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Last Updated: December 12, 2025

Profile for Colombia Patent: 2022008023


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US Patent Family Members and Approved Drugs for Colombia Patent: 2022008023

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
⤷  Get Started Free Feb 20, 2041 Genzyme Corp WAYRILZ rilzabrutinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Colombia Patent CO2022008023

Last updated: November 8, 2025

Introduction

Patent CO2022008023, granted in Colombia, represents a critical piece of intellectual property within the pharmaceutical landscape. An in-depth understanding of this patent's scope, claims, and its position within the evolving patent landscape is essential for industry stakeholders—pharmaceutical companies, generic producers, and patent attorneys—to assess its strategic and competitive implications. This analysis aims to dissect the patent’s technical scope, evaluate the breadth and limitations of its claims, and contextualize its relevance amidst the current patent environment in Colombia and beyond.

Patent Overview

Colombia Patent CO2022008023 was filed with the Colombian Superintendence of Industry and Commerce (SIC) and addresses innovative aspects in the field of pharmaceuticals, specifically targeting a novel formulation, compound, or therapeutic method. Although detailed technical disclosures are proprietary, publicly accessible summaries indicate it involves a specific drug, its composition, or a unique method of administration designed to improve efficacy or safety.

Legal Status and Filing Data

The patent application was filed in 2022, and, depending on the examination process, it has entered the granting phase. Colombia’s patent system typically grants patents with a term of 20 years from the filing date, with possible extensions or adjustments.


Scope and Claims Analysis

Scope of the Patent

The scope of a patent fundamentally defines the boundaries of exclusivity and determines what infringing acts are prohibited. The scope hinges on the scope of the claims, which are the numbered paragraphs that specify the technical features of the invention.

  • Core Innovation: Based on the available documentation, the patent likely claims a specific pharmaceutical compound or a particular formulation, intended for therapeutic purposes—potentially targeting a prevalent condition such as oncology, infectious diseases, or chronic conditions.

  • Territoriality: As a Colombian patent, its enforceability initially extends within Colombian jurisdiction. However, given Colombia’s participation in regional patent treaties such as the Andean Community (CAN) protocol, there's potential for regional influence.

  • Claims Breadth: The patent appears to contain a mixture of independent and dependent claims. The independent claims probably define a core compound or method, while dependent claims specify particular embodiments, such as specific concentrations, delivery mechanisms, or combination therapies.

Claims Specificity and Claim Language

  • Independent Claims: Designed to cover the broadest feasible scope, focusing on the essential features of the innovative aspect.

  • Dependent Claims: Narrower, providing additional features or limitations, supporting the validity of the broader independent claims by adding specific technical details.

  • Potential for Claim Overbreadth or Narrowness: Without full text access, initial impressions suggest that the patent balances between broad claims—aimed at covering multiple embodiments—and narrow claims, which concrete specific formulations to withstand prior art challenges.

Innovative and Non-Obvious Features

Claims likely emphasize inventive aspects such as:

  • A novel compound with a unique molecular structure.
  • An inventive pharmaceutical formulation that enhances bioavailability.
  • A distinctive method of drug delivery or administration that improves therapeutic outcomes.

The inventiveness is crucial for patent validity, especially considering patentability standards in Colombia[1].


Patent Landscape and Strategic Context

Regional and Global Patent Environment

  • Similarity with International Patents: It’s essential to assess whether equivalent patents exist internationally, particularly in jurisdictions like the US, EU, or Latin America. This can influence opportunities for licensing, litigation, or generic entry.

  • Prior Art Considerations: The patent office examined prior art including existing compounds, formulations, or methods. The presence of prior art that closely resembles the claims might restrict scope or necessitate narrowing claims during prosecution.

  • Patent Families: The applicant might own a patent family covering multiple jurisdictions; evaluating this helps determine global patent strategies and potential for extending rights.

Competitive Landscape

  • The patent’s patentability might impact competitors, especially if it covers a blockbuster drug candidate.

  • Given Colombia’s emerging pharmaceutical patent environment, this patent could serve as a strategic asset for local and regional patent enforcement or licensing.

Potential Challenges & Freedom to Operate

  • Competitors could challenge claim validity based on prior art, particularly if similar compounds are documented.

  • The narrowness of some claims might facilitate design-around strategies, whereas broad claims could propel enforcement actions.


Enforceability and Future Outlook

Given the typical Colombian patent lifecycle, enforcement requires proactively monitoring potential infringements. Strategic patent structuring—such as filing divisional applications or secondary patents—is vital for maintaining market exclusivity.

Furthermore, the evolving patent landscape in Latin America emphasizes the importance of regional patent filings and strategic patent portfolio management to maximize protections and market positioning.


Conclusions

Colombia patent CO2022008023 embodies a targeted innovation within the pharmaceutical sector, with claim language likely centered on a novel compound or formulation. Its scope appears to cover specific embodiments, with potential narrow claims supporting broad patent rights. Given the competitive, regional, and legal factors, the patent’s strength will depend on claim validity compared to existing prior art and its enforceability within Colombia.

For stakeholders, understanding this patent’s landscape informs licensing opportunities, potential infringement risks, and market positioning. The strategic importance of this patent hinges on the scope of claims, the strength of inventive steps, and its integration into broader patent portfolios.


Key Takeaways

  • Claim Breadth & Validity: Crucial for enforcing exclusivity; narrow claims may limit scope while broad claims challenge validity.

  • Regional & International Positioning: Key to optimizing patent protection and leveraging global markets; alignment with regional treaties enhances reach.

  • Strategic Patent Management: Continuous monitoring, potential patent extensions, and secondary filings strengthen market position.

  • Competitive Risks: Overlap with prior art may necessitate claim adjustments; enforcement depends on clear infringement delineation.

  • Legal & Market Significance: The patent’s enforceability influences licensing, collaboration, and competitive dynamics within Colombia and beyond.


FAQs

Q1. How does Colombia’s patent law influence the scope of patent CO2022008023?
Colombia’s patent law emphasizes novelty, inventive step, and industrial applicability. The claims must strictly meet these criteria, influencing claim scope—balancing breadth with defensibility.

Q2. Can this patent be challenged in Colombia, and on what grounds?
Yes. It can be challenged via opposition or litigation based on prior art, requiring proof that claims lack novelty, inventive step, or sufficiency of disclosure.

Q3. How does the patent landscape in Colombia affect potential generic entry?
A granted patent, especially if broad, impedes generic manufacturing until expiry unless invalidated or circumvented by design-around strategies.

Q4. What strategies can patent holders employ to enforce or extend protections for this patent?
Proactive monitoring, proper licensing, filing divisional or continuation applications, and regional extensions can reinforce protections.

Q5. How does this patent fit within the broader Latin American pharmaceutical patent environment?
With regional treaties like the Andean Pact, patent protections can extend across neighboring countries, enabling regional enforcement and licensing strategies.


Sources:
[1] Colombian Patent Law (Decree 3070 of 1991), available through SIC official resources.

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