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Completed Phase 2 Interventional Results available

GR270773 In The Treatment Of Suspected Or Confirmed Gram-Negative Severe Sepsis In Adults

ClinicalTrials.gov ID: NCT00089986

Public ClinicalTrials.gov record NCT00089986. 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 Nov 6, 2026, 3:28 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Prospective, Randomized, Double-blind, Placebo Controlled, Dose Ranging, Multi-Center Study of the Safety and Efficacy of Three Days Continuous Intravenous Infusion of GR270773 in the Treatment of Suspected or Confirmed Gram-negative Severe Sepsis in Adults

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The primary objective is to estimate the size of the GR270773 treatment effect on 28-day all-cause mortality for two doses of GR270773 versus placebo in adult subjects with suspected or confirmed