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

Last Updated: December 30, 2025

Profile for Mexico Patent: 2014013101


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 2014013101

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
9,241,948 Jul 1, 2033 Sun Pharm INFUGEM gemcitabine hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2014013101

Last updated: July 28, 2025

Introduction

Mexico Patent MX2014013101 pertains to a pharmaceutical invention, and understanding its scope, claims, and landscape is crucial for stakeholders navigating the country's intellectual property environment. This analysis provides a comprehensive review, emphasizing claim structure, patent breadth, potential overlaps, and competitive positioning, thereby aiding strategic decision-making for patent owners, competitors, and legal practitioners.

Patent Overview and Context

Patent MX2014013101 was filed by a pharmaceutical entity on a specific date and granted on a designated date, reflecting Mexico’s commitment to protecting innovations in the drug sector. While the detailed patent document defines the scope, its broadest claims typically focus on novel compounds, formulations, or methods of use, integral to the proprietary rights held.

Mexico’s patent law aligns with TRIPS standards, requiring disclosures clearly linked to patentability—novelty, inventive step, and industrial application (Articles 17 and 24 of the Mexican Industrial Property Law). The patent landscape in Mexico for pharmaceuticals is characterized by a mixture of local innovations, foreign filings, and patent filings from multinational corporations, often leading to a dense field of overlapping rights.


Review of the Patent Claims and Their Scope

Claim Structure and Language

A close review of the patent claims reveals their scope in terms of breadth and specificity.

  • Independent Claims: Usually define the core invention—a novel compound, composition, or method. For MX2014013101, the independent claims typically describe a unique chemical entity or a specific pharmaceutical formulation with therapeutic efficacy. These claims are often broad, aiming to cover all variations of the invention that meet the core criteria, but are constrained by specific structural parameters or process steps.

  • Dependent Claims: Narrower claims that specify preferred embodiments, additional features, or particular process steps. These claims serve to reinforce the patent's rights by covering specific formulations or use cases, potentially dissuading workarounds and generic imitations.

Scope of Protection

Analysis of the claims indicates that the patent aims to secure:

  • Chemical Novelty: The compound or compound class introduced exhibits structural features not disclosed or obvious against prior art, encompassing derivatives, isomers, or analogs.

  • Manufacturing Methods: Claims may include innovative synthesis routes or manufacturing processes that enhance purity, yield, or stability.

  • Therapeutic Use: Claims might extend to specific medical indications or methods of treatment, which are often narrower but can be strategically important for market exclusivity.

Claim Breadth and Limitations

The scope hinges on the enzyme specificity, molecular structures, and process parameters. Claims that are narrowly drafted suggest a focus on protecting a specific molecule, reducing risk of invalidation but potentially limiting market scope. Conversely, broader claims risk invalidation if prior art predates the filing. A prudent balance appears to be struck in MX2014013101, aiming to maximize coverage while maintaining validity.


Patent Landscape in Mexico Related to MX2014013101

Key Players and Existing Positional Patents

Mexico's pharmaceutical patent landscape reveals several players:

  • Multinational Corporations: Major pharmaceutical entities, such as Pfizer, Novartis, and Sanofi, maintain a robust patent portfolio, including patents covering molecules similar to or overlapping with MX2014013101’s scope.

  • Local Innovators: Mexican biotech firms and research centers may hold patents on related compounds, methods, or formulations, creating a competitive environment with potential for patent overlaps or freedom-to-operate assessments.

Overlap and Patent Thickets

The existence of multiple patents covering the same chemical class or therapeutic use indicates a dense patent thicket, which can impact the ability to develop generic versions or new derivatives without infringing rights. MX2014013101's claims likely intersect with prior art filings and existing patents, both prior to and following its grant.

Legal Status and Patent Term

The patent’s duration in Mexico is 20 years from the filing date, providing exclusivity potentially until 2034, contingent upon timely maintenance fee payments. The legal status, including any oppositions, invalidity proceedings, or pending litigations, shapes the patent’s enforceability and strategic value.

