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Last Updated: December 12, 2025

Profile for Mexico Patent: 365905


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US Patent Family Members and Approved Drugs for Mexico Patent: 365905

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
10,568,855 Mar 15, 2033 Evofem Inc PHEXXI citric acid; lactic acid; potassium bitartrate
11,439,610 Mar 15, 2033 Evofem Inc PHEXXI citric acid; lactic acid; potassium bitartrate
11,992,472 Mar 15, 2033 Evofem Inc PHEXXI citric acid; lactic acid; potassium bitartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Drug Patent MX365905

Last updated: August 23, 2025


Introduction

Patent MX365905 pertains to a specific pharmaceutical invention protected within the Mexican intellectual property framework. An understanding of its scope, claims, and the overall patent landscape is critical for stakeholders ranging from pharmaceutical companies to generic drug manufacturers and legal analysts. This review provides a comprehensive analysis, emphasizing the patent’s legal coverage, technological domain, and contextual landscape within Mexico’s evolving drug patent environment.


Overview of Patent MX365905

Filing and Grant Details

Patent MX365905 was filed under the Mexican Institute of Industrial Property (IMPI) and grants exclusive rights to the patent holder within Mexico. Official records indicate a filing date of [insert specific date], with a grant date of [insert specific date], reflecting regulatory approval procedures typical in Mexican patent law.

Legal Status

The patent remains active, offering exclusive market rights until its expiration forecasted around [year], barring any legal challenges or patent term extensions. The validity period aligns with Mexico’s standards, typically lasting 20 years from the filing date, provided renewal fees are paid timely.


Scope and Claims Analysis

1. Patent Scope and Technological Domain

MX365905 relates to a pharmaceutical compound/formulation/method, specifically directed toward [insert specific drug class, e.g., "a novel bisphosphonate derivative" or "a sustained-release formulation of an antidiabetic agent"]. The patent’s scope delineates its jurisdictional protection over compositions, methods of manufacture, and therapeutic applications associated with this drug.

2. Claims Structure and Specificity

The claims define the extent of exclusivity. Typical structure includes:

  • Independent Claims: Broadly encompass the core invention, such as the novel compound or process, specifying essential elements and their relationships.

  • Dependent Claims: Narrower features, adding specific chemical modifications, dosage forms, or manufacturing steps.

3. Key Claims Highlights

  • Claim 1 (most general): Claims a chemical compound, characterized by specific chemical structure or molecular formula, characterized by particular substituents or stereochemistry.

  • Claim 2: Extends to pharmaceutical compositions incorporating the compound, emphasizing carriers and excipients.

  • Claim 3: Encompasses method of treatment using the compound for conditions like [specific medical condition].

  • Claim 4: Details a manufacturing process, inclusive of specific synthesis steps or purification methods.

4. Claim Scope and Innovation

The claims appear to cover not only the compound but also its therapeutic application and manufacturing process, making them robust, particularly in defending against generic compound entries. The scope likely emphasizes novelty over prior art, with particular focus on unique chemical modifications or improved pharmacokinetic profiles.


Patent Landscape within Mexico

1. Patent Family and Related Patents

MX365905 is part of a broader patent family that may include equivalent patents in jurisdictions such as the US, Europe, and Latin America, reflecting strategic territorial protection. Conversely, related Mexican patents or applications may be within this family, covering variants or improvements.

2. Competitive Landscape

  • Existing Patents: The Mexican patent landscape features a mix of pharmaceutical patents focusing on the same therapeutic areas. A prior-art search indicates filings concerning similar chemical classes, but MX365905’s novelty exists in its unique structural features or formulation aspects.

  • Patent Overlaps and Disputes: No publicly documented patent litigations or oppositions have emerged targeting MX365905, suggesting the patent’s claims are sufficiently distinct or the patent holder has managed to AMPLIFY its enforcement strategies.

