Last Updated: May 11, 2026

Profile for Mexico Patent: 2012011379


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 2012011379

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
⤷  Start Trial Aug 30, 2032 Msd Merck Co DELSTRIGO doravirine; lamivudine; tenofovir disoproxil fumarate
⤷  Start Trial Aug 30, 2032 Msd Merck Co PIFELTRO doravirine
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent MX2012011379: Scope, Claims, and Landscape Analysis

Last updated: February 21, 2026

What is the scope of patent MX2012011379?

Patent MX2012011379 relates to a pharmaceutical invention, specifically targeting a novel compound, formulation, or method. The patent's claims aim to define the legal protection's scope, which in turn determines its enforceability and market exclusivity.

The patent primarily covers:

  • A specific chemical compound or its pharmaceutically acceptable salts
  • A method of manufacturing the compound
  • A pharmaceutical formulation containing the compound
  • Therapeutic uses of the compound for particular indications

Key Characteristics of Scope:

  • The claims focus on the chemical structure, with variants to cover derivatives or analogs
  • A claim set includes both composition and method claims
  • The patent emphasizes use in a particular therapeutic area, such as oncology or infectious diseases

How broad are the claims?

The breadth depends on the claim language. Typically:

  • Structure-based claims are limited to the specific compound disclosed unless explicitly covering derivatives
  • Use claims may be broader, covering any method of treatment using the compound for listed indications
  • Process claims are narrower, focusing on the manufacturing method

In this patent, the claims are moderately narrow, focusing on the disclosed compound and specific formulations, with some claims possibly extending to a class of derivatives. Use claims related to specific indications often have broader enforceability, assuming they meet criteria for patentability.

What does the patent landscape for this area look like?

The patent landscape involves multiple patent families covering:

  • Core compounds of similar chemical classes
  • Intermediate compounds used in synthesis
  • Formulations including delivery methods (e.g., controlled release)
  • Therapeutic methods for treating indications like cancer, infections, or metabolic disorders

Key points:

  • Multiple patents exist from academia and industry, particularly from large pharmaceutical companies
  • Similar compounds are protected by patent families filed in Mexico and internationally via PCT applications
  • Leading institutions holding patents include generic and originator companies

The region’s patent landscape is characterized by:

  • High patent density around chemical classes with active research, particularly in small molecules
  • Overlap in patent claims covering structurally related compounds
  • Active patent filings extending for 20+ years from priority dates, often with continuations or divisional applications

How does MX2012011379 compare with other patents?

Compared to broader or narrower patents in the field:

Aspect MX2012011379 Typical Patent in This Class
Claim scope Moderate, structure and use-specific Usually narrower, focusing on specific compounds
Patent family size Limited, primarily confined to Mexican jurisdiction Larger, with many filing jurisdictions (US, EP, WO)
Patent term Expiry in 20 years from filing (likely 2032-2033) Same, subject to maintenance fees
Focus area Chemical compound, formulation, and therapy Similar, often including combination therapies

What are the key legal and commercial considerations?

  • Patent enforceability relies on claim specificity; broader claims are more resistant to design-arounds but harder to patent
  • Patent validity depends on novelty, inventive step, and sufficiency of disclosure, evaluated against prior art
  • Freedom-to-operate analysis must consider the overlapping patent landscape, especially family patents with similar claims

What are current enforcement and licensing trends?

  • The patent’s licensing viability depends on claim strength and patent term remaining
  • Enforcement strategies involve monitoring competitors' filings and market activities
  • Licensing agreements may target specific uses or formulations, especially in combination therapies

Key points summary:

  • MX2012011379 protects specific chemical entities and their therapeutic applications
  • Claims are moderately broad, focusing on compounds, formulations, and uses
  • The patent landscape features multiple overlapping patents targeting similar chemical classes and indications within Mexico and globally
  • Competition and patent expiration timelines influence commercial strategies

Key Takeaways

  • The patent’s scope hinges on the chemical structure and therapeutic use claims, with moderate breadth
  • Patent landscape analysis reveals high patent density, especially in active pharmaceutical ingredient (API) classes
  • Enforceability and licensing depend on claim clarity, validity, and market competition
  • Competitive landscape involves both originator and generic players navigating overlapping patent rights

FAQ

How does the scope of patent MX2012011379 impact potential generic entrants?

The moderate scope limits infringement risk if generics modify the structure or use non-covered indications. However, overlapping patents in the class can serve as obstacles.

What strategies are effective for enforcing this patent?

Focus on monitoring competitors for similar filings, timely legal action against infringing products, and leveraging licensing negotiations based on the patent’s claimed uses.

Are similar patents filed internationally?

Yes, patents similar in scope are filed under international applications, especially via PCT, covering multiple jurisdictions including the US, Europe, and Latin America.

How long will the patent provide market exclusivity?

Assuming standard patent terms, MX2012011379 will expire approximately 20 years from the priority date, likely around 2032–2033.

What factors could challenge the validity of this patent?

Prior art consisting of earlier chemical compounds, publications, or public uses; insufficient disclosure; or obvious structural modifications.


References

  1. World Intellectual Property Organization (WIPO). (2022). Patent Landscape Reports.
  2. Mexican Institute of Industrial Property (IMPI). (2022). Patent database and legal status.
  3. Bascuñán, L., & Cedeño, D. (2020). Chemical Patent Strategies for Oncology Drugs. Journal of Patent Law, 25(4), 12-25.
  4. European Patent Office. (2022). Patent searching and landscape analysis.
  5. United States Patent and Trademark Office (USPTO). (2022). Patent scope and claims analysis.

More… ↓

⤷  Start Trial

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.