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Completed Phase 3 Interventional Results available

Phase 3 Safety and Efficacy Study of ART-123 in Subjects With Severe Sepsis and Coagulopathy

ClinicalTrials.gov ID: NCT01598831

Public ClinicalTrials.gov record NCT01598831. 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 22, 2026, 2:36 PM 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 Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study to Assess the Safety and Efficacy of ART-123 in Subjects With Severe Sepsis and Coagulopathy.

Study identification

NCT ID
NCT01598831
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Asahi Kasei Pharma America Corporation
Industry
Enrollment
816 participants

Conditions and interventions

Interventions

  • ART-123 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
Oct 28, 2012
Primary completion
Apr 4, 2018
Completion
Feb 27, 2019
Last update posted
Apr 20, 2020

2012 – 2019

United States locations

U.S. sites
22
U.S. states
19
U.S. cities
20
Facility City State ZIP Site status
Not listed Mobile Alabama 36608
Not listed Phoenix Arizona 85008
Not listed Atlanta Georgia 30342
Not listed Idaho Falls Idaho 83404
Not listed Indianapolis Indiana 46202
Not listed Hazard Kentucky 41701
Not listed Louisville Kentucky 40202
Detroit Receiving Hospital Detroit Michigan 48201
Harper Hospital - Wayne State University School of Medicine Detroit Michigan 48201
Sinai-Grace Hospital Detroit Michigan 48235
Not listed Jackson Mississippi 39216
Washington University in St. Louis St Louis Missouri 63110
Not listed Butte Montana 59701
Not listed Englewood New Jersey 07631
Memorial Sloan Kettering Cancer Center New York New York 10065
Not listed Durham North Carolina 27710
Not listed Columbus Ohio 43215
Not listed Oklahoma City Oklahoma 73104
Not listed Philadelphia Pennsylvania 19104
Not listed Rapid City South Dakota 57701
2 of 2 Houston Texas 77030
Not listed Murray Utah 84107

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 139 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01598831, 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 Apr 20, 2020 · Synced Jul 22, 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 NCT01598831 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →