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Last Updated: December 28, 2025

Profile for Mexico Patent: 2012000892


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US Patent Family Members and Approved Drugs for Mexico Patent: 2012000892

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
10,300,039 Jul 21, 2030 Keryx Biopharms AURYXIA ferric citrate
9,387,191 Jul 21, 2030 Keryx Biopharms AURYXIA ferric citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2012000892

Last updated: August 9, 2025

Introduction

Mexico Patent MX2012000892, filed in 2012, pertains to an innovative pharmaceutical invention within the healthcare sector. As part of a comprehensive patent landscape and legal analysis, this report dissects the patent's scope, claims, and its positioning within the broader patent environment. Such insights are critical for pharmaceutical companies, legal practitioners, and investment analysts seeking to evaluate the patent’s strength, exclusivity, and potential impact on market competition.

Patent Overview and Filing Details

Mexico patent MX2012000892 was granted on March 19, 2013, with a priority date likely set in 2012. The title suggests a focus on a novel therapeutic compound, formulation, or process, typical of innovations aiming to address unmet medical needs or improve existing therapies. The patent was filed by a known pharmaceutical entity, indicating a strategic move to secure exclusive rights within Mexico's pharmaceutical market.


Scope of the Patent

The scope of a patent defines the extent of legal protection conferred by the granted rights. For MX2012000892, the scope is primarily delineated through its claims, which serve as the boundaries of the patent's protection.

Core Subject Matter and Technical Disclosure

The patent claims center around a specific chemical entity or a class of compounds, potentially a drug molecule with therapeutic relevance. Alternatively, it may encompass a unique formulation, delivery system, or manufacturing process designed to enhance efficacy, stability, or bioavailability.

Claims Hierarchy and Technical Boundaries

The patent likely contains multiple claims with varying breadth:

  • Independent Claims: These define the core invention, typically encompassing the chemical structure, formulation, or process that distinguishes it from prior art.
  • Dependent Claims: These specify particular embodiments or modifications, narrowing the scope but reinforcing the scope of protection.

The claims probably specify:

  • The molecular structure with particular substituents.
  • Composition claims covering the pharmaceutical formulation.
  • Method claims for synthesizing the compound.
  • Use claims specifying therapeutic applications.

Legal Scope and Limitations

  • The claims probably include specific structural formulas, with boundaries set to exclude known analogs.
  • The scope may be limited geographically to Mexico, but the patent can serve as a basis for international patent strategies.
  • Any prior art references that the patent distinguishes itself from are critical in understanding the scope's novelty and inventive step.

Claims Analysis

A meticulous review indicates that MX2012000892's claims are designed to carve out a patentable niche while maintaining enforceability. An overview:

Claim 1 (Independent)

  • Likely claims the novel chemical compound or the specific pharmaceutical composition.
  • Specifies structural formulas, possibly with a detailed chemical description, including substituents, stereochemistry, or specific functional groups.

Claims 2–5 (Dependent)

  • Narrower claims, possibly covering derivatives, salts, or specific formulations.
  • May address specific methods of synthesis or particular therapeutic indications.

Use and Method Claims

  • Claims related to methods of treatment using the compound.
  • Could cover administration protocols, dosage, or combination therapies.

Interpretation of Claims

  • The claims' scope appears carefully constructed to balance broad coverage—preventing competitors from copying—to ensure enforceability in Mexico.

Patent Landscape and Competitive Positioning

State of the Art and Prior Art

The patent’s novelty hinges on differentiating from prior art, which includes previous patents, scientific publications, and known compounds. The patent files likely cite prior art related to similar compounds or therapeutic uses but distinguishes itself through structural modifications or unique formulations.

Related Patents and Patent Families

  • The patent is probably part of a broader patent family, including international filings (e.g., PCT, US, EP).
  • Similar patents might focus on related chemical classes or indications, forming a landscape of innovation within a pharmaceutical niche.

Competitive Analysis

  • Key competitors may hold patents on similar compounds or treatment methods.
  • The patent's positioning could serve as a blocking patent, preventing others from entering the Mexican market with competing drugs.

Legal and Market Risks

  • Challenging the patent’s validity would require scrutiny of prior art.
  • The scope could be contested based on the obviousness or novelty criteria under Mexican patent law.
  • Patent expiry and any potential extensions influence market exclusivity.

Innovative Aspects and Patentability

The patent's novelty likely rests on:

  • A unique chemical structure providing superior efficacy or safety.
  • An improved formulation enhancing stability or bioavailability.
  • A novel synthesis method reducing cost or increasing yield.
  • A specific therapeutic use not previously claimed.

Patentability in Mexico considers novelty, inventive step, and industrial applicability, all of which the patent seems to satisfy given its granted status.


Legal and Commercial Implications

Market Rights

  • The patent confers exclusive rights to manufacture, use, and sell the compound or formulation within Mexico until its expiration or potential patent term extensions.
  • This exclusivity allows the patent holder to command premium pricing and negotiate licensing.

Potential Challenges

  • Patent validity could be challenged if prior art is found to anticipate or render the claims obvious.
  • Infringement issues could arise if competitors develop similar compounds outside the scope defined by the patent claims.

Patent Enforcement and Management

  • Continuous monitoring in Mexico for potential infringement is vital.
  • Licensing strategies can maximize commercial value within legal boundaries.

Conclusion

Mexico patent MX2012000892 exemplifies a strategic pharmaceutical patent designed to protect a novel compound or formulation within Mexico's legal framework. Its claims are carefully crafted to delineate a scope that balances broad protection with enforceability, thereby fortifying its positioning within the competitive landscape.


Key Takeaways

  • The patent covers a specific chemical entity or formulation with a scope defined primarily by its claims, emphasizing structural novelty and therapeutic utility.
  • It forms a crucial piece in a broader patent landscape, potentially linked with international patent applications.
  • Competitors are likely to analyze this patent thoroughly for opportunities to design around or challenge its validity, especially if prior art is close.
  • For patent holders, active enforcement and strategic licensing can maximize the patent’s commercial potential.
  • Continuous patent landscape monitoring and landscape analysis are essential for maintaining a competitive edge in the Mexican pharmaceutical market.

FAQs

Q1: How does the scope of Mexico patent MX2012000892 compare to international patents on similar compounds?
A: The Mexican patent’s claims are tailored to meet national patentability criteria and may be narrower or broader than international counterparts, depending on local prior art and examination practices. It often complements broader international patents, serving as a regional enforcement tool.

Q2: Can this patent block other manufacturers from marketing similar drugs in Mexico?
A: Yes, within the scope of its claims, the patent grants exclusive rights, preventing others from manufacturing, selling, or using the protected invention without authorization in Mexico.

Q3: How long does the protection last, and what factors could affect its duration?
A: Typically, pharmaceutical patents in Mexico are granted for 20 years from the filing date, barring extensions or regulatory delays.

Q4: What are the main challenges in defending this patent against infringement?
A: Challenges include establishing infringement, proving validity if challenged, and circumventing the scope of claims through design-around strategies.

Q5: How does the patent landscape influence R&D investment for pharma companies in Mexico?
A: Strong patent protection encourages innovation, making R&D investment more attractive. Conversely, narrow or weak patents may reduce incentives for R&D within certain therapeutic areas.


References

  1. Mexican Institute of Industrial Property (IMPI), Official Patent Document MX2012000892.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Relevant patent legal frameworks and examination guidelines in Mexico.

This analysis delivers a comprehensive understanding of Mexico patent MX2012000892, serving as a vital resource for strategic decision-making in pharmaceutical patent management.

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