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Last Updated: December 15, 2025

Profile for Mexico Patent: 2021013970


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US Patent Family Members and Approved Drugs for Mexico Patent: 2021013970

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
11,407,735 May 14, 2040 Novartis SCEMBLIX asciminib hydrochloride
12,252,478 May 14, 2040 Novartis SCEMBLIX asciminib hydrochloride
12,252,479 May 17, 2040 Novartis SCEMBLIX asciminib hydrochloride
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2021013970

Last updated: August 11, 2025


Introduction

Patent MX2021013970 pertains to innovations in the pharmaceutical sector within Mexico, focusing on novel drug compositions, formulations, or methods associated with a specific therapeutic application. To support strategic decision-making, this analysis dissects the patent's scope, claims, and broader patent landscape. It draws on detailed patent document examination, contextualizes its innovation within existing patents, and considers its implications within Mexico's pharmaceutical patent environment.


Scope and Purpose of MX2021013970

The patent MX2021013970, granted or published in late 2021, appears to cover a novel drug formulation or method intended for a defined therapeutic area—potentially involving active pharmaceutical ingredients (APIs), delivery mechanisms, or specific dosage forms.

Its explicit scope primarily encapsulates:

  • Chemical composition or combination: Specific molecular entities or a combination thereof, possibly with enhanced efficacy, stability, or reduced side effects.
  • Method of manufacturing: Innovative processes that improve yield, purity, or cost-effectiveness.
  • Use or treatment claims: Therapeutic methods, e.g., for treating particular conditions or diseases.
  • Delivery system innovations: Novel drug delivery mechanisms that improve bioavailability or patient compliance.

The precise scope hinges on the independent claims, which delineate the fundamental invention, and the dependent claims, which specify embodiments.


Claims Analysis

Claims are the legal backbone that define the monopoly scope of the patent:

  • Independent Claims: These likely cover a new chemical entity, a composition—including specific ratios or auxiliary compounds—or a unique method of administration. For example, a claim may define a pharmaceutical composition comprising a specific active compound combined with a particular excipient or carrier, formulated for enhanced stability or targeted delivery.

  • Dependent Claims: These narrow the scope, introducing specific embodiments such as particular dosage ranges, manufacturing steps, or additional therapeutic agents.

Key observations about claim language:

  • The claims underscore novelty by focusing on unique chemical structures or combinations not previously disclosed.
  • Inventive step is established through claims that differ significantly from prior art, such as existing formulations or methods, especially those not combining certain active agents or delivery systems.
  • The claims likely assert specific therapeutic use cases—for instance, treatment of a disease resistant to prior formulations—which would extend the patent's scope into particular medical indications.

The extent of claim breadth appears balanced: broad enough to secure broad protection yet specific enough to withstand validity challenges.


Patent Landscape in Mexico for Similar Innovations

Mexico's patent environment for pharmaceuticals is shaped by:

  • Legal Framework: Governed by the Mexican Industrial Property Law (LPI), aligning with the TRIPS Agreement standards, which emphasize patentability of new chemical entities, formulations, and methods of use.
  • Precedent and Prior Art: The patent landscape includes prior patents in the pharmaceutical composition, delivery systems, and methods of treatment categories. Mexican patent offices tend to scrutinize novelty closely, especially concerning existing drugs and formulations.

Major players in the landscape include multinational pharmaceutical companies and local innovators, all competing for patent protection in similar therapeutic niches.

Impacted patents include:

  • Prior art compositions for the same therapeutic use.
  • Patents for delivery mechanisms similar to those claimed in MX2021013970.
  • Use-specific patents that may overlap, potentially challenging the scope’s novelty.

Patentability considerations:

  • To avoid infringement issues and ensure enforceability, the patent claims should demonstrate significant inventive features over the Mexican prior art.
  • Patent examiners frequently evaluate claims against databases such as IMPI's (Mexican Institute of Industrial Property) repository and international patent databases.

Overlap and Potential Challenges

  • Overlap with existing patents: The key challenge to MX2021013970’s enforceability is potential overlap with prior art—specifically, earlier patents filing for similar compounds, formulations, or therapeutic methods.

  • Patentability of claims: Given the strict examination standards, claims that overly rely on known chemical entities or standard formulations may face novelty or inventive step rejections, unless they introduce surprising advantages or unexpected results.

  • Legal considerations: Some claims—particularly method claims—may encounter limitations due to compulsory licensing or prior art disclosures.


Strategic Implications

  1. Patent Scope Optimization: It’s vital that the patent claims are carefully drafted to encompass the full scope of the invention without encroaching on prior art, emphasizing novel aspects such as unique delivery mechanisms or unexpected therapeutic benefits.

  2. Building a Robust Patent Portfolio: Companies should consider filing additional patents for improvements, formulations, or alternative uses to strengthen market protection.

  3. Monitoring Competitors: Active surveillance of patent filings by competitors in Mexico will inform prosecution strategies and potential litigations.

  4. Regulatory Alignment: Aligning the patent claims with regulatory considerations ensures that patent protection complements clinical and commercialization activities.


Conclusion

Patent MX2021013970 represents a strategic intellectual property asset in Mexico's pharmaceutical landscape. Its scope centers on a novel drug composition or method with a carefully drafted set of claims designed to secure broad yet defensible protection. Success in maintaining its enforceability hinges upon its ability to distinguish itself from prior art through inventive features and precise claim drafting.

The patent landscape in Mexico remains dynamic, with increasing patent filings in pharmaceuticals emphasizing the importance of early and comprehensive patent strategies. As the Mexican market matures, robust patent protections such as MX2021013970 provide a significant competitive advantage.


Key Takeaways

  • MX2021013970’s claims likely cover a novel pharmaceutical composition or method; precise claim drafting enhances enforceability.
  • The Mexican patent landscape is competitive, requiring continuous monitoring for overlapping prior art.
  • Patentability hinges on demonstrating genuine novelty and inventive step, especially given stringent Mexican patent examination standards.
  • Companies should consider strategic portfolio expansion, including filings for improvements and alternative uses.
  • Regulatory and patent strategies must be integrated to optimize drug exclusivity and market penetration.

FAQs

Q1: What types of claims are most common in Mexican pharmaceutical patents like MX2021013970?
A1: Common claims include composition claims (covering chemical entities or combinations), process claims (methods of manufacture), and use claims (therapeutic applications). Their scope varies from broad to specific.

Q2: How does Mexican patent law handle pharmaceutical patent scope regarding prior art?
A2: Mexican law emphasizes novelty and inventive step, requiring patent claims to be distinctly different from existing prior art, whether domestic or international.

Q3: Can MX2021013970 be challenged post-grant?
A3: Yes, third parties can file opposition or invalidity actions based on prior art or other grounds within Mexican legal procedures, especially within the opposition window after publication.

Q4: What strategies can reinforce MX2021013970’s patent protection?
A4: Filing secondary patents for formulations, methods, or new therapeutic uses, combined with vigilant patent monitoring, fortifies the patent portfolio.

Q5: How important is claim specificity for patent enforcement in Mexico?
A5: Very important. Clear, specific claims improve enforceability, reduce vulnerability to invalidation, and clarify the scope of protection against infringement.


References:

  1. Mexican Industrial Property Law (LPI).
  2. IMPI Patent Examination Guidelines.
  3. Patent MX2021013970 documentation and claims (hypothetical reference based on available data).

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