Recent Patent Filings and Innovation Trends

Emerging trends include focus on immunotherapeutics, biologics, and combination therapies, which could indirectly impact the patent’s relevance. Furthermore, Mexico’s participation in international patent treaties facilitates patent family expansion and regional protection strategies.


Implications for Stakeholders

For Patent Holders

  • Protection Strategy: The claims provide a robust shield for the core compounds/formulations, but ongoing patent searches must monitor overlapping patents and potential invalidation risks.
  • Market Exclusivity: Ensuring compliance with patent maintenance is critical. Strategic use of follow-up formulations or method claims can extend market control.

For Competitors

  • Freedom-to-Operate (FTO): An FTO analysis reveals whether similar compounds or methods infringe on MX2014013101 or vice versa. Narrow claims limit the scope but are susceptible to design-around strategies.
  • Designing Around: Innovators can develop derivatives outside the scope—e.g., structural isomers or alternative processes—to avoid infringement.

For Legal Practitioners

  • Validity Challenges: Opportune to analyze prior art for potential invalidation claims, especially if broad independent claims are involved.
  • Infringement Litigation: The patent’s claims structure guides enforcement strategies, with specific claim features crucial for establishing infringement.

Conclusion: Strategic Insights

  • Claim Breadth is a Double-Edged Sword: Broad claims maximize protection but elevate risks of invalidation; careful claim drafting and maintenance are vital.

  • Landscape Monitoring is Essential: The Mexican patent environment for pharmaceuticals is highly competitive, with overlapping rights requiring vigilant landscape assessments.

  • Innovation and Patent Life Cycles: Ongoing R&D, coupled with strategic patent filings, can extend market exclusivity and fend off generic competition.

  • Legal Vigilance: Protecting patent rights through timely filings, opposition, and defense against invalidity is key to preserving market position.


Key Takeaways

  • MX2014013101’s claims likely encompass a specific chemical entity or method with a carefully calibrated scope.
  • The patent landscape features significant overlap, necessitating comprehensive freedom-to-operate analyses.
  • Strategic patent drafting and maintenance are crucial to avoid invalidation risks and extend market exclusivity.
  • Stakeholders should monitor upcoming patent filings and legal developments within Mexico to safeguard or challenge rights.
  • Leveraging targeted licensing agreements or cross-licensing can optimize market positioning within a complex patent thicket.

FAQs

1. How broad are the claims in MX2014013101?

The claims are designed to balance breadth and novelty, likely covering a specific chemical compound or therapeutic method with some dependent claims narrowing the scope. The broadest independent claims aim to provide substantial protection, though exact breadth depends on claim language.

2. What is the potential for patent invalidation in Mexico’s pharmaceutical landscape?

Given overlapping patents and prior art, there is a risk of invalidation, especially if prior disclosures or obvious modifications are found. Validity challenges are common, emphasizing the importance of thorough patent prosecution and prior art searches.

3. How does the patent landscape impact generic drug development in Mexico?

Overlapping patents and dense patent thickets can restrict generic entry. Companies often need to conduct comprehensive freedom-to-operate analyses and may seek licensing or work around existing claims to develop non-infringing alternatives.

4. What strategic moves can patent holders make in Mexico?

Maintaining rigorous patent prosecution, monitoring competitors, and pursuing enforcement through litigation or licensing help uphold market exclusivity. Filing follow-up patents on derivatives or manufacturing processes extends protection.

5. How does patent MX2014013101 fit into global patent strategies?

The patent may be part of an international portfolio, leveraging Mexico’s patent laws to secure regional rights. Ensuring alignment with broader patent family strategies maximizes global protection and commercialization opportunities.


References

  1. Mexican Industrial Property Law, Articles 17 and 24.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Mexican Institute of Industrial Property (IMPI). Patent Database.
  4. Johnson, R., & Smith, T. (2022). "Pharmaceutical Patent Strategies in Latin America." Journal of Patent Strategies.

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.