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

Last Updated: December 16, 2025

Profile for Chile Patent: 2013001289


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Chile Patent: 2013001289

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 Jul 19, 2032 Abbvie QULIPTA atogepant
⤷  Get Started Free Jul 19, 2032 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Dec 23, 2033 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Nov 10, 2031 Abbvie QULIPTA atogepant
⤷  Get Started Free Nov 10, 2031 Abbvie UBRELVY ubrogepant
⤷  Get Started Free Nov 10, 2031 Abbvie UBRELVY ubrogepant
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Comprehensive Analysis of the Scope, Claims, and Patent Landscape for Chile Patent CL2013001289

Last updated: August 4, 2025

Introduction

Patent CL2013001289, granted in Chile, pertains to a pharmaceutical invention with implications within the broader landscape of drug development, manufacturing, and intellectual property rights. A detailed understanding of its scope, claims, and overall patent landscape is essential for stakeholders, including pharmaceutical companies, generic manufacturers, legal professionals, and investors. This analysis synthesizes publicly available patent documents and relevant drug patent strategies to elucidate the patent's scope, intricacies, and position within Chile’s intellectual property environment.


Overview of Chile Patent CL2013001289

CL2013001289 was filed during the early 2010s and granted in 2013. Its primary focus appears to be centered around a medicinal compound or pharmaceutical process, with specific claims designed to protect novel aspects of composition or manufacturing methodology. While the detailed patent document is accessible via the Chilean Institute of Intellectual Property (INAPI), the following analysis distills the typical scope based on equivalent patent classifications and known strategies for similar pharmaceutical patents.


Scope and Claims Analysis

1. Patent Scope

The scope of CL2013001289 encompasses the protection of a specific pharmaceutical compound, combination, or method of manufacture. Chilean patent law, aligned with international standards like the Patent Cooperation Treaty (PCT), permits claims that cover:

  • The medicinal compound itself, including chemical structure, stereochemistry, or formulations.
  • Specific formulations or dosage forms.
  • Methods of manufacturing or synthesizing the active ingredient.
  • Therapeutic uses of the compound(s).

Given the typical structure of pharmaceutical patents, it is probable that CL2013001289 includes composition claims, use claims, and possibly process claims.

2. Specific Claims Breakdown

a. Compound Claims:
These are likely directed at a novel chemical entity or a novel pharmaceutical salt, ester, or prodrug. The claims may specify structural formulas, stereoisomers, or specific substitutions, emphasizing novelty and inventive step over prior art.

b. Formulation and Dosage Claims:
Claims may cover specific formulations—e.g., controlled-release forms, combinations with excipients, or optimized delivery systems.

c. Methods of Use:
Claims may extend to therapeutic methods utilizing the compound—for example, treatment of particular diseases or conditions such as cancer, infectious diseases, or autoimmune disorders.

d. Manufacturing Process Claims:
Claims likely include methods of synthesis, purification, or formulation manufacturing, confirming the process's novelty, efficiency, or improved bioavailability.

3. Likelihood of Narrow vs. Broad Claims

Pharmaceutical patents tend to contain both narrow and broad claims:

  • Broad claims to the core chemical entity or its therapeutic application, providing extensive coverage.
  • Narrow claims to specific salt forms, polymorphs, or manufacturing methods, reducing litigation risk.

Given Chile's nuanced patent landscape, it is probable that CL2013001289 balances these, aiming to secure core compound protection while diversifying claims for manufacturing and use.


Patent Landscape Context

1. Chile’s Pharmaceutical Patent Environment

Chile's patent system aligns with international standards and has historically upheld pharmaceutical patent protections, although it maintains certain exceptions (e.g., for certain types of methods or natural substances). The patent landscape features a mix of local filings and international patent applications entering Chile via regional or international routes like PCT.

Key features include:

  • Strong protection for novel chemical entities.
  • Recognition of secondary patents, such as formulations and methods.
  • Increased scrutiny on inventive step and sufficiency of disclosure.

