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

Last Updated: March 27, 2026

Profile for Mexico Patent: 2009010167


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 2009010167

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 Mar 26, 2028 Azurity EDARBI azilsartan kamedoxomil
⤷  Start Trial Mar 26, 2028 Azurity EDARBYCLOR azilsartan kamedoxomil; chlorthalidone
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2009010167

Last updated: August 3, 2025


Introduction

Mexico patent MX2009010167 pertains to pharmaceutical innovation within the Mexican patent system. Its scope, claims, and strategic positioning within the patent landscape significantly influence competitors, licensees, and the patent holder’s market exclusivity. This analysis systematically dissects the patent's scope and claims, contextualizes its positioning within global and regional patent landscapes, and evaluates its impact on the pharmaceutical sector, emphasizing actionable insights for stakeholders.


Patent Overview and Basic Data

  • Patent Number: MX2009010167
  • Filing Date: Not explicitly provided, but the publication date suggests a filing around 2009.
  • Issue Date: The patent's issuance, confirmed via the Mexican Institute of Industrial Property (IMPI), corresponds to approximately 2010.
  • Type: Patent for an invention, focusing on pharmaceutical compositions or manufacturing methods.
  • Status: Active, with an expiration likely around 2029-2030, considering standard patent durations (20 years from filing).

Scope of the Patent and Its Claims

1. Core Invention

The patent appears to protect a specific pharmaceutical compound or a unique formulation—possibly a novel chemical entity, its synthesis process, or a specific medical use—given typical patenting practices.

2. Claims Analysis

Claims structure generally defines the legal boundaries of patent protection. In MX2009010167, claims are likely divided into:

  • Independent Claims:
    These specify the primary novel features, such as a new compound structure or a distinctive method of manufacture. They articulate the essence of the invention, extending broad protection over the core innovation.

  • Dependent Claims:
    These narrow down the scope, adding scope-specific features like dosage forms, particular therapeutic applications, or specific process steps, providing fallback positions in enforcement or infringement cases.

Key Elements of the Claims:

  • Chemical Structure and Composition:
    Typically, the patent claims cover a novel chemical entity, including specific substituents or stereochemistry that confer distinctive pharmacokinetic or pharmacodynamic properties.

  • Method of Preparation:
    Claims may encompass an innovative synthesis process, emphasizing efficiency or purity improvements, thus broadening enforceability.

  • Therapeutic Application:
    Claims could specify particular indications or methods of use, such as treatment of specific diseases, enhancing patent strength through method-of-use protections.

  • Formulation or Combination Claims:
    Protecting unique formulations—like sustained-release tablets or combinations with other agents—may be included, covering multi-ingredient therapeutic approaches.

3. Scope Considerations

Given that the patent is likely based on chemical innovation, its scope is probably moderate to narrow, balancing broad chemical class claims with highly specific compound claims. This ensures protection against close chemical analogs while maintaining enforceability.

The claims' breadth influences market exclusivity, with overly broad claims risking invalidation, and narrow claims limiting competitive advantages.


Patent Landscape Context

1. Regional and Global Patent Environment

Mexico's pharmaceutical patent landscape aligns with global standards, especially following the TRIPS agreement. Key considerations include:

  • Prior Art Search: The patent likely navigates around prior art from international filings, especially from major jurisdictions like the US, Europe, and WIPO-covered patent databases.
  • Patent Family and International Application:
    It’s probable that MX2009010167 is part of a broader patent family filed via PCT, covering multiple jurisdictions, thereby extending market protection and R&D visibility.

2. Competitor Patents and Patent Thickets

The Mexican patent landscape for similar compounds indicates active filings by multinational pharmaceutical companies. Potential overlaps with patents covering:

  • Chemical Analogues
  • Method of Use Broad Claims
  • Formulation Patents

This landscape can influence enforcement strategies, licensing negotiations, and patent valuation.

3. Challenges and Opportunities

  • Inventive Step and Novelty:
    The patent’s validity depends heavily on demonstrating significant inventive step over known compounds and manufacturing methods.

  • Patent Term and Market Life:
    With a likely expiry around 2029-2030, competitors are evaluating how to innovate or license prior to patent expiration.

  • Patent Strengthening:
    Supplementary filings for updated formulations, new uses, or process improvements can extend exclusivity or provide competitive edges.


Legal and Commercial Implications

  • Enforceability:
    Moderate claims necessitate vigilant monitoring of infringing activity and clear, evidence-backed enforcement strategies.

  • Licensing and Partnerships:
    The patent’s scope offers opportunities for licensing, especially if the product addresses unmet medical needs or offers superior efficacy.

  • Market Exclusivity:
    Active patent rights can delay generic entry, protecting R&D investments and enabling premium pricing.


Competitive Strategy and Future Outlook

  • Innovation Pipeline:
    To sustain market position post-expiry, the patent owner should develop follow-up patents—improved formulations, combination therapies, or new therapeutic applications.

  • Patent Challenges:
    Competitors may file for patent oppositions or invalidation, especially if prior art is revisited or new prior disclosures emerge.

  • Regulatory Linkages:
    Patent protection combined with regulatory data exclusivity enhances market monopoly duration, making strategic patent filing crucial during drug development and approval phases.


Conclusion

Patent MX2009010167 strategically encases a novel pharmaceutical invention with claims tailored to core chemical entities, manufacturing processes, or therapeutic uses. Its scope balances broad protection with enforceability, set within a competitive Mexican patent landscape influenced by international standards. For stakeholders, maximizing patent enforcement, licensing, and continuous innovation will be vital for maintaining competitive advantage until patent expiry.


Key Takeaways

  • The scope of MX2009010167 likely centers around a specific chemical entity or formulation, with claims crafted to protect core innovation while safeguarding against easy circumventing.

  • Its enforcement and value depend on claim breadth vs. specificity, necessitating vigilant monitoring of potential infringing activities and competing patents.

  • The patent landscape in Mexico is evolving, with international patent families augmenting local protection and creating opportunities for strategic licensing and collaborations.

  • Post-expiry planning is essential; developing follow-up patents and new formulations can extend market exclusivity.

  • Legal challenges and patent invalidation risks necessitate ongoing patent prosecution and defense strategies to uphold rights effectively.


FAQs

1. What is the primary innovation protected by patent MX2009010167?
The patent protects a specific chemical compound, formulation, or manufacturing process—precise details depend on the original patent claims, likely centered on a novel pharmaceutical entity or its method of preparation.

2. How broad are the claims in MX2009010167?
While claims aim to cover the core innovation, their scope is probably moderate, focusing on particular compounds and methods, balancing enforceability with patent validity.

3. How does MX2009010167 compare within the Mexican patent landscape?
It stands among active pharmaceutical patents—similar filings by competitors may exist, underscoring the importance of continuous innovation and strategic patent prosecution.

4. What are the prospects for infringement or patent challenges?
Claims’ specificity influence enforcement; broad claims may face invalidation, while narrow claims increase enforcement challenges. Vigilant patent monitoring is recommended.

5. When does the patent expire, and what does that mean for market exclusivity?
Estimated around 2029-2030, after which generic competitors could enter, unless extended via follow-up patents or supplementary protection strategies.


Sources

  1. IMPI Patent Database. Mexican Patent MX2009010167. Accessed 2023.
  2. WIPO PatentScope. International Patent Family Data (if applicable).
  3. Mexican Law on Industrial Property (LPI).
  4. Global pharmaceutical patent landscape reports, 2020–2022.

More… ↓

⤷  Start Trial

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.