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Last Updated: December 31, 2025

Profile for Colombia Patent: 2024013947


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US Patent Family Members and Approved Drugs for Colombia Patent: 2024013947

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 17, 2041 Springworks GOMEKLI mirdametinib
⤷  Get Started Free Apr 9, 2043 Springworks GOMEKLI mirdametinib
⤷  Get Started Free Feb 17, 2041 Springworks GOMEKLI mirdametinib
⤷  Get Started Free Mar 16, 2043 Springworks GOMEKLI mirdametinib
⤷  Get Started Free Mar 16, 2043 Springworks GOMEKLI mirdametinib
⤷  Get Started Free Feb 17, 2041 Springworks GOMEKLI mirdametinib
⤷  Get Started Free Mar 16, 2043 Springworks GOMEKLI mirdametinib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Colombia Patent CO2024013947

Last updated: August 2, 2025


Introduction

The patent application CO2024013947, granted in Colombia, addresses a novel pharmaceutical invention. Its scope, claims, and positioning within the existing patent landscape play a crucial role in establishing patent rights, market exclusivity, and competitive advantage. This analysis offers a comprehensive review of the patent’s claims, elucidates its scope, and situates it within the broader Colombian patent landscape relevant to pharmaceuticals.


Patent Overview and Basic Attributes

  • Application Number: CO2024013947
  • Application Date: [Insert Application Date] (Assuming recent and aligned with current filings)
  • Grant Date: [Insert Grant Date] (assuming recent)
  • Inventors / Assignees: [Insert if available]
  • Patent Type: Utility patent (most likely in pharmaceuticals)

This patent likely pertains to a new chemical entity, a novel formulation, or a method of manufacturing or use. Based on the number structure, this patent seems part of Colombia’s recent pharmaceutical innovation environment, often aligned with local and regional patent strategies.


Scope of the Patent

The scope of a patent is primarily delineated through its claims sections. While exact claims from CO2024013947 are not available here, typical pharmaceutical patents encompass:

  • Compound Claims: Cover specific chemical entities or derivatives.
  • Method Claims: Specify novel processes for synthesizing compounds.
  • Use Claims: Cover methods of treating diseases or conditions with the compound.
  • Formulation Claims: Protect specific pharmaceutical compositions.

Given standard practices, this patent most likely concentrates on a chemical compound with a unique structure and its specific therapeutic applications, potentially targeting a particular disease (e.g., cancer, infectious diseases, or metabolic disorders).

The scope is intended to be broad enough to prevent competitors from producing similar compounds or utilizing alternative methods of synthesis and application, but sufficiently detailed to satisfy novelty and inventive step criteria.


Claims Analysis

1. Independent Claims:
Typically define the core innovation—likely a novel chemical structure or a pharmaceutical composition. For example, a claim might specify:

  • "A compound of formula I," followed by a detailed chemical structure.
  • A method of preparing the compound involving specific reagents and conditions.
  • A method of treating a disease using the compound.

2. Dependent Claims:
These narrow the scope to particular embodiments, such as specific substitutions, formulations, or therapeutic indications. They offer fallback positions if broad independent claims are invalidated.

3. Novelty and Inventive Step:
Claims must demonstrate unexpectedly improved efficacy, reduced side effects, or novel mechanisms of action compared to prior art. If the patent claims a new chemical entity, the novelty hinges on prior art references failing to disclose identical or similar compounds.

4. Potential Limitations and Defenses:
Possible limitations include the presence of prior art disclosing similar structures or uses. Defensive strategies may involve emphasizing unique structural features or unexpected therapeutic benefits.

Potential Scope and Limitations

Given Colombia's patent standards, the patent likely emphasizes:

  • The novelty of the specific chemical structure, including unique substitution patterns.
  • Improved pharmacokinetic or pharmacodynamic properties.
  • Specific therapeutic use cases with demonstrated efficacy.

Any claims overly broad risk rejection or invalidation, whereas overly narrow claims may limit commercial scope.


Patent Landscape in Colombia for Pharmaceutical Innovations

Colombia’s patent environment, governed by the Superintendencia de Industria y Comercio (SIC), has seen an evolving landscape emphasizing innovation in pharmaceuticals, aligned with TRIPS obligations and regional harmonization. Key characteristics include:

  • High Standards for Patentability: Requiring novelty, inventive step, and industrial applicability.
  • Focus on Chemical and Biological Inventions: Patentability extends to new compounds, formulations, and uses.
  • Challenges from Patentability Exclusions: Exclusion of methods of medical treatment per Supreme Court decisions, limiting method claims but not compound claims.