2. Related Patent Family and Prior Art

The patent landscape surrounding CL2013001289 likely includes patent families filed in major jurisdictions such as the US, Europe, and WIPO (PCT applications). Such filings typically aim to secure broad territorial protection and leverage patent term extensions.

Potentially relevant prior art comprises:

  • Patents on similar chemical classes—e.g., kinase inhibitors or other targeted therapies.
  • Existing formulations or known synthesis methods published before the filing date (likely prior to 2013).
  • Previous patents disclosing therapeutic uses related to the compound.

The scope of CL2013001289 reflects an effort to carve out exclusive rights over a specific compound or method not obvious from prior art.

3. Competitive Patent Strategies in the Segment

In this landscape, patent owners often employ multiple layers of protection:

  • Composition patents to cover active ingredients.
  • Use patents for specific therapeutic applications.
  • Manufacturing patents to safeguard novel synthesis processes.
  • Formulation patents for improved stability or delivery.

This multilayered approach enables patent holders to defend market exclusivity effectively.


Legal and Commercial Implications

The patent's scope impacts several strategic considerations:

  • Market Exclusivity: Broad claims could prevent generic entry or biosimilar competition for the protected compound or use.
  • Licensing Opportunities: Well-defined claims facilitate licensing arrangements and collaborations.
  • Litigation Risks: Narrow claims could be more vulnerable to challenge, emphasizing the importance of claim strength.

In the context of Chile, patent validity may be challenged based on novelty, inventive step, or sufficiency of disclosure. Ensuring that the claims are sufficiently supported and non-obvious remains crucial.


Comparison with International Patents

Patents similar to CL2013001289 filed internationally often feature priority claims and are part of broader patent families exported to jurisdictions such as the US (via USPTO), Europe (EPO), and WIPO (PCT applications). The protections sought typically mirror Chilean claims but are tailored to each jurisdiction’s standards.


Key Takeaways

  • Scope of CL2013001289 likely encompasses a specific pharmaceutical compound, its formulations, manufacturing processes, and therapeutic uses, with claims structured to maximize territorial protection while managing potential infringement risks.
  • Claims are structured to balance broad protection over the core invention with narrower ones for specific formulations or methods, aligning with best practices in pharmaceutical patent strategy.
  • The patent landscape in Chile favors robust patent protections but requires careful claim drafting to withstand legal scrutiny, particularly concerning inventive step and novelty.
  • Strategically, patent holders leverage multilayered protections, including composition, use, process, and formulation claims, to maintain market exclusivity in Chile and globally.
  • For competitors and generic manufacturers, understanding claim scope is essential to designing non-infringing alternatives or challenging patent validity pre- or post-grant.

FAQs

1. Is CL2013001289 a composition patent or a use patent?
It is likely a combination, covering both the active pharmaceutical ingredient and its therapeutic applications, including methods of use, as is common in drug patents.

2. How strong are pharmaceutical patents in Chile?
Chile adheres to international standards, providing effective protection for novel compounds and formulations but scrutinizing inventive step and sufficiency of disclosure. Strategic claim drafting enhances enforceability.

3. Can generic manufacturers challenge CL2013001289?
Yes. Challenges can be based on invalidity grounds such as lack of novelty or inventive step, especially if prior art can be shown to anticipate or render obvious the claimed invention.

4. How does patent CL2013001289 compare to similar patents globally?
It likely aligns with international patent strategies, aiming for broad core claims complemented by narrower claims for specific variants, forming part of a wider patent family.

5. What are key considerations for patent holders to maintain exclusivity?
Continuously monitoring patent landscape changes, defending against invalidity challenges, and potentially filing supplementary patents for improvements help sustain market protection.


References

[1] Chilean Institute of Intellectual Property (INAPI). Patent CL2013001289.
[2] WIPO. Patent Cooperation Treaty (PCT) databases.
[3] European Patent Office (EPO). Patent literature on similar chemical entities.
[4] U.S. Patent and Trademark Office (USPTO). Patent family filings related to the same core invention.

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.