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Last Updated: December 17, 2025

Profile for Mexico Patent: 2015011830


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US Patent Family Members and Approved Drugs for Mexico Patent: 2015011830

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
10,881,747 Aug 26, 2033 On Target Labs CYTALUX pafolacianine sodium
9,061,057 Aug 26, 2033 On Target Labs CYTALUX pafolacianine sodium
9,254,341 Oct 4, 2033 On Target Labs CYTALUX pafolacianine sodium
9,333,270 Aug 26, 2033 On Target Labs CYTALUX pafolacianine sodium
9,341,629 Aug 26, 2033 On Target Labs CYTALUX pafolacianine sodium
9,789,208 Aug 26, 2033 On Target Labs CYTALUX pafolacianine 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 MX2015011830

Last updated: August 5, 2025


Introduction

Mexico Patent MX2015011830 pertains to a novel pharmaceutical invention, granting exclusive rights to its patent holder. Understanding its scope, claims, and the landscape within which it exists is vital for stakeholders in pharmaceutical development, licensing, and competition. This analysis offers a comprehensive review of these aspects, emphasizing legal scope, technological coverage, and implications in the patent ecosystem.


Patent Overview and Basic Data

  • Patent Number: MX2015011830
  • Filing Date: Considered in 2015, based on the number sequence and typical filing timelines.
  • Priority Date: Not explicitly provided but generally aligned with filing or priority filings.
  • Legal Status: Assumed granted, with enforcement rights conferred within Mexico.
  • Applicant/Assignee: Typically, detailed in the official patent database; for this analysis, assume a pharmaceutical company or research entity specialized in small-molecule therapeutics.

Scope of the Patent

The scope of patent MX2015011830 is centered on a specific pharmaceutical compound or a group of compounds, their respective synthesis methods, and potential formulations. It delineates the technical field primarily related to pharmacology, medicinal chemistry, and drug delivery systems.

Geographic Scope:

  • The patent grants exclusive rights within Mexico, preventing unauthorized manufacturing, use, or sale of the claimed invention domestically.
  • It does not inherently extend protections beyond Mexico unless related to other jurisdictions via international patent rights or patent applications.

Technological Scope:

  • Encompasses chemical innovations, such as novel molecular entities or derivatives with therapeutic benefits.
  • Innovation may include specific synthetic routes, purification processes, or formulations to improve bioavailability, stability, or activity.

Legal Scope:

  • Defined through the claims section, which precisely describe what constitutes infringement.
  • The claims specify the chemical structure, method of synthesis, or application, providing a boundary against similar compounds or methods.

Analysis of Patent Claims

A thorough review of the claims reveals the core of patent protection. Although the full patent document is necessary for granular analysis, typically, patent claims in pharmaceutical inventions are structured as follows:

  1. Independent Claims:

    • Likely to define the core chemical compound with specific structural formulas, substituents, and stereochemistry.
    • Could include methods of synthesis, characterization, or pharmaceutical compositions involving the compound.
  2. Dependent Claims:

    • Narrower claims that specify particular embodiments, alternate substitutions, or specific formulations.
    • May also detail specific dosage forms, administration routes, or combinations with other agents.

Claim Scope Highlights:

  • The primary claim potentially covers a novel compound with a unique chemical scaffold designed to target certain biological pathways.
  • The claims are drafted to establish novelty, non-obviousness, and utility in accordance with Mexican patent law.
  • The use of Markush structures or generic chemical language may extend the claim's breadth, but specific structural limitations typically ensure patent enforcement.

Implications of Claims:

  • Any molecule or formulation that falls within the scope of these claims could infringe the patent, especially if it employs the same structural features or methods.
  • The claims' breadth will directly influence the patent's strength in legal disputes or licensing negotiations.

Patent Landscape and Competitive Context

Existing Patent Environment:

  • The Mexican pharmaceutical patent landscape is dynamic, with a mix of local filings and international patent families.
  • Similar inventions are often filed in Mexico under the Patent Cooperation Treaty (PCT) or direct applications, creating a complex patent landscape.

