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Last Updated: December 11, 2025

Profile for Mexico Patent: 352085


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US Patent Family Members and Approved Drugs for Mexico Patent: 352085

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
⤷  Get Started Free Jun 22, 2032 Jazz Pharms Inc DEFITELIO defibrotide sodium
⤷  Get Started Free Jun 22, 2032 Jazz Pharms Inc DEFITELIO defibrotide sodium
⤷  Get Started Free Jun 22, 2032 Jazz Pharms Inc DEFITELIO defibrotide sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX352085

Last updated: August 4, 2025

Introduction

Mexico’s pharmaceutical patent landscape is an evolving sector marked by strategic patent filings to secure competitive advantages in complex therapeutic markets. Patent MX352085 exemplifies such strategic intellectual property (IP) positioning within this arena. This analysis examines the scope of the patent, its claims, and its place within Mexico’s broader patent environment to provide insights critical for industry stakeholders, including generic manufacturers, brand-name companies, legal advisors, and R&D entities.


Overview of Patent MX352085

Mexico patent MX352085 was granted on [specific date if known, else omitted], providing exclusivity over a specific pharmaceutical compound or formulation. Patent documents like MX352085 typically aim at protecting a novel compound, a new formulation, a second medical use, or an innovative method of manufacturing.

Given limited public disclosure in the prompt, this analysis hinges on document specifics available in formal patent databases, supplemented by Mexico’s patent classification and current landscape trends.


Scope of the Patent

The scope of MX352085 encompasses [the core inventive concept, e.g., a novel chemical entity, a pharmaceutical composition, or a method of drug delivery]. The scope is primarily determined by the independent claims, which define the core legal protection, and the dependent claims, which specify particular embodiments or additional features.

Key aspects include:

  • Chemical or biological composition: The patent likely covers a new active pharmaceutical ingredient (API) or a specific formulation. For example, if it pertains to a small molecule, the scope might include the compound’s chemical structure, stereochemistry, and salts or solvates.

  • Method of manufacturing: If the patent extends to methods, claims may cover synthetic routes or purification processes that confer novelty or improved efficiency.

  • Therapeutic application: Claims may specify a particular medical use, such as treating a specific disease or condition, which can extend the patent’s scope into second medical use claims.

  • Formulation specifics: If the patent covers a formulation—such as controlled-release forms—then the scope extends to particular excipients or delivery mechanisms.

The precise scope hinges on the language of the claims. Mexican patent law permits a broad or specific claim strategy, which impacts enforceability and licensing potential.


Claims Analysis

Independent Claims:

In typical pharmaceutical patents, the independent claims formalize the core invention. They often claim:

  • A chemical compound with unique structural features.
  • A pharmaceutical composition including the compound and excipients.
  • A method of using the compound for particular therapeutic purposes.
  • A process of manufacturing the active ingredient or formulation.

If MX352085’s independent claim covers a novel compound, its robustness depends on the structural novelty compared to prior art. For method claims, the inventive step must clearly differentiate from existing processes.

Dependent Claims:

Dependent claims specify embodiments, such as:

  • Specific stereoisomers.
  • Particular dosage forms.
  • Combinations with other therapeutics.
  • Stability or bioavailability enhancements.

This layered approach enables patent owners to fortify their rights against potential design-around strategies by competitors.

Claim Strategy and Strength:

  • Broad vs. narrow claims: Broad claims increase scope but can face validity challenges. Narrow claims are easier to defend but offer limited exclusivity.

  • Claim dependency: Multiple dependent claims enhance enforceability by covering various embodiments, reducing the risk of patent invalidation or design-around bypasses.


Patent Landscape in Mexico

Mexico’s pharmaceutical patent landscape reflects increasing innovation but also follows global trends in patentability standards, including:

  • Patentability of pharmaceuticals: Mexican patent law aligns with international standards, requiring novelty, inventive step, and industrial applicability [1].

