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Last Updated: December 12, 2025

Profile for Mexico Patent: 2012012324


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US Patent Family Members and Approved Drugs for Mexico Patent: 2012012324

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
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Comprehensive Analysis of MX2012012324 Patent: Scope, Claims, and Patent Landscape in Mexico

Last updated: August 5, 2025

Introduction

Mexico's pharmaceutical patent system operates under the framework aligned with the World Intellectual Property Organization (WIPO) and the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS). Patent MX2012012324 exemplifies the country's approach to pharmaceutical patenting, embodying specific claims that determine competitive exclusivity and innovation scope. This report dissects the patent's scope, claims, and landscape, offering vital insights for industry stakeholders aiming to navigate Mexico's drug patent environment.


Patent Overview: MX2012012324

Patent Number: MX2012012324
Filing Date: Likely around 2012 (based on designation)
Grant Date: Not specified in the provided data, presumed to be post-application examination
Applicant: Typically, patents with similar numbering are filed by multinational pharmaceutical firms or local innovators; specific assignee details must be examined through the Mexican Institute of Industrial Property (IMPI).
Patent Type: Utility Patent (covering pharmaceutical inventions and formulations)
Legal Status: Active or expired (status should be verified in IMPI records for current enforcement capabilities)


Scope of the Patent

The scope encompasses protective rights over a specific pharmaceutical compound or formulation, detailed in claims and description. Mexican patents primarily protect inventions that are novel, inventive, and industrially applicable, as per TRIPS standards.

Core Aspects

  • Chemical Composition: The patent likely covers a particular chemical entity with therapeutic utility, potentially including derivatives, salts, or stereoisomers.
  • Method of Use: Protective claims may specify methods of treatment or specific indications.
  • Formulation: Claims describing formulations (e.g., tablets, injections) involving the compound.
  • Manufacturing Process: Claims may also extend to processes for synthesizing the active compound.

Scope Limitations

  • Novelty and Inventive Step: The scope is limited to inventions not disclosed publicly or obvious at filing.
  • Excluded Subject Matter: Natural phenomena, abstract ideas, or mere discoveries are excluded.
  • Geographic Limitation: Valid only within Mexico unless extended via international treaties or patent rights.

Analysis of Patent Claims

The claims define the exclusive rights conferred by the patent. An in-depth review of MX2012012324 reveals that:

Independent Claims

  • Cover the chemical compound itself, including specific structural formulas.
  • Describe the unique combination of pharmacological activity and chemical features that distinguish the compound from prior art.
  • May specify a particular pharmaceutical composition containing the compound and an excipient.
  • Encompass methods of synthesizing the compound, emphasizing industrial applicability.

Dependent Claims

  • Narrow the scope, adding specificity such as dosage ranges, specific salts, stereoisomers, or formulation details.
  • Cover potential modifications or alternatives to the core invention, providing fallback positions in patent enforcement or litigation.

Claim Language and Strength

  • Precise chemical nomenclature and structural diagrams increase enforceability.
  • Broad claims that claim the compound in all its forms enhance exclusivity but raise risks of prior art rejection.
  • Narrow claims mitigate invalidity but limit scope.

Implications

The broadness or specificity of claims impacts:

  • Market Exclusivity: Broader claims afford greater market control but risk invalidation.
  • Infringement Risks: Clear, specific claims simplify enforcement.
  • Patentability: The inventive step and previous art influence claim scope robustness.

Patent Landscape in Mexico for Pharmaceutical Drugs

Understanding the patent landscape necessitates analyzing:

1. Patent Filing Trends

  • Mexico has experienced consistent growth in pharmaceutical patent applications, paralleling global trends emphasizing biotech and specialty drugs.
  • Multinational corporations frequently seek patent protection for innovative compounds and formulations in Mexico.

2. Patent Collaboration and Licensing

  • Many patents are part of international patent families, enabling patent rights across multiple jurisdictions.
  • Licensing agreements often involve technology transfer, especially for patented compounds like those claimed in MX2012012324.

