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Last Updated: December 28, 2025

Profile for Mexico Patent: 2012006311


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US Patent Family Members and Approved Drugs for Mexico Patent: 2012006311

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 Jan 15, 2031 Abbvie RINVOQ LQ upadacitinib
⤷  Get Started Free Jan 15, 2031 Abbvie RINVOQ upadacitinib
⤷  Get Started Free Aug 16, 2033 Abbvie RINVOQ LQ upadacitinib
⤷  Get Started Free Aug 16, 2033 Abbvie RINVOQ upadacitinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent MX2012006311: Scope, Claims, and Landscape

Last updated: August 12, 2025

Introduction

Patent MX2012006311 pertains to a pharmaceutical invention filed and granted in Mexico, aiming to secure exclusive rights over a novel drug-related innovation. An understanding of its scope, claims, and the broader patent landscape is vital for stakeholders such as pharmaceutical companies, generic manufacturers, and legal entities to navigate market entry, licensing, or litigatory strategies.

This analysis provides a comprehensive review of patent MX2012006311's scope and claims, contextualized within Mexico's patent system, and examines its position within the global pharmaceutical patent landscape.


Patent Overview and Status

Patent Number: MX2012006311
Filing Year: 2012 (based on patent number and typical filing timelines)
Grant Status: Likely granted (as indicated by the patent number format and timing)
Patent Office: Mexican Institute of Industrial Property (IMPI)

While publicly available information on the patent's specific claims is limited without detailed official records, typical patent filings in the pharmaceutical domain encompass compound claims, formulation claims, uses, or methods of manufacturing.


Scope and Claims

1. Broadness of Claims

The scope of patent MX2012006311 hinges on the specific claims articulated by the applicant. Generally, pharmaceutical patents may encompass:

  • Compound claims: Claiming a new chemical entity or a novel polymorph of an existing compound.
  • Use claims: Protecting a particular therapeutic application or a new medical indication.
  • Formulation claims: Covering pharmaceutical compositions, methods of delivery, or specific excipient combinations.
  • Process claims: Methods for synthesizing the active compound or formulation.

Given the patent's title and typical practices, it likely includes a combination of composition and use claims, aimed at protecting a specific drug or treatment method.

2. Claim Structure and Limitations

  • Independent Claims: Typically, cover the core invention—e.g., a new chemical compound or therapeutic use.
  • Dependent Claims: Narrower, often describing specific formulations, dosages, or methods.

The scope's breadth directly impacts the patent's enforceability and potential for generics’ challenge. A well-drafted patent balances broad protection with sufficient specificity to withstand legal scrutiny.

3. Key Aspects of the Claims

  • Novelty: The claims likely focus on a compound or application that is not previously disclosed in prior art, including scientific literature and patents.
  • Inventive Step: Demonstration that the claimed invention involves an inventive step over existing compounds or methods.
  • Industrial Applicability: The claims would specify use in therapeutic contexts, emphasizing utility and efficacy.

Patent Claims and Their Strategic Importance

1. Compound Claims

If the patent claims a new chemical entity, its scope can significantly impact the competitive landscape. Compound claims are generally strong if the novelty and inventive steps are well-supported, potentially barring direct competitors from manufacturing similar molecules.

2. Use Claims

Use claims extend protection beyond compounds to specific indications. They are advantageous when the patent owner seeks to prevent others from commercializing a known compound for particular indications, thus broadening market control.

3. Formulation and Method Claims

By claiming specific formulations or methods of treatment, the patent secures rights over commercial aspects such as optimized delivery or manufacturing techniques, critical for market differentiation.


Patent Landscape in Mexico for Similar Pharmaceuticals

1. National Innovation Environment

Mexico's pharmaceutical patent landscape has evolved to encourage innovation, aligning with international agreements like TRIPS. The country has a dense network of patents covering chemical compounds, formulations, and uses.

2. Key Competitors and Patent Holders

Major international pharmaceutical firms, alongside local players, hold patents on innovative drugs. The dominance of patents on blockbuster drugs results in a crowded landscape where new filings often seek narrow claims or unique formulations.

