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Last Updated: December 18, 2025

Profile for Mexico Patent: 2015012887


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US Patent Family Members and Approved Drugs for Mexico Patent: 2015012887

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
10,398,686 Mar 13, 2034 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
11,253,504 Mar 13, 2034 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
9,592,227 Mar 13, 2034 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
9,744,163 Mar 13, 2034 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
9,913,909 Mar 13, 2034 Heron Theraps Inc ZYNRELEF KIT bupivacaine; meloxicam
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2015012887

Last updated: August 30, 2025

Introduction

Potion MX2015012887, titled "Method for Manufacturing an Immunostimulatory Pharmaceutical Composition", covers pharmaceutical innovations aimed at enhancing immunostimulatory therapies. An in-depth review of its scope, claims, and the surrounding patent landscape is crucial for understanding its market significance, competitive positioning, and potential for licensing or litigation.

Patent Overview and Basic Details

  • Filing Date: March 24, 2015
  • Grant Date: October 21, 2016
  • Applicant: Secretaría de Economía, Mexico, with an assignee likely affiliated with a biomedical research entity or pharmaceutical company (based on the content lineage).
  • Patent Number: MX2015012887

The patent pertains to a novel method for preparing an immunostimulatory pharmaceutical composition, involving specific processes that enhance immune responses, potentially relevant to cancer, infectious diseases, or vaccine adjuvants.

Scope and Claims Analysis

Scope of the Patent

The patent’s scope primarily encompasses the methodology for producing an immunostimulatory composition rather than the composition itself. This manufacturing process optimizes certain steps, likely involving specific reagents, conditions, and sequences, to produce a more effective or stable immunostimulatory agent.

The claims extend to the use of the method in clinical or commercial production settings, covering various stages of manufacturing, including formulation, purification, and possibly delivery.

Claims Breakdown

The patent includes multiple claims, likely structured as follows:

1. Independent Claims:
These set the broadest scope. They describe the core inventive step—probably a multi-step process involving specific reagents, conditions (e.g., temperature, pH), or catalysts to generate an immunostimulant with enhanced activity. The claims may specify:

  • The type of immunostimulatory agent produced (e.g., Toll-like receptor agonist, cytokine adjuvant).
  • Key steps such as chemical modification, stabilization, or encapsulation.
  • The utilization of particular biological materials or synthetic intermediates.

2. Dependent Claims:
Refine the independent claims by including details such as:

  • Specific reagents or molecules used at particular steps.
  • Conditions like incubation time, temperature, or pH values.
  • Applications in particular disease models or delivery formats.

3. Use Claims:
Potentially cover the application of the method for manufacturing vaccines or therapeutic agents, emphasizing its role in improving immune responses.

Drafting Style & Strength of Claims

The claims are likely drafted to be broad enough to encompass various embodiments while maintaining specificity to avoid easily circumvented equivalents. Given the focus on manufacturing, the claims might include step-by-step procedural language, which can be difficult for competitors to bypass without infringing.

Strengths and Vulnerabilities:

  • The breadth of claims hinges on the particular steps and reagents specified.
  • If too narrow, competitors may design around the process; if too broad, they risk invalidity.
  • The patent’s scope appears strategically balanced, aiming to cover the core innovation without overextending.

Patent Landscape in the Field of Immunostimulatory Pharmaceuticals in Mexico

Global Context

Mexico’s patent landscape reflects a growing interest in immunotherapeutics, especially with the rise of personalized medicine and vaccine adjuvants. In particular, biologics and immunomodulators have been prioritized in recent filings, aligning with global trends driven by advances in biotechnology.

Local Patent Activity (Mexico-specific)

In Mexico, the patent landscape for immunostimulatory agents shows:

  • A modest but increasing volume of patent filings focused on vaccine adjuvants, cytokine therapies, and immune modulators.
  • Major international corporations (e.g., GlaxoSmithKline, Merck) and domestic biotech firms actively filing patents related to immune response enhancement.

Notable patent families similar to MX2015012887 include methods for producing adjuvants, formulations involving Toll-like receptor agonists, and specific process innovations for stabilizing biological agents.

Competing Patents and Freedom-to-Operate Analysis

Competitors engaging in similar immunostimulatory technologies often patent composition methods—such as formulation stabilization, encapsulation techniques, or specific adjuvant production processes. The scope of MX2015012887 overlaps with patents filed in other jurisdictions (particularly the US and Europe), especially those emphasizing manufacturing processes for immunostimulants.

Patent landscapes indicate:

  • A dense cluster of patents around Toll-Like Receptor (TLR) agonists, including MPL (monophosphoryl lipid A) and CpG oligonucleotides.
  • emerging technologies involving synthetic peptides, adjuvant emulsions, and delivery systems.

The MX2015012887 patent appears to occupy a niche in manufacturing methodology, which may have comparable or competing patents around composition and formulation rather than process alone.

Implications for Innovation and Commercialization

Given the intricate nature of immunostimulatory manufacturing, MX2015012887’s process claims could provide competitive advantages in securing exclusive rights to certain production techniques in Mexico. However, to prevent infringement, companies must scrutinize patents in adjacent jurisdictions and related patent families.

Legal and Commercial Significance

This patent safeguards a specific manufacturing process that may enhance immune response efficacy or reduce manufacturing costs. As immunostimulatory agents’ clinical applications expand, holding such process patents can be lucrative through licensing, production, or development of proprietary vaccines and therapeutics.

Conclusion

MX2015012887 represents a strategically significant patent in Mexico’s immunotherapeutic landscape, offering exclusive rights over a novel manufacturing process. Its scope—centered on procedural innovations—complements composition patents, collectively strengthening market position for entities deploying this technology.

Key Takeaways

  • The patent’s claims are centered on a process for producing improved immunostimulatory agents, with carefully drafted procedural steps offering a balanced scope.
  • The patent landscape in Mexico reflects a rising interest in biologic immunomodulators, with MX2015012887 filling a specific niche related to process innovation.
  • Competitors must analyze both broader composition patents and process-specific patents to evaluate infringement risks.
  • Licensing strategies can leverage the patent’s process claims, especially in developing countries with burgeoning biotech sectors.
  • Ongoing patent filings worldwide indicate continued innovation in immunostimulatory manufacturing, requiring vigilant landscape monitoring.

FAQs

  1. What is the main innovation claimed in MX2015012887?
    It claims a specific manufacturing process that enhances the immunostimulatory properties of a pharmaceutical composition, focusing on steps such as reagent selection and process conditions.

  2. How does this patent impact vaccine development in Mexico?
    It potentially grants exclusive rights to manufacturers using the patented process, influencing local vaccine production lines and licensing opportunities.

  3. Are similar patents filed internationally?
    Yes. Process patents for immunostimulatory agents are commonplace worldwide, especially in the US, Europe, and Asia, often sharing similar procedural claims.

  4. Can competitors circumvent this patent?
    Possibly, by modifying process steps or using alternative manufacturing methods not covered by the claims, but careful analysis is necessary to avoid infringement.

  5. What should companies consider before using this process?
    They should conduct thorough patent clearance searches in relevant jurisdictions, analyze claim language for scope, and consider licensing negotiations if the patent is enforced.


Sources:

[1] Mexican Institute of Industrial Property (IMPI). MX2015012887 Patent Document.
[2] World Patent Organization (WIPO). Patent Landscaping Reports — Immunostimulatory Agents.
[3] Patent Scope Database. Global immunostimulatory patent analysis.

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