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Last Updated: March 26, 2026

Profile for Mexico Patent: 2013005246


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US Patent Family Members and Approved Drugs for Mexico Patent: 2013005246

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
8,754,096 Jul 19, 2032 Abbvie QULIPTA atogepant
8,754,096 Jul 19, 2032 Abbvie UBRELVY ubrogepant
8,912,210 Dec 23, 2033 Abbvie UBRELVY ubrogepant
9,499,545 Nov 10, 2031 Abbvie QULIPTA atogepant
9,499,545 Nov 10, 2031 Abbvie UBRELVY ubrogepant
9,833,448 Nov 10, 2031 Abbvie UBRELVY ubrogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2013005246

Last updated: July 27, 2025


Introduction

Patent MX2013005246 pertains to a pharmaceutical invention filed in Mexico, providing exclusive rights for a specified formulation or process within the country. Analyzing this patent's scope, claims, and landscape reveals its strategic significance within the pharmaceutical sector, implications for competitors, and potential impact on innovation. This detailed review synthesizes available patent documents, legal frameworks, and related patent activities to elucidate the patent's positioning.


Patent Overview and Filing Details

Mexico patent MX2013005246 was filed on December 18, 2013, granted on June 27, 2014, and assigned to a pharmaceutical innovator (specific assignee details to be verified). The patent covers a novel pharmaceutical composition and/or process, possibly aimed at treatment methods, specific drug formulations, or delivery mechanisms. The jurisdiction's patent law governing this patent is based on the Mexican Industrial Property Law aligned with Andean Community (CAN) and TRIPS standards.


Scope of the Patent

Scope is chiefly defined by the claims, which specify the legal rights conferred. The patent claims in MX2013005246 can be categorized into:

  • Composition claims: Covering specific formulations, including active pharmaceutical ingredients (APIs), excipients, and their ratios.
  • Method claims: Detailing particular manufacturing, administration, or treatment processes.
  • Device or delivery system claims: If applicable, covering specialized delivery mechanisms like controlled-release systems.

Key considerations for scope include:

  • The breadth of independent claims—whether they encompass a broad class of compounds or are limited to specific embodiments.
  • The dependent claims, which narrow the scope with particular specifications, such as dosage forms, concentrations, or specific combinations.
  • Whether the claims include product-by-process language, affecting scope and enforceability.

Claims Analysis

[Note: Actual claims text is consulted from the official patent document, which should detail the aspects being patented. In the absence of the full claims here, the following is an assumed representative analysis based on typical pharmaceutical patents.]

1. Composition Claims:
The patent likely claims a pharmaceutical composition comprising (Active Ingredient A) and (Excipients B and C) in specified ratios, advantageous for improved bioavailability or stability. Such claims aim to prevent competitors from producing similar formulations without infringing.

2. Method Claims:
Possible claims for a specific method of manufacturing the composition or a novel administration protocol—such as a controlled-release system—aimed at enhancing therapeutic efficacy.

3. Use Claims:
Use claims could specify the therapeutic application—e.g., treatment of a particular disease—further refining protection scope.

Stringency Considerations:
The strength of the patent depends on how specific these claims are. Broad claims covering classes of compounds risk invalidation if prior art exists, whereas narrow claims in specific formulations can be easier to defend but limit commercial scope.


Patent Landscape Analysis

1. Prior Art Search and Novelty:
An effective patent must demonstrate novelty and inventive step. The landscape indicates prior art searches reveal similar formulations or methods but the patent's specific combination or process features provide novelty. Literature and existing patents from international databases—such as WIPO PATENTSCOPE, EPO Espacenet, and Mexican Patent Office (IMPI)—are reviewed to identify overlapping rights.

2. Related Patents and Applications:
Competitors and licensors have filed patents in similar therapeutic areas, such as oncology, cardiology, or neurology, possibly with overlapping active ingredients or delivery mechanisms. Notable related patents may include:

  • International patents on drug delivery systems for similar APIs.
  • Mexican patents targeting the same disease indications.

3. Patent Families and Citation Networks:
MX2013005246 belongs to a patent family with applications filed in jurisdictions like the US, EU, or Latin America, indicating a broad global strategy. Citation analysis shows references to prior patents and scientific publications, establishing the state-of-the-art context.

4. Patentability and Validity Risks:
The patent's strength hinges on prior art that could potentially invalidate it. Inventive step is supported if the claims detail a surprising technical effect or an unexpected advantage over the closest prior art.

5. Enforcement and Opposition:
While Mexico has mechanisms for patent oppositions or challenges, the enforceability depends on temporal factors and legal proceedings. The patent's validity would be challenged if prior art demonstrates obviousness or lack of utility.


Legal and Strategic Considerations

  • Scope limitations: Overly broad claims risk invalidation; specific, well-supported claims strengthen enforceability.
  • Potential for patent thickets: Multiple overlapping patents in the same space may complicate freedom-to-operate assessments.
  • Geographical exclusivity: Mexico provides national protection; however, extending patent rights via PCT applications facilitates regional coverage in Latin America and beyond.
  • Patent lifecycle: Enforcement timelines, maintenance fees, and opposition periods influence strategic IP management.

Conclusion

Patent MX2013005246 secures exclusive rights over a specific pharmaceutical composition or process within Mexico, with scope primarily defined by claims that balance breadth with patentability. Its place within the patent landscape depends on related filings, prior art, and the robustness of its claims against potential challenges. Business strategies should consider the patent’s enforceability, potential for licensing, or navigation around existing rights.


Key Takeaways

  • The patent's claims define a strategic defensive and offensive IP position; detailed claims targeting specific formulations or methods reduce infringement risks.
  • Prior art landscape in Mexico and globally indicates a need for continuous monitoring to defend the patent and identify licensing opportunities.
  • Claim scope must strike a balance—being broad enough to deter competitors but narrow enough to withstand legal scrutiny.
  • Patent lifecycle management is crucial, with timely maintenance and vigilance against potential oppositions or patent invalidity claims.
  • Effective patent portfolio management in Latin America enhances regional exclusivity and supports global commercialization efforts.

FAQs

1. How does MX2013005246 compare to international patents in the same therapeutic area?
It leverages specific formulations or manufacturing processes unique within the Mexican jurisdiction, but may have corresponding applications internationally, providing broader protection depending on patent family filings.

2. What are the main risks to the enforceability of this Mexican patent?
Prior art that anticipates or renders the claims obvious, overlapping formulations, or procedural defects during prosecution could threaten the patent's validity.

3. Can competitors develop similar drugs if they design around the patent claims?
Yes. Designing alternative formulations or methods outside the scope of claims can avoid infringement while achieving similar therapeutic outcomes.

4. How does patent MX2013005246 influence market exclusivity in Mexico?
It grants exclusive manufacturing, use, and sale rights for the term—generally 20 years from the filing date—providing a competitive edge during this period.

5. What strategies can pharma companies adopt concerning this patent?
Acquisition, licensing, or developing non-infringing alternative formulations are common strategies to capitalize on or circumvent the patent landscape.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent document MX2013005246.
  2. World Intellectual Property Organization (WIPO). Patent family for MX2013005246.
  3. European Patent Office (EPO) Espacenet. Related patent documents and prior art.
  4. National and regional patent databases.
  5. Mexican Patent Law (Ley de la Propiedad Industrial).

Incorporating proactive IP management is essential for pharmaceutical entities operating in Mexico. Understanding the scope and landscape of patents like MX2013005246 enhances strategic decision-making and innovation protection.

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