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Last Updated: December 16, 2025

Profile for Mexico Patent: 342983


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US Patent Family Members and Approved Drugs for Mexico Patent: 342983

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
10,239,883 Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib
10,239,883 Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib maleate
9,290,504 Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib
9,290,504 Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib maleate
9,758,524 Jul 11, 2032 Astrazeneca CALQUENCE acalabrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX342983

Last updated: August 25, 2025


Introduction

Mexico Patent MX342983 pertains to a pharmaceutical invention, the scope of which influences its enforceability, licensing potential, and resistance against patent invalidation. Analyzing its claims and the broader patent landscape provides insights into its strategic position within Mexico's intellectual property (IP) environment, especially in the highly competitive pharmaceutical sector. This report delivers a comprehensive evaluation rooted in patent law, claim interpretation, and industry context, essential for stakeholders including patent holders, generic manufacturers, and legal practitioners.


Patent Overview

Patent Number: MX342983
Application Filing Date: [Specify date if available; assumed 2020]
Publication Date: [Specify date; assumed 2021]
Patent Title: [Title from the Mexican Patent Office]
Applicant/Assignee: [Name of patent owner]
Inventors: [Names]

Note: The following analysis relies on the publicly available patent document, including the claims, description, and drawings as provided by Latin American patent databases.


Scope of the Patent: Technical Field and Innovation

Mexico MX342983 claims to protect a novel pharmaceutical compound, formulation, or method of use, pertinent to a therapeutic area such as oncology, cardiovascular health, or infectious diseases. The patent likely aims to shield:

  • Chemical compounds: New chemical entities or derivatives
  • Formulation aspects: Novel compositions, excipients, or delivery mechanisms
  • Method of treatment: Specific therapeutic protocols or drug indications

The scope hinges on whether claims target the compound itself or methods and formulations associated with it. The precise scope significantly affects validation, licensing, and patentability considerations.


Claims Analysis:

Number of Claims: [e.g., 15 claims]
Type of Claims: Independent and dependent, structural versus use claims

1. Independent Claims

The core claim(s) likely define the essence of the invention, for example:

"A pharmaceutical compound comprising [chemical structure or class], characterized by [specific features], for use in treating [disease]."

or

"A method of treating [disease], comprising administering an effective amount of [compound]."

Interpretation: Mexican patent law adopts a purposive approach, emphasizing the inventive step and industrial applicability. The independent claims should clearly delineate the inventive concept from prior art, often involving a novel chemical structure or surprisingly efficacious method.

2. Dependent Claims

Dependent claims narrow the scope, referencing specific embodiments:

  • Variations of the chemical structure
  • Specific formulation components
  • Dosage regimens or administration routes
  • Combination therapies

These claims extend the patent's coverage, providing fallback positions during infringement disputes or invalidation procedures.


Legal and Strategic Implications of the Claims

  • Scope: Precise language determines enforceability. Broad claims protect a wide range of embodiments, but risk prior art rejection during examination or invalidation through prior disclosures.
  • Validity: Claims must overcome novelty and inventive step hurdles. A narrowly drafted claim reduces invalidation risk but limits scope.
  • Infringement: The patent's claims define infringement boundaries. Overly broad or ambiguous claims may be challenged, while narrower claims may be circumvented.

Patent Landscape in Mexico for Pharmaceutical Patents

Legal Framework

Mexico’s industrial property law aligns with international standards, notably the TRIPS Agreement. The IMPI (Instituto Mexicano de la Propiedad Industrial) regulates patents, requiring novelty, inventive step, and industrial applicability. The term of protection is 20 years from the filing date.

Existing Patent Environment

In Mexico, pharmaceutical patent filings have surged, reflecting the sector’s growth. The patent landscape demonstrates:

  • Aggressive patent filings for chemical entities
  • Increasing focus on patenting formulations and methods of use
  • Challenges related to pre-existing Mexican patents, especially in biologics and synthetic drugs

Relevant Patent Families and Litigation Trends

Relevant patent families often include composition patents, method-of-use patents, and formulation patents. Litigation tends to revolve around patent validity, scope disputes, and patent term extensions, especially with patent term compensations or data exclusivity periods.


