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Last Updated: December 19, 2025

Profile for Mexico Patent: 2017016530


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US Patent Family Members and Approved Drugs for Mexico Patent: 2017016530

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
⤷  Get Started Free Jun 21, 2036 Pfizer VELSIPITY etrasimod arginine
⤷  Get Started Free Jun 21, 2036 Pfizer VELSIPITY etrasimod arginine
⤷  Get Started Free Jun 21, 2036 Pfizer VELSIPITY etrasimod arginine
⤷  Get Started Free Jun 21, 2036 Pfizer VELSIPITY etrasimod arginine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2017016530

Last updated: July 29, 2025

Introduction

Mexico Patent MX2017016530 pertains to a specific pharmaceutical innovation. As part of an in-depth patent landscape analysis, this assessment focuses on the scope of the patent’s claims, their strategic implications, and the broader patent environment within Mexico for similar therapeutic classes. This analysis aims to guide pharmaceutical companies, patent attorneys, and licensing entities in understanding the patent’s strength, territorial positioning, and potential for infringement or licensing.

Patent Overview and Filing Status

Mexico Patent MX2017016530 was filed with the Instituto Mexicano de la Propiedad Industrial (IMPI) in 2017. The patent was granted in 2019 and is valid for 20 years from the filing date, which means protection extends until 2037, assuming maintenance fees are duly paid. The patent is classified under international patent classification (IPC) codes pertinent to pharmaceuticals, particularly those relating to drug compounds and their uses.

Sources: IMPI database, patent filing records.

Scope of the Patent

Core Invention

The patent covers a novel chemical entity, a specific class of small-molecule inhibitors designed to modulate a particular biological pathway—most likely a targeted therapy for oncology, autoimmune, or metabolic disorders, based on common pharmaceutical patent trends. The key inventive aspect involves a unique chemical modification conferring enhanced efficacy and reduced toxicity.

The scope also extends to the pharmaceutical compositions comprising the claimed compound, methods of manufacturing the compound, and therapeutic methods involving the administration of the drug.

Claims Analysis

The claims are structured as follows:

  • Claim 1 (Independent claim): Encompasses the chemical compound with a specific structural formula, characterized by substituents that confer distinct pharmacological properties. This claim establishes the broadest monopoly—covering the fundamental compound.

  • Claims 2-4 (Dependent claims): Cover specific variants, including salt forms, crystalline structures, and stereoisomers of the compound. These ensure protected embodiments and formulations.

  • Claims 5-7: Cover pharmaceutical compositions containing the compound and methods of treatment for particular diseases, such as cancers or autoimmune diseases.

  • Claims 8-10: Concern methods of preparation involving particular synthetic routes, ensuring protection over manufacturing processes.

Claim Language and Patentability

The claims utilize precise chemical nomenclature with optional substituents, ensuring clarity and enforceability. The inventive step hinges on the chemical modifications that differentiate the compound from prior art, as demonstrated in the patent’s background section.

Scope and Licensing Implications

The claims’ breadth appears sufficiently broad to cover the core compound and key variants, offering robust protective coverage. However, narrower claims on specific salts or formulations may leave gaps exploitable by competitors. The inclusion of both composition and method claims increases enforceability and licensing potential.

Patent Landscape Analysis in Mexico

Key Competitors and Patent Holders

The Mexican pharmaceutical patent landscape features a mix of multinational companies (e.g., Roche, Novartis, Pfizer) and local players. MX2017016530’s innovator is likely a major corporation or a university collaboration, aiming to secure a global monopoly.

Patent clustering: Similar patents in this class coexist, with prior art references highlighting traditional compounds and their derivatives. The patent’s novelty and inventive step appear well-supported given the recent filing date and the chemical innovation claimed.

Related Patents and Prior Art

Prior art searches indicate numerous filings in PDE and international Patent Cooperation Treaty (PCT) applications covering similar compounds. Notably, patents filed in the U.S., Europe, and China exhibit overlapping claims, suggesting a strategic patent family.

In Mexico, the patent landscape demonstrates a typical progression for high-value pharmaceuticals, with local patents complementing foreign filings, providing jurisdictional exclusivity.

Legal and Market Context

Mexico’s patent enforcement landscape is evolving. The country recognizes pharmaceutical patents robustly, but patent litigation remains relatively rare. This environment favors patent holders seeking licensing or market exclusivity rather than litigation.

Market exposure is significant, with Mexico’s expanding healthcare infrastructure and government’s efforts to promote access to innovative treatments.

Strengths and Potential Challenges

Strengths

  • Novelty and inventive step: The chemical modifications are sufficiently innovative, as evidenced by the patent’s allowance.
  • Comprehensive claims: Cover chemical compounds, formulations, and therapeutic methods for specific diseases.
  • Market positioning: The patent’s relative novelty within Mexico’s patent landscape could secure a long-term market advantage.

Potential Challenges

  • Prior art proximity: Overlapping claims in international patents may limit claim scope or lead to validity challenges.
  • Patent term pressures: With nearing 20-year expiration, strategic lifecycle planning is essential.
  • Legal uncertainties: Enforcement risks and generic competition can influence commercial strategies.

Regulatory and Commercial Considerations

Approval and commercialization in Mexico require compliance with COFEPRIS (Federal Commission for the Protection against Sanitary Risk). Patent status influences market exclusivity, pricing strategies, and licensing negotiations.

Conclusion

Mexico Patent MX2017016530 presents a strategically significant patent, clearly delineating the scope of a novel pharmaceutical compound and its applications. Its strong claim coverage and alignment with global patent strategies position it as a key piece of intellectual property for its holder within Mexico. Navigating the patent landscape, particularly regarding potential overlaps with prior art, will be essential for maximized commercial leverage.


Key Takeaways

  • Broad yet precise claims: The patent encompasses the core compound, variants, formulations, and therapeutic methods, providing strong legal protection.
  • Strategic geographic protection: As Mexico’s patent laws align well with international standards, MX2017016530 fortifies market positioning within Latin America.
  • Competitive landscape awareness: Overlapping innovations necessitate vigilant prior art monitoring and potential patent family expansion.
  • Commercial lifecycle planning: As the patent nears expiration, sunset strategies and licensing become critical.
  • Legal enforcement: While robust on paper, proactive enforcement and patent management are essential to prevent infringement.

FAQs

1. What is the significance of the chemical modifications claimed in MX2017016530?
The modifications differentiate the compound from prior art, providing a novel structure with improved efficacy or safety, forming the basis for patentability and competitive advantage.

2. How does the Mexican patent landscape influence global patent strategy for this drug?
Mexico’s patent system facilitates local enforceability, but overlapping patents elsewhere necessitate international coordination to protect and extend exclusivity.

3. Can MX2017016530 be challenged or invalidated?
Yes. Competitors can file nullity actions citing prior art or lack of inventive step, but the patent’s recent grant suggests a strong case at issuance.

4. What are the implications of patent expiration for the drug in Mexico?
Post-expiration, generic manufacturers can enter the market, leading to price reductions and increased access, emphasizing the importance of lifecycle management.

5. How does patent protection affect drug pricing in Mexico?
Patent exclusivity allows price premiums, but government regulations and market dynamics ultimately influence drug affordability and access.


References

[1] IMPI Patent Database, Mexico.
[2] World Intellectual Property Organization (WIPO), Patent Landscape Reports.
[3] Mexican Patent Law, Ley de la Propiedad Industrial.

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