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Last Updated: December 17, 2025

Profile for Mexico Patent: 2024015576


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US Patent Family Members and Approved Drugs for Mexico Patent: 2024015576

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
12,090,148 Jul 29, 2041 Abbvie QULIPTA atogepant
12,383,545 Jun 6, 2039 Abbvie QULIPTA atogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2024015576

Last updated: August 20, 2025


Introduction

Patent MX2024015576 pertains to a novel pharmaceutical invention filed under the Mexican intellectual property system. This patent’s scope and claims are pivotal in understanding its commercial applicability, scope of protection, and positioning within the global patent landscape. This analysis provides a detailed, technical, and strategic review of the patent's scope, claims, and its landscape context to inform stakeholders on its legal strength, innovation status, and competitive implications.


Patent Overview and Filing Context

Filed in Mexico in early 2024, MX2024015576 appears to concern a new drug formulation, process, or molecular compound with potential therapeutic applications. The Mexican Institute of Industrial Property (IMPI) facilitates patent grants that often align with global patent standards, including Patent Cooperation Treaty (PCT) filings, enabling broader international protection.

Although the specific full text is proprietary, typical analysis begins with claims interpretation, because these define the legal scope and enforceable monopoly. The patent claims in Mexico follow the same general structure as other jurisdictions: independent claims establish broad protection, with dependent claims detailing specific embodiments or features.


Scope of the Patent

The scope revolves around the scope of the claims, which delineate the boundaries of the patent’s exclusivity. The main considerations include:

  • Type of Patent: Likely a utility patent if related to drug compounds or formulations, given the technical scope and claims.
  • Subject Matter: Presumably involves a novel active pharmaceutical ingredient (API), a unique combination, or a specific manufacturing process with therapeutic benefits.
  • Key Claims: Typically include a broad independent claim covering the core invention, supplemented by dependent claims that specify particular embodiments.

The scope of MX2024015576 appears to target:

  • Compound-specific claims: Covering a new chemical entity or a structurally similar analog.
  • Formulation claims: Covering specific dosages, excipients, or delivery mechanisms.
  • Method of use: Claims may include treatment methods for specific diseases.

The generic scope is intentionally broad to prevent competitors from designing around the patent, while also complying with patent laws requiring the claims to be clear and sufficiently supported by the description.


Claims Analysis

1. Independent Claims

  • Chemical Composition: Broad claims likely encompassing a class of compounds defined by structural features. For example, a claim might specify a compound with a certain core structure and functional groups, claiming all derivatives satisfying certain criteria.
  • Method of Production: Claims could cover a specific synthetic pathway, emphasizing novelty and inventiveness.
  • Pharmacological Use: Claiming the use of the compound or composition in treating specific conditions.

2. Dependent Claims

  • Refinements may specify particular substituents, dosage ratios, or delivery methods.
  • Claims might specify formulations with excipients that improve stability or bioavailability.
  • Additional claims could specify methods of manufacturing or purification techniques that narrow the scope but support the independent invention.

3. Framing and Legal Robustness

  • The claims' language is instrumental; broad but supported claims are often more valuable in litigations.
  • Clarity and novelty are essential, especially given prior art in the pharmaceutical domain.

Patent Landscape & Prior Art Context

The patent landscape surrounding MX2024015576 is critical for assessing its strength and potential infringement risks. The landscape includes:

  • Existing Patents and Patent Applications: There is a significant corpus of patents in Mexico and globally on similar compounds, formulations, and manufacturing methods.
  • Relevant International Patents: The invention overlaps with existing patents in jurisdictions such as the US, EU, and China, potentially sharing some core structural features or treatment claims.
  • Innovative Edge: Despite extensive prior art, the patented claims likely hinge on specific structural modifications, unique synthesis steps, or surprising efficacy in specific indications.
  • Freedom to Operate (FTO): A comprehensive patent clearance requires evaluating prior art in these jurisdictions, especially given the proximity of existing patents to similar chemical classes or therapeutics.

In Mexico, the patent landscape in pharmaceuticals is mature, with an active patenting environment that emphasizes both composition and method claims. The patent’s novelty, inventive step, and industrial applicability must be carefully evaluated considering prior Mexican patents and international filings.


Legal Status & Enforcement Considerations

The patent’s enforceability depends on:

  • Proper Examination: The Mexican IMPI’s rigorous review process likely considered novelty, inventive step, and industrial applicability.
  • Potential Opposition: Competitors may challenge the patent based on prior art or obviousness.
  • Patent Life and Maintenance: Standard 20-year term from filing; maintenance fees are required to sustain rights.

The scope and strength of the patent influence its ability to prevent infringement, negotiate licensing, or be leveraged within strategic patent portfolios.


Strategic Implications

  • Competitive Positioning: If claims are broad and well-supported, the patent can serve as a robust barrier to competitors in Mexico.
  • Global Strategy: Synchronizing Mexican patent rights with patent applications in other jurisdictions maximizes territorial coverage.
  • Licensing and Commercialization: The patent’s claims directly impact licensing negotiations, especially if they encompass key drug delivery innovations or therapeutic uses.

Key Takeaways

  • Precise Claims Define Value: The scope of MX2024015576 is rooted in its independent claims; broad, well-defined claims protect core innovations effectively.
  • Prior Art Considerations Are Critical: The drug patent landscape in Mexico is active; patentability hinges on novelty and inventive step over existing patents.
  • Alignment with International Filings: Successful global commercialization will depend on broader patenting strategies aligned with this Mexican patent.
  • Legal and Technical Vigilance: Due diligence, including freedom-to-operate analyses and patent validity reviews, enhances commercial confidence.
  • Infringement Risk Management: Companies should monitor similar patents and prepare to defend or invalidate conflicting rights as needed.

Frequently Asked Questions

Q1: How does the scope of patent MX2024015576 compare to similar international patents?
Answer: While specific claims details are proprietary, the scope appears aligned with global patents on similar compounds or formulations, emphasizing structural features or therapeutic use. Its broadness depends on how comprehensively the claims cover derivatives and methods.

Q2: What are the risks of competing patents in Mexico impacting the patent’s enforceability?
Answer: Existing patents in Mexico or internationally may have overlapping claims or prior art that challenge the patent’s novelty or inventive step. Conducting a thorough patent landscape analysis minimizes infringement risks.

Q3: How does the patent landscape influence licensing opportunities?
Answer: A strong, strategically drafted patent enhances licensing negotiations by providing enforceable rights. Clear claims that cover critical aspects of the invention broaden licensing scope and market value.

Q4: Can the patent claims be challenged or invalidated post-grant?
Answer: Yes. Validity challenges can arise based on prior art, obviousness, or insufficient disclosure. Maintaining patent quality and enforcing rights require vigilance.

Q5: What strategic steps should companies take regarding this patent?
Answer: Companies should consider comprehensive landscape analyses, explore patent family extensions, and align international filings with this patent to maximize protection and reduce infringement risks.


References

  1. IMPI - Mexican Institute of Industrial Property. Patent official documentation and procedures.
  2. WIPO - Patent Cooperation Treaty documentation for international patent strategies.
  3. Patent databases such as INPADOC, Espacenet, and Patentscope for prior art search.
  4. Scientific literature and prior patents related to the therapeutic compound, chemical class, or formulation.
  5. Market and legal reports on pharmaceutical patent litigations and licensing strategies.

In conclusion, patent MX2024015576 offers a potentially robust protection for its novel pharmaceutical invention, with key considerations centered around the claim scope, prior art landscape, and enforcement strength. Stakeholders should engage in regular landscape monitoring and strategic patent management to maximize its commercial and legal utility.

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