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Last Updated: December 31, 2025

Profile for Mexico Patent: 347290


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US Patent Family Members and Approved Drugs for Mexico Patent: 347290

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
8,679,544 Apr 23, 2030 Zyla ZORVOLEX diclofenac
8,999,387 Apr 23, 2030 Zyla ZORVOLEX diclofenac
9,017,721 Apr 23, 2030 Zyla ZORVOLEX diclofenac
9,173,854 Apr 23, 2030 Zyla ZORVOLEX diclofenac
9,180,095 Apr 23, 2030 Zyla ZORVOLEX diclofenac
9,180,096 Apr 23, 2030 Zyla ZORVOLEX diclofenac
9,186,328 Apr 23, 2030 Zyla ZORVOLEX diclofenac
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX347290

Last updated: September 4, 2025


Introduction

Mexico Patent MX347290, granted by the Mexican Institute of Industrial Property (IMPI), pertains to a proprietary pharmaceutical invention. Understanding its scope, claims, and the surrounding patent landscape is crucial for stakeholders including pharmaceutical companies, generic drug manufacturers, legal professionals, and investors aiming to navigate the Mexican pharmaceutical patent environment effectively.

This analysis offers a comprehensive overview of MX347290, focusing on its legal scope, claim structure, and position within the patent ecosystem, emphasizing strategic implications and potential challenges.


Patent Overview and Legal Status

Registration Details:

  • Patent Number: MX347290
  • Filing Date: [Exact date needed; presumed around early 2010s based on typical patent term durations]
  • Grant Date: [Date needed]
  • Expiry Date: Typically 20 years from filing, subject to maintenance fees and legal extensions.

Patent Term and Maintenance:
The patent likely remains in force if properly maintained through timely fee payments. Its active status signifies protection over the claimed invention, barring unauthorized commercial use within Mexico.


Scope of the Patent

Core Focus:
MX347290 claims revolve around a novel pharmaceutical composition involving a specific active ingredient or combination, which may be a formulation intended to improve efficacy, stability, bioavailability, or reduce side effects.

Scope of Protection:
The patent's scope is defined by its claims. In Mexico, claims are categorized into independent and dependent claims, with the former establishing broad protection and the latter offering narrower, specific embodiments.

  • Independent Claims:
    Typically, these cover the core inventive concept—e.g., a specific chemical compound, a unique formulation, or a process for manufacturing.

  • Dependent Claims:
    These refine the independent claims by adding particular features such as dosage forms, manufacturing steps, or specific compound variants.


Analysis of the Claims

Without the full text, the analysis relies on publicly available information and patent databases such as IMPI’s official records and global patent databases (e.g., WIPO PATENTSCOPE, INPADOC).

Claim Type & Breadth:

  • Likely claims encompass both composition-of-matter and method-of-use aspects.
  • They probably specify the chemical structure or a novel combination, potentially including salts, polymorphs, or formulations.

Key Elements to Note:

  1. Novelty and Inventive Step:
    The claims must demonstrate novelty over prior art. In pharmaceuticals, this often involves demonstrating a new therapeutic effect or a surprising technical advantage.

  2. Scope Limitations:
    Mexican patent law limits claims to what is sufficiently disclosed; overly broad claims may invoke invalidity or opposition. The scope is primarily confined to the language used in the claims, emphasizing the importance of their precise drafting.

  3. Claim Interpretation:
    Under Mexican law, claims are interpreted in light of their description, context, and the patent specifications, with a focus on safeguarding the covered inventive core.


Patent Landscape in Mexico

Mexico presents an evolving but robust patent environment for pharmaceuticals, balancing innovation incentives with public health considerations.

Key Trends:

  • Patentability of Pharmaceuticals:
    The Mexican Industrial Property Law (LPI) aligns with TRIPS standards, permitting patent protection for new chemical entities, formulations, and innovative manufacturing processes.

  • Patent Challenges & Litigation:
    Patent disputes are increasingly prevalent, especially concerning secondary patents and formulations. The Mexican Patent Office (IMPI) and courts scrutinize patent validity, especially in cases involving widely used drugs.

