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Last Updated: December 15, 2025

Profile for Mexico Patent: 350011


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US Patent Family Members and Approved Drugs for Mexico Patent: 350011

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
9,173,881 Aug 12, 2029 Actelion UPTRAVI selexipag
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX350011

Last updated: July 27, 2025

Introduction

Mexico Patent MX350011 emerges as a critical intellectual property asset within the pharmaceutical patent landscape of Mexico. Understanding its scope, claims, and the surrounding patent environment encompasses strategic importance for pharmaceutical innovators, generic manufacturers, and legal professionals seeking insight into market exclusivity, patent strength, and potential challenges.

This analysis offers a comprehensive review of the patent's scope, the intricacies of its claims, and an overview of the patent landscape in Mexico related to this patent, ensuring stakeholders can make informed decisions grounded in current patent law and market dynamics.


Overview of Mexico Patent MX350011

Patent Identification and Basic Details

  • Patent Number: MX350011
  • Application Filing Date: [Specific date, if known]
  • Grant Date: [Specific date, if known]
  • Applicants/Owners: [Assumed or specific assignee]
  • Legal Status: Active/granted, with potential continuations or related patents—[assumed or confirmed]

Note: Precise details such as filing and grant dates should be confirmed from the Mexican Institute of Industrial Property (IMPI) databases or official patent records.


Scope of Patent MX350011

Patent Subject Matter

MX350011 appears to pertain to a pharmaceutical compound or a formulation, likely involving a novel active ingredient, a unique formulation, or a specific method of manufacturing a drug. Such patents often intend to secure exclusivity over a new chemical entity or a novel therapeutic use.

The scope extends to:

  • Chemical Composition: Detailing specific molecular structures or combinations.
  • Method of Preparation: Claiming novel synthesis or processing techniques.
  • Therapeutic Use: Covering specific indications or medical applications.
  • Formulation Claims: Covering specific formulations or delivery systems.

Detailed scope depends on the breadth afforded by the specific enumeration of claims; typically, the patent aims to cover the core inventive concept while excluding prior art.

Legal and Technical Breadth

The patent's scope must balance breadth with specificity:

  • Broad Claims: Encompass entire classes or mechanisms of action to deter competition.
  • Dependent Claims: Narrow scope, focusing on specific embodiments or process details.

This strategic structuring influences enforceability and the potential for patent invalidation or license challenges.


Claims Analysis

Claim Structure and Focus

Generally, patents in this domain delineate claims along the following lines:

  1. Compound Claims: Covering the chemical compound in its most general form, including specific substitutions or structural features.
  2. Method of Use: Protecting therapeutic methods involving the compound.
  3. Manufacturing Claims: Detailing synthesis or formulation techniques.
  4. Combination Claims: Protecting the compound or formulation when combined with other agents.

A typical broad claim might read:

“A pharmaceutical compound comprising [specific chemical structure], effective for treating [indication].”

Supporting dependent claims refine the scope, citing specific chemical derivatives, dosages, or administration routes.

Claim Interpretation and Validity Aspects

  • Novelty and Inventive Step: Claims must demonstrate non-obviousness over prior Mexican and international prior art.
  • Specificity: Overly broad claims risk invalidation if prior art discloses similar compounds or methods.
  • Compliance: Claims should meet formal requirements, including clarity, conciseness, and precise wording.

Claim Scope Implications

  • Enforcement: Narrow or specific claims diminish scope but strengthen validity.
  • Infringement: Broader claims increase the likelihood of infringement but risk invalidation certificate if challenged.

Patent Landscape in Mexico for Related Drugs

Market and Legal Context

Mexico's pharmaceutical patent landscape reflects a balance between fostering innovation and allowing generic entry. The country adheres to the Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS), providing 20-year patent terms from the filing date.

Patent Trends

  • Patent Filing Trends: Increasing filings for novel active ingredients post-2010, especially in oncology, cardiology, and infectious diseases.
  • Patent Duration and Litigation: Patents like MX350011 often face infringement challenges or licensing negotiations.

Major Patent Clusters and Competitive Dynamics

  • Chemical and Biological Patents: Snippets of MX350011 face competition or potential infringement from patents covering similar compounds or formulations.
  • Patent Thickets: Multiple overlapping patents can encumber market entry; MX350011's claims may intersect with earlier patents or applications, requiring diligent freedom-to-operate analyses.

Legal Challenges and Patent Term Extensions

While Mexico permits patent term extensions in specific cases, generally, patent life remains at 20 years from filing. Observations:

  • Litigation History: MX350011 may have been involved in opposition or invalidation proceedings, common in the Mexican pharma sector.
  • Patent Amendments or Re-examinations: Implemented to refine scope or address prior art.

Strategic Implications for Stakeholders

For Innovators

  • Valuable Asset: The potential breadth of claims can secure market exclusivity.
  • Patent Enforcement: Vigorously defend claims against infringement and invalidity challenges.

For Generics and Competitors

  • Freedom to Operate: Must analyze patent claims meticulously to navigate around the patent.
  • Design-around Strategies: Focus on compounds or methods outside MX350011's scope.

For Legal and Regulatory Entities

  • Patent Validity: Continuous monitoring of prior art and prior filings influences enforceability.
  • Patent Term Management: Timely filings and strategic amendments optimize patent lifespan.

Conclusion & Key Takeaways

  • MX350011 likely claims a specific pharmaceutical compound or formulation with therapeutic utility, with a scope defined by its detailed claims structure.
  • The patent's strength hinges on the novelty, non-obviousness, and precise claim phrasing; broad claims offer market advantages but pose invalidation risks.
  • The patent landscape in Mexico reveals an active environment, with overlapping patents and strategic filings governing market dynamics.
  • Stakeholders should conduct comprehensive freedom-to-operate analyses and monitor potential patent challenges to mitigate risks.
  • Close attention to claim language and patent prosecution history enhances strategic decision-making for innovators and competitors alike.

FAQs

  1. What is the typical lifespan of patent MX350011?
    The patent generally enjoys a 20-year term from its filing date, subject to maintenance fee payments and potential extensions in specific situations.

  2. Can MX350011 be challenged for invalidity in Mexico?
    Yes, third parties can initiate invalidation proceedings based on prior art, lack of novelty, or inventive step, potentially limiting or nullifying the patent.

  3. How broad are the claims typically found in similar pharmaceutical patents in Mexico?
    It varies; some patents claim broad chemical classes, while others focus narrowly on specific compounds or formulations. Broader claims offer more market protection but are more vulnerable.

  4. What strategies do companies use to navigate patent landscapes like that surrounding MX350011?
    Companies perform detailed patent landscape analyses, seek design-arounds, file additional patents, or negotiate licenses to mitigate infringement risks.

  5. Is foreign patent protection necessary for pharmaceuticals marketed in Mexico?
    Yes, for exclusivity in Mexico, local patent protection is vital. International patents do not automatically extend to Mexico; separate filings are required under Mexican law.


References

  1. IMPI Official Patent Database – For detailed patent documents, filing, and prosecution history records.
  2. Mexican Patent Law (Ley de la Propiedad Industrial) – Provides legal framework for patent rights, validity, and enforcement.
  3. WIPO Patent Landscape Reports – Offers insights into global patent filing trends relevant to Mexican filings.
  4. Pharmaceutical Patent Analysis Reports – Industry-specific reports for patent scope, litigation, and strategic considerations.

Note: Specific data points such as filing and grant dates along with detailed claim language should be verified against official IMPI documentation for accuracy.

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