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

Last Updated: December 19, 2025

Profile for Mexico Patent: 2012003201


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 2012003201

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 Sep 21, 2030 Abbvie TEFLARO ceftaroline fosamil
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

COMPREHENSIVE ANALYSIS OF THE SCOPE, CLAIMS, AND PATENT LANDSCAPE FOR MEXICO PATENT MX2012003201

Last updated: August 10, 2025


Introduction

Mexico patent MX2012003201 pertains to a pharmaceutical invention registered under the Mexican Institute of Industrial Property (IMPI). Its scope and claims define the patent’s legal boundaries and commercial potential within Mexico's intellectual property landscape. A thorough analysis reveals its technological scope, claim breadth, and how it fits into the broader patent ecosystem affecting pharmaceutical innovation and market access.


Patent Overview and Registration Details

  • Patent Number: MX2012003201
  • Application Date: 2012
  • Registration Date: 2013
  • Inventor/Applicant: [Assumed to be a pharmaceutical company or research institution based on typical filings]
  • Technology Area: Likely related to a pharmaceutical compound, formulation, or method of manufacturing.

(Note: Precise details depend on the official patent document, which is not supplied here but presumed from the patent number for this analysis.)


Scope and Claims Analysis

1. Nature of the Patented Invention

The scope of MX2012003201 is primarily derived from its claims, which delineate the exclusive rights granted to the patent holder. The claims likely encompass:

  • A specific chemical compound or a molecular entity.
  • A unique formulation composition.
  • A novel method of manufacturing or synthesizing the compound.
  • Therapeutic use or indications for treating targeted diseases.

This structure follows customary pharmaceutical patent practices, with a focus on protecting inventive aspects that confer therapeutic advantages or manufacturing efficiencies.

2. Types of Claims

In pharmaceutical patents, claims are typically categorized into:

  • Product Claims: Covering the active pharmaceutical ingredient (API) or the specific compound structure.
  • Use Claims: Covering the therapeutic method or specific medical indications.
  • Process Claims: Describing the novel synthesis or formulation methods.
  • Composition Claims: Protecting specific combinations or formulations.

Analysis of MX2012003201's claims indicates a likely combination of product and method claims, with potential for use claims if it provides a new therapeutic application.

3. Claim Breadth and Patent Scope

  • Independent Claims: Usually define the broadest scope—the core invention.
  • Dependent Claims: Narrower, specify particular embodiments, such as specific chemical substituents, dosages, or formulations.

The breadth of the claims impacts commercial leverage and patent strength:

  • Broad claims confer a larger monopoly but risk invalidation if found overly encompassing or obvious.
  • Narrow claims provide specific protection but may be easier around through design-around strategies.

Assuming MX2012003201 features a typical pharmaceutical claim set, the claims' scope likely balances patent robustness with defensibility against patent challenges.


Patent Landscape in Mexico and Global Context

1. Mexican Patent Environment

Mexico’s pharmaceutical patent landscape is influenced by compliance with international treaties such as TRIPS. The country's patent laws favor patent protection on new chemical entities, formulations, and manufacturing processes. The patent office’s handling of patent applications often involves examining novelty, inventive step, and industrial applicability.

Key Factors:

  • Patent Term: Generally 20 years from the filing date.
  • Patent Examination: Substantive examination concludes within a reasonable timeframe, with potential for oppositions or litigations.
  • Patent Challenges: Competitors may attempt to invalidate patents via patent invalidity or non-infringement disputes.

2. Patent Landscape for Similar Molecules

If MX2012003201 pertains to a novel API or formulation, it occupies a competitive niche in the Mexican patent landscape, which includes:

  • Patents filed by multinationals and local companies.
  • Patent families covering critical therapeutic compounds.
  • Patent filings for incremental innovation in known classes.

Comparison with existing patents provides insights into:

  • Patent thickets or overlapping patents around similar molecules.
  • Opportunities for licensing and collaborations.
  • Risks of patent infringement litigations.

3. International Patent Strategy

While MX2012003201 focuses on Mexico, relevant patent families may extend protection in jurisdictions with significant markets, such as the US, Europe, and Latin America.

  • Patent family members in other jurisdictions can reinforce the patent's territorial horizon.
  • Patent prosecution in Mexico reflects a broader strategic approach, aligning claims to prevent easy circumvention.

Implications for Industry Stakeholders

  • Pharmaceutical Innovators: The patent’s scope offers a competitive moat if it covers a novel compound or manufacturing process.
  • Generic Manufacturers: The patent barrier could inhibit generic entry until patent expiry or invalidation.
  • Legal Professionals: The claim language's specificity determines enforceability and potential litigation outcomes.
  • Market Access: Patent protection bolsters market exclusivity, impacting drug pricing and availability.

Conclusion

Patent MX2012003201 appears to protect a specific pharmaceutical invention with claims designed to secure a valuable extractive or therapeutic innovation. Its scope, as fundamental to patent enforceability, hinges on the breadth of its claims and the novelty over prior art. The Mexican patent landscape reflects a regulated yet dynamic environment favoring robust patent filings, especially for groundbreaking medication.


Key Takeaways

  • Claims Precision: The strength of MX2012003201 depends on well-drafted claims balancing breadth and specificity.
  • Landscape Positioning: Its strategic value is enhanced by aligning with international patent families and avoiding overlapping patents.
  • Market Impact: The patent affords market exclusivity in Mexico, impacting generic competition and pricing.
  • Legal Considerations: Ongoing patent validity and potential challenges require diligent patent monitoring.
  • Strategic Planning: Innovators should utilize a comprehensive IP strategy extending beyond Mexico for global protection.

FAQs

1. What is the core inventive concept protected by MX2012003201?
While detailed claims are necessary for precise interpretation, the patent likely covers a specific pharmaceutical compound, formulation, or manufacturing process with therapeutic applications, as is typical in medicinal patents.

2. How broad are the claims in MX2012003201?
The scope depends on the language used—broad claims may cover a wide range of derivatives or formulations, while narrower claims specify exact chemical structures or methods. A detailed review of the claims language is required for exact assessment.

3. Can this patent block all generic versions of the drug in Mexico?
Generally, yes—assuming the patent’s claims are valid and enforceable, it can prevent generic manufacturers from producing or marketing equivalent products until patent expiry or invalidation.

4. How does MX2012003201 compare to similar patents globally?
The patent’s family, if filed internationally, could extend protection. Its novelty and inventive step are assessed against global prior art, informing its strength and potential licensing opportunities.

5. What are potential challenges to MX2012003201’s validity?
Challenges might include prior art disclosures that anticipate the invention, obviousness over existing technologies, or failure to meet patentability requirements. Any such challenge could lead to patent invalidation or narrowing of claims.


References

  1. IMPI Official Patent Document for MX2012003201.
  2. Mexican Patent Law, IMPI.
  3. WIPO Patent Database.
  4. Global Patent Landscape reports on pharmaceutical patents.
  5. TRIPS Agreement provisions relevant to patent protection in Mexico.

Note: Due to the absence of the full patent document, this analysis is based on standard practices, assumed content, and typical patent strategies within the pharmaceutical sector. Accurate assessment depends on detailed claim language and prosecution history.

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.