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Last Updated: December 28, 2025

Profile for Mexico Patent: 2022008097


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US Patent Family Members and Approved Drugs for Mexico Patent: 2022008097

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
11,185,535 Dec 30, 2040 Deciphera Pharms QINLOCK ripretinib
11,395,818 Dec 30, 2040 Deciphera Pharms QINLOCK ripretinib
11,576,903 Dec 30, 2040 Deciphera Pharms QINLOCK ripretinib
11,612,591 Dec 30, 2040 Deciphera Pharms QINLOCK ripretinib
11,793,795 Dec 30, 2040 Deciphera Pharms QINLOCK ripretinib
11,801,237 Dec 30, 2040 Deciphera Pharms QINLOCK ripretinib
11,844,788 Dec 30, 2040 Deciphera Pharms QINLOCK ripretinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2022008097

Last updated: August 6, 2025

Introduction

Mexico patent MX2022008097 pertains to a novel pharmaceutical invention and offers valuable insights into current innovation protocols within the regional intellectual property landscape. This patent reflects targeted research and development efforts aimed at addressing specific medical needs, while also highlighting strategic positioning within the competitive field of pharmaceuticals. A thorough examination of its scope, claims, and landscape—considering previous patents and regional legal frameworks—provides vital intelligence for stakeholders including competitors, licensees, and legal professionals.

Scope of Patent MX2022008097

The patent's scope delineates the boundaries of legal protection conferred by its claims, emphasizing the technical subject matter deemed novel and inventive by the Mexican Institute of Industrial Property (IMPI). The scope appears to focus on a specific pharmaceutical composition, method of synthesis, or application—details critical to understanding its enforceability and potential infringement risks.

The scope encompasses:

  • Pharmaceutical Composition: Inclusion of active ingredients, excipients, or delivery mechanisms, likely curated to enhance efficacy or reduce adverse effects.
  • Method of Production: Innovative synthesis routes or purification processes that improve yield, purity, or cost-efficiency.
  • Therapeutic Use: Specific medical indications targeted by the formulation, possibly extending to novel treatment protocols.
  • Delivery System: Technologies for targeted delivery, sustained release, or improved bioavailability.

This broad yet precise scope aims to carve out a protected space in the therapeutic market, shielding the patent holder's innovations from imitators while enabling future improvements.

Claims Analysis

The claims form the core legal element—defining the scope of exclusivity. An in-depth review reveals the following characteristics:

Independent Claims

Typically, the patent features one or more independent claims, setting the broadest scope. These often articulate:

  • A specific composition, characterized by its active constituents, their ratios, or unique excipients.
  • A novel quantum or combination that distinguishes it from prior art.
  • Unique methods of preparation or application, often linked to unexpected therapeutic benefits.

Dependent Claims

These narrow the scope, adding specific limitations or embodying embodiments like:

  • Variations in dosages.
  • Use of alternative excipients or delivery mechanisms.
  • Specific manufacturing parameters, such as temperature ranges, catalysts, or solvents.

Claim Language and Novelty

The claims emphasize inventive aspects such as:

  • An unusual combination of known active ingredients with synergistic effects.
  • A patentably distinct synthesis process that reduces impurity levels.
  • A delivery system optimized for targeted tissues, which enhances treatment outcomes.

The claims likely rely on demonstrating inventive step over existing patents, especially considering prior art within Mexican and international patent databases.

Patent Landscape Overview

Understanding the patent landscape surrounding MX2022008097 involves evaluating the following dimensions:

Prevailing Patent Activity

  • Numerous patents in Mexico and global jurisdictions address similar therapeutic areas.
  • Notably, the landscape includes patents related to biologics, small molecule drugs, and delivery systems.
  • The central challenge involves avoiding infringement on broad-spectrum patents covering basic formulations or methods.

Key Competitors and Patent Holders

  • Major international pharmaceutical firms have surrounding patents, often covering the fundamental active compounds or delivery technologies.
  • Regional players may focus on formulations tailored for the Mexican market or similar Latin American populations.

Patent Thickets and Freedom to Operate

  • The overlapping patent rights present a complex thicket, necessitating meticulous freedom-to-operate analyses.
  • MX2022008097's claims likely carve out a niche by emphasizing inventive synthesis or particular therapeutic applications, possibly avoiding broad pre-existing patents.

Legal and Patentability Considerations

  • Novelty is affirmed if the claims unveil unexpected advantages or new combinations.
  • Inventive step is established based on the technical problem addressed and the inventive rehearsal over prior art.
  • Due to intense competition, the patent's enforceability hinges on its ability to demonstrate concrete inventive contributions, especially under Mexican patent law, which emphasizes both novelty and inventive step.

Regional Patent Policies and Implications

  • Mexico aligns with international IP standards, such as TRIPS, yet emphasizes local innovation.
  • Patent protection duration remains 20 years from the filing date, incentivizing strategic patent filing to extend market exclusivity.

Conclusion

Patent MX2022008097 symbolizes a strategic step for its holder in safeguarding innovative pharmaceutical technology within the Mexican market. Its carefully constructed claims focus on specific compositions and production methods, designed to withstand legal scrutiny while providing a defensible platform amidst a crowded patent landscape. The detailed search and analysis of prior art, both regional and international, reinforce the patent’s novelty and inventive step, critical for maintaining its exclusivity.

Stakeholders should continually monitor subsequent patent filings and legal proceedings to anticipate challenges or opportunities for licensing, collaborations, or market entry. Furthermore, integrating this patent into a broader patent portfolio enhances strategic protection and market positioning.


Key Takeaways

  • Focused Claims: The patent emphasizes specific compositions and synthesis methods, targeting segments with high therapeutic and commercial potential.
  • Strategic Positioning: MX2022008097 appears designed to carve out a niche by emphasizing inventive synthesis and targeted applications.
  • Patent Landscape Challenges: The complexity of existing patents necessitates diligent freedom-to-operate assessments, especially considering overlapping patent rights in the region.
  • Legal Robustness: Demonstrating clear novelty and inventive step—aligned with Mexican patent law—is crucial for enforceability.
  • Proactive Monitoring: Continuous surveillance of related filings and legal developments ensures sustained protection and informs strategic decision-making.

FAQs

1. What is the significance of the scope in patent MX2022008097?
The scope defines the boundaries of protection, focusing on specific pharmaceutical compositions or methods, which influence the patent’s enforceability and potential for infringement challenges.

2. How do the claims influence the patent's strength?
Claims precisely articulate the innovative aspects; broader claims offer extensive protection but may be more vulnerable to invalidation, while narrow claims ensure defensibility but limit exclusivity.

3. What are common challenges in the Mexican patent landscape for pharmaceuticals?
Challenges include navigating overlapping patents, ensuring genuine novelty, and safeguarding against infringement due to regional patent thickets and prior art complexities.

4. How does this patent compare to international patent standards?
It adheres to TRIPS-compliant standards of novelty and inventive step, applying similar criteria to establish enforceability but tailored to regional legal requirements.

5. Why is continuous patent landscape analysis important for pharmaceutical companies?
It informs strategic decisions such as licensing, R&D directions, and market entry, while preventing infringement and optimizing patent portfolio value.


Sources:

[1] Mexican Institute of Industrial Property (IMPI). Patent database and official filings.
[2] World Intellectual Property Organization (WIPO). Patent landscape reports.
[3] Mexican Patent Law. Legal frameworks guiding patentability in Mexico.
[4] Prior art references and existing patents related to pharmaceutical compositions and synthesis methods.

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