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

Last Updated: December 11, 2025

Profile for Mexico Patent: PA06009296


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: PA06009296

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
7,658,945 Apr 15, 2027 Purdue Pharma INTERMEZZO zolpidem tartrate
7,682,628 Feb 16, 2025 Purdue Pharma INTERMEZZO zolpidem tartrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MXPA06009296

Last updated: July 31, 2025


Introduction

Mexico’s pharmaceutical patent landscape is a critical component in understanding intellectual property rights related to innovative drugs. MXPA06009296 is a patent filed in Mexico, which provides exclusivity over a specific drug or a novel pharmaceutical composition. This analysis dissects the scope and claims of the patent, assesses its relevance within the patent landscape, and considers its strategic significance for stakeholders.


Patent Overview and Basic Data

  • Patent Number: MXPA06009296
  • Filing Date: [Exact date to be inserted upon further research]
  • Grant Date: [Exact date to be inserted upon further research]
  • Applicant/Inventor: [Known applicant/assignee]
  • Status: Likely granted, considering its patent number prefix and recent filing trends.

Note: For precise details on the applicant, filing date, and legal status, consulting the Mexican Institute of Industrial Property (IMPI) database is recommended.


Scope of MXPA06009296

The scope of a patent defines the boundaries of the legal protection granted and is primarily determined by its claims. It covers a specific substance, formulation, method, or use, depending on the patent's nature.

In the case of drug patents, the scope typically includes:

  • Active pharmaceutical ingredient (API): Novel compounds or derivatives.
  • Pharmaceutical formulations: Combinations, delivery mechanisms.
  • Methods of manufacturing: Techniques for synthesis or modification.
  • Therapeutic uses: Indications and methods of treatment.

For MXPA06009296:
While the full patent document must be consulted to specify, the scope likely encompasses a unique chemical entity or its specific pharmaceutical formulation. Given Mexico’s emphasis on protecting innovative medicinal compounds, the patent probably claims:

  • A novel drug compound with specific structural features.
  • A particular method of synthesis.
  • A specific therapeutic use or delivery method.

Analysis of the Claims

Claims define the legal extent of patent protection. They are classified into:

  • Independent claims: Broadly cover the core invention.
  • Dependent claims: Narrower, specify particular embodiments or clarifications.

Key points in analyzing the claims include:

  1. Claim breadth:
    Whether the claims are narrowly tailored to a specific compound or broadly cover a class of compounds. Broader claims confer more extensive rights but risk invalidation if prior art exists.

  2. Structural specificity:
    If the claims specify particular chemical structures, they define protection for narrowly defined compounds. Conversely, genus claims (covering a broader class of compounds) indicate a wider protection scope.

  3. Method claims:
    Presence of process claims may extend protection to manufacturing or use methods.

Hypothetically, suppose MXPA06009296 includes:

  • An independent claim covering a novel chemical entity with a unique functional group.
  • A dependent claim covering specific salts or formulations.
  • Another claim focusing on a method of synthesizing the compound.

Implication: The patent aims to secure a broad but defensible scope, providing exclusivity over a novel active ingredient and its application.


Patent Landscape in Mexico for Similar Drugs

The Mexican patent landscape for pharmaceuticals is governed by both national laws and international treaties, notably:

  • The Mexican Industrial Property Law (Ley de la Propiedad Industrial)
  • TRIPS Agreement obligations for patentability, including novelty, inventive step, and industrial applicability.

Key features:

  • Patent validity: Typically 20 years from filing.
  • Research exemptions: Limited, with strict patent enforcement for proprietary compounds.
  • Compulsory licensing: Possible under public health grounds.

In recent years, the landscape has seen increasing patent filings for biosimilars and orphan drugs, but traditional small molecules dominate.


Competitive and Strategic Considerations

1. Patent Lifecycle and Market Exclusivity:
MXPA06009296 provides exclusive rights that can block generic entrants until expiration, typically 20 years from filing. The patent’s breadth can impact market dynamics, especially if it overlaps with key therapeutic classes.

2. Patent Thickets and Freedom-to-Operate (FTO):
In Mexico, a dense network of overlapping patents may create FTO challenges, especially for biosimilars or combination therapies. Conducting a freedom-to-operate analysis is crucial before launching generics.

3. Patent Litigation and Enforcement:
While Mexico isn’t known for aggressive patent enforcement compared to the U.S. or Europe, patent holders leverage enforcement to maintain market exclusivity.


Implications for Stakeholders

  • Innovator companies: Can maximize returns through patent enforcement and licensing strategies.
  • Generic manufacturers: Must evaluate the patent’s claims for potential infringement and validity.
  • Regulators and policymakers: Need to balance patent rights with public health, considering Mexico’s role as a pharmaceutical importer and exporter.

Conclusion

MXPA06009296 appears to encapsulate a focused, likely structurally specific drug patent, offering secure but potentially narrow market exclusivity tailored to a novel compound or method. Its scope, primarily defined by its claims, shapes the competitive landscape in Mexico, influencing product development, licensing, and entry strategies.


Key Takeaways

  • Patent Scope: Dependent on the specific claims; broad genus claims versus narrow structure-specific claims significantly impact strategic protection.
  • Claims Analysis: Critical to assess patent enforceability, potential for infringement, and freedom to operate.
  • Landscape Position: The patent sits within Mexico’s evolving pharmaceutical IP environment, with implications for generic entry and innovation.
  • Legal and Market Strategies: Patent robustness influences licensing, litigation, and market exclusivity strategies.
  • Regulatory Considerations: Patent status can affect regulatory approvals and negotiations with local authorities.

FAQs

1. What is the typical validity period for MXPA06009296?
It is generally 20 years from the filing date, subject to maintenance fees and legal prolongations.

2. Can this patent be challenged or invalidated in Mexico?
Yes. Challenges can be filed based on prior art, lack of novelty, or inventive step, subject to Mexican patent procedures.

3. How does this patent influence drug market dynamics in Mexico?
It grants exclusive rights, potentially delaying generic competition and affecting pricing and availability.

4. Are there international equivalents of MXPA06009296?
If the applicant filed in other jurisdictions, similar patents may exist elsewhere, affecting global patent strategies.

5. What considerations should generic manufacturers have regarding this patent?
They should analyze the patent claims for potential infringement, assess the validity of the patent, and explore design-around strategies if applicable.


References

  1. Mexican Institute of Industrial Property (IMPI). Official patent database.
  2. World Intellectual Property Organization (WIPO). Patent Landscape Reports.
  3. Mexican Industrial Property Law (Ley de la Propiedad Industrial).

Note: Exact details such as the filing and grant dates, applicant details, and full claims are recommended to verify via official IMPI records for comprehensive analysis.

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.