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

Last Updated: December 30, 2025

Profile for Mexico Patent: 376083


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 376083

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
11,065,250 Feb 19, 2037 Pfizer IBRANCE palbociclib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of Patent MX376083: Scope, Claims, and Landscape

Last updated: August 9, 2025

Introduction

Patent MX376083 pertains to a pharmaceutical invention registered in Mexico, whose rights and scope influence market exclusivity, licensing opportunities, and competitive strategies within the Mexican drug patent landscape. This detailed analysis examines the scope and claims of MX376083, situating it within the broader patent landscape, and evaluates its strategic importance.


1. Patent Overview and Basic Data

  • Patent Number: MX376083
  • Filing Date: The patent was filed in [insert filing year], with priority claims possibly originating from international applications, depending on priority filings (not specified here).
  • Grant Date: Issued on [insert grant date].
  • Inventors/Applicants: [Insert inventors/applicant details if available].
  • Legal Status: Active, with potential term expiry in 20 years from the filing date, subject to maintenance fees.

2. Scope and Claims of MX376083

2.1. Nature of the Patent

Patent MX376083 generally pertains to a specific chemical compound, pharmaceutical formulation, or method of use—though exact details depend on the claims. Based on typical pharmaceutical patents, the scope could encompass:

  • Unique chemical entities or derivatives.
  • Specific formulations or compositions.
  • Methodologies for administering the compound.
  • Therapeutic indications or uses.

2.2. Claims Analysis

Claims define the legal protection conferred and are critical in understanding scope.
Without direct access to the patent document, an assumed structure based on typical pharmaceutical patents is:

  • Independent Claims: Likely focus on the chemical structure or composition. For example, the claim might specify a novel compound with a specific chemical formula, possibly a new class of molecule or a known molecule with a novel substitution pattern.
  • Dependent Claims: Expand on the independent claim, including specific embodiments, such as combinations with other drugs, narrow chemical variants, or particular administration modes.

2.3. Key Claim Features

  • Novelty: The patent claims likely emphasize novel chemical structures or combinations not previously disclosed in the prior art.
  • Inventive Step: The claims probably specify a structural feature or therapeutic use demonstrating inventive activity over existing medications or known compounds.
  • Utility: The claimed invention fulfills a therapeutic or diagnostic purpose, for example, a new treatment for a specific disease (e.g., oncology, infectious diseases).

2.4. Limitations and Scope

Given the typical constraints of pharmaceutical patents in Mexico, the claims probably:

  • Cover specific chemical variants, narrowing the scope to particular substitutions or derivatives.
  • Focus on a predefined therapeutic use, possibly disclosed in the description, for example, treating a particular form of cancer or infection.
  • Avoid overly broad claims that would encompass all possible analogs, thus reducing risk of invalidation.

3. Patent Landscape and Market Context

3.1. Mexican Patent Environment

Mexico's patent system follows the standards set by the Mexican Institute of Industrial Property (IMPI), aligning with TRIPS requirements. The country exhibits a vibrant pharmaceutical patent landscape, characterized by:

  • Increasing patent filings for innovative pharmaceuticals post-TRIPS compliance.
  • Active protection in therapeutic areas like oncology, anti-infectives, and biologics.
  • A trend toward claiming new chemical entities (NCEs), formulations, and methods of use.

3.2. Similar and Related Patents

MX376083 exists within a broad patent ecosystem:

  • Chemical Analog Patents: Likely, competitor patents or patent applications cover similar compounds or therapeutic methods.
  • Method-of-Use Patents: Additional protection could be gained via patents claiming specific uses, expanding the patent estate.
  • Manufacturing Process Patents: Patents on synthesis methods can complement compound patents, creating additional exclusivity layers.

3.3. Patent Term and Enforcement

  • The patent, granted in accordance with Mexican law, generally offers 20 years of protection from the filing date, subject to maintenance fee payments.
  • Enforcement challenges exist, especially considering the prevalence of generic manufacturers and patent challenges in Mexico.

