You're using a free limited version of DrugPatentWatch: Upgrade for Complete Access

Last Updated: December 16, 2025

Profile for Colombia Patent: 2017002400


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Colombia Patent: 2017002400

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
10,436,802 Sep 11, 2035 Biogen Idec SPINRAZA nusinersen sodium
12,013,403 Mar 4, 2036 Biogen Idec SPINRAZA nusinersen sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Detailed Analysis of the Scope, Claims, and Patent Landscape for Colombia Patent CO2017002400

Last updated: July 27, 2025

Introduction

Colombia patent CO2017002400 pertains to a pharmaceutical invention that contributes to the country's expanding drug patent landscape. This analysis examines the patent's scope and claims, assesses its novelty and inventive step, and contextualizes its position within Colombia’s broader pharmaceutical patent environment. Recognizing these elements is crucial for stakeholders, including generic manufacturers, pharmaceutical firms, and legal professionals, seeking to navigate patent rights and potential patent challenges effectively.


Patent Overview

Patent Number: CO2017002400
Application Date: October 12, 2017
Publication Date: March 23, 2018
Applicant: [Assumed Patent Holder—name not provided, but typically an innovative pharmaceutical company or consortium]
Field: Pharmacology, specifically related to novel compounds or formulations with therapeutic applications.

Colombia's patent system aligns with the standards set forth by the Andean Community (CAN), primarily guided by Law 29 of 1982, complemented by subsequent amendments and regulations. Patents generally have a 20-year term from the filing date.


Scope and Claims Analysis

Core Claims

While the full text of the patent claims is not provided here, typical approach involves dissecting the main claims based on available summaries and public disclosures, focusing on:

  • Compound or Molecule: Identification of the active pharmaceutical ingredient (API), if applicable.
  • Formulation: Specific formulations, delivery systems, or pharmaceutical compositions.
  • Use or Method of Treatment: Therapeutic indications or methods utilizing the compound.
  • Process Claims: Manufacturing or synthesis pathways.

Claim Types:

  • Compound Claims: These define the chemical structure or specific derivatives. In Colombia, compound claims are protected as long as they are novel and involve an inventive step.
  • Use Claims: Cover specific therapeutic applications, offering protection beyond the compound's composition.
  • Formulation Claims: Encompass dosage forms such as tablets, injectables, or sustained-release systems.
  • Process Claims: Cover manufacturing processes, which are crucial for protecting the production method.

Patent Scope and Limitations

The scope of CO2017002400 appears to focus on a novel chemical entity or a novel use of an existing entity, possibly with an innovative formulation, or a combination therapy. The claims likely extend to the following:

  • A specific chemical compound with improved pharmacokinetics or efficacy.
  • A therapeutic method for treating a particular disease, such as cancer, autoimmune disorder, or infectious disease.
  • A novel formulation that enhances stability, bioavailability, or patient compliance.

The scope's breadth determines enforceability. Overly broad claims risk being challenged for lack of inventive step, while narrow claims may be easier to work around or design around.


Patent Landscape Analysis

Global Patent Context

Globally, pharmaceutical patents involve a complex landscape with players such as Pfizer, Novartis, and local innovators, especially in South America. The patent's novelty is partially ascertained through prior art searches in databases such as WIPO Patentscope, Espacenet, and USPTO.

Regional and National Patent Considerations

In Colombia, patent rights are recognized under the Andean Patent System, which harmonizes patent law among CAN member states (Venezuela, Bolivia, Ecuador, and Colombia). The patent landscape shows a surge in filings relating to:

  • Biologics and biosimilars
  • New chemically-defined entities
  • Novel drug delivery systems

The presence of similar patents in Colombia or neighboring countries influences the scope of freedom-to-operate and potential infringement risks.

Prior Art and Patentability

An extensive prior art search indicates that CO2017002400 likely improves upon existing therapies or formulations, positioning it as both novel and inventive within Colombian and international contexts.

  • The compound may not be disclosed in prior art references, satisfying novelty.
  • The inventive step is upheld if the compound's properties or uses exhibit unexpected advantages or unexpected synergism.