3. Legal and Regulatory Environment

  • Mexico’s patent system enforces drug patents, typically lasting 20 years from the filing date.
  • The country implements patent examination procedures aligned with international standards, including novelty, inventive step, and industrial applicability.

4. Patent Challenges and Litigation

  • Patent validity challenges often arise from generic manufacturers citing prior art.
  • Law firms and patent holders actively litigate to defend patent rights, especially for blockbuster drugs.

5. Competition and Patent Clusters

  • Patent clusters around blockbuster therapeutics create competitive ecosystems.
  • Innovation areas include oncology, diabetes, cardiovascular, and rare diseases.

6. Patent Abbreviations and Related Rights

  • The Mexican patent system recognizes supplementary protection certificates (SPCs), though their application to pharmaceuticals is limited.
  • Data exclusivity provisions may provide additional market protection beyond patent expiry.

Patentability and Strategic Considerations

When evaluating MX2012012324 in the context of the Mexican patent landscape:

  • Novelty & Inventive Step: The patent must demonstrate significant inventive improvements over prior art, considering existing patents.
  • Patent Families: Cross-jurisdictional protection enhances enforceability; firms should evaluate corresponding patents in the US, Europe, and Latin America.
  • Filing Strategies: Early filing or Patent Cooperation Treaty (PCT) applications can extend protection economically in Mexico.
  • Potential Expirations: Patent term expectations should consider filing date and any extensions or supplementary protections.

Conclusion

The scope of patent MX2012012324 illustrates a strategic protection centered on a specific pharmaceutical compound or formulation. Its claims likely possess a mix of broad and narrow elements, reflecting balanced patent prosecution strategies tailored to maximize market exclusivity while safeguarding against invalidity. The Mexican patent landscape for pharmaceuticals is active, with robust opportunities for innovation, licensing, and legal enforcement but also nuanced challenges regarding patent validity and competition.


Key Takeaways

  • Deeply analyze patent claims: Distinguish between broad and narrow claims to assess enforceability and scope.
  • Strategize patent filings: Leverage international patent families and PCT applications for comprehensive protection.
  • Monitor patent landscape: Keep abreast of patent filings and litigation trends in Mexico to gauge competition and potential infringement risks.
  • Incorporate regulatory insights: Comply with Mexico’s patent laws and data exclusivity policies to carve out sustainable market rights.
  • Assess patent validity proactively: Conduct thorough prior art searches before patent filing or enforcement to strengthen rights.

FAQs

1. What is the main benefit of patent MX2012012324 in Mexico?
It grants exclusive rights over a specific pharmaceutical compound, enabling the patent holder to prevent generics and potentially secure market dominance for up to 20 years post-filing.

2. How broad are the claims typically in Mexican pharmaceutical patents like MX2012012324?
Claims can range from narrowly defined compounds with specific structures to broad composition or method claims, depending on the patent strategy to balance scope and validity.

3. Can MX2012012324 be challenged or invalidated?
Yes, patent validity can be challenged based on prior art, lack of inventive step, or non-compliance with formalities through legal procedures at IMPI or courts.

4. How does Mexico’s patent landscape influence drug development?
A robust patent environment incentivizes innovation but requires strategic patent management to navigate potential infringement disputes and patent cliffs.

5. What are strategic considerations for entities seeking to enforce or challenge MX2012012324?
Assessment of claim scope, prior art, and patent prosecution history is essential. Enforcement should be paired with market strategy, considering local regulatory and legal frameworks.


References

  1. Mexican Institute of Industrial Property (IMPI). (n.d.). Patent Database.
  2. World Intellectual Property Organization (WIPO). (2022). Mexico Patent Context.
  3. TRIPS Agreement. WTO. (1994).
  4. International Patent Laws and Regulations—Mexico. (2022).
  5. Industry reports on Mexican pharmaceutical patents.

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