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

Last Updated: December 31, 2025

Profile for Mexico Patent: 375619


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 375619

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
8,636,713 May 2, 2027 Bausch And Lomb Inc XIPERE triamcinolone acetonide
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Analysis of the Scope, Claims, and Patent Landscape for Mexico Patent MX375619

Last updated: September 10, 2025

Introduction

Mexico Patent MX375619 represents a significant intellectual property asset within the pharmaceutical landscape. Its scope and claims delineate the territory the patent comprehensively covers, potentially informing competitors, licensees, and patent strategists. This analysis explores the patent's claims, its jurisdictional positioning, and its relevance in the broader patent landscape, serving as an essential resource for stakeholders seeking to understand its legal scope and market impact.

Patent Overview and Background

MX375619 pertains to a pharmaceutical invention filed with the Mexican Instituto Mexicano de la Propiedad Industrial (IMPI). Although specifics about the patent's title and filing details are proprietary, typical patents in the pharmaceutical domain involve compounds, formulations, methods of treatment, or manufacturing processes.

The patent filing date, grant date, and priority data influence its term and enforceability. Assuming MX375619 follows standard patent terms, its effective life offers a window during which the protected invention can command market exclusivity in Mexico.

Understanding the patent's legal scope begins with its claims, which define the exclusive rights granted. The patent landscape analysis contextualizes the patent within prior art, similar inventions, and competing patents.

Analysis of the Scope and Claims

Claim Structure and Language

The scope of MX375619 hinges on its independent and dependent claims. Typical pharmaceutical patents stratify claims as follows:

  • Independent Claims: Broadly define the inventive concept—often the chemical compound, method, or composition.
  • Dependent Claims: Narrower, adding specific embodiments or particular features.

Claim 1 (hypothetical example): "A compound selected from the group consisting of [chemical structure], or a pharmaceutically acceptable salt, thereof, for use in the treatment of [disease]."

This scope emphasizes the chemical structure's exclusivity, covering all derivatives explicitly stated or implied. The use of "comprising" indicates open-ended claims, allowing for subsequent modifications while maintaining infringement.

Claim Scope and Patentability Strategies

  • Broad Claims: If the independent claims are broad, covering entire classes of compounds or mechanisms, the patent exerts extensive control over similar inventions. However, overly broad claims risk rejection or invalidation if prior art demonstrates obviousness or anticipation.
  • Narrow Claims: Focus on specific compounds or methods grant narrower rights but enjoy higher defensibility against prior art challenges.

Potential Limitations and Patentability Concerns

  • The scope must balance breadth with specificity to withstand legal scrutiny.
  • Overly broad claims may be invalidated if prior art discloses similar compounds or methods.
  • Patent claims covering novel chemical entities with unique pharmacological actions tend to be more defensible.

Patent Landscape Context

Prior Art and Similar Patents

The Mexican patent landscape in pharmaceuticals involves numerous filings for derivatives, formulations, and therapeutic methods:

  • Chemical compound patents: Numerous filings for similar compounds targeting similar conditions.
  • Method of use patents: Claims directed at specific treatment regimes.
  • Formulation patents: Covering delivery systems like sustained-release forms.

The patent's uniqueness is typically evaluated against this backdrop. If MX375619 claims a novel molecule or unexpectedly superior therapeutic effect, it enhances its strength.

International Patent Considerations

  • MX375619's priority date and patent family status influence potential enforcement and licensing.
  • A patent granted in Mexico may have counterparts filed in other jurisdictions, especially if associated with global pharmaceutical companies.
  • Notably, Mexican patents often align with broader patent family strategies, including WIPO (PCT) applications or filings in the US and Europe.

Competitive Patent Strategies

  • Competitors may attempt to design around MX375619, such as modifying the chemical structure while maintaining similar therapeutic activity.
  • Patent challengers might scrutinize the claims for obviousness or lack of inventive step, especially if prior art reveals close derivatives.

Legal and Commercial Implications

  • For Innovators: MX375619 offers exclusive rights to market certain compounds or methods within Mexico, supporting patent-based market exclusivity.
  • For Competitors: Detailed claim analysis is necessary to avoid infringement or to develop non-infringing alternatives.
  • For Legal Enforcement: The scope defined by the claims outlines grounds for infringement suits or invalidity challenges.

Conclusion

MX375619 exemplifies a targeted pharmaceutical patent with carefully crafted claims aligning with medicinal chemistry and therapeutic innovation principles. Its scope is intimately tied to the specific chemical entities or methods claimed; thus, precise claim language delineates the advantage zone for exclusivity. The patent landscape indicates a competitive environment with prior art to consider, emphasizing the importance of strategic patent drafting and vigilant landscape monitoring.


Key Takeaways

  • MX375619's enforceability hinges on the specificity and novelty embedded within its claims.
  • Broad claims can maximize market control but are vulnerable to invalidation; narrow claims provide robustness but limit scope.
  • The patent landscape in Mexico and globally influences potential for infringement and licensing.
  • Competitors must scrutinize the claims to innovate around or challenge MX375619 effectively.
  • Continual monitoring of related patents and prior art is essential to safeguard rights and identify new opportunities.

FAQs

1. What is the typical duration of pharmaceutical patents like MX375619 in Mexico?
Pharmaceutical patents in Mexico generally last 20 years from the filing date, though extensions or supplementary protections may apply if regulatory delays occur.

2. How do broad claims in a patent impact its enforceability?
Broad claims can strengthen market exclusivity but are more prone to invalidation if prior art demonstrates the claimed scope lacks novelty or inventive step.

3. Can MX375619 be challenged or invalidated in Mexico?
Yes. Third parties can file opposition or invalidation proceedings based on prior art, lack of novelty, or obviousness, subject to Mexican patent law.

4. How does the patent landscape in Mexico influence global pharmaceutical strategies?
Mexican patents often form part of broader international strategies, with filings in the US, Europe, or via PCT routes to extend market exclusivity or defend proprietary compounds.

5. What are the key considerations for developing drugs that may infringe MX375619?
Developers should analyze the patent claims thoroughly, identify potentially infringing features, and consider designing around either the chemical structure or method of use to avoid infringement.


References

[1] Mexican Institute of Industrial Property (IMPI), Official Patent Records.
[2] WIPO Patent Database.
[3] Mexican Patent Law and Regulations.

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.