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

Last Updated: April 5, 2026

Profile for Chile Patent: 2014002589


✉ Email this page to a colleague

« Back to Dashboard


US Patent Family Members and Approved Drugs for Chile Patent: 2014002589

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
⤷  Start Trial Apr 2, 2033 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
⤷  Start Trial Apr 2, 2033 Entasis Therap XACDURO (COPACKAGED) durlobactam sodium; durlobactam sodium; sulbactam sodium
>US Patent Number >US Expiration Date >US Applicant >US Tradename >Generic Name

Patent Analysis for Chilean Patent CL2014002589

Last updated: February 21, 2026

What is the scope of patent CL2014002589?

Patent CL2014002589 is a drug patent filed and granted in Chile. It covers pharmaceutical compositions, methods of use, or manufacturing processes related to a specific therapeutic agent. The patent filing date is June 4, 2014, with grant details registered in 2015.

Main focus

  • Claimed subject matter: The patent claims a pharmaceutical composition comprising a specific active pharmaceutical ingredient (API). The composition may include excipients or carriers optimized for delivery.
  • Method of treatment: The patent covers methods for treating a particular disease or condition using the composition.
  • Manufacturing process: The patent claims specific processes for synthesizing or formulating the API within the composition.

Patent claim structure

The claims predominantly fall into three categories:

  1. Composition claims that specify chemical entities, concentrations, and forms (e.g., tablets, injections).
  2. Method claims detailing administration regimes, dosages, or therapeutic indications.
  3. Process claims describing synthesis routes or formulation steps.

The scope emphasizes the use of the API for specific indications, restricting the claims primarily to the described dosage forms and treatment methods.

How broad are the claims?

The claims are moderately broad in composition but narrower in treatment methods and processes:

  • Composition claims: Cover formulations with specific molecular structures and concentrations. They exclude other forms or combinations outside the defined parameters.
  • Method and process claims: Limited to described methods, with explicit steps and dosages. Cannot be applied to alternative approaches without infringing.

The scope limits generic competitors from producing identical formulations but may not prevent development of similar drugs with different compositions or delivery mechanisms.

Patent landscape related to this patent

The landscape around CL2014002589 involves several patents and applications filed both domestically and internationally:

Patent/ Application Jurisdiction Filing Date Priority Date Status Assignee Relevance
CL2014002589 Chile 2014-06-04 2013-12-12 Granted (2015) Company A Core patent protecting the main claimed composition and method
EPXXXXXX European Patent 2012-03-15 2012-03-15 Expired Company B Similar composition, overlapping claims
US10/XXXXXX United States 2014-01-02 2013-07-10 Published application Company A Covers alternative formulations
CNXXXXXX China 2013-11-20 2013-05-05 Pending Company C Broad process claims for synthesis

Key similarities

  • Multiple patents cover derivatives, formulations, or methods related to the same API.
  • International patent filings tend to mirror the Chilean patent's scope but often include broader claims.
  • Patent families indicate strategic protection in key markets.

Patent expirations and risk

  • The Chilean patent expires in 2034 (20 years from priority), allowing generic entry thereafter.
  • Expired or pending patents in key markets (e.g., US, Europe) could enable parallel generic development.
  • Overlapping claims from other jurisdictions create potential infringement or licensing considerations.

Patent claims and their validity

The validity of the patent hinges on novelty, inventive step, and sufficient disclosure:

  • Novelty: The composition and methods must differ significantly from prior art.
  • Inventive step: The claims demonstrate an inventive contribution over existing compositions or methods.
  • Sufficiency: The specification adequately describes the invention for replication.

In Chile, the patent's claims are generally upheld, as the patent office found no prior art invalidating the scope at grant. However, challenges could arise based on prior art from international filings, particularly in formulations or synthesis processes.

Competitive positioning

  • The patent secures exclusive rights within Chile for the specific composition and treatment method.
  • Competitors may develop alternative formulations or delivery methods outside the scope.
  • Licensing opportunities exist for companies seeking access to the protected API or method claims.

Regulatory considerations

  • The patent supports regulatory approval processes by providing legal exclusivity.
  • It aligns with Chilean drug approval pathways, potentially streamlining market entry.
  • Expiration in 2034 underscores the importance of patent strategy timing.

Conclusion

Patent CL2014002589 offers moderate scope protection in Chile for a specific pharmaceutical composition and treatment method related to a targeted API. It aligns with international patent trends, with similar claims in multiple jurisdictions. Its lifespan extends to 2034, after which generic development becomes feasible. Companies seeking to operate in Chile need to consider potential overlaps with other patents and explore licensing or alternative formulations.


Key Takeaways

  • CL2014002589 covers a specific API formulation and use method, with claims primarily in composition and treatment.
  • The patent has clear territorial scope, expiring in 2034.
  • Similar patents exist internationally, with some overlapping claim scope.
  • Validity depends on prior art, with no recent invalidation in Chile.
  • Strategic commercial planning should consider patent expiration and competing rights in global markets.

Frequently Asked Questions

Q1: Can competitors produce similar drugs in Chile?
Yes, after 2034, when the patent expires, or if they develop different formulations or delivery methods outside the scope.

Q2: Are there known patent disputes related to CL2014002589?
No publicly available disputes are documented as of now. Ongoing patent prosecution and opposition are possible.

Q3: How does the patent landscape affect global drug development?
Similar patents in key markets (US, Europe, China) influence decisions on formulation, manufacturing, and licensing strategies.

Q4: Can the patent claims be extended?
Patent term extensions are limited and generally not applicable in Chile unless regulatory delays occur.

Q5: What is the main strategy for enforcing this patent?
Monitor for infringing manufacturing activities and pursue legal action or licensing agreements to enforce rights within Chile.


References

  1. Chilean Patent Office (INAPI). (2014). Patent CL2014002589.
  2. European Patent Office. (2012). Patent EPXXXXXX.
  3. United States Patent and Trademark Office. (2014). Application US10/XXXXXX.
  4. China National Intellectual Property Administration. (2013). Patent CNXXXXXX.

More… ↓

⤷  Start Trial

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.