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Last Updated: December 18, 2025

Profile for Mexico Patent: 2024003960


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US Patent Family Members and Approved Drugs for Mexico Patent: 2024003960

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 Aug 5, 2041 Pfizer PAXLOVID (COPACKAGED) nirmatrelvir; ritonavir
⤷  Get Started Free Oct 31, 2041 Pfizer PAXLOVID (COPACKAGED) nirmatrelvir; ritonavir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2024003960

Last updated: July 30, 2025


Introduction

Understanding the scope and claims of patent MX2024003960, granted in Mexico, provides critical insights for stakeholders involved in pharmaceutical innovation, licensing, and competitive intelligence. This patent’s strategic positioning within Mexico’s intellectual property landscape influences market entry, R&D investment, and litigation risks. This analysis delivers a comprehensive review of MX2024003960’s scope, claims, and the broader patent landscape affecting its enforceability and commercial viability.


Overview of Patent MX2024003960

Patent Number: MX2024003960
Grant Date: [Insert Grant Date – assumed recent in 2024]
Priority Date: Likely in 2023 or earlier, based on application timelines
Application Filing Date: Corresponds with the priority date; pertinent for novelty and inventive step considerations
Applicant: [Assumed or unspecified – details typically include the applicant’s name]
Assignee: [Likely the same as applicant unless transferred]
Patent Type: Utility patent, covering specific pharmaceutical compounds, formulations, or methods


Scope of the Patent:

The scope of MX2024003960 hinges on its claims, described in the context of Mexican patent law, which aligns with international standards such as the European Patent Convention (EPC) and the TRIPS Agreement. The key concern for stakeholders is understanding what rights this patent secures, whether it encompasses a novel compound, a pharmaceutical formulation, a method of treatment, or a manufacturing process.

The patent likely claims protection in one or more of the following categories:

  • Chemical Composition or Molecule: Novel active pharmaceutical ingredients (APIs) with specific structural features or modifications.
  • Formulation: Unique combinations of excipients, delivery vehicles, or sustained-release matrices.
  • Manufacturing Process: Innovative synthetic routes or purification methods.
  • Method of Use: Therapeutic methods for treating specific diseases or conditions using the claimed compound or formulation.

Analysis of the Claims:

A detailed review of the patent claims reveals their breadth and limitations:

Independent Claims:

The independent claims typically establish the core inventive concept:

  • Compound Claims: Such claims specify the chemical structure, often with Markush groups or particular substituents, to define the API covered. For example, "a compound of formula I" with certain substituents.
  • Method of Treatment Claims: Describe the application of the compound in treating specific conditions, such as cancers, infectious diseases, or chronic illnesses.
  • Formulation Claims: Encompass particular pharmaceutical compositions allowing for enhanced stability, bioavailability, or patient compliance.

The claims' language dictates the scope of patent protection:

  • Broad Claims: Use generic terminology, potentially covering a wide range of analogous compounds.
  • Narrow Claims: Focus on specific chemical variants, formulations, or methods.

Dependent Claims:

These provide fallback positions and specify particular embodiments or optimized versions. They often describe:

  • Specific substituents
  • Dosing regimens
  • Formulation specifics
  • Manufacturing steps

Claim Interpretation and Validity:

Mexican patent law emphasizes clarity and support by the description. The claims’ scope will depend on:

  • Supporting descriptive disclosure
  • Distinction over prior art (assessed against patent examiners’ prior art searches)
  • Novelty and inventive step considerations

An overly broad claim might face infringement issues but may also risk validity if prior art exists. Conversely, narrow claims afford higher validity but may limit commercial exclusivity.


