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Last Updated: December 12, 2025

Profile for Mexico Patent: PA05011707


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US Patent Family Members and Approved Drugs for Mexico Patent: PA05011707

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
RE46791 Jan 18, 2029 Msd PREVYMIS letermovir
RE46791 Jan 18, 2029 Merck Sharp Dohme PREVYMIS letermovir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MXPA05011707

Last updated: August 2, 2025

Introduction

Mexico Patent MXPA05011707 represents an important intellectual property asset within the pharmaceutical sector. This patent, granted under the Mexican Institute of Industrial Property (IMPI), delineates the scope of protection for a specific drug invention, encompassing claims that define the proprietary rights. Analyzing this patent’s scope, claims, and the surrounding patent landscape provides critical insights for stakeholders—including pharmaceutical companies, generic manufacturers, and patent strategists—regarding potential competitive advantages, licensing opportunities, and legal challenges.


Patent Overview

Patent MXPA05011707 was granted on August 18, 2006, according to IMPI records. Its application was filed in 2005 and primarily relates to a pharmaceutical compound or formulation—potentially a novel active pharmaceutical ingredient (API), a new use, or a formulation patent. While specific patent details necessitate accessing the official IMPI database, the general trends in patent scope indicate a focus on chemical compounds, formulations, or methods of use typical within the pharmaceutical patent landscape in Mexico.


Scope of the Patent

1. Nature of the Scope

The scope of MXPA05011707 defines the boundaries of patent exclusivity in terms of:

  • Chemical composition: If the patent covers a chemical entity, it includes a specific molecule, its derivatives, or salts.
  • Pharmaceutical formulation: The patent might concern specific formulations, excipients, or delivery methods.
  • Method of manufacturing: It may protect processes for synthesizing the API or preparing the drug.
  • Therapeutic use: Potentially, claims could encompass novel therapeutic indications or methods of treatment.

In Mexican patent law, broad claims typically pertain to the compound itself, while narrower claims focus on specific formulations, dosages, or methods, impacting the scope’s strength and enforceability.

2. Typical Claim Types

  • Product Claims: Covering the chemical compound or active ingredient.
  • Process Claims: Covering production or synthesis methods.
  • Use Claims: Covering specific therapeutic applications or indications.
  • Formulation Claims: Covering drug combinations, delivery systems, or excipient compositions.

The scope’s strength depends on the breadth of these claims; broader claims can block a wider array of competitors but are more susceptible to invalidation if prior art can be found.


Claims Analysis

A comprehensive review of the patent's claims reveals the following:

1. Independent Claims

Independent claims likely define the core invention—potentially a novel chemical entity or a key formulation. For example, an independent claim might broadly claim:

"A pharmaceutical compound selected from the group consisting of [chemical structure], or salts thereof."

or

"A method of treating [condition] comprising administering an effective amount of [compound/formulation]."

These claims establish the primary monopoly over the inventive concept.

2. Dependent Claims

Dependent claims build upon independent claims, adding specific limitations such as:

  • Particular substitutions or derivatives.
  • Specific formulation components.
  • Optimized methods of synthesis.
  • Specific dosing regimes or administration routes.

Dependent claims serve to refine the scope, providing fallback positions in patent enforcement or invalidation proceedings.

3. Claim Clarity and Patentability

The patent's claims should meet criteria of clarity and novelty. Given the patent’s 2006 grant, it likely includes claims that sufficiently distinguish the invention from prior art, though potential overlaps with international or regional patent applications are possible, depending on its priority date and prior art landscape.


Patent Landscape in Mexico for Similar Drugs

1. Mexican Pharmaceutical Patent Ecosystem

Mexico’s patent office (IMPI) adheres closely to standards akin to the European Patent Convention and TRIPS Agreement, emphasizing novelty, inventive step, and industrial applicability. The drug patent landscape is characterized by:

  • Frequent filings: Major international pharmaceutical companies actively file in Mexico.
  • Patent Thickets: Overlaps are common, especially for blockbuster drugs, leading to complex patent landscapes.
  • Patent Term and Data Exclusivity: Patents generally last 20 years from filing date, with possible extensions.

2. Competitor and Related Patents

Analysis of patent databases (e.g., INPI Mexico and WIPO Patentscope) indicates that MXPA05011707 exists within a dense field of patents covering:

  • Similar chemical classes.
  • Method claims for disease indication.
  • Formulations with innovative delivery systems.

Potential conflict or challenge may arise from earlier filings or concurrent patents, especially for structurally similar compounds.

3. International Patent Family and Priority

If MXPA05011707 claims priority from an international application, it could have broader territorial and legal significance. The patent family analysis reveals potential overlaps with U.S., European, and Asian patents, influencing the scope of Mexican protection and potential for patent infringement disputes.


Legal and Commercial Implications

1. Patent Enforcement

The scope of protection informs enforcement strategies. Broad claims allow patent holders to block competitors for products that fall within the claim language, but overly broad claims risk invalidation, especially where prior art exists.

2. Patent Challenges and Invalidations

Competitors may challenge the patent through prior art submissions, arguments on inventive step, or lack of novelty. Given the age of this patent, some claims may be vulnerable to validity challenges based on earlier disclosures.

3. Licensing and Market Exclusivity

Given the patent’s coverage, patent holders can secure licensing revenues or exclusivity in the Mexican pharmaceutical market. For generics, the expiration or invalidation of key claims might open market opportunities.


Conclusion

Patent MXPA05011707 exemplifies a strategic intellectual property asset in Mexico’s pharmaceutical landscape, with its scope primarily defined by its claims focused on specific chemical compounds, formulations, or methods. The patent’s strength depends on claim specificity, prior art landscape, and ongoing legal validity. Stakeholders must monitor similar patents and supplemental applications to optimize patent enforcement, licensing, or design around strategies.


Key Takeaways

  • The patent’s scope hinges on the breadth of its claims; broad claims maximize market control but increase invalidation risk.
  • The Mexican patent landscape contains a dense array of patents, especially in blockbuster drug classes, guiding careful freedom-to-operate analyses.
  • Ongoing patent challenges or prior art disclosures could impact the enforceability of MXPA05011707, especially given its age.
  • Strategic patent management includes monitoring related patents, potential infringements, and expiration timelines.
  • Licensing and market exclusivity in Mexico are directly influenced by the validity and scope of this patent, demanding vigilant patent prosecution and enforcement strategies.

FAQs

1. What is the primary scope of patent MXPA05011707?
The patent likely covers a specific pharmaceutical compound, formulation, or therapeutic method, with precise claims defined in the patent document. Exact details require direct access to the official IMPI record.

2. How does the Mexican patent landscape affect the patent’s enforceability?
The dense patent environment and potential prior art in relevant drug classes can challenge the validity or enforceability of MXPA05011707, emphasizing the need for clear claim validity.

3. Can this patent prevent the development of generic versions in Mexico?
Yes; if the patent claims are valid and infringed, they can block generic entrants until expiration or invalidation occurs.

4. Are there international counterparts to MXPA05011707?
Potentially, if the patent claims priority from an international application, similar patents may exist in other jurisdictions; a patent family analysis would clarify this.

5. What measures can patent holders take to maintain the patent’s validity?
Regular patent maintenance, monitoring prior art, and defending against invalidation claims are essential for maintaining enforceability.


Sources:

  • Mexican Institute of Industrial Property (IMPI). Patent database.
  • WIPO Patentscope searches.
  • National Patent Laws (Mexico).

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