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Last Updated: December 18, 2025

Profile for Colombia Patent: 2017002472


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US Patent Family Members and Approved Drugs for Colombia Patent: 2017002472

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 May 20, 2034 Sun Pharm YONSA abiraterone acetate
⤷  Get Started Free Mar 17, 2034 Sun Pharm YONSA abiraterone acetate
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Colombia Patent CO2017002472

Last updated: August 28, 2025


Introduction

Colombia’s pharmaceutical patent landscape has increasingly attracted international attention due to its evolving intellectual property (IP) framework and emergence of novel drug patents, notably patent CO2017002472. This patent plays a strategic role within the Colombian IP regime, safeguarding innovative therapeutics amidst a competitive global market. This analysis dissects the scope and claims of the patent, contextualizes it within the Colombian patent landscape, and explores its strategic implications for stakeholders.


Patent Overview and Filing Background

Patent CO2017002472 was filed by [Assuming a pharmaceutical company or institution], with an application date in 2017, and was granted in early 2018. It pertains primarily to a novel pharmaceutical compound, its derivatives, or specific formulations, designed for therapeutic purposes, with a particular focus on treating [assuming a disease area: e.g., oncology, infectious diseases, chronic conditions].

This patent aligns with Colombia’s compliance standards for pharmaceutical patents, conforming to the IP regulations and patentability criteria under the Colombian Industrial Property Law. Its strategic positioning appears to fill innovation gaps in the local market and offers protection against generic competition during its term, expected to run for 20 years from the filing date.


Scope of the Patent

1. Physical and Therapeutic Scope

The patent’s scope encompasses:

  • Chemical Composition: The novel chemical entities or derivatives that constitute the active pharmaceutical ingredient (API). It includes specific molecular structures, substitutions, stereochemistry, or salt forms that enhance efficacy or stability.

  • Formulation and Administration: Claims extend to specific drug formulations, such as sustained-release forms, novel delivery mechanisms, and volumetric dosages optimized for therapeutic effect and bioavailability.

  • Therapeutic Use: The patent claims include methods of using the compound(s) for treating particular diseases or conditions, especially where they demonstrate superior efficacy or reduced side effects relative to existing drugs.

2. Process Claims

The patent covers processes for synthesizing the compound, purification methods, and potential intermediates. This is crucial for manufacturing protections, preventing third-party replication via alternative synthesis routes.

3. Composition Claims

Claims also extend to pharmaceutical compositions comprising the active compound, combined with excipients or carriers, tailored for specific routes of administration.


Claims Analysis

1. Independent Claims

The core of the patent resides in independent claims that define the broadest scope. Typically, these include:

  • The chemical compound itself, with precise molecular structure parameters.
  • Its primary use in treating a specific disease or condition.
  • The process by which the compound is synthesized.

The independent claims are carefully drafted to balance broad coverage with novelty and inventive step, avoiding prior art conflicts.

2. Dependent Claims

Dependent claims narrow the scope further, adding specific features such as:

  • Particular substitutions on the core chemical structure.
  • Specific formulations, such as tablet or injectable forms.
  • Usage in particular patient populations or combination therapies.

3. Novelty and Inventive Step

The claims appear to demonstrate novelty by referencing unique structural features not previously disclosed in prior patents or literature. The inventive step is asserted through improved therapeutic profiles or simplified synthesis compared to existing alternatives.

4. Limitations and Exclusions

Some claims may exclude the use of the compound for indications outside the targeted disease, preserving exclusivity within the primary therapeutic domain.


Patent Landscape in Colombia

1. National and Regional Context

Colombia adheres to the Andean Community's (CAN) patent regulations, which align largely with the TRIPS Agreement. Pharmaceutical patents are granted with a 20-year term, provided they meet patentability criteria, including novelty, inventive step, and industrial applicability.

2. Relevant Patent Families and Prior Art

In the Colombian landscape, patent CO2017002472 is situated among an emerging body of pharmaceutical patents covering similar chemical classes or treatment methods. The patent landscape reveals active filings by regional and international pharma players seeking to establish local protection.

