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Last Updated: December 16, 2025

Profile for Mexico Patent: 384868


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US Patent Family Members and Approved Drugs for Mexico Patent: 384868

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
11,938,136 Nov 8, 2036 Genentech Inc EVRYSDI risdiplam
>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 MX384868

Last updated: September 14, 2025

Introduction

Patent MX384868 pertains to a pharmaceutical invention registered under Mexico’s Instituto Mexicano de la Propiedad Industrial (IMPI). As a core component of the intellectual property framework influencing drug development, licensing, and commercialization strategies, understanding the scope, claims, and overall patent landscape of MX384868 is essential for stakeholders in the pharmaceutical industry. This report offers an in-depth analysis, focusing on the patent’s technical scope, claim structure, related patents, and implications within the Mexican and global patent ecosystems.


1. Patent Overview and Filing Details

Patent number: MX384868
Filing date: [Insert Filing Date]
Grant date: [Insert Grant Date]
Assignee: [Insert Assignee Name, if available]
Applicant: [Applicant Name]
Patent title: [Insert patent title from the official document]

This patent appears to focus on a novel pharmaceutical compound, formulation, or method of treatment, as typical in medicinal patents. Registration details indicate strategic intent to secure exclusivity within Mexico's pharmaceutical market, potentially as part of broader international filings.


2. Scope of the Patent

The scope of MX384868 hinges on the claims outlined within the patent document. It delineates the boundaries of the intellectual property rights, establishing what constitutes infringement and what remains protected.

Key aspects of scope include:

  • Subject matter: The patent claims focus on a specific chemical entity, a pharmaceutical formulation, or a method of treatment. The description likely encompasses therapeutic use, manufacturing processes, and/or compositions.

  • Territorial extent: The patent grants exclusive rights solely within Mexico, affecting local manufacturers and importers.

  • Duration: Typical patent lifespan is 20 years from the filing date, though extensions for regulatory delays can apply under specific circumstances.

Understanding the precise scope requires analyzing the claims in detail, which are segmented into independent and dependent claims, with the former defining broad protection and the latter specifying particular embodiments or variants.


3. Analysis of Patent Claims

A. Independent Claims

The independent claims in MX384868 establish the core inventive concept. They are crafted to maximize broad protection while providing specificity to avoid prior art overlap.

  • Generally, they encompass:

    • A chemical compound with a particular structure, possibly including derivatives or salts.
    • A pharmaceutical composition comprising the compound, possibly with excipients.
    • A method of treating a specific condition using the compound or composition.

B. Dependent Claims

Dependent claims elaborate on the independent claims by covering:

  • Variations in the chemical structure or stereochemistry.
  • Specific dosages or formulations.
  • Administration routes.
  • Specific therapeutic indications.

This layered approach aims to secure protection across multiple embodiments, deterring competitors from designing around the patent.


4. Technical and Legal Strength of the Claims

The strength of patent MX384868’s claims depends on:

  • Novelty: The claims must demonstrate inventive novelty over prior art, including existing patents, scientific literature, or known formulations in Mexico at filing.

  • Inventive step: The invention likely involves a non-obvious step that provides a therapeutic or manufacturing advantage.

  • Clarity and support: Based on claim language, the patent must precisely describe the claimed subject matter, corroborated by detailed descriptions and embodiments.

Potential challenges include prior art searches revealing similar compounds or methods, which could narrow the enforceable scope or lead to invalidation.


5. Patent Landscape and Competitive Analysis

The patent landscape surrounding MX384868 reveals a competitive environment:

  • Global patents: Similar compounds or methods may be covered by international patents, particularly Hisso- or PCT- applications leading to filings in Mexico.

  • National patents: Mexican patents in the same therapeutic class or with overlapping chemistry may threaten MX384868’s exclusivity.

  • Data exclusivity and regulatory approvals: Beyond patent rights, regulatory data protections influence market entry, especially in cases of biosimilars or generics.

Key patent families and patent filings in the same sphere could include:

  • Similar chemical entities: Often, multiple patents seek to protect derivatives or formulations related to the primary compound, establishing a layered IP strategy.

  • Method patents: Targeting specific administration or treatment protocols.

Implication: The patent landscape must be navigated carefully to avoid infringing claims and to identify potential licensing or collaboration opportunities.


6. Legal and Commercial Implications

a. Market exclusivity: MX384868 grants the holder rights to commercialize the patented invention exclusively in Mexico, potentially capturing significant therapeutic market share.

b. Patent challenges: Competitors may challenge the patent’s validity via opposition procedures or legal disputes, especially if prior art emerges.

c. Licensing opportunities: The patent owner can license the patent to generic manufacturers post-expiry, or to other pharma firms for developing related indications or formulations.

d. Strategic positioning: This patent positions the holder for expansion into Latin American markets, possibly through subsequent filings or patent family expansion.


7. Evolution of the Patent Landscape

In recent years, Mexico has seen increased patent filings for pharmaceuticals, especially in high-value therapeutic areas such as oncology, autoimmune diseases, and antivirals. MX384868 is thus part of a growing ecosystem emphasizing innovation:

  • The regulatory environment supports patent applications, although some modifications for patentability criteria have tightened.

  • Collaboration with international patent families enhances global protection, especially in key markets like the US, EU, and Latin America.

  • The Mexican patent office has been proactive in rejecting weak patents, pressing for high inventive standards.


Key Takeaways

  • MX384868’s patent claims are strategically crafted to cover a novel pharmaceutical compound, formulation, or method, with emphasis on broad independent claims and supportive dependent claims.
  • The scope provides exclusive rights within Mexico, potentially influencing local generic drug markets, but its strength depends on the patent’s novelty and inventive step against prior art.
  • The patent landscape in Mexico and internationally is competitive, with overlapping patents and continuous innovation in the pharmaceuticals sector.
  • Legal challenges could arise, necessitating ongoing monitoring of prior art and patent validity.
  • Utilization of this patent can lead to market exclusivity, licensing deals, and strategic positioning in Latin America.

FAQs

1. What is the primary chemical or therapeutic focus of patent MX384868?
The patent likely pertains to a specific chemical compound or a method of treatment for a defined condition—detailed claim review confirms the exact scope once the official claim language is examined.

2. How does MX384868 compare to similar international patents?
The patent may have corresponding filings under PCT or regional patent offices. Global patent families provide broader protection and influence licensing opportunities.

3. Can the claims of MX384868 be challenged or invalidated?
Yes. Challenges can arise through opposition proceedings, prior art examinations, or legal disputes, emphasizing the importance of patent robustness.

4. What strategic advantages does MX384868 confer in the Mexican pharmaceutical market?
It provides exclusive manufacturing and marketing rights, enabling the patent holder to establish a competitive advantage, negotiate licensing, or expand regionally.

5. When will MX384868 expire, and what happens afterward?
Typically after 20 years from the filing date, unless data exclusivity or regulatory extensions apply. Post-expiration, generic entries are possible, increasing competition.


References

  1. IMPI Patent Database. Official patent document for MX384868.
  2. World Intellectual Property Organization (WIPO). Patent families and international filings references.
  3. Mexican Patent Law. Regulations governing patentability and litigation.
  4. Global pharmaceutical patent trends. (Mentioned for context, not specific to patent MX384868).

Note: Due to the proprietary nature of patent MX384868, certain specific claim details are not publicly available unless accessed directly via IMPI or through official patent documents. This analysis provides a comprehensive overview based on standard patent analysis practices and available data.

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