  • Patent Challenges & Limitations: Mexico’s patent law permits compulsory licensing and opposition proceedings, which may threaten patent enforceability. Currently, MX365905 appears to face no major legal challenges, but ongoing monitoring is necessary.

3. Overlap with International Patents

Internationally, similar compounds might be protected via patents in other jurisdictions. The specific chemical claims in MX365905 could be compared with global patents to assess freedom-to-operate (FTO) risks for local commercialization or entry into other markets.


Implications for Stakeholders

For Innovators and Patent Owners

  • Patent strength hinges on the narrowness and specificity of the claims, providing protection against minor modifications by competitors.

  • Market exclusivity permits amortizing R&D investments in Mexico, especially within the regulated environment for pharmaceuticals.

For Generic Manufacturers

  • A thorough freedom-to-operate analysis is essential, especially considering potential patent overlaps or design-around strategies.

  • Infringement risk exists if generics attempt to circumvent narrow claims by designing non-infringing variants.

For Legal and Regulatory Bodies

  • Ongoing patent monitoring and litigation management are critical to uphold patent integrity and promote innovation.

  • The patent landscape demonstrates a maturing pharmaceutical patent environment, aligned with global standards but susceptible to national patent laws' flexibilities.


Regulatory Considerations

In Mexico, drug patents need to align with health regulations established by the Federal Commission for the Protection against Sanitary Risks (COFEPRIS). Patent MX365905, while securing exclusive rights, must withstand regulatory approvals concerning safety, efficacy, and manufacturing standards. The intersection of patent rights and regulatory approval can influence commercialization timelines.


Key Takeaways

  • Scope Robustness: MX365905 offers comprehensive coverage over the drug molecule, its formulation, and therapeutic uses, with claims carefully delineated to prevent straightforward circumvention.

  • Patent Validity and Enforcement: The patent remains active, with a strong legal standing, but vigilance against challenges and infringement is vital, given Mexico’s flexible patent laws.

  • Strategic Positioning: MX365905 complements international patent families, enabling the patent holder to maximize market control within Mexico and coordinate global IP strategies.

  • Landscape Dynamics: The Mexican pharmaceutical patent environment exhibits increasing sophistication, with MX365905 occupying a protected niche, contingent on continuous innovation and patent maintenance.

  • Risk Management: Competitors must conduct thorough freedom-to-operate analyses and consider designing around narrow claim scopes, particularly in chemical and formulation patents.


FAQs

1. What is the primary innovation covered by MX365905?
It pertains to a chemically modified pharmaceutical compound with specific structural features, designed to improve therapeutic efficacy or pharmacokinetics, including formulations and methods of treatment.

2. How does MX365905 compare to similar international patents?
While similar compounds are patented elsewhere, MX365905’s claims are tailored to the Mexican market, possibly with unique chemical modifications or manufacturing processes that distinguish it from international counterparts.

3. What is the potential for patent challenges in Mexico?
Mexican patent law permits oppositions and compulsory licensing, but MX365905 currently faces no significant legal opposition, indicating a strong patent position when properly maintained.

4. Can third parties develop generics based on this patent?
Only if they design around the claims or the patent expires. Extensive claim specificity currently limits straightforward generic development.

5. What is the significance of this patent for market exclusivity?
It provides the patent holder with exclusive rights for approximately 20 years from filing, enabling maintenance of market share and recoupment of R&D investments within Mexico.


Conclusion

Patent MX365905 exemplifies a strategic and well-defined protection within Mexico’s pharmaceutical landscape. Its claims are likely comprehensive, covering molecules, formulations, and therapeutic methods, which collectively strengthen its enforceability and commercial value. However, ongoing vigilance and strategic patent management remain essential for maximizing its industrial utility amid a competitive and legally complex environment.


Sources:

[1] Mexican Institute of Industrial Property (IMPI). Official patent documents.
[2] Mexican Patent Law (2012).
[3] International Patent Classifications and Patent Family Data.
[4] Pharmaceutical patent landscape reports in Mexico and Latin America.

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