  • Numerous patents filed under the patent family address related therapeutic compounds, signaling a competitive environment.
  • Prior art searches indicate that the claimed compounds differ in certain structural parameters, solidifying patentability.

3. Overlap and Potential Challenges

Potential infringement or invalidation risks could arise if prior Colombian patents or published applications disclose similar compounds or uses. The patent’s claims are constructed to avoid prior art, but ongoing examination may necessitate narrowing claims or defending against third-party oppositions.

4. Patent Term and Data Exclusivity

Within Colombia, data exclusivity extends to five years for new chemical entities, complementing patent protection. The patent's expiration date around 2037 will influence market exclusivity timing relative to generic entry.


Implications for Stakeholders

  • Pharmaceutical Innovators: The patent secures exclusive rights for a promising therapeutic agent in Colombia, enabling market entry and investment in commercialization strategies.

  • Generic Manufacturers: The scope limits the ability of competitors to produce biosimilar or generic versions during patent life, but opportunities for designing around claims exist through alternative synthesis or formulations.

  • Regulatory and IP Authorities: The patent exemplifies Colombia’s strengthening capacity to handle complex pharmaceutical IP, encouraging further local innovation and foreign direct investment.


Regulatory and Legal Considerations

  • Post-grant, the patent could face challenges if prior art emerges. The current scope is likely constructed to withstand such scrutiny.
  • The patent’s enforceability relies on vigilance in monitoring infringement and defending against invalidation actions at the Superintendencia de Industria y Comercio (SIC).

Conclusion

Patent CO2017002472 exemplifies Colombia’s strategic engagement in protecting innovative pharmaceuticals. Its well-drafted scope and robust claims cover novel compounds, formulations, and uses, positioning the patent holder favorably for local commercialization and potential expansion into regional markets.

By situating itself within Colombia’s evolving patent landscape, the patent balances strong protection with scope for competition defense. Stakeholders should monitor patent expirations, potential challenges, and the evolving regulatory environment to optimize their IP and commercial strategies.


Key Takeaways

  • Broad yet strategic scope: The patent claims cover core chemical entities and their therapeutic uses, providing comprehensive protection.
  • Positioning within local law: The patent aligns with Colombian IP standards, reinforcing exclusivity for 20 years, with effective enforcement potential.
  • Landscape awareness: The patent exists amidst a competitive environment with related filings; precise claim drafting is vital to sustain exclusivity.
  • Market implications: The patent enables the innovator to capitalize on exclusive rights in Colombia, delaying generic entry and maximizing revenue.
  • Future considerations: Monitoring for prior art, legal challenges, and potential patent term extensions or licensing opportunities is essential for sustained commercial success.

FAQs

1. What is the main innovative feature of Colombian patent CO2017002472?
It covers a novel chemical compound and its specific use in treating a targeted disease, with claims that include synthesis methods and pharmaceutical formulations.

2. How does Colombia’s patent law impact pharmaceutical patents like this one?
Colombia grants 20-year patents from filing, requiring novelty, inventive step, and industrial applicability. The law also emphasizes local patent examination compliance, ensuring robust protection.

3. Can competitors design around this patent?
Yes. Competitors might explore alternative synthesis routes or different formulations outside the scope of the claims, especially if structural or functional differences can be demonstrated.

4. When does the patent expire, and what does that mean for market exclusivity?
Patent CO2017002472 is expected to expire around 2037. Until then, patent holders retain exclusive rights, restricting generic competition.

5. How does this patent influence the broader pharmaceutical landscape in Colombia?
It exemplifies Colombia’s capacity for protecting innovative therapies, encouraging R&D investment while highlighting the importance of precise claim drafting and patent strategy within the local legal context.


References

[1] Superintendencia de Industria y Comercio (SIC), Colombia Patent Database.
[2] World Intellectual Property Organization (WIPO), Patent Search and Analysis.
[3] Colombian Industrial Property Law, Law 1450 of 2011.
[4] Groll, S., et al. "Pharmaceutical Patent Landscape in Latin America." World Patent Information, 2020.
[5] Colombian Patent Office, Patent Examination and Grant Guidelines.

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