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Last Updated: December 17, 2025

Profile for Mexico Patent: PA04006917


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US Patent Family Members and Approved Drugs for Mexico Patent: PA04006917

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
8,101,659 Jan 15, 2025 Novartis ENTRESTO SPRINKLE sacubitril; valsartan
8,101,659 Jul 15, 2025 Novartis Pharms Corp ENTRESTO sacubitril; valsartan
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MXPA04006917

Last updated: August 4, 2025

Introduction

Mexico’s patent system plays a vital role in safeguarding pharmaceutical innovations, fostering R&D, and ensuring market exclusivity. The patent MXPA04006917, granted for a pharmaceutical invention, warrants a comprehensive review to understand its scope, claims, and the broader patent landscape within Mexico’s pharmaceutical patent domain. This analysis offers insights crucial for pharmaceutical companies, generic entrants, and legal professionals navigating Mexico's patent environment.


Patent Overview and Background

Patent Number: MXPA04006917
Application Filing Date: Likely around 2004-2006 (based on patent numbering conventions and grant date estimates)
Grant Date: Approximately 2006-2007
Applicant/Assignee: [Details not specified; hypothetical or derived from public records]
Title: [Assumed to relate to a specific pharmaceutical compound or formulation based on similar patents]

This patent addresses a pharmaceutical invention, potentially a novel compound, a specific formulation, or a method of use—common categories for patents in the biomedical field. Its specific scope is defined in its claims, which delineate the boundaries of patent protection.


Scope of the Patent

The scope of MXPA04006917 is primarily delineated by its claims. Patent claims define the legal boundaries, determining what others cannot make, use, sell, or distribute without infringing on the patent. Analyzing the scope involves examining independent claims and their dependent claims, clarifying whether the patent covers:

  • Chemical compounds: Novel molecules with therapeutic activity
  • Pharmaceutical formulations: Specific compositions, dosages, or delivery methods
  • Methods of use or treatment: Specific therapeutic indications or administration protocols
  • Manufacturing processes: Techniques to produce the active compound or formulation

Given the data, the patent’s scope likely covers a novel chemical entity or a unique formulation, with claims possibly extending to methods of treatment employing the inventive compound or composition.


Claims Analysis

In patent documents, claims are categorized as independent and dependent:

Independent Claims

These establish broad protective boundaries, often covering:

  • The chemical entity itself: For example, a compound with a specific structure or functional groups.
  • Method of synthesis or production: Detailing steps or conditions to manufacture the compound.
  • Therapeutic use: Methodologies employing the compound for treating specific conditions.

Dependent Claims

These narrow the scope, adding specific features such as:

  • Specific substituents or pharmacokinetic properties.
  • Particular formulations or dosage forms.
  • Improved stability or bioavailability profiles.

Potential Claim Language

While exact claim language is unavailable without accessing the patent text, typical pharmaceutical patents encompass:

  • Structural formulae of the compound(s).
  • Specific chemical modifications or substituents.
  • Methodologies for preparing the compound.
  • Use claims for specific diseases or indications.

Implications of the Claims

The scope hinges on how broad or narrow these claims are:

  • Broad claims provide extensive protection but face higher invalidity risks.
  • Narrow claims reduce infringement risk but may be easier for competitors to circumvent.

In the Mexican context, patent claims must meet novelty and inventive step criteria, aligning with international standards under TRIPS.


Patent Landscape in Mexico

Pharmaceutical Patent Environment

Mexico adheres to the Patent Law for Inventions (2019), aligned with TRIPS. The patent landscape features:

  • Growth in pharmaceutical patent filings, especially in areas like oncology, antivirals, and biologics.
  • Increased patent examination rigor, focusing on inventive step and novelty.
  • Challenges against evergreening: Many patents target incremental changes, demanding detailed claims analysis.

Comparison with Similar Patents

MXPA04006917 sits within a landscape of patents covering:

  • Similar chemical classes: Such as kinase inhibitors, anti-inflammatory agents, etc.
  • Formulation patents: Combining active ingredients with excipients for enhanced delivery.
  • Method patents: Covering novel therapeutic protocols.

Patent Term and Maintenance

The typical patent term in Mexico lasts 20 years from filing, but patent maintenance requires periodic fee payments. Extended protection can be obtained through patent term extensions under certain conditions, especially for drugs.

Legal Challenges and Litigation

In Mexico, patent enforcement involves:

  • Administrative opposition: Filed within six months of grant, challenging validity.
  • Patent infringement litigation: Handled via specialized courts.
  • Compulsory licensing: Possible for public health reasons, which is crucial amid patent disputes.

Implications for Stakeholders

  • Innovators: Must evaluate if MXPA04006917’s claims sufficiently cover their innovations or if they face potential infringement.
  • Generic manufacturers: Need to assess patent validity, scope, and expiry for entry strategies.
  • Legal firms: Should analyze claim breadth and landscape to advise on patent defenses or challenges.
  • Regulatory bodies: Monitor patent compliance during drug approval process.

Conclusion

Patent MXPA04006917 exemplifies Mexico’s active pharmaceutical patent domain, with scope likely centered on a specific chemical entity or formulation. Its claims establish a possibly broad or narrow barrier, depending on claim drafting, influencing market exclusivity and competitive dynamics. The Mexican patent landscape is dynamic, increasingly aligned with international standards, yet remains sensitive to challenges like patent validity and enforcement issues.


Key Takeaways

  • Scope Clarity: The patent’s scope depends heavily on claim language; broad claims offer extensive protection but risk invalidation, while narrow claims are safer but less encompassing.
  • Landscape Context: MXPA04006917 operates amid a growing and complex pharmaceutical patent landscape in Mexico, with active innovation and enforcement.
  • Strategic Considerations: Patent holders should actively monitor patent validity and potential infringers; newcomers must thoroughly analyze the scope for freedom-to-operate.
  • Legal and Regulatory Trends: Continued reforms and TRIPS alignment enhance patent robustness, but challenges like patentability of incremental changes persist.
  • Enforcement and Litigation: Patent disputes in Mexico typically involve administrative and judicial proceedings, emphasizing the need for precise patent drafting and strategic litigation planning.

FAQs

1. What is the typical duration of patent protection for pharmaceuticals in Mexico?
Mexico grants patents lasting 20 years from the filing date. Maintenance fees are required periodically to retain enforcement rights.

2. How does Mexico assess patent novelty and inventive step?
Following TRIPS standards, Mexico requires that inventions be new, involve an inventive step, and have industrial applicability. Patent examiners evaluate claims for novelty over prior art and inventive merit.

3. Can existing patents be challenged or invalidated in Mexico?
Yes. Patents can be challenged through administrative opposition within six months of grant or via judicial nullity proceedings, especially if they fail to meet patentability criteria.

4. Are formulation patents easily circumvented in Mexico?
Formulation patents might be circumvented if competitors develop alternative compositions or delivery methods not covered by claims. Narrow claims increase the risk of design-around strategies.

5. How does Mexico’s patent landscape influence global pharmaceutical strategies?
Mexico’s patent landscape offers opportunities for securing exclusive rights but requires careful design of claims to prevent infringement and to comply with local legal standards.


Sources

  1. IMPI - Mexican Institute of Industrial Property. Official patent database and legal framework references.
  2. TRIPS Agreement. World Trade Organization standards influencing Mexican patent law.
  3. Patent Documentation. Mexican patent documents accessible via IMPI or related patent databases.
  4. Legal Analysis Reports. Sector reports analyzing pharmaceutical patent trends in Mexico.
  5. Industry Publications. Articles on patent strategies and litigation in Mexican pharmaceutical landscape.

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