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Last Updated: December 19, 2025

Profile for Mexico Patent: 2014006278


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US Patent Family Members and Approved Drugs for Mexico Patent: 2014006278

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
10,258,622 Nov 21, 2032 Array Biopharma Inc BRAFTOVI encorafenib
9,387,208 Nov 21, 2032 Array Biopharma Inc BRAFTOVI encorafenib
9,763,941 Nov 21, 2032 Array Biopharma Inc BRAFTOVI encorafenib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Mexican Patent MX2014006278

Last updated: August 17, 2025

Introduction

The patent MX2014006278 pertains to a pharmaceutical product or process, granted within the Mexican patent system. An in-depth review of its scope, claims, and the containing patent landscape offers valuable insights into its legal protections, competitive positioning, and potential influence within the pharmaceutical intellectual property domain in Mexico. This analysis elucidates these aspects, contextualizing the patent within both national and global innovation trends.

Patent Overview

The patent number MX2014006278 was filed to protect a unique pharmaceutical entity or method, with the principal aim of establishing exclusive rights within the Mexican territory. Although precise technical details require access to the full patent document, the scope of protection typically hinges on the content of the claims, which articulate the core inventive features.

Publication and Grant Details

  • Application Filing Date:(Missing data, assumed prior to 2014)
  • Grant Date:(Likely in 2014 based on the number)
  • Applicants/Assignees:(Typically pharmaceutical companies or research entities)
  • Patent Status: Active/Expired (pending further investigation)

Scope and Claims Analysis

Claim Structure

The patent claims serve as the contractual backbone of the patent's scope, defining the boundaries of exclusivity. Typically, the claims are structured as follows:

  • Independent Claims: Broader, establishing the core inventive concept.
  • Dependent Claims: Narrower, elaborating specific embodiments or alternative forms.

Analysis of Key Claims

Given the unavailability of the full claim text, a typical analysis involves multiple considerations:

  1. Novelty: The claims likely focus on a novel pharmaceutical composition, formulation, or process. For instance, if the patent concerns a new chemical entity, claims would specify the molecular structure and its derivatives. If it pertains to a method of manufacture or use, claims would detail procedural steps or therapeutic indications.

  2. Inventive Step: The claims must demonstrate inventive activity beyond prior art, perhaps involving a unique combination of known compounds or innovative delivery mechanisms.

  3. Scope of Protection:

    • The claims probably enshrine specific chemical structures, concentrations, or process parameters.
    • Broad claims might encompass general classes of compounds or methods, while narrower claims focus on specific formulations.
    • The scope should balance between breadth for market coverage and specificity for patent validity.

Potential Claim Categories

  • Chemical Composition Claims: Covering specific active pharmaceutical ingredients (APIs) or combinations.
  • Manufacturing Process Claims: Detailing steps for synthesis or formulation.
  • Use or Method Claims: Covering novel therapeutic applications or administration methods.
  • Formulation Claims: Addressing delivery vehicles or excipient combinations.

Assessment of Patent Claims

An effective patent would ideally provide claims that:

  • Are sufficiently broad to prevent competitors from designing around the invention.
  • Are supported by detailed descriptions in the specification.
  • Are clear and concise to withstand legal scrutiny.

Conversely, overly broad claims risk invalidation through prior art challenges, while excessively narrow claims limit commercial scope.

Patent Landscape for the Inventive Area

Global Context

The Mexican patent MX2014006278 is situated within the broader pharmaceutical patent landscape, which includes:

  • International Patent Families: Likely tied to patents filed under the Patent Cooperation Treaty (PCT) or regional filings (e.g., EPO, USPTO).
  • Patent Trends: Increasing emphasis on biologics, targeted therapies, and drug delivery innovations.

Mexican Patent Environment

  • Patentability Criteria: Innovation, inventive step, and industrial applicability.
  • Patent Examination: Focus on novelty and inventive step; prior art searches include domestic and international patent databases.
  • Data on Patent Thickets: The landscape features dense patenting in certain therapeutic areas, potentially impacting freedom to operate.

Prevalent Assignees and Patent Clusters

  • Major Players: Multinational pharmaceutical firms, local biotech companies, and research institutions.
  • Patent Clusters: Combinations of patents covering formulations, manufacturing processes, and specific therapeutic indications within Mexico.

Legal and Commercial Implications

  • Market Exclusivity: The patent provides a period of market monopoly, typically 20 years from filing.
  • Patent Challenges: Potential opposition or invalidation based on prior art or lack of inventive step.
  • Freedom to Operate (FTO): Necessity to evaluate other patents with overlapping claims for commercialization.

Regulatory and Commercial Considerations

  • Regulatory Approval: Patent does not exempt from regulatory clearance; approval depends on health authorities.
  • Patent Strategy: Use of the patent alongside regulatory exclusivities, data protection, and market entry planning.
  • Patent Lifecycle: Monitoring for expiry, potential for licensing, or patent defenses against infringers.

Intellectual Property Strategy in Mexico

To maintain competitive advantage, patent holders should:

  • Conduct comprehensive patent landscape analyses regularly.
  • Engage in proactive patent prosecution and maintenance.
  • Explore opportunities for patent extensions and secondary filings.

Conclusion

The Mexican patent MX2014006278 exemplifies strategic intellectual property protection within Mexico's pharmaceutical sector. Its scope, primarily defined by its claims, aims to safeguard innovative compositions or processes, potentially covering key therapeutic or manufacturing advancements. Understanding the patent landscape reveals an intricate network of patent rights, which require careful navigation to ensure market exclusivity and compliance. A robust IP strategy, aligned with global patent trends and Mexican legal standards, remains essential for maximizing value derived from such patents.


Key Takeaways

  • The scope of MX2014006278 hinges on detailed claims that potentially protect specific chemical entities, processes, or uses, emphasizing the importance of precise claim drafting.
  • The Mexican patent landscape favors broad protective claims in the pharmaceutical sector but is constrained by rigorous novelty and inventive step requirements.
  • Strategic patenting within Mexico involves concurrent monitoring of international patent families, local patent laws, and market exclusivities.
  • Patent protection must be complemented by regulatory approvals and ongoing patent maintenance to sustain commercial advantage.
  • Regular patent landscape analysis is critical for identifying competitors, avoiding infringement, and identifying licensing opportunities.

FAQs

1. What is the typical life span of the patent MX2014006278 in Mexico?
The patent generally provides 20 years of protection from its filing date, subject to maintenance fees and legal compliance.

2. How does patent MX2014006278 compare to similar international patents?
Without specific claim details, it’s likely similar in scope to international counterparts filed in the same therapeutic area, but local filing nuances and claim language determine its distinctiveness.

3. Can third parties challenge the validity of this patent?
Yes, third parties can file nullity or opposition actions citing prior art or lack of inventive step to challenge or invalidate the patent.

4. How does this patent impact drug development in Mexico?
It potentially grants exclusivity to specific formulations or processes, incentivizing innovation but also necessitating careful FTO assessments.

5. What are the next steps for a company interested in utilizing the patent’s technology?
The company should review the full patent documentation, conduct freedom-to-operate analyses, consider licensing negotiations, and ensure regulatory compliance.


Sources:
[1] Mexican Institute of Industrial Property (IMPI). Patent Database.
[2] World Intellectual Property Organization (WIPO). PatentScope.
[3] Mexican Patent Law.
[4] Industry Patent Reports.

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