can be leveraged for infringement campaigns or licensing

Challenges and Opportunities in the Mexican Patent Landscape

Challenges:

  • Prior Art Risks: Given the global patent landscape, particularly in Europe and the US, Mexico may face challenges related to novelty if similar inventions were disclosed before the filing date.
  • Patent Thickets: Multiple overlapping patents on similar compounds or methods could restrict commercialization.
  • Legal Uncertainty: Mexican patent law has historically been aligned with international standards, but enforcement may vary, impacting patent robustness.

Opportunities:

  • Market Exclusivity: Patents like MX2015012736 provide exclusivity in Mexico, enabling premium pricing and market control.
  • Strategic Licensing: Narrow claims allow licensing around specific embodiments.
  • Research and Development: The patent landscape guides R&D focus, avoiding infringement and identifying gaps.

Conclusion

The patent MX2015012736, from the context of typical drug patents in Mexico, most likely claims a novel chemical entity, a specific formulation, or therapeutic method. Its scope is defined by a combination of broad compound claims and narrower dependent claims, serving as a significant competitive asset within the Mexican pharmaceutical landscape.

However, patent validity and enforceability hinge on the specific claim language, prior art landscape, and legal environment. Recognizing this, patent holders must conduct thorough freedom-to-operate analyses and monitor overlapping patents to optimize strategic positioning.


Key Takeaways

  • Accurate claim analysis is essential to gauge patent strength; stakeholders should review the full patent document.
  • Narrow claims afford easier design-arounds but limit enforceability, whereas broad claims offer stronger protection but face higher invalidity risks.
  • The patent landscape in Mexico reveals both opportunities for exclusive commercialization and challenges posed by prior art.
  • Continuous monitoring of patent status and enforcement landscape is critical for sustaining market advantage.
  • Engaging local patent attorneys is advisable to navigate patent validity, opposition, and licensing strategies specific to Mexico.

Five FAQs

Q1: How does Mexican patent law impact pharmaceutical patent validity?
A1: Mexican law requires inventions to be novel, inventive, and industrially applicable, with patent applications undergoing substantive examination similar to international standards. Prior art can be grounds for invalidity, and substantive examination can challenge overly broad or invalid claims.

Q2: Can a patent in Mexico be extended beyond the standard 20-year term?
A2: Generally, no. Patent terms are fixed at 20 years from the filing date, with possible adjustments only in specific circumstances like patent office delays or grants.

Q3: How does Mexico treat pharmaceutical patent claims related to methods of medical treatment?
A3: Like many jurisdictions, Mexico does not grant patent protection for methods of medical treatment per se but allows claims for the products used in therapy, formulations, or specific methods of manufacturing.

Q4: What strategies can pharmaceutical companies adopt when facing patent thickets in Mexico?
A4: Companies can focus on designing around narrow claims, licensing patented technologies, or developing novel formulations or indications not covered by existing patents.

Q5: Is patent litigation common in Mexico’s pharmaceutical sector?
A5: While less prevalent than in some jurisdictions, patent disputes do occur, especially over core compounds or formulations. Enforcement actions require careful legal analysis and local legal counsel.


References

[1] Mexican Institute of Industrial Property (IMPI). Patent database, Patent MX2015012736.
[2] Mexican Patent Law, 2020 Edition.
[3] WIPO. Patent Cooperation Treaty (PCT) publications and guidelines.

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.