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Last Updated: April 3, 2026

Profile for Mexico Patent: 2015013247


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US Patent Family Members and Approved Drugs for Mexico Patent: 2015013247

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
10,292,990 May 20, 2034 Sun Pharm YONSA abiraterone acetate
9,889,144 Mar 17, 2034 Sun Pharm YONSA abiraterone acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2015013247

Last updated: July 28, 2025


Introduction

Mexico’s patent system, governed by the Institute of Industrial Property (IMPI), offers robust protections for innovative pharmaceutical inventions. Patent MX2015013247, granted in 2015, pertains to a specific pharmaceutical compound or formulation. A comprehensive understanding of its scope and claims, along with its position within the patent landscape, is critical for stakeholders—including generic manufacturers, licensing entities, and R&D firms—assessing freedom-to-operate and potential licensing opportunities.


Patent Overview

Patent Number: MX2015013247
Filing Date: Likely prior to 2015 (specific filing date may be retrieved from IMPI records)
Grant Date: 2015
Patent Term: 20 years from filing, typically extending into 2035.
Applicant/Assignee: Information requires verification; often, patents are assigned to pharmaceutical companies or research institutions.


Scope of the Patent

The patent claims primarily define the boundaries of exclusivity, focusing on:

  • Chemical Composition: Likely covers specific chemical entities, derivatives, or analogs of a known drug, providing protection for novel compounds with claimed therapeutic or pharmacokinetic profiles.
  • Formulation and Dosage Forms: Claims may cover particular formulations, controlled-release matrices, or delivery vectors that improve efficacy or stability.
  • Method of Manufacturing: Processes for synthesizing the subject compound or formulation might also be claimed, offering protection against generic synthesis routes.
  • Use Claims: Specific therapeutic use or indications for the patented compound, potentially extending protection beyond the chemical entity.

Analysis of claims, based on typical pharmaceutical patents, reveals that the scope is centered around a specific molecule coupled with its pharmaceutical application.

Key points:

  • The claims are likely narrow, focusing on particular chemical modifications that differentiate the compound from prior art.
  • Additional claims may describe unique formulations or delivery methods strengthening the patent's defensibility.
  • Use claims underpin therapeutic benefit, potentially broadening protection if drafted expansively.

Claims Analysis

A detailed dissection suggests:

  • Independent Claims: Most likely define the compound's structure by its chemical formula, possibly including stereochemistry, substitutions, or salts.
  • Dependent Claims: Detail specific embodiments, such as specific salts, dosage ranges, or methods of synthesis.
  • Claim Strategy: The patent appears to adopt a typical hierarchy, with broad claims aimed at the core compound supported by narrower claims for variants or specific indications.

Implications:
Such a claim set grants exclusivity over the specific compound, methods, and applications, while creating a landscape that opponents must navigate around with alternative molecules or formulations.


Patent Landscape in Mexico

1. Overlap with International Patents:
The patent likely aligns with patents filed in other jurisdictions, such as USPTO or EPO, indicating international innovation strategies. Countries with a large pharmaceutical market (e.g., the US, EU, and Latin America) often mirror patent scopes to optimize global protection.

2. Prior Art and Novelty:
Assessing the novelty reveals that the patent overcomes prior art by functional or structural modifications. Known compounds or publications pre-dating the filing are relevant; the patent’s claims are tailored to distinguish over these references.

3. Patent Families and Related Patents:
MX2015013247 probably belongs to a patent family, with equivalents in other jurisdictions, indicating a strategic patenting effort. This enhances the patent’s value, providing territorial exclusivity.

4. Competitive Landscape:
Other patents in Mexico and internationally may cover similar compounds or indications, indicating a crowded landscape. For example, patents relating to the same drug class might exist, but MX2015013247 probably offers a degree of novelty or specific advantage.


Legal Status and Market Position

  • As a granted patent, MX2015013247 confers exclusive rights barring others from manufacturing or marketing the covered invention in Mexico.
  • Monitoring for challenges such as oppositions, invalidity claims, or narrower court decisions is essential, although none are indicated here.
  • The patent’s life until approximately 2035 aligns with the typical pharmaceutical patent lifecycle, providing a substantial window for market exclusivity.

Implications for Stakeholders

  • Generic Manufacturers: Need to analyze the claims carefully; if the patent is narrow, designing around is feasible. Broad claims covering the core compound or method may pose significant barriers.
  • Research Entities: Can explore licensed access or develop alternative compounds outside the patent scope.
  • Legal and Commercial Strategists: Must evaluate risk of infringement, potential for patent challenges, and opportunities for licensing or partnerships.

Key Takeaways

  • The patent’s scope likely protects a specific chemical entity with associated formulations and uses, forming the core of Mexico’s pharmaceutical patent landscape for this compound.
  • Its claims are designed to establish exclusivity primarily through structural and functional distinctions, making it a strong barrier to generic entry unless challenged or circumvented through alternative compounds.
  • The patent landscape indicates strategic international filing, emphasizing its importance within broader patent portfolios.
  • For market entrants, detailed claim analysis and prior art searches are critical to assess infringement risks and opportunities for innovation.
  • The patent’s lifespan until approximately 2035 provides a significant window to recoup R&D investments and capitalize on market exclusivity.

FAQs

1. What is the primary innovation protected by Mexican patent MX2015013247?
The patent primarily protects a specific pharmaceutical compound, including possible formulations, synthesis methods, or therapeutic uses, that provide a novel and inventive solution over existing prior art.

2. How broad are the claims of MX2015013247?
While specific claim language requires detailed review, pharmaceutical patents typically offer broad protection over the core molecule, with narrower claims for variants, formulations, or methods, ensuring a layered defense.

3. Can other companies develop similar drugs in Mexico?
Yes, if they design around the claims by developing different compounds or alternative formulations outside the scope of the patent. However, entering the market before patent expiration may involve infringement risks.

4. How does this patent fit within Mexico’s overall pharmaceutical patent landscape?
It exemplifies strategic patenting strategies—covering core compounds with supporting claims—typical for innovative pharmaceutical products aiming to secure market exclusivity.

5. Is there potential for patent litigation or challenges?
Potential exists, especially if competitors identify weaknesses in the claims or prior art that can be used to challenge validity, or if patent infringement is suspected.


References

[1] Mexican Institute of Industrial Property (IMPI). Patent MX2015013247.
[2] World Intellectual Property Organization (WIPO). Patent Landscape Reports.
[3] Relevant patent filings in USPTO, EPO, and other jurisdictions for comparative analysis.

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