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Completed Phase 3 Interventional

Efficacy & Safety of Resatorvid in Adults With Severe Sepsis

ClinicalTrials.gov ID: NCT00143611

Public ClinicalTrials.gov record NCT00143611. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 5:29 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Pivotal, Multicenter, Multinational, Randomized, Double-Blind, Placebo-Controlled Study To Evaluate The Efficacy And Safety of TAK-242 in Adults With Severe Sepsis

Study identification

NCT ID
NCT00143611
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Takeda
Industry
Enrollment
277 participants

Conditions and interventions

Conditions

Interventions

  • Resatorvid Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2005
Primary completion
Jan 31, 2007
Completion
Jan 31, 2007
Last update posted
Feb 1, 2012

2005 – 2007

United States locations

U.S. sites
49
U.S. states
28
U.S. cities
49
Facility City State ZIP Site status
Not listed Birmingham Alabama
Not listed Mobile Alabama
Not listed Phoenix Arizona
Not listed Scottsdale Arizona
Not listed Escondido California
Not listed Los Angeles California
Not listed Orange California
Not listed Poway California
Not listed San Diego California
Not listed Colorado Springs Colorado
Not listed New Haven Connecticut
Not listed Newark Delaware
Not listed Atlantis Florida
Not listed Bay Pines Florida
Not listed Jacksonville Florida
Not listed Miami Florida
Not listed Orlando Florida
Not listed Sarasota Florida
Not listed Atlanta Georgia
Not listed Augusta Georgia
Not listed Chicago Illinois
Not listed Peoria Illinois
Not listed Indianapolis Indiana
Not listed Des Moines Iowa
Not listed Louisville Kentucky
Not listed Shreveport Louisiana
Not listed Portland Maine
Not listed Baltimore Maryland
Not listed Springfield Massachusetts
Not listed Kalamazoo Michigan
Not listed Kansas City Missouri
Not listed St Louis Missouri
Not listed Butte Montana
Not listed Englewood New Jersey
Not listed Buffalo New York
Not listed New York New York
Not listed Rochester New York
Not listed Greensboro North Carolina
Not listed Winston-Salem North Carolina
Not listed Akron Ohio
Not listed Columbus Ohio
Not listed Oklahoma City Oklahoma
Not listed Greenville South Carolina
Not listed Nashville Tennessee
Not listed Fort Worth Texas
Not listed Galveston Texas
Not listed Houston Texas
Not listed Lubbock Texas
Not listed Bellevue Washington

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 95 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00143611, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 1, 2012 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00143611 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →