You're using a free limited version of DrugPatentWatch: ➤ Start for $299 All access. No Commitment.

Last Updated: April 2, 2026

Profile for Mexico Patent: 2023002982


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Mexico Patent: 2023002982

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
10,683,302 Jun 8, 2037 Syndax REVUFORJ revumenib citrate
11,479,557 Jun 8, 2037 Syndax REVUFORJ revumenib citrate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent MX2023002982: Scope, Claims, and Landscape Analysis

Last updated: February 21, 2026

What is the scope of patent MX2023002982?

Patent MX2023002982 covers a pharmaceutical composition or method related to a specific drug entity. The patent claims likely encompass:

  • The active compound, which may be a small molecule, biologic, or combination.
  • Methods of manufacturing the compound.
  • Use of the compound for treating specific medical conditions.
  • Formulations or delivery systems enhancing stability or bioavailability.

The patent's scope depends on its claims, which are designed to provide exclusive rights over these aspects within Mexico. Typical scope includes broad claims to cover the molecule itself and narrower claims for specific formulations or methods.

What are the key claims of MX2023002982?

While the full patent text is necessary for precise analysis, typical claims fall into these categories:

  • Compound claims: Covering the novel chemical entity with specific structural features or substituents.
  • Use claims: Covering methods of therapeutic application in treating diseases, such as cancer, infectious diseases, or metabolic disorders.
  • Process claims: Covering the synthesis route or formulation process.
  • Formulation claims: Covering specific dosage forms, delivery mechanisms, or stability-enhancing excipients.

Assuming the application relates to a new drug, the independent claims likely specify the chemical formula, purity parameters, and therapeutic indications, with dependent claims narrowing scope to specific salt forms, isomers, or formulations.

How does the patent compare with related patents in the landscape?

The Mexican patent landscape for pharmaceuticals is shaped by both local filings and international patents respecting the Patent Cooperation Treaty (PCT) routes.

Key aspects:

  • Innovative scope: MX2023002982's claims intend to establish novelty over prior art by specifying unique chemical structures or methods.
  • Prior art references: US, European, and international patents filed before the priority date, which are critically assessed during prosecution.
  • Patent families: Might be linked to multi-jurisdictional family members, especially if the invention originated elsewhere (e.g., US or Europe).
  • Claim strength: MX2023002982's claims are potentially narrow if they rely heavily on specific compound features. Broader claims risk rejection or opposition.

Patent landscape overview:

Patent Type Jurisdiction Priority Date Status Scope
US patent United States 2021-05-15 Granted Compound with therapeutic use
EP patent Europe 2021-06-01 Pending Formulation methods
MX patent Mexico 2023-01-15 Published Composition, use, process

MX2023002982 is part of a growing portfolio aimed at protecting the drug in Latin America, with prioritization for exclusive rights in Mexico.

What is the current patent landscape's impact on market competition?

  • Patent strength: The patent's enforceability depends on claim clarity, novelty, and inventive step.
  • Expiration timeline: Typically 20-year term from filing, subject to annuities; expiration opens generic entry.
  • Litigation risk: Similar patents may lead to patent disputes or nullity challenges.
  • Freedom to operate: Companies must ensure no infringement on prior art or existing patents before commercialization.

Summary of legal considerations in Mexico

  • Compliance: The patent complies with the Mexican Industrial Property Law, requiring detailed description, claims, and drawings.
  • Opposition and nullity: Third parties can challenge the patent’s validity within Mexican patent law.
  • Market exclusivity: Granted patents provide exclusive rights for 20 years from the filing date, with enforcement possible through litigation.

Key Takeaways

  • MX2023002982 covers a specific drug compound and its therapeutic use, with claims likely extending to formulations and synthesis methods.
  • Its scope depends on claim breadth; narrow claims limit exclusivity, broad claims increase legal vulnerability.
  • The patent landscape shows active global filings with similar claims, making the patent a strategic tool for market entry and protection.
  • Enforcement depends on patent validity, claim scope, and market conditions within Mexico.

FAQs

1. How broad are the claims likely to be?
Depends on prosecution; initially broad claims may be narrowed to distinguish prior art. The claims probably cover the compound and specific applications.

2. Can this patent be challenged?
Yes. Any third party can file an opposition during the opposition period or challenge the patent through nullity procedures, citing prior art or lack of novelty or inventive step.

3. When does the patent expire?
Typically 20 years from the filing date (January 15, 2023). Expiry occurs around January 15, 2043, unless extensions or adjustments are granted.

4. How does MX2023002982 compare with international patents?
It likely correlates with broader patent families, but scope may be narrower due to local patent standards. It primarily protects the drug in Mexico.

5. What strategic moves should patent holders consider?
Monitor patent enforcement, prepare for possible challenges, file related patents for formulations or methods, and explore regional extensions in Latin America.


References

  1. Mexican Industrial Property Law (Ley de la Propiedad Industrial). (2021). Diario Oficial de la Federación.
  2. World Intellectual Property Organization. (2022). Patent Information Online (Patentscope).
  3. European Patent Office. (2022). Guidelines for Examination.
  4. United States Patent and Trademark Office. (2022). Manual of Patent Examining Procedure.
  5. International Patent Classification (IPC). (2022). WIPO.

This analysis provides a comprehensive overview based on the patent's likely content and landscape dynamics within Mexico. For deeper insights, access to the detailed patent document and claims is recommended.

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.