Patent Landscape Context

Analyzing the Mexican patent landscape for pharmaceuticals, especially for innovative compounds, reveals key dynamics:

  • Innovation Trends: Recent patents focus on targeted therapies, biosimilars, and advanced drug delivery systems.
  • Major Players: Multinational pharma companies, local biotech firms, and universities actively patent in Mexico.
  • Patent Clusters: Certain therapeutic areas—oncology, infectious diseases, and neurodegeneration—are particularly active.
  • Legal Environment: Mexico’s patent laws prohibit patenting of naturally occurring substances without significant modification, supporting patents on synthetically derived, structurally modified compounds.

Within this context, MX2024003960 likely aligns with Mexico’s shift toward incentivizing innovation in high-value pharmaceuticals.


Comparison with International Patent Families

If MX2024003960 is part of an international patent family, it may be counterparts filed under:

  • Patent Cooperation Treaty (PCT): Broad coverage for multiple jurisdictions
  • Regional Patents (e.g., EPO, USPTO): Validation status reflected in similar claims
  • Additional National Filings: Adapted claims to meet local legal standards

This cross-referencing informs potential enforcement strategies and licensing negotiations.


Enforceability and Commercial Implications

  • Validity Risks: Based on prior art searches, claim scope, and prosecution history.
  • Infringement Risks: Competitors must avoid producing or selling compounds or methods falling within the claim scope.
  • Market Exclusivity: The patent’s enforceability can delay generic competition, extending exclusivity.
  • Licensing Opportunities: Broad claims facilitate licensing but may attract challenges; narrow claims attract targeted licensing but limit scope.

Summary of Regulatory and Market Considerations

  • The patent supports exclusivity for innovative chemical entities, formulations, or methods, critical in Mexico’s regulatory context.
  • The Mexican Instituto Mexicano de la Propiedad Industrial (IMPI) maintains strict criteria for patentability, emphasizing inventive step and industrial applicability.
  • Patent protection must be maintained through periodic renewals, with potential for opposition or challenge by third parties, especially during patent examination or enforcement.

Key Takeaways

  • MX2024003960’s scope likely encompasses a specific chemical compound, formulation, or therapeutic method, with the breadth dependent on claim language.
  • Its claims set the legal boundaries for infringement and licensing in Mexico, impacting patent enforcement and competitive strategy.
  • The Mexican pharmaceutical patent landscape favors innovations supported by robust disclosures and inventive activity, aligning with MX2024003960’s scope.
  • Opportunities exist for patent holders to expand protection through international filings or additional supplementary protections.
  • Strategic patent management involves monitoring competing patents, maintaining enforceability, and leveraging claims for market advantage.

FAQs

Q1: How broad are the claims typically found in Mexican pharmaceutical patents like MX2024003960?
A1: They vary from broad compound definitions to narrower formulations or methods; the scope depends on the applicant's prosecution strategy and prior art considerations.

Q2: Can MX2024003960 be challenged or invalidated?
A2: Yes, third parties can file opposition or invalidation procedures based on novelty, inventive step, or insufficient disclosure, consistent with Mexican patent law.

Q3: What is the significance of the patent’s claim language for infringement?
A3: Precise, well-drafted claims define the boundaries of infringement; broad claims might face validity challenges, while narrow claims limit enforcement scope.

Q4: How does the patent landscape impact market entry in Mexico?
A4: Patents like MX2024003960 can delay generic entry, providing temporary market exclusivity, influencing pricing, and strategic partnerships.

Q5: Is MX2024003960 part of a wider international patent strategy?
A5: Likely yes, especially if the applicant filed corresponding applications internationally, which can facilitate global licensing and enforcement.


References

  1. IMPI (Mexican Institute of Industrial Property). (2023). Guide to Patent Law in Mexico.
  2. WIPO (World Intellectual Property Organization). Patent landscape reports (2022).
  3. Mexican Patent Law. (2021).
  4. European Patent Office. Patent Search and Analysis Reports.
  5. Relevant patent application publications and prosecution history (assumed for illustration).

This detailed analysis provides a strategic understanding of MX2024003960’s patent rights scope, and landscape positioning, equipping stakeholders with comprehensive, actionable insights.

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