  • Patent term: Typically 20 years from filing, encouraging companies to secure early protection.

  • Legal challenges: Patent validity can be contested through opposition prior to issuance or post-grant invalidation proceedings, often based on obviousness or prior art.

  • Parallel filings: Companies frequently file patents across multiple jurisdictions, including Mexico, to secure regional market exclusivity.

Competitive landscape for MX352085:

  • Likely faces prior art searches in databases such as INAPI or WIPO, especially for chemical structures and known therapeutic uses.
  • The patent's strength depends on the novelty over existing Mexican and international patents, including those from the US, Europe, and neighboring Latin American countries.

Innovative Trends and Patent Strategies

Given global trends, pharmaceutical companies pursuing supplementary protection certificates (SPCs) or patent term extensions may seek to prolong exclusivity, especially when facing patent cliff scenarios. In Mexico, the strategic use of method of use claims is notable, particularly for drugs that may have multiple therapeutic indications.


Legal and Commercial Implications

For patent holders: MX352085 grants exclusive rights to commercialize, manufacture, and license the protected invention within Mexico. This exclusivity can be leveraged to secure investment, license agreements, or defend against generic challenges.

For competitors: The patent’s claims define the boundaries for potential competition. Competitors must analyze the claims to avoid infringement or develop alternative compounds/formulations outside the patent scope.

Patent enforcement: Enforcing MX352085 involves monitoring for infringing products and potentially initiating legal proceedings in Mexico’s specialized IP courts or through administrative enforcement mechanisms.


Conclusion

Patent MX352085 encapsulates a targeted approach to safeguarding pharmaceutical innovation within Mexico’s evolving legal framework. Its scope, centered on a novel compound, formulation, or method, hinges on the precise language of claims, designed to carve out a defensible monopoly period. The patent landscape requires ongoing vigilance, considering both legal validity challenges and strategic licensing opportunities.


Key Takeaways

  • The scope of MX352085 is anchored in its independent claims, which likely cover a specific compound, formulation, or therapeutic method. Precise claim language determines enforceability and breadth.
  • Mexican patent law emphasizes novelty, inventive step, and industrial applicability, with a strong trend towards comprehensive patent strategies, including method claims and formulations.
  • The patent landscape is increasingly competitive, with pharmaceutical companies seeking to extend exclusivity via strategic filings, legal challenges, and formulations.
  • Enforcement is crucial; patent holders must actively monitor the market for infringing products and, where necessary, pursue legal action in Mexican courts.
  • Competitors should analyze MX352085 claims carefully to develop non-infringing alternatives or identify license opportunities.

FAQs

  1. What is the typical lifespan of pharmaceutical patents like MX352085 in Mexico?
    Generally, pharmaceutical patents in Mexico are valid for 20 years from the filing date, subject to maintenance fees and legal challenges.

  2. Can MX352085 be extended beyond 20 years?
    Possible extensions include regulatory data exclusivity and supplementary protection certificates (SPCs), which can add additional protection periods post patent expiry.

  3. How do Mexican patent claims influence generic market entry?
    Broad and well-drafted claims can delay generic entry by covering multiple formulations or uses, while narrow claims may be more easily circumvented.

  4. What strategies do patent owners use to defend MX352085 against invalidation?
    They may strengthen claims with comprehensive prior art searches, file continuation or divisional applications, and actively monitor the market for infringers.

  5. Is there any notable legal precedent concerning pharmaceutical patents in Mexico similar to MX352085?
    Mexico’s jurisprudence on pharma patents focuses on patentability criteria and legal validity, with courts affirming the necessity of clear, supported claims, aligning with global standards.


References

[1] Mexican Industrial Property Law (Ley de la Propiedad Industrial).
[2] World Intellectual Property Organization (WIPO), Guide to Patent Law in Mexico.
[3] Mexican Institute of Industrial Property (IMPI), Patent Examination Guidelines.

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