Existing Patent Landscape:

  • Numerous patents for innovative drugs targeting infectious diseases, metabolic disorders, and oncology.
  • A steadily increasing number of pharmaceutical patent applications, reflecting Colombia’s expanding R&D capacity.
  • Previous patent conflicts often revolve around inhalation devices, formulations, and compound structures.

Implications for CO2024013947:

  • Must carefully navigate prior art references in Colombia’s patent applications and granted patents.
  • Should emphasize unique structural features or innovative therapeutic applications to withstand challenges.
  • Could face opposition based on health policies favoring access, which may invoke compulsory licensing or patent exceptions.

Legal and Commercial Significance

Legal Factors:

  • The patent sustains exclusivity for 20 years from filing, incentivizing investment in R&D.
  • It provides a basis to prevent unauthorized manufacture, use, or sale within Colombia.
  • Enforceability depends on robust claims and clear delineation of scope.

Commercial Factors:

  • The patent supports marketing exclusivity, enabling premium pricing strategies.
  • It enhances licensing opportunities, attracting regional partners.
  • The scope influences generic entry; narrower claims may ease biosimilar or generic competition.

Challenges and Opportunities

Challenges:

  • Prior Art Clearance: Ensuring no existing patents or publications undermine validity.
  • Patent Thinness: Broad or vague claims risk invalidation.
  • Regulatory Hurdles: Obtaining marketing approval in Colombia may require demonstrating patent-supported therapeutic claims.

Opportunities:

  • Regional Expansion: Patent rights can be extended through patent family filings in Latin America.
  • Strategic Licensing: The patent could serve as an asset for licensing agreements within Colombia and neighboring markets.
  • Patent Enforcement: Strong claims enable litigation against infringers, securing market position.

Key Takeaways

  • Scope & Claims: Likely centered on a novel chemical entity with specific therapeutic applications, with claims tailored to emphasize structural uniqueness and efficacy.
  • Patent Landscape: The Colombian pharmaceutical patent environment is dynamic, with increasing filings; patent strategy should focus on carve-outs that withstand prior art and legal scrutiny.
  • Commercial Strategy: The patent's strength depends on well-defined claims, securing market exclusivity and enabling regional patent family development.
  • Legal Navigation: Must address local patent law nuances, especially in biological and chemical patentability, and prepare for possible opposition or validity challenges.
  • Policy Impact: Colombian regulations favor innovation but also balance public health needs, which may influence enforcement and licensing strategies.

FAQs

Q1: What makes a chemical compound patentable under Colombian law?
A1: The compound must be novel, involve an inventive step, and be industrially applicable. The chemical structure must not be disclosed in prior art, and the invention must demonstrate a non-obvious technical advancement.

Q2: How does the scope of claims impact patent enforcement in Colombia?
A2: Broader claims offer greater protection but risk invalidation if overly encompassing or not adequately supported by the description. Narrow claims may be easier to defend but limit exclusivity.

Q3: Can method of use claims be protected in Colombia?
A3: Yes, but Colombia’s courts typically restrict patentability of methods of medical treatment, focusing on the compound and formulation claims. Use claims must be crafted carefully to stay within legal bounds.

Q4: How does Colombia’s patent landscape influence pharmaceutical innovation?
A4: The evolving environment offers opportunities but requires careful strategy; robust patent claims, thorough prior art searches, and regional patent filings are essential for competitive advantage.

Q5: What are best practices for maintaining patent validity in Colombia?
A5: Regular patent maintenance, diligent enforcement, and strategic narrowing of claims can ensure longevity. Monitoring for potential challenges or invalidations is also vital.


References

  1. Colombian SCI Patent Law and Regulations. Superintendencia de Industria y Comercio.
  2. World Intellectual Property Organization (WIPO) Patent Search.
  3. Colombian Patent Office (SIC) Official Documentation.
  4. TRIPS Agreement – World Trade Organization.
  5. Industry Reports on Pharmaceutical Patent Trends in Latin America.

More… ↓

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