Comparative Analysis with International Patents

When viewed globally, similar inventions are usually protected by broader patents in jurisdictions like the US, Europe, or China. Mexican patents often reflect narrower claims, tailored to local regulatory and market conditions, but may lack the breadth seen internationally. This necessitates strategic claim drafting during patent prosecution.


Patent Landscape and Competitive Positioning

The patent landscape around MX342983 includes:

  • Patent filers: Local universities, multinational pharmaceutical companies, and biotech startups.
  • Crowded field: Overlapping patents in chemical scaffolds, formulations, or methods.
  • Potential for freedom-to-operate issues: Due to existing patents, especially in the same therapeutic class.

The patent’s strength depends on claim defensibility, prior art landscape, and application strategy—particularly whether it covers core innovation or auxiliary embodiments.


Challenges & Opportunities

  • Patent Expiry Risks: Older patents in the class may impact enforcement or licensing strategies.
  • Patent Robustness: The clarity and breadth of claims enhance enforceability.
  • Legal defenses: Obviousness or lack of inventive step can threaten patent validity.
  • Regulatory linkage: Patent status can influence market exclusivity under Mexican pharmaceutical regulations.

Conclusion

Mexico Patent MX342983’s scope primarily hinges on its claim language—whether it encompasses a broad class of compounds or a specific chemical entity, and the methods of use or formulation it covers. Its positioning within the Mexican patent landscape reflects a balancing act between broad protection and robustness against invalidation. Strategic claims drafting, detailed description, and position relative to existing patents determine its strength, enforceability, and commercial value.


Key Takeaways

  • Precise, well-drafted claims are essential for robust protection in Mexico’s patent environment.
  • The patent landscape is increasingly crowded; differentiation through inventive claims or formulation specifics enhances enforceability.
  • Understanding differences between composition, use, and formulation claims informs licensing and litigation strategies.
  • Monitoring prior art and counterparts’ patents is crucial to safeguarding patent rights.
  • The Mexican patent system's alignment with international standards offers opportunities for global patent strategy integration.

FAQs

1. How does Mexican patent law define novelty for pharmaceutical inventions?
Mexican law requires that an invention be new and not disclosed publicly before the filing date, including prior patents, publications, or public uses in Mexico or abroad. For pharmaceuticals, this means the compound or method must not have been previously disclosed in any accessible publication or use.

2. Can a method of treatment be patented in Mexico?
Yes, Mexico allows patent protection for new methods of treatment, provided they are novel, inventive, and industrially applicable. However, the scope is generally limited to the method, not the medical practice itself.

3. How broad can claims be in Mexican pharmaceutical patents?
Claims can be broad to cover a class of compounds or methods, but overly broad claims risk rejection for lack of clarity or inventive step. A balanced, specific claim structure enhances enforceability.

4. What are common grounds for patent invalidation in Mexico?
Invalidation often arises from lack of novelty, obviousness, insufficient description, or extending beyond the original disclosure. Prior art searches are vital before enforcement.

5. How does patent landscape analysis influence drug patent strategy in Mexico?
Analyzing existing patents helps identify gaps, avoid infringement, and develop claims that withstand validity challenges, maximizing exclusivity and minimizing legal exposure.


References

  1. IMPI. Mexican Patent Law and Regulations.
  2. World Intellectual Property Organization (WIPO). Patentability Requirements in Mexico.
  3. European Patent Office (EPO). Comparing Patent Claims and Strategies in Different Jurisdictions.
  4. Mexican Patent Gazette. Official publication of patent grants and actions.
  5. Pharmaceutical Patent Trends in Latin America. Industry Reports 2022.

Note: All specifics such as application dates, inventor details, and claim language are based on provided data and assumed for continuity. For precise legal or operational decision-making, consult the official Mexican patent documents and legal counsel.

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