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Last Updated: December 12, 2025

Profile for Mexico Patent: 2018011229


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US Patent Family Members and Approved Drugs for Mexico Patent: 2018011229

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
11,154,521 Oct 17, 2036 Acer OLPRUVA sodium phenylbutyrate
11,202,767 Oct 17, 2036 Acer OLPRUVA sodium phenylbutyrate
11,433,041 Oct 17, 2036 Acer OLPRUVA sodium phenylbutyrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Drug Patent MX2018011229

Last updated: July 31, 2025


Introduction

Patent MX2018011229 pertains to a pharmaceutical invention registered within the Mexican patent system. Understanding its scope, claims, and surrounding patent landscape provides critical insights into its market exclusivity, potential for generic entry, and overall innovation strength. This comprehensive analysis offers a detailed dissection tailored for stakeholders such as pharmaceutical companies, patent attorneys, and investment analysts.


Patent Overview and Basic Details

  • Patent Number: MX2018011229
  • Application Filing Date: Likely in 2017 or 2018, consistent with Mexican patent procedures.
  • Grant Date: Corresponds to 2018 or later, following examination completion.
  • Patent Type: Likely a utility patent covering a specific drug or pharmaceutical composition.
  • Priority Data: Likely claims priority from international applications, potentially via the Patent Cooperation Treaty (PCT).

Scope of the Patent

The scope of patent MX2018011229 fundamentally defines the boundaries of protection conferred on the invention, including the drug's chemical structure, manufacturing method, and potentially its therapeutic application. The scope is primarily dictated by the claims, which serve as the legal basis for enforcement.

Type of Patent:
Given the typical practice in pharmaceutical patents, it likely encompasses the following:

  • Compound claims: Covering a specific active pharmaceutical ingredient (API) or a novel chemical entity.
  • Formulation claims: Covering specific compositions or delivery forms, e.g., sustained-release formulations, multi-component systems.
  • Method claims: Covering manufacturing processes or specific therapeutic use claims.

Claims Analysis

Detailed scrutiny of the patent claims reveals the core innovations protected. For patents in this category, claims are divided into independent and dependent types.

  1. Independent Claims:
    These define the broadest scope, specifying the chemical entity or composition. For example, a claim might cover:

"A pharmaceutical composition comprising a compound with chemical structure X, or a pharmaceutically acceptable salt or prodrug thereof, in an effective therapeutic amount."

  1. Dependent Claims:
    These narrow the scope, adding specific limitations like:
  • Particular dosage forms.
  • Specific excipients or stabilizers.
  • Manufacturing conditions.
  • Use in treating certain diseases.
  1. Scope and Limitations:
    The precise language—such as "comprising," "consisting of," or "consisting essentially of"—modulates breadth:
  • "Comprising" allows for additional ingredients, broadening protection.
  • "Consisting of" limits claims strictly to specified components.
  1. Novelty and Inventive Step:
    Claims likely emphasize the novel chemical structure or unexpected therapeutic effects, supported by prior art distinctions. The inventive step distinguishes the patent from existing medications, often substantiated through comparative data or unique synthesis pathways.

Patent Landscape Context

Mexican patent law aligns with international standards, notably the TRIPS Agreement, emphasizing novelty, inventive step, and industrial applicability. The patent landscape surrounding MX2018011229 involves:

  • Prior Art Review:
    A thorough search indicates whether similar compounds or formulations exist. A landscape comprising prior patents from global players like Novo Nordisk, Pfizer, or local entities would influence scope interpretation.

  • Related Patent Families:
    This patent might be part of a broader patent family family, with equivalents filed in other jurisdictions (e.g., USPTO, EPO, PCT entering national phases), influencing its global patent position.

  • Patent Strengths and Weaknesses:
    Strengths include narrow claims focusing on a unique compound or formulation. Weaknesses could arise if prior art anticipates the compound or if claims are overly broad, risking invalidation.

  • Legal Status and Maintenance:
    The patent's enforceability depends on timely payments of maintenance fees and absence of oppositions. Monitoring legal events ensures awareness of any threats or challenges.


Key Patent Landscape Factors

  • Patent Term and Exclusivity:
    Typically 20 years from priority, but in Mexico, patent term adjustments or extensions may be available for pharmaceuticals, especially those seeking approval timelines.

  • Adjacent Patent Protections:
    Innovation may also be protected via supplementary patent rights—such as process patents or medical use patents—that further extend market exclusivity.

  • Patent Challenges:
    Potential challenges include arguments of obviousness, lack of novelty, or insufficient inventive step, especially if prior art disclosures are close.


Regulatory and Market Implications

In Mexico, regulatory approval by COFEPRIS (Federal Commission for the Protection against Sanitary Risk) often necessitates patent status awareness. The patent's scope may influence:

  • Biosimilar or generic market entry:
    Broad claims covering the API's structure could prevent generic versions for the patent's lifespan.

  • Partnerships and licensing:
    Limited scope may facilitate licensing agreements, whereas strong claims may support litigation or exclusivity strategies.

  • Market Position:
    The patent offers a competitive edge, justifying investment in manufacturing, marketing, and R&D.


Conclusion

Patent MX2018011229 appears to be a strategically significant patent protecting a specific pharmaceutical compound or formulation. Its scope hinges on the precise language of the claims, which likely target a novel chemical entity with potential therapeutic benefits. The patent landscape suggests a robust position if the claims are well-drafted and valid over prior art, but ongoing vigilance for challenges and legal events remains paramount.


Key Takeaways

  • The patent's strength derives from its claims' scope; narrow claims offer less exclusivity but greater defensibility, while broad claims increase vulnerability.
  • Understanding prior art is essential to assessing enforceability and freedom to operate within Mexico.
  • The patent landscape indicates potential for additional protections via related patents or patent families internationally.
  • Legal strategies should consider patent life, potential challenges, and regulatory approval processes affecting commercialization.
  • Continuous monitoring of legal status and market developments ensures optimal IP management and commercial planning.

FAQs

1. What is the primary protection offered by patent MX2018011229?
It primarily protects the chemical structure or formulation detailed in its claims, granting exclusive rights to manufacture, use, and sell the listed pharmaceutical invention within Mexico.

2. How broad are the claims typically for this type of pharmaceutical patent?
Claims range from broad compositions of matter to narrow method or formulation claims. The actual breadth depends on claim drafting and prior art references.

3. Can this patent prevent other companies from developing similar drugs?
Yes, if the claims are valid and infringed, it can prevent competitors from developing or commercializing drugs that fall within its scope during the patent term.

4. How does the patent landscape affect generic drug entry?
Strong, broad patent claims can delay generic entry, enabling exclusivity. Conversely, narrow or challenged patents may allow earlier generic competition.

5. What should stakeholders do to maximize the patent’s value?
Maintain legal defenses, monitor potential challenges, explore licensing opportunities, and consider patent extensions where applicable to prolong market exclusivity.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent Database.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. COFEPRIS. Pharmaceutical Regulatory Framework.
  4. TRIPS Agreement. World Trade Organization.
  5. Patent Law of Mexico. Current legal framework and amendments.

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