  • Patent Term & Extensions:
    The patent term aligns with international standards, with possible extensions for regulatory delays, although these are less common for pharmaceuticals in Mexico compared to other jurisdictions.

  • Parallel Patent Strategies:
    To extend market exclusivity, patentees often file supplementary protections, patent term extensions, or leverage data exclusivity provisions.


Contextual Position of MX347290 within the Patent Space

Comparison with Prior Art:
If MX347290 claims a composition or molecular structure, similar prior art likely exists, with patentability hinging on demonstrating inventive step and overcoming obviousness.

Potential for Generic Entry:
Once the patent expires or is challenged successfully, generic manufacturers are positioned to enter the Mexican market. Current patent scope determines the extent of patent barriers.

Regulatory & IP Regulations Impact:
Mexico’s health authorities (COFEPRIS) require data exclusivity and may influence patent enforcement, particularly for innovative formulations or new uses.


Legal and Commercial Implications

For Patent Holders:

  • The scope of MX347290 provides a foundation for exclusive market rights.
  • Conducting validity assessments and monitoring potential infringement are crucial for enforcement.

For Competitors:

  • A detailed review of the claims can identify potential non-infringing alternatives or areas for designing around.
  • The patent landscape analysis guides strategic planning, such as pursuing licensing, filing secondary patents, or challenging the patent.

Challenges & Risks:

  • Patent infringement allegations—especially if broad claims are involved—pose litigation risks.
  • Regulatory delays or opposition proceedings may impact patent enforceability.

Key Takeaways

  • Claim Precision Defines Scope:
    The patent’s enforceability hinges on the clarity and breadth of its claims. Regular review of claim language is vital for strategic enforcement and potential litigations.

  • Patent Landscape Dynamics:
    Mexico’s pharmaceutical patent environment is active, with increasing scrutiny of secondary patents. MX347290’s position must be contextualized within existing prior art to assess strength and vulnerabilities.

  • Market and Regulatory Considerations:
    Patent protection confers exclusivity but must be balanced with regulatory data requirements, especially for new formulations or indications.

  • Legal Challenges and Strategies:
    Patent holders should prepare for possible oppositions or invalidity defenses, maintaining detailed documentation of inventive steps and clinical data.

  • Monitoring and Enforcement:
    Continuous monitoring of competitors’ activities and vigilant enforcement are essential to sustain market advantages and maximize patent lifespan.


FAQs

1. What is the scope of protection offered by Mexican patent MX347290?
It covers specific pharmaceutical compositions and methods as detailed in its claims, primarily protecting the inventive structure, formulation, or use described. Its scope depends on claim language, with independent claims offering broader coverage.

2. How does MX347290 compare to similar patents in Mexico?
Its uniqueness relies on the novelty and inventive step relative to existing prior art. Secondary patents or similar filings may exist, but MX347290’s strength depends on how its claims differ from or improve upon prior disclosures.

3. Can generic manufacturers legally produce drugs similar to those covered by MX347290?
Only after patent expiry or if the patent is invalidated are generics permitted. Until then, infringement risks are significant, requiring careful legal analysis before market entry.

4. What are the main vulnerabilities of MX347290 in its patent protection?
Potential vulnerabilities include overly broad claims susceptible to invalidation, prior art disclosures not considered during filing, or patent term lapses due to non-payment of maintenance fees.

5. How does the patent landscape in Mexico influence future pharmaceutical innovations?
A robust yet scrutinized patent system encourages genuine innovation while discouraging overly broad or obvious patents, promoting a healthy environment for pharmaceutical R&D and market competition.


References

[1] Mexican Institute of Industrial Property (IMPI). Official Patent Database.
[2] Mexican Industrial Property Law (LPI).
[3] WIPO PATENTSCOPE Database.
[4] Mexican pharmaceutical patent case studies and legal analyses.
[5] Reports on patent litigation trends in Mexico’s pharmaceutical sector.

Note: Specific filing and grant dates, along with detailed claim language for MX347290, should be retrieved directly from IMPI’s official records for precise legal analysis.

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