3. Patent Challenges and Litigation

Mexican patent law permits third-party challenges through invalidation procedures, especially if patents are deemed overly broad, lack inventive step, or are not sufficiently novel.

4. Patent Term and Data Exclusivity

Pharmaceutical patents in Mexico generally have a 20-year term from filing, with possible extensions. Data exclusivity periods may further influence generic entry.


Implications for the Pharmaceutical Industry

The scope of MX2012006311's claims define its protective value. Broad claims covering a novel compound or therapeutic use provide a competitive moat, whereas narrow claims may be easier for competitors to circumvent through design-around strategies.

Local patent landscapes indicate ongoing innovation, but also raise the risk of patent thickets and litigation—especially for blockbuster or high-value drugs.


Global Context and Comparability

While this analysis centers on Mexico, similar patents worldwide often face comparable challenges regarding claim scope and enforcement. Cross-referencing with patent filings in jurisdictions like the US or EU can reveal strategies for global patent protection; however, each jurisdiction's legal standards impact enforceability.


Conclusion

Patent MX2012006311 exemplifies a typical pharmaceutical patent securing exclusive rights through claims that likely encompass novel compounds, uses, or formulations. Its scope critically hinges on the drafting quality, claim breadth, and underlying inventive step. Within Mexico’s patent landscape, such patents contribute to a robust ecosystem but are subject to legal scrutiny and challenges, especially as the pharmaceutical industry increasingly emphasizes broad, enforceable rights.

For industry stakeholders:

  • patentees: Focus on crafting claims that balance breadth with specificity to withstand validity challenges.
  • competitors: Analyze claim scope to identify potential design-around opportunities.
  • legal practitioners: Monitor patent challenges and validity proceedings to safeguard or challenge patent rights effectively.

Key Takeaways

  • Claim strategy is pivotal: Broad claims enhance protection but may invite invalidation; narrow claims are easier to defend but limit scope.
  • Patent landscape is competitive: Mexico hosts active pharmaceutical patenting, with high stakes on innovation and legal validity.
  • Global positioning matters: Alignment of claims with international standards can support patent enforcement across jurisdictions.
  • Challenging patents: Validation, opposition, and invalidation processes are critical tools within Mexico's patent system.
  • Continual monitoring: The evolving patent environment necessitates ongoing review of patent validity and third-party rights.

Frequently Asked Questions (FAQs)

1. What is the significance of a pharmaceutical patent like MX2012006311 in Mexico?

It grants exclusive rights to manufacture, market, and use the protected pharmaceutical invention within Mexico, providing a competitive advantage and potential licensing opportunities.

2. How does claim scope influence the enforceability of the patent?

Broader claims provide wider protection but are more susceptible to invalidation if not fully supported by inventive activity; narrower claims are easier to defend but offer limited coverage.

3. Can a competitor produce a similar drug if they work around the claims of MX2012006311?

Yes. Designing around the patent—such as developing a different compound, formulation, or therapeutic use—can circumvent the claims if they are sufficiently narrow.

4. How does Mexican patent law compare to other jurisdictions for pharmaceutical patents?

Mexico's patent system aligns with international standards like TRIPS but may differ in aspects like patent term adjustments or opposition procedures. The general principles of novelty, inventive step, and industrial applicability are consistent.

5. What strategies can patent holders adopt to enhance their patent portfolio in Mexico?

They should aim for comprehensive claims covering compounds, uses, and formulations, conduct thorough prior art searches, and consider filing divisional or continuation applications to extend protection.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent Law and Examination Guidelines.
  2. World Intellectual Property Organization (WIPO). Patent Cooperation Treaty (PCT) System.
  3. Ginarte, J.C., & Galindo, A. (1992). "Determinants of Patent Rights: A Cross-National Study." Research Policy.
  4. European Patent Office. Patentability of Pharmaceuticals.
  5. United States Patent and Trademark Office (USPTO). Patent Examination Guidelines for Pharmaceutical Patents.

(Note: Specific claims and detailed legal status of MX2012006311 are subject to official patent documents and legal databases.)

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