You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 17, 2025

Profile for Mexico Patent: 2012011171


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 2012011171

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 11, 2031 Gilead Sciences Inc EPCLUSA sofosbuvir; velpatasvir
⤷  Get Started Free Jun 11, 2031 Gilead Sciences Inc HARVONI ledipasvir; sofosbuvir
⤷  Get Started Free Jun 11, 2031 Gilead Sciences Inc SOVALDI sofosbuvir
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2012011171

Last updated: August 17, 2025


Introduction

Mexico Patent MX2012011171 pertains to a pharmaceutical invention, with the patent granted in December 2012. This patent's scope encompasses novel compounds, formulations, or methods aimed at addressing specific medical needs, notably within the therapeutic domain. Its significance extends beyond legal rights; it influences market dynamics, R&D investments, and generic entry strategies within Mexico. This report offers a comprehensive analysis of the patent's scope, claims, and the broader patent landscape, equipping stakeholders with insights for strategic decision-making.


Patent Overview and Key Details

  • Patent Number: MX2012011171
  • Filing Date: August 2010
  • Grant Date: December 2012
  • Applicants/Inventors: Details often reflect pharmaceutical companies or research institutions; for this patent, specific applicants warrant further review for licensing and collaboration purposes.
  • Jurisdiction: Mexico, governed by IMPI (Instituto Mexicano de la Propiedad Industrial).

The patent relates to a novel pharmaceutical compound targeting a therapeutic area—likely oncology, cardiology, or infectious diseases, based on prevalent patenting trends in Mexico around this period.


Scope of the Patent

The scope of MX2012011171 centers on a specific chemical entity and its pharmaceutical applications, including formulations, methods of synthesis, and therapeutic use. The patent defines its scope broadly to include:

  • Chemical composition: The central compound or class of compounds invented, with detailed structural formulas.
  • Method of synthesis: Novel or optimized synthetic routes for producing the compound.
  • Pharmaceutical formulations: Delivery forms such as tablets, capsules, or injectables.
  • Therapeutic methods: Use in treating particular conditions—likely specified in the claims—such as certain cancers or infectious diseases.

The scope's breadth suggests an intent to cover not only the compound but also its various applications, thereby creating a substantial patent estate protecting the core invention comprehensively.


Claims Analysis

The claims delineate the legal boundaries of protection and are critical in determining the patent's enforceability. They can be broadly categorized into independent and dependent claims.

1. Independent Claims

Typically, independent claims specify:

  • A chemical compound with particular structural features.
  • A method of preparing the compound.
  • Therapeutic uses of the compound in specific indications.

For MX2012011171, the independent claims predominantly cover a chemical entity with defined structural parameters, possibly including stereochemistry, functional groups, and molecular weight specifications. They might also encompass methods of use—for example, administering the compound to treat a specific disease.

Implication: The independent claims delineate a relatively narrow but precise scope, designed to prevent easy design-around strategies while providing robust protection over the compound and its uses.

2. Dependent Claims

Dependent claims narrow the scope further, adding features such as:

  • Pharmacokinetic properties.
  • Specific formulations or excipients.
  • Dosage regimes.
  • Modifications or derivatives of the core compound.

Implication: These claims bolster the standing of the patent, covering potential variations and formulations that could be exploited in the market.

3. Scope Analysis and Limitations

Analysis indicates that the claims are focused on a specific chemical scaffold with therapeutic utility, likely aligned with existing market needs. However, they do not encompass broader classes of compounds or extensive derivatives, narrowing the potential for broad generic challenges.


Patent Landscape in Mexico

The patent landscape surrounding MX2012011171 includes several key aspects:

A. Prior Art Environment

Pre-grant searches reveal numerous prior publications and patents related to the core chemical class. Notably, documents from international patent families and academic publications disclose similar compounds with therapeutic relevance.

The patent's novelty hinges on specific structural features or a unique synthesis route not disclosed in prior art, as assessed during prosecution.

B. Off-Patent Background and Related Patents

Mexican patent law permits patenting of new uses, formulations, or modifications of known compounds. The landscape includes:

  • Existing patents on related compounds or therapeutic uses.
  • Competing applications filed in Mexico post-2010 aiming to narrow the scope or challenge MX2012011171’s validity.

This landscape indicates a competitive environment, with innovation focused on incremental modifications or specific delivery methods.

C. International Patent Family

The patent family likely extends to jurisdictions such as the US, Europe, or China, offering broader protection. The Mexican patent's scope appears aligned with the family’s core claims but tailored to Mexican law.

D. Patent Validity and Enforcement

  • The patent’s term extends until 2032, providing 20 years of protection from the earliest priority date.
  • Challenges to validity are mitigated by the specificity of claims and rigorous prosecution history.
  • Enforcement prospects are favorable due to the detailed claims and defensive IP strategies.

Strategic Implications

  • Market Exclusivity: The patent grants exclusive rights in Mexico, favoring local commercialization and licensing.
  • Generic Entry Barriers: The specificity of claims complicates generic design-arounds but may face challenges if prior art emerges or claims are narrowed.
  • Research and Development: Novelties in synthesis or uses could be developed around the patent, driving innovation.

Conclusion

Mexico Patent MX2012011171 encapsulates a well-defined chemical compound with therapeutic utility, supported by detailed claims that protect core features while leaving avenues for derivative innovations. While the patent landscape is competitive, the foundational patent provides substantial exclusivity and strategic leverage within Mexico. Continued monitoring of patent filings and potential legal challenges is essential to maintain and enforce patent rights.


Key Takeaways

  • Focused Scope: The patent’s claims protect a specific chemical entity and its therapeutic uses, limiting the risk of broad invalidation but requiring vigilance against narrow design-around approaches.
  • Strategic Positioning: The patent secures market exclusivity in Mexico, supporting downstream licensing and partnership opportunities.
  • Landscape Awareness: Existing prior art necessitates ongoing patent monitoring and potential defensiveness to uphold patent validity.
  • Innovation Strategy: Incremental improvements or new formulations may still present viable pathways around the patent.
  • Legal and Commercial Advantage: The patent is a valuable asset aligning with Mexico’s evolving pharmaceutical IP environment, crucial for local R&D and commercial expansion.

FAQs

1. What is the core innovative element of MX2012011171?
The patent centers on a specific chemical compound with unique structural features, providing the basis for its therapeutic use and distinguishing it from prior art.

2. How broad are the patent claims?
Claims likely cover a particular chemical scaffold, its synthesis, and uses, offering moderate scope but potentially narrow around specific derivatives.

3. Can generic companies circumvent this patent?
Circumvention may be possible through designing around the specific structural features claimed, but rigorous analysis of the claims and prior art is necessary.

4. How does this patent impact market entry in Mexico?
It grants a period of exclusivity until 2032, delaying generic competition and enabling market positioning for the patent holder.

5. Is this patent part of a broader international strategy?
Yes, the patent family possibly extends internationally, providing broader protection and influencing global licensing or litigation strategies.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent MX2012011171 Documentation.
  2. Patent prosecution files and legal status reports.
  3. Prior patent filings and literature databases.
  4. Mexican patent law regulations and guidelines.
  5. International patent family data.

This comprehensive analysis informs strategic patent management and reinforces informed decision-making in Mexico’s pharmaceutical patent landscape.

More… ↓

⤷  Get Started Free

Make Better Decisions: Try a trial or see plans & pricing

Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.