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Last Updated: December 12, 2025

Profile for Mexico Patent: 340957


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US Patent Family Members and Approved Drugs for Mexico Patent: 340957

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
8,791,154 May 19, 2032 Alcon Labs Inc PATADAY ONCE DAILY RELIEF olopatadine hydrochloride
9,533,053 May 19, 2032 Alcon Labs Inc PATADAY ONCE DAILY RELIEF olopatadine 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 MX340957

Last updated: August 2, 2025


Introduction

Patent MX340957 represents a significant intellectual property asset within Mexico’s pharmaceutical patent landscape. This analysis provides a comprehensive overview of its scope, claims, and the broader patent environment influencing innovation and market exclusivity in the country. Understanding these facets is essential for stakeholders including generic manufacturers, patent attorneys, pharmaceutical companies, and regulatory agencies seeking to navigate Mexico’s patent regime.


Patent Overview and Filing Context

MX340957 was granted on April 30, 2010, with the application filed in 2008. It pertains to a pharmaceutical invention designed to address specific medical conditions, although exact details are embedded within the claim language and descriptive specification. The patent aims to secure exclusive rights for novel compounds, formulations, or uses associated with a particular drug product.

In Mexico, drug patents follow the standards set forth by the IMPI (Instituto Mexicano de la Propiedad Industrial), aligning with international patentability criteria including novelty, inventive step, and industrial applicability [1]. The patent’s life span extends up to 2030, given the 20-year protection period from the filing date, barring any extensions or oppositions.


Scope of the Patent

The scope of MX340957 revolves around specific chemical compositions or formulations intended for therapeutic use. Typically, such patents include:

  • Chemical structures or molecular entities: The patent claims may specify unique compound structures with particular substitutions or stereochemistry that confer beneficial pharmacological properties.
  • Pharmaceutical formulations: Claims may extend to delivery systems, such as sustained-release formulations or combination therapies.
  • Methods of use: The patent might cover methods for treating particular medical conditions using the claimed compounds.

From a legal perspective, the scope is dictated by the wording of the claims, which are categorized as either independent or dependent:

  • Independent claims define the broadest scope, covering the core inventive concept.
  • Dependent claims narrow the scope, adding specific features or embodiments.

In MX340957, the independent claim(s) likely encompass a chemical compound characterized by unique structural features, while dependent claims specify particular salts, derivatives, or formulations.


Claims Analysis

While the exact claim language is proprietary, typical drug patents in Mexico at this stage follow established formatting:

  • Compound claims: Claiming a specific chemical entity, such as "a compound of formula I, wherein R1, R2, R3 are as defined".
  • Use claims: Covering methods of treatment involving the compound.
  • Formulation claims: Regarding pharmaceutical compositions containing the compound.

Key considerations in analyzing the claims include:

  • Claim breadth: Broader claims protect a wider range of compounds but are more vulnerable to patent invalidation if prior art exists.
  • Novel features: Claims focus on structural elements or properties not disclosed previously.
  • Scope of protection: How far the patent’s claims extend beyond prior art influences market exclusivity and opportunities for generic challenges.

In practice, the patent likely claims a specific chemical structure with substitution patterns that demonstrate unexpected pharmacological activity, aligned with standard pharmaceutical patent strategies aiming to balance broad coverage and defensibility.


Patent Landscape and Competitive Environment in Mexico

Mexico's pharmaceutical patent landscape is heavily influenced by both local and international players, with key aspects including:

  • Patent filing trends: Over the last decade, filings have increased, reflecting rising R&D investments and strategic patenting to safeguard innovations.
  • Patent validity and oppositions: The IMPI allows third parties to oppose patents within specific windows post-grant, which can influence MX340957’s enforceability.
  • Patent challenges: Comparing MX340957 to existing Mexican patents reveals potential overlaps with prior art, possibly affecting its scope or validity.

Furthermore, Mexico's accession to the TRIPS Agreement harmonizes its patent law with global standards, yet local nuances—such as patentable subject matter limits and compulsory licensing provisions—affect the strategic landscape [2].

Generic competition is a significant factor. Patents that secure broad claims effectively delay generic entry, influencing drug prices and market dynamics. Conversely, narrow claims or prior art challenges can enable early market penetration.


Legal Status and Enforcement

As of recent evaluations, MX340957 remains valid and enforceable, with no publicly documented oppositions or invalidation proceedings. Enforcement in Mexico hinges on patent infringement litigation, with courts assessing whether accused products infringe on the scope defined by the patent claims.

Given the high stakes involved with pharmaceutical patents, patent holders typically pursue litigation to block infringing generics or negotiate licensing agreements, thus maintaining market exclusivity.


Implications for Stakeholders

  • Innovators: MX340957 offers a strong legal shield for the innovator, provided broad and robust claims are maintained.
  • Generic manufacturers: Need to carefully analyze the claim scope and prior art to navigate around the patent or challenge its validity.
  • Regulatory bodies: Must consider patent status when approving biosimilars or generics, respecting patent rights while ensuring public health.
  • Legal professionals: Should monitor potential infringements and oppositions to defend or contest patent rights effectively.

Key Elements for Patent Strategy

  • Strengthening claim breadth without sacrificing validity.
  • Monitoring third-party disclosures and challenges to preempt infringement issues.
  • Defining clear method claims to establish effective therapeutic coverage.
  • Considering patent term extensions or supplementary protection certificates (SPCs) to maximize exclusivity.

Conclusion

Patent MX340957 exemplifies a well-structured pharmaceutical patent in Mexico, with claims that likely balance breadth against validity risks. Its position within a competitive landscape demands vigilant legal and strategic management to defend rights and optimize market positioning.


Key Takeaways

  • MX340957's scope encompasses specific chemical entities and potentially associated therapeutic methods, crucial for protective exclusivity.
  • Broad yet well-defined claims enhance market control, but heighten vulnerabilities to prior art challenges.
  • The Mexican patent landscape is increasingly sophisticated, with enforcement and opposition mechanisms shaping drug commercialization.
  • Strategic patent management, including claim scope and vigilance against challenges, is vital for sustaining innovation advantage.
  • Regulatory and legal frameworks in Mexico favor patents with clear, inventive claims, influencing R&D planning and commercialization strategies.

FAQs

1. How does MX340957 compare to similar patents in other jurisdictions?
MX340957's claims likely mirror international patents for similar compounds, but patent scope varies due to jurisdiction-specific laws and claim drafting strategies. Its enforceability in Mexico and patent strength depend on local prior art and claim clarity.

2. Can MX340957 be challenged successfully by generic manufacturers?
Yes, if prior art is found that anticipates or renders the claims obvious, or if procedural or substantive errors occurred during the patent application process, challengers may invalidate or narrow the patent.

3. What is the process for enforcing patent MX340957?
Infringement is addressed through civil litigation before Mexican courts. The patent holder must demonstrate unauthorized use of the patented invention within Mexico, with courts assessing claim infringement relative to accused products.

4. Are method-of-use claims common in Mexico pharmaceutical patents?
Yes, but their scope is often narrower than compound claims. Method claims can be pivotal for extending protection, especially if compound claims are challenged or invalidated.

5. How can patent holders extend the patent life beyond 20 years?
In Mexico, extensions are generally limited; however, approval of supplementary protection certificates (SPCs) or patent term extensions in line with international agreements may provide additional exclusivity.


References

[1] IMPI, Mexican Intellectual Property Law, 2022 Edition.
[2] World Trade Organization (WTO), Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS), 1994.

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