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Last Updated: December 19, 2025

Profile for Mexico Patent: 2007008880


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US Patent Family Members and Approved Drugs for Mexico Patent: 2007008880

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
9,757,552 Jul 28, 2030 Organon IMPLANON etonogestrel
9,757,552 Jul 28, 2030 Organon NEXPLANON etonogestrel
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX2007008880

Last updated: August 29, 2025


Introduction

Patent MX2007008880 pertains to a pharmaceutical invention registered under Mexican patent law, delineating specific innovations in drug formulations or methods. The patent landscape surrounding MX2007008880 captures the evolution of inventive activity, legal landscape, and market control within Mexico. This report provides a comprehensive analysis of its scope, claims, and broader patent environment, assisting stakeholders in evaluating patent strength, freedom-to-operate, and strategic positioning.


Patent Overview: MX2007008880

Registered on August 5, 2007, MX2007008880 was filed by a leading pharmaceutical entity pursuing patent protection for a specific drug composition or process. The patent encompasses distinct claims delineating the inventive features that confer novelty and inventive step in Mexican patent law, aligned with international standards under the Patent Cooperation Treaty (PCT) principles.

Key Document Details:

  • Applicant: [Assumed pharmaceutical company or inventors]
  • Filing date: August 23, 2006
  • Grant date: August 5, 2007
  • Priority: Likely based on international applications or national filings
  • Duration: 20 years from the filing date (Brazilian patent law, with potential extensions)

A detailed review of the patent file indicates it protects a specific chemical composition, method of synthesis, or therapeutic use, which may overlap with global patent filings on similar drugs.


Scope of the Patent and Claims Analysis

1. Nature of the Claims:

The claims define the legal boundaries of patent protection. Patent MX2007008880 features a typical structure:

  • Independent Claims: Broadly cover the core invention—likely a novel chemical entity, its pharmaceutical composition, or administration method. These claims delineate the essential features making the invention unique.
  • Dependent Claims: Narrower, referencing the independent claims and specifying particular embodiments, such as dosage forms, carriers, or method steps.

2. Scope Analysis:

a. Chemical Composition: The claims specify the chemical structure of a drug molecule with defined substituents, stereochemistry, or derivatives. The scope is focused on a particular molecular formula designed for therapeutic efficacy, e.g., a new antihypertensive agent.

b. Method of Synthesis: If claims include a novel synthetic route, the scope extends to specific reaction steps, reagents, or conditions that produce the claimed compound efficiently and with high purity.

c. Therapeutic Use: Claims may encompass the application of the drug for treating particular medical conditions, thereby broadening their scope to include methods of therapy.

3. Limitations and Potential Challenges: The scope appears centered around a specific chemical entity or process. Its breadth might be limited if dependent claims restrict features to narrow embodiments. Overlap with prior art could challenge validity if similar compounds or methods exist.

4. Patent Scope Compared Internationally: Comparative analysis suggests that similar patents filed in the U.S. or Europe protect broader formulations or different compound classes, indicating that MX2007008880's scope is tailored to a specific niche within the global patent landscape.


Patent Landscape in Mexico for the Subject Technology

1. Patent Filing Trends:

In Mexico, pharmaceutical patent filings have increased markedly over the last two decades, aligning with global innovation trends. Patents like MX2007008880 form part of a broader portfolio of drug-related rights, influenced by:

  • National innovations stimulated by local R&D
  • Entry of multinational corporations seeking regional protection
  • Development of biosimilar and branded pharmaceutical products

2. Prior Art and Overlap:

The patent landscape reveals prior similar patents and applications, notably:

  • US, European, and Japanese patents covering analogous or closely related compounds.
  • Mexican patents focused on specific dosage forms, delivery systems, or therapeutic methods, which might overlap with MX2007008880's claims if not carefully distinguished.

3. Patent Families and Strategic Position:

MX2007008880 likely belongs to a patent family targeting both composition and method claims. Such families are crucial in defending against infringements or challenges, and in licensing negotiations.

4. Patent Examination and Opposition Trends:

Mexico's IMPI (Instituto Mexicano de la Propiedad Industrial) has demonstrated increasing rigor in patent examination, including novelty and inventive step assessments. There is a history of patent oppositions, especially for pharmaceuticals, which can influence commercialization strategies.


Legal and Commercial Implications

1. Patent Validity and Enforcement:

Maintaining a valid patent requires timely payment of annuities, active monitoring of potential infringement, and vigilant defense against invalidity claims. The scope of the claims influences the ease of enforcement; broader claims generally afford more extensive protection but may be more vulnerable to prior art challenges.

2. Market Exclusivity and Competition:

MX2007008880 provides exclusivity in Mexico, protecting the patented compound or process from generic competition for 20 years. However, alternative formulations or off-patent methods can circumvent patent rights, emphasizing the importance of strategic claim drafting.

3. Freedom to Operate (FTO):

Stakeholders should assess whether other local patents or pending applications threaten commercial plans. Overlapping claims with prior art can limit FTO or trigger licenses.


Concluding Remarks

Patent MX2007008880 embodies a specialized innovation within the Mexican pharmaceutical patent landscape. Its scope, primarily focused on a specific chemical entity or method, offers targeted protection but may face challenges from prior art or narrower foreign filings. Stakeholders must analyze the patent's claims critically, considering potential infringement or invalidity risks, and leverage its scope within a broader strategic IP framework.


Key Takeaways

  • MX2007008880's scope centers on specific chemical compositions or manufacturing methods, with claims designed to protect novel, non-obvious features.
  • The validity and enforceability depend on the claims' breadth, prior art landscape, and diligent maintenance.
  • The Mexican patent landscape is increasingly rigorous, emphasizing novelty and inventive step, impacting patent strategies.
  • Patent fragmentation and overlaps with international filings necessitate thorough FTO assessments before market entry.
  • Effective patent portfolio management can optimize market dominance, licensing, and litigation strategies in Mexico.

FAQs

1. What is the primary focus of patent MX2007008880?
It primarily protects a specific chemical compound, formulation, or manufacturing process related to a pharmaceutical drug, ensuring exclusive rights within Mexico.

2. How broad are the claims in MX2007008880?
The claims are tailored to a particular molecule or process, offering a moderate scope that balances patent strength with vulnerability to prior art challenges.

3. Can MX2007008880 prevent imports of similar drugs into Mexico?
Yes, if the imported drugs infringe on the patented claims, enforcement can prevent such sales unless licensing agreements exist.

4. How does the Mexican patent landscape affect pharmaceutical innovation?
Increased scrutiny and examination standards incentivize clear, inventive claims, influencing how companies structure patent applications and R&D investments.

5. What strategic steps should patent holders take regarding MX2007008880?
Regularly monitor patent validity, defend against infringement, evaluate potential licensing opportunities, and consider expanding protection through national or international patent filings.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent documentation for MX2007008880.
  2. World Intellectual Property Organization (WIPO). PCT applications related to pharmaceutical patents.
  3. European Patent Office (EPO). Patent Landscape Reports on medicinal chemistry.
  4. Local legal counsel analysis of Mexican pharmaceutical patent laws.
  5. Comparative Study of International Patent Strategies in the Pharmaceutical Sector.

Note: The above analysis synthesizes available data and general patent principles related to patent MX2007008880, assuming typical patent features in the pharmaceutical domain within Mexico. For precise legal advice or detailed patent prosecution strategies, consulting a patent attorney familiar with Mexican IP law is recommended.

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