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

Last Updated: December 18, 2025

Profile for Colombia Patent: 2023004141


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Colombia Patent: 2023004141

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 Sep 10, 2041 Bristol KRAZATI adagrasib
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope and Claims and Patent Landscape for Colombia Patent CO2023004141

Last updated: July 29, 2025


Introduction

Patent CO2023004141 pertains to a pharmaceutical invention filed and granted within Colombia, contributing to the country's expanding patent landscape in the biotech and pharmaceutical sectors. This analysis dissects the scope and claims of the patent, assesses its positioning within Colombia's patent ecosystem, and identifies relevant precedents and overlapping patents to understand its strength, novelty, and potential competitive impact.


Patent Overview

Patent Number: CO2023004141
Filing Date: [Exact date not provided but assumed recent based on numbering]
Grant Date: [Not provided, indicating recent approval or publication]
Applicant: [Applicant details not provided, typically a pharmaceutical company or research institution]
Title: [Title not provided; assume related to a new drug compound, formulation, or therapeutic method]

The patent likely relates to a novel pharmaceutical compound or a specific formulation, method of use, or manufacturing process. Colombia’s patent law aligns with the TRIPS Agreement, emphasizing patentability of new inventions with novelty, inventive step, and industrial application.


Scope and Claims

Scope of the Patent

The scope defines the legal boundaries of the patent rights, centered around the specific invention’s novelty and inventive contribution. While the exact claims are not provided, a typical patent in this domain includes:

  • Compound Claims: Patent claims covering specific chemical entities, structures, or variants—possibly a new molecular formula or a derivative with therapeutic properties.
  • Method Claims: Claims related to methods of synthesis, formulation, or treatment involving the compound.
  • Use Claims: Specific therapeutic applications, e.g., treatment of particular diseases or medical conditions.
  • Formulation Claims: Specific pharmaceutical compositions, delivery systems, or excipient combinations.

Claim Types and Their Likelihood

  • Independent Claims: Cover core compound or method, defining the primary innovation.
  • Dependent Claims: Cover specific embodiments, such as salts, polymorphs, dosing regimes, or administration routes.

In Colombia, claims must clearly differentiate the invention from prior art, and a robust set of dependent claims strengthens patent scope, reducing loopholes for invalidation.


Analysis of Key Claims

1. Chemical Structure or Composition Claims

If the patent covers a novel chemical entity, claims likely define the compound’s molecular formula, specific substitutions, or stereochemistry. The scope will depend on how broadly these claims are drafted; broader claims increase market protection but risk invalidation if prior art exists.

2. Therapeutic Application Claims

Claims dedicated to medical use or treatment methods—such as administering the drug to treat a particular disease—are common and can extend patent life by covering various therapeutic indications.

3. Manufacturing Process Claims

Claims that specify innovative synthesis pathways, purification techniques, or formulation methods provide additional layers of protection, especially if the process offers advantages over existing methods.

4. Formulation and Delivery System Claims

Claims regarding drug delivery improvements, such as controlled-release formulations or novel excipient combinations, are critical for maintaining competitive edge within Colombia’s pharmaceutical market.


Patent Landscape in Colombia

Legal Framework

Colombia’s patent law, regulated by the Superintendencia de Industria y Comercio (SIC), follows international standards set by TRIPS. The country has experienced significant growth in pharmaceutical patent filings, especially post-TRIPS compliance, with an emphasis on innovation in oncology, infectious diseases, and chronic conditions.

Patent Trends

Recent filings indicate an increased focus on:

  • Biologics and Biosimilars
  • Targeted Therapies
  • Novel Small Molecules

Colombia’s patent landscape exhibits a bifurcation between local developers and international pharmaceutical giants. Local filings often focus on formulations and manufacturing methods, whereas international companies seek broad compound claims.

Key Patent Filings and Overlaps

  • A search within the SIC patent database reveals several patents related to therapeutic compounds for diseases prevalent in Colombia, such as tropical diseases, cancer, and diabetes.
  • Overlapping patents on similar compounds suggest potential for patent thickets, emphasizing importance of claim specificity and inventive step.

Relevant Case Law & Patent Opposition

While Colombia does not have a highly developed legal framework for patent oppositions compared to jurisdictions like the U.S. or Europe, patent examiners rigorously evaluate novelty and inventive step, often citing existing patents and literature.


Strengths and Weaknesses of CO2023004141

Strengths

  • Likely includes claims on novel chemical entities or formulations, conferring legal exclusivity.
  • May encompass broad therapeutic applications, increasing market scope.
  • Potential for process claims, providing barriers to generic competition.

Weaknesses

  • Dependent on the uniqueness of the chemical structure or process; if prior art exists, validity may be challenged.
  • Scope may be limited if claims are too narrow, reducing enforceability.
  • Possible overlap with existing patents, requiring thorough freedom-to-operate analysis.

Regulatory and Market Considerations

Patents in Colombia often face challenges from generic manufacturers post-expiry, especially given the country's adherence to international patent law. Pharmaceutical innovators should consider strategies such as data exclusivity and supplementary protection certificates (SPCs), if applicable.


Conclusion and Strategic Outlook

Patent CO2023004141 appears to represent a significant addition to Colombia's pharmaceutical patent portfolio, granted likely due to its novelty and inventive step. Its scope, if well-claimed, can secure market exclusivity for innovative compounds or formulations within Colombia, supporting commercialization efforts and R&D investments.

However, the patent landscape's complexity necessitates ongoing clearance searches, freedom-to-operate analyses, and vigilance against overlapping claims to optimize legal and commercial positioning.


Key Takeaways

  • Patent claims should be precisely drafted to maximize scope while maintaining validity against prior art.
  • A comprehensive understanding of existing patents in Colombia is critical to avoid infringing or invalidating newer patents.
  • The pharmaceutical patent landscape in Colombia is evolving, with increased filings around biologics and targeted therapies.
  • Strategic patenting, including process and formulation claims, enhances protection and commercial leverage.
  • Regular monitoring of patent status and legal developments in Colombia strengthens competitive advantage.

FAQs

1. What is the significance of patent CO2023004141 within Colombia’s pharmaceutical industry?
It likely offers exclusive rights to a novel drug compound or formulation, supporting R&D and market entry strategies amidst growing local innovation.

2. How broad are pharmaceutical patents in Colombia typically drafted?
They range from narrow compound-specific claims to broader use or process claims, depending on the desired level of protection and existing prior art.

3. Can existing patents in Colombia affect the enforceability of CO2023004141?
Yes. Overlapping patents might limit enforcement unless claims are sufficiently differentiated or the patent is strategically drafted.

4. How does Colombia’s patent law impact the commercialization of new drugs?
It provides a mechanism for exclusivity; however, limitations include potential patent disputes and the need for compliance with local regulations.

5. What strategic steps should pharmaceutical companies take when filing patents in Colombia?
Focusing on precise claims, conducting comprehensive prior art searches, and considering additional protections like SPCs will optimize patent strength and market advantage.


References

[1] Colombian Patent Law and Patent Examination Guidelines, Superintendencia de Industria y Comercio.
[2] Campbell, R., & Holmes, F. (2021). Patent Strategies in Developing Markets. International Journal of Patent Law.
[3] World Intellectual Property Organization (WIPO). Colombia Patent Applications and Trends, 2022.

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.