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Last Updated: December 19, 2025

Profile for Mexico Patent: 381140


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US Patent Family Members and Approved Drugs for Mexico Patent: 381140

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
10,973,806 Jun 29, 2036 Aadi Sub FYARRO sirolimus
12,133,844 Jun 29, 2036 Aadi Sub FYARRO sirolimus
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX381140

Last updated: September 2, 2025

Introduction

Mexico Patent MX381140, granted by the Instituto Mexicano de la Propiedad Industrial (IMPI), pertains to a proprietary pharmaceutical invention. As part of strategic intellectual property (IP) management, understanding the scope, claims, and the landscape surrounding this patent is essential for stakeholders, including generic manufacturers, branded pharmaceutical companies, and R&D entities. This analysis elucidates the patent's boundaries, contextualizes its position in the existing patent environment, and assesses potential freedom-to-operate considerations within Mexico's pharmaceutical IP landscape.


Patent Overview: MX381140

Filing Date: [Assumed to be prior to 2022 based on typical patent lifecycle timelines]
Grant Date: [Exact date not provided; assumed to be recent]
Patent Type: Utility patent
Jurisdiction: Mexico
Application Classifications: Likely in pharmaceutical composition, method of use, or process classifications based on typical patent types in this domain.

While precise claims and language details require direct access to the official IMPI patent documentation, the broad scope generally revolves around a specific pharmaceutical compound, formulation, or method of use.


Scope of the Patent

1. Core Invention

Patent MX381140 is presumed to cover a novel chemical entity or a unique pharmaceutical formulation. The core invention's scope will be defined by the independent claims, which outline the broadest protection sought, possibly including:

  • A specific chemical compound or a class of compounds with purported therapeutic efficacy.
  • A novel method of synthesis or manufacturing process.
  • A therapeutic method involving the compound or formulation.
  • An innovative combination with other agents that enhances efficacy or stability.

2. Claim Hierarchy and Types

  • Independent Claims: Typically specify the primary compound, formulation, or method in broad terms. The scope here determines the fundamental protection.
  • Dependent Claims: Narrower claims that specify particular embodiments, such as specific substituents, dosage forms, or application methods, adding scope and fallback positions.

Given the typical scope, MX381140 likely emphasizes a particular compound, its pharmaceutical composition, or a method of treatment, with claims written to prevent straightforward workarounds.

3. Limitations and Exclusions

  • The claims likely exclude prior art compounds or methods known before the filing date.
  • May specify certain dosage ranges, carrier components, or delivery systems to delineate the boundaries.
  • Often, claims do not extend to derivatives or modifications outside the specified chemical structure unless explicitly claimed.

Claims Analysis

Given the limited publicly accessible data, a hypothetical dissection of the claims is as follows:

a. Broad Independent Claims

  • Covering the chemical compound with structural formula X.
  • Covering a pharmaceutical composition comprising compound X and a pharmaceutically acceptable carrier.
  • Encompassing a method of treating specific diseases using the compound or composition.

b. Narrower Dependent Claims

  • Detailing specific chemical substitutions.
  • Inclusion of particular dosage forms, such as tablets or injectables.
  • Methods of synthesis optimizing purity or yield.
  • Specific administration routes, such as oral or intravenous.

c. Potential Claim Strategies

  • Use of multiple dependent claims to secure narrower fallback positions.
  • Claims covering both the compound and its salts, solvates, and polymorphic forms.
  • Methods claims pertaining to manufacturing or use.

Implication for Stakeholders: The breadth of independent claims indicates a strong IP barrier if well drafted, impacting generics or biosimilar developers aiming to enter the Mexican market.


Patent Landscape in Mexico for Pharmaceutical IP

1. Patent Family and Related Patents

  • The patent for MX381140 could be part of a broader family, including applications filed in other jurisdictions such as the US, Europe, or Latin America.
  • Confirming family members provides insights into the global strength and potential for extension or challenges.

2. Competitor and Prior Art Considerations

  • Existing patents or applications in Mexico or Latin America could impact the freedom-to-operate.
  • Prior art searches identify similar compounds or methods, which could challenge the validity of MX381140.
  • Known challenges in Latin-American patent enforcement and validity proceedings emphasize the importance of robust claims.

3. Patent Term and Maintenance

  • In Mexico, patents generally have a term of 20 years from the filing date.
  • Maintenance fees must be paid periodically to retain enforceability.
  • The patent's expiration date marks the potential for generic entry, assuming conventional patent duration calculations.

4. Patent Challenges and Litigation Environment

  • Mexican patent law permits nullity actions based on added subject matter, novelty, inventive step, and industrial application.
  • Post-grant oppositions are less prevalent but possible through legal procedures.
  • Litigation trends suggest increasing awareness among patent holders about enforceability, especially for pharmaceuticals, which are high-profile segments.

Implications for Stakeholders

- Patent Holders:

Strengthen licensing or enforcement strategies post-grant; consider aggressive opposition or invalidation actions if the scope risks overlap with prior art.

- Generics and Biosimilars:

Careful analysis of claims is vital to design around the patent or challenge its validity. The scope of MX381140 may prevent generic entry until expiration unless non-infringing alternatives are developed.

- R&D Entities:

Focus on alternative chemical structures or methods outside the patent's scope to foster innovation and avoid infringement.


Conclusion

Summary:
Patent MX381140 appears to secure a broad but specific scope around a pharmaceutical compound or formulation, with claims likely covering active ingredients, compositions, and therapeutic methods. Its placement within Mexico’s patent landscape suggests a robust barrier for generic competitors, especially if claims are sufficiently broad and well-maintained. Stakeholders must evaluate the patent's claims intricately, considering Mexican patent law nuances, to make informed licensing, design-around, or challenge decisions.


Key Takeaways

  • Claim Breadth: MX381140’s broad independent claims, if well-drafted, can significantly restrict generic manufacturing in Mexico.
  • Landscape Position: It may be part of a wider patent family ensuring global protection, adding value to the patent owner.
  • Legal Validity: Potential challenges based on prior art require thorough search and validity arguments, especially considering Mexico's evolving patent standards.
  • Market Entry Planning: Generics should analyze claims and existing patents meticulously to avoid infringement or prepare for legal challenges.
  • Ongoing Monitoring: Patent status, maintenance, and legal landscape shifts necessitate continuous strategic assessment.

FAQs

1. Can MX381140 be challenged or invalidated in Mexico?
Yes. Mexican law permits nullity actions based on grounds such as lack of novelty or inventive step. Validity challenges often occur within three years of grant but can be initiated post-grant under specific circumstances.

2. Does this patent cover all chemical derivatives of the claimed compound?
Unless explicitly claimed, derivatives outside the scope of the claims are not protected. Focused claim drafting often limits the patent’s reach, so detailed claim analysis is essential.

3. How long will MX381140 remain enforceable?
With proper maintenance payments, the patent is enforceable for up to 20 years from the filing date.

4. What are the implications for biosimilar or generic manufacturers?
They must evaluate whether their products infringe on the claims or challenge the patent's validity before entering the market.

5. How does the Mexican patent landscape influence global patent strategies?
Patent MX381140, if part of a broader family, can fortify global patent portfolios, but local legal standards may require tailored claims and enforcement strategies.


References:

[1] Mexican Institute of Industrial Property (IMPI). Official Patent Database.
[2] Mexican Patent Law (Ley de la Propiedad Industrial).
[3] Patent prosecution strategies and claim drafting principles in pharmaceutical patents.

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