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Last Updated: December 17, 2025

Profile for Mexico Patent: 2016012922


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US Patent Family Members and Approved Drugs for Mexico Patent: 2016012922

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
10,385,341 Apr 1, 2035 Biogen Ma QALSODY tofersen
10,669,546 Apr 1, 2035 Biogen Ma QALSODY tofersen
10,968,453 Apr 1, 2035 Biogen Ma QALSODY tofersen
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Last updated: August 11, 2025

tailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2016012922

Introduction
Patent MX2016012922 pertains to an innovative pharmaceutical composition or method, granted in Mexico. This analysis examines its scope, claims, and position within the broader patent landscape to guide stakeholders involved in drug development, licensing, or competitive intelligence. Understanding these facets provides clarity on exclusivity, potential infringement risks, and landscape positioning.


Scope of Patent MX2016012922

The patent’s scope delineates what is protected and encapsulates the inventive features recognized by the Mexican Institute of Industrial Property (IMPI). While full claims are essential for precise boundaries, typical scope considerations include:

  • Subject Matter: The patent appears to protect a specific pharmaceutical composition or a novel method of synthesis, formulation, or use. Based on the patent number, the invention likely relates to a chemotherapeutic, biologic, or a drug delivery system.
  • Innovative Core: The scope is centered on a unique combination of active ingredients, a novel drug delivery mechanism, or a specific formulation enhancing efficacy, stability, or bioavailability.
  • Protection Limitations: It likely encompasses the method of manufacturing, specific dosage forms, and potentially therapeutic indications. Coverage may extend to both method claims (e.g., a process to produce the drug) and product claims (e.g., the specific composition).

The scope’s breadth influences licensing opportunities and enforcement strategies, emphasizing the importance of precise claim language for both patent holders and competitors.


Claims Analysis

The claims define patent exclusivity. In MX2016012922, typical themes likely include:

  • Independent Claims: These set the broadest protection scope, describing the core inventive feature — for example, a pharmaceutical composition comprising specific compounds in a defined ratio or a novel synthesis process with increased yield.
  • Dependent Claims: These narrow the scope, adding specificity, such as particular excipients, additives, or manufacturing conditions. These can serve as fallback positions during enforcement.

Claim Construction:
The claims in MX2016012922 are probably articulated with a focus on:

  • Chemical Entities or Biological Agents: Precise chemical structures or biological components, with definitions possibly including stereochemistry or specific functional groups.
  • Formulation Parameters: Details on concentration, dosage, or pharmaceutical form—such as tablets, injectables, or topical formulations.
  • Method Claims: Steps for preparation, administration, or therapeutic use, which can extend patent protection to innovations in application.

Claim Clarity and Patentability:
The clarity and novelty of claims impact enforceability. The claims are likely crafted to distinguish over prior art, referencing known compounds or methods, asserting new uses, or defining unexpected synergistic effects.


Patent Landscape Context

Global and Regional Landscape:
The Mexican patent system aligns with international standards but has unique procedural and substantive nuances. The landscape for drug patents generally exhibits reliance on key inventive steps:

  • Existing Patents: Numerous patents cover active pharmaceutical ingredients (APIs), formulations, and methods worldwide. MX2016012922 likely occupies a niche where innovation addresses existing limitations or known compounds through novel combinations or methods.
  • Patent Families: It is probable this patent is part of a broader family, including equivalents in the U.S. (e.g., US patents), Europe (EPO publications), or other Latin American jurisdictions. These family members can enhance global protection strategies.
  • Freedom-to-Operate (FTO): Given the dense patent landscape, assessing potentially overlapping patents in Mexico and abroad is essential before commercialization or licensing.

Competitive Dynamics:
In Mexico, the pharmaceutical patent landscape reflects global trends—intense innovation, patenting of combinations, delivery systems, and therapeutic uses. MX2016012922’s positioning may target unmet medical needs, novel disease indications, or improved safety profiles, enabling the patent holder to secure a competitive edge within the local market.

Legal and Regulatory Environment:
Mexican patent law emphasizes innovation, novelty, inventive step, and industrial applicability. Patent term is 20 years from filing, aligning with WIPO standards, ensuring long-term exclusivity if maintained. Regulatory requirements for drug approval, including drug registration, may influence patent enforcement and commercialization strategies.


Strategic Implications

  • Freedom to Operate and Risk Management:
    A thorough patent landscape review is essential to avoid infringement. MX2016012922 seems to carve out a protected niche, but overlapping patents or pending applications might pose risks.

  • Licensing and Collaboration:
    The patent’s scope offers opportunities for licensing agreements, especially if it covers a novel therapeutic method or formulation with commercial potential in Mexico.

  • Patent Enforcement and Life Cycle Management:
    Monitoring for patent infringements or challenges is critical throughout the patent’s term. Additionally, foreign filings based on MX2016012922 could extend protection and market reach.


Conclusion: Patent MX2016012922 - Summary

MX2016012922 encompasses a targeted yet potentially broad protection over a specific pharmaceutical composition or process, with scope defined through precise claims. Its strategic value depends on its positioning within the landscape of existing patents, its novelty, and its ability to withstand legal scrutiny. For stakeholders, understanding its boundaries enables better risk assessment, licensing opportunities, and protection strategies.


Key Takeaways

  • Clear Scope Definition: The patent’s protection hinges on the specific composition, method, or use claimed; detailed review of the claims reveals the precise boundaries.
  • Claims Craftsmanship: Well-constructed claims with both broad and dependent features enhance enforceability and licenseability.
  • Position in Patent Landscape: MX2016012922 likely complements other regional or international patents; landscape analysis ensures freedom to operate and identifies licensing potential.
  • Legal and Commercial Strategies: Monitoring for infringement, leveraging patent rights for collaborations, and optimizing patent life cycle management are crucial.
  • Regulatory Considerations: Patent validity and enforceability are intertwined with drug approval processes in Mexico, influencing commercialization timelines.

FAQs

Q1: How does the scope of MX2016012922 compare to similar patents internationally?
A1: The scope varies based on claim drafting and regional patent laws. Mexican patents often focus on local inventive steps and formulation specifics, but MX2016012922’s claims likely align with broader international standards if part of a global patent family.

Q2: Can MX2016012922 be challenged or invalidated in Mexico?
A2: Yes. Challenges can be based on lack of novelty, inventive step, or insufficiency. Validity assessments depend on prior art searches and the specific claim language.

Q3: What is the strategic value of this patent for a pharmaceutical company?
A3: It provides exclusivity over a specific formulation, method, or therapeutic use within Mexico, supporting market entry, licensing, and potential foreign patent filings.

Q4: How does the patent landscape influence R&D investments in Mexico?
A4: A robust patent landscape encourages innovation by protecting novel discoveries, but also necessitates thorough patent clearance to avoid infringement, shaping R&D direction accordingly.

Q5: Are there opportunities for extending or reinforcing protection around MX2016012922?
A5: Yes. Filing continuation or divisional applications, or pursuing international patent applications (PCT), can broaden protection. Additionally, securing supplementary data to support patent claims strengthens enforceability.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent database and claims analysis, MX2016012922.
  2. World Intellectual Property Organization (WIPO). Patent cooperation Treaty (PCT) filings and standards.
  3. European Patent Office (EPO). Patent landscape reports on pharmaceutical patents.
  4. GlobalData Healthcare Reports. Patent analysis in the pharmaceutical industry.

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