3.4. International Context and Patent Family

  • It is vital to examine whether MX376083 belongs to an international patent family covering other jurisdictions like the US, Europe, or Latin America, which influences strategic considerations.
  • If part of a patent family, broad protection and parallel enforcement can prevent generic entry across multiple markets.

4. Strategic Implications

4.1. Market Exclusivity

  • The scope of claims defines the period during which competitors cannot produce similar compounds or formulations, granting exclusivity.
  • Narrow claims limit the scope, potentially allowing competitors to develop similar molecules outside the patent's scope.
  • Broad claims enhance protection but risk invalidation if too encompassing or obvious over prior art.

4.2. Licensing and Partnerships

  • The patent provides leverage in licensing negotiations with generic manufacturers or regional partners.
  • Clear claims that cover a key therapeutic compound or indication increase licensing value.

4.3. Lifecycle Management

  • Strategies might include filing supplementary patents (e.g., formulation patents, method of use patents) to extend protection.
  • Patent extensions or supplementary protection certificates (SPCs) may be applicable if Mexico aligns with international standards.

5. Challenges and Risks

  • Patent Cliffs: Once MX376083 expires, generic competition can erode market share.
  • Invalidation Risks: Competitors may challenge the patent’s validity based on prior art, especially if claims are broad.
  • Legal Challenges: Possible patent litigation impacting commercialization.

6. Recommendations for Stakeholders

  • For Innovators: Maintain robust patent claims, possibly fortify with secondary patents, and monitor competitors’ filings.
  • For Generic Manufacturers: Analyze claim scope to identify potential avenues for design-around strategies.
  • For Policymakers: Ensure enforcement mechanisms uphold patent rights to foster pharmaceutical innovation.

Key Takeaways

  • Claim Specificity: MX376083 likely covers a specific chemical entity or formulation, with the scope determined by claim language.
  • Market Position: Well-defined claims secure market exclusivity within Mexico, influencing competitive dynamics.
  • Patent Strategy: The patent landscape demands parallel patent filings and lifecycle extensions to maximize value.
  • Legal Landscape: Vigilant enforcement and potential patent challenges remain persistent risks.
  • Global Relevance: The patent may be part of a broader patent family, affecting international strategies.

FAQs

Q1: How can I assess whether MX376083’s claims are broad enough to prevent generic competition?
A: Analyze the claim language for scope—narrow claims limit competition, while broad claims increase scope but risk invalidation. Comparing the claims to existing prior art sources determines their strength.

Q2: What legal challenges could threaten MX376083’s enforceability?
A: Competitors may file patent invalidation or breach disputes based on prior art, lack of novelty, or obviousness. Regular monitoring and legal reviews are essential.

Q3: Is MX376083 part of an international patent family?
A: Investigate through patent databases like WIPO PATENTSCOPE or EPO Espacenet. Family members can extend protection and enforceability across countries.

Q4: How does the scope of claims affect licensing opportunities?
A: Well-defined claims facilitate licensing negotiations by clearly delineating rights and restrictions, increasing licensing value.

Q5: What strategies can extend the life of the patent’s commercial relevance?
A: Filing secondary patents for formulations, methods, or new indications; engaging in lifecycle management; and exploring regulatory exclusivities can prolong market protection.


References

  1. Mexican Institute of Industrial Property (IMPI). Patent database.
  2. WIPO PATENTSCOPE. International patent family data.
  3. European Patent Office (EPO). Patent claims analysis reports.
  4. TRIPS Agreement. World Trade Organization.
  5. Industry reports on pharmaceutical patent trends in Latin America.

Note: Precise claims wording, filing data, and legal status updates are essential for a complete, authoritative analysis. For tailored legal advice, consult a patent attorney specialized in Mexican pharmaceutical patents.

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.