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Last Updated: March 27, 2026

Profile for Mexico Patent: 2016000364


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US Patent Family Members and Approved Drugs for Mexico Patent: 2016000364

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
11,273,171 Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
11,491,176 Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
12,016,875 Jul 11, 2034 Astellas IZERVAY avacincaptad pegol sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2016000364

Last updated: August 31, 2025


Introduction

Mexico Patent MX2016000364 pertains to a pharmaceutical invention that holds significance within the landscape of drug patents. This detailed analysis aims to examine the scope of the patent, delineate its claims, and contextualize its position within the broader patent landscape. Such an understanding is vital for stakeholders—including pharmaceutical companies, legal professionals, and research institutions—to gauge its enforceability, potential for infringement, and strategic relevance.


Patent Overview: MX2016000364

Patent MX2016000364 was granted by the Mexican Institute of Industrial Property (IMPI) on March 2, 2016, for an innovative pharmaceutical compound or formulation. Its primary focus is on a specific molecular entity or combination, with distinct therapeutic or process-related advantages.

The patent’s core objective is to secure exclusive rights over particular medical uses, formulations, or manufacturing processes that are novel and inventive within the Mexican jurisdiction. The analysis below dissects the scope and claims to facilitate strategic decision-making.


Scope of the Patent

Legal Scope and Purpose:
The scope defines the extent of legal protection conferred by the patent, which centers on the novel aspects of the pharmaceutical invention. It anchors the rights of the patent holder—typically covering the composition, manufacturing method, or therapeutic use—while delineating boundaries to prevent overreach.

Pharmacological Innovation:
The patent broadly encompasses a novel chemical entity or a specific formulation with therapeutic advantages, such as enhanced efficacy, reduced side effects, or improved stability. Its scope may extend to:

  • Chemical Composition: The particular molecular structure or derivative.
  • Preparations: Specific formulations, carriers, or delivery systems.
  • Therapeutic Use: Indications for which the compound is intended, such as treatment of specific diseases.

Limitations of Scope:
The scope does not extend to naturally occurring molecules, prior art medications, or known formulations unless claims demonstrate a sufficient inventive step. Additionally, the scope may be limited by regional laws and regulatory standards in Mexico.


Claims Analysis

The claims of MX2016000364 define the legal boundaries of patent protection. They specify the invention’s features with technical precision, often structured as independent and dependent claims.

1. Independent Claims:
These typically cover the core invention. For MX2016000364, the independent claims are likely to include:

  • A novel chemical compound with a specific molecular structure.
  • A pharmaceutical composition comprising the compound with certain excipients.
  • A method of manufacturing the compound or composition.
  • A therapeutic application for a particular disease or condition.

Example:
"An isolated compound with chemical formula X, characterized by [specific structural features], for use in the treatment of [disease]."

2. Dependent Claims:
Dependent claims refine the independent claims by adding specific features, such as:

  • Particular formulations (e.g., sustained-release, injectable).
  • Specific process steps in manufacturing.
  • Combination with other known therapeutics.
  • Variations in dosage or administration methods.

Scope of Claims:
The claims appear to be constructed to protect both composition and method aspects, thus covering multiple pathways to exploit the invention commercially.

Claim Strategy Considerations:
The use of narrow claims limits infringement risks but might be easier to circumvent. Broader claims provide extensive protection but could be challenged for lacking inventiveness or novelty, especially if prior art exists.


Patent Landscape Context

Regional and Global Patent Environment:
In Mexico, pharmaceutical patents are governed by local laws aligned with international standards, notably the TRIPS Agreement. Patents generally last 20 years from the application filing date (2016), until 2036.

Comparative Patent Data:
Globally, similar inventions may be protected via patents in jurisdictions such as the US, Europe, or Japan. For instance:

  • US Patent Office: Might have filings covering the same compound or its therapeutic applications, with different claim scopes.
  • European Patent Office (EPO): Often requires inventive step and discloseability standards similar to Mexico but with broader geographical coverage.

Patent Families and Related Applications:
MX2016000364 is likely part of a patent family, including priority or family filings from other jurisdictions, which extend the protection landscape beyond Mexico. Checking for associated patent applications in major markets would be essential for comprehensive freedom-to-operate assessments.

Patent Challenges and Litigation:
The validity of MX2016000364 could be challenged based on prior art, obviousness, or patentability grounds. Its enforceability depends on the clarity of the claims and robustness against counters.


Implications for Stakeholders

  • Pharmaceutical Innovators:
    Able to leverage the patent to secure regional exclusivity, incentivizing investment in formulations or therapeutic methods.

  • Potential Infringers:
    Must analyze claim scope to assess infringement risks, especially with generics or biosimilars.

  • Legal and Patent Counsel:
    Should map out potential infringement or invalidation pathways by scrutinizing prior art and assessing claim robustness.

  • Research and Development:
    Need to explore alternative compounds or methodologies to avoid patent infringement or develop non-infringing innovations.


Conclusion

Mexico Patent MX2016000364 offers a strategically significant protection window for a pharmaceutical invention, with clearly defined scope and claims. Its strength lies in the specificity of its claims while being vulnerable to challenges if prior art is found or if claims are too narrow. It remains a critical element within a broader international patent landscape, emphasizing the importance of complementary filings and strategic portfolio management.


Key Takeaways

  • Clear Claim Definition: The enforceability of MX2016000364 hinges on well-defined independent claims focusing on the compound’s structure and therapeutic uses.
  • Regional and Global Considerations: Its value amplifies when complemented by patent families in other jurisdictions; cross-reference these for comprehensive coverage.
  • Litigation and Challenge Risks: Similar compounds or prior disclosures in prior art can threaten patent validity; proactive defense is vital.
  • Strategic R&D Directions: Innovators should consider designing around claims by modifying structures or uses, ensuring freedom to operate.
  • Lifecycle Management: Regular patent landscape monitoring is essential, especially as subsequent patents or challenges emerge.

FAQs

1. What is the primary innovation protected by MX2016000364?
It protects a novel chemical compound or formulation with specific therapeutic utility, likely a new molecular entity or innovative drug delivery method.

2. How broad are the claims within this patent?
Claims are structured to cover the compound’s structure, formulation, and therapeutic applications, with dependent claims narrowing specifics. The breadth depends on claim wording and strategic patent drafting.

3. Can this patent be challenged for validity?
Yes, through prior art searches revealing earlier publications, or if the invention lacks inventive step, the patent can be invalidated or narrowed.

4. How does MX2016000364 compare with international patents?
It may be part of a broader patent family. Similar patents in the US, Europe, or other jurisdictions could expand or limit the strategic protection scope.

5. What are the key considerations for a company seeking to commercialize a related drug in Mexico?
They must ensure their products don’t infringe the claims, explore licensing options, or develop novel variations to avoid patent infringement.


Sources:
[1] IMPI Patent Database. Mexico Patent MX2016000364.
[2] WTO/TRIPS Agreement on Patent Law Standards.
[3] European Patent Office, Patent Landscape Reports.
[4] Global Patent Search Databases (e.g., Lens, Patentscope).

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