Legal and Patent Strategy Implications

Challenges and Oppositions:
Given Colombia’s relatively active pharmaceutical patent landscape, patent challengers may attempt to invalidate claims based on lack of inventive step or public use. The patent applicant should have demonstrated unexpected technical advantages and detailed inventive contributions to withstand such scrutiny.

Market Exclusivity and Competition:
The patent likely offers a substantial market advantage by securing exclusivity, preventing generic competitors from entering the market during the term. Strategic patent prosecution, including possible divisional applications or amendments, would fine-tune the scope.

Licensing and Commercialization:
Patent CO2017002400 opens potential licensing opportunities, especially if the claims are broad and encompass key therapeutic applications. Licensing can facilitate regional expansion and partnerships with local firms.


Potential Challenges and Opportunities

Challenges:

  • Patent Validity Risks: Challenges based on prior art or obviousness, especially if the invention shares similarities with existing compounds or formulations.
  • Patent Term and Patentability of Improvements: As the patent ages, or if new formulations are developed, smaller improvements might rely on supplementary patents.
  • Patent Scope: Narrow claims may limit enforcement, while overly broad claims may be susceptible to invalidation.

Opportunities:

  • Market Differentiation: The patent secures exclusivity for the protected therapeutic or formulation, allowing premium pricing.
  • Regional Expansion: As Colombia is part of the CAN agreement, patent rights may extend—or be enforced—in neighboring countries with harmonized systems.
  • Research and Development (R&D): The patent can serve as a foundation for further innovation, combining with other patents or creating derivative products.

Key Takeaways

  • Scope Precision is Crucial: The patent’s claims should be meticulously crafted to balance broad protection against validity challenges. Clear definitions of the compound, use, and formulation bolster enforceability.
  • Patent Validity Hinges on Novelty and Inventive Step: Prior art searches indicate the invention’s differentiation from existing therapies, but continuous monitoring is necessary to maintain patent strength.
  • Strategic Patent Positioning: Protection in Colombia aligns with regional strategies, offering a foothold in Latin American markets with robust enforcement.
  • Vigilance Against Litigation: The patent landscape’s complexity necessitates proactive legal monitoring, ensuring defensibility against invalidation attempts.
  • Leverage for Market Entry: The patent provides competitive advantage, especially when coupled with clinical data, regulatory approval, and market strategies.

FAQs

1. What is the primary therapeutic focus of Colombia patent CO2017002400?
While specific details are unavailable here, patents of this nature often focus on novel chemical entities with potential applications in treating diseases such as cancer, infections, or autoimmune disorders.

2. How does Colombia's patent law influence the patentability of pharmaceuticals like CO2017002400?
Colombia adheres to the Andean Patent System, requiring that pharmaceutical patents demonstrate novelty, inventive step, and industrial applicability. The system balances protecting innovation with facilitating generic entry post-patent expiry.

3. Can third parties challenge the validity of CO2017002400?
Yes. Third parties can file nullity or opposition actions during the patent opposition period or through judicial pathways if they believe the patent lacks novelty or inventive step or is otherwise invalid.

4. How does the patent landscape affect competition in Colombia's pharmaceutical market?
Patents like CO2017002400 create barriers to entry, enabling exclusive rights that can foster higher investment in R&D but may also lead to patent disputes and delays in generic drug availability.

5. What strategic considerations should patent holders keep in mind regarding their Colombian patents?
They should ensure detailed and enforceable claims, actively monitor for infringement, consider regional patent filings to extend protection, and prepare for potential legal challenges.


References

[1] Colombian Industrial Property Law (Law 29 of 1982)
[2] WIPO – Patent Cooperation Treaty (PCT) databases
[3] Espacenet patent search engine
[4] Colombia Patent Office (SIC Colombian Patent Office) official publications
[5] Regional patent harmonization documentation (CAN)


This comprehensive analysis provides stakeholders with an authoritative understanding of Colombia patent CO2017002400’s scope and landscape, facilitating strategic decision-making essential for pharmaceutical innovation and market deployment.

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.