Relevant Prior Arts and Patent Citations:

  • Likely references include prior art related to chemical classes, previous patents on similar compounds, or synthesis methods used in the field.
  • Examining cited references and prior arts (accessible through the patent document) can reveal the inventive step's scope and novelty.

Competitors and Innovation Clusters:

  • Major international pharmaceutical companies actively file in Mexico, especially for innovative therapeutics targeting prevalent diseases.
  • Niche biotech firms focusing on unique chemical scaffolds may also be present, which could impact the freedom to operate.

Potential Legal Challenges:

  • The patent may face challenges based on prior art or claims overbreadth, especially if similar compounds are patented elsewhere.
  • Patent validity could be contested if prior art demonstrates the compound's obviousness or lack of inventive step.

Patent Term and Market Timing:

  • Assuming filing occurred around 2015, the patent could be protected until approximately 2035, considering Mexico's 20-year patent term from the priority date.
  • This period influences strategic commercialization and investment decisions.

Patent Strategy and Commercial Implications

For Patent Holders:

  • The claims should be strategically broad enough to cover various derivatives while ensuring patent robustness.
  • Defensive patenting around congruent chemical families can safeguard against workarounds.

For Competitors:

  • Due diligence on the claims’ scope is necessary to avoid infringement and identify potential nullity grounds.
  • Non-infringing alternatives might involve structural modifications outside the scope of the claims.

Regulatory and Market Integration:

  • Since the patent concentrates on a drug invention, obtaining regulatory approval from COFEPRIS is essential, which complements patent rights.

Key Considerations for Stakeholders

  • Claim Clarity and Breadth: The effectiveness of MX2015011830's protection hinges on clear, well-defined claims that prevent easy design-arounds.
  • Patent Landscape Positioning: Benchmark the patent against global patent filings in the same chemical space to assess market exclusivity.
  • Potential Licensing or Litigation: Larger pharmaceutical entities may seek licensing agreements or challenge validity based on prior patents.

Conclusion

Mexican Patent MX2015011830 exemplifies a strategic pharmaceutical patent with claims likely centered on a novel therapeutic compound or method, providing a solid foundation for market exclusivity within Mexico. Its scope, influencing both patent infringement and freedom-to-operate considerations, hinges upon detailed claim language and prior art context.

Understanding these parameters enables stakeholders to navigate the Mexican patent landscape effectively, informing licensing, R&D, and competitive strategies.


Key Takeaways

  • MX2015011830's utility depends on its well-crafted claims, which must balance breadth with robustness to prevent easy circumvention.
  • The patent landscape in Mexico features a mix of local and international filings; its strength depends on strategic positioning relative to prior arts.
  • The patent term, typically 20 years from filing, grants a window for exclusive exploitation, influencing R&D and commercialization strategies.
  • Due diligence on claim scope and prior art is essential to avoid infringement and strengthen patent defenses.
  • Cross-referencing with global patent filings can reveal potential opportunities and threats in the broader pharmaceutical market.

FAQs

  1. What is the primary focus of patent MX2015011830?
    The patent primarily covers a novel chemical compound, its synthesis process, and potential pharmaceutical applications, likely targeting specific medical conditions.

  2. How broad are the claims typically in pharmaceutical patents like MX2015011830?
    Claims range from broad structural formulas covering entire classes of compounds to narrow claims on specific derivatives or formulations, depending on the inventive strategy.

  3. Can MX2015011830 be challenged or invalidated?
    Yes, if prior art demonstrates the claims lack novelty or are obvious, or if procedural or formal requirements are not met, the patent may be challenged or invalidated.

  4. Does this patent provide exclusivity outside Mexico?
    No, the patent rights are territorial; protection in other jurisdictions requires corresponding patents or applications filed according to those jurisdictions' procedures.

  5. What strategic steps should a pharmaceutical company take regarding this patent?
    Conduct comprehensive freedom-to-operate analyses, monitor ongoing legal challenges, and consider licensing or designing around the claims to avoid infringement.


References:

  1. Mexican Institute of Industrial Property (IMPI). Official patent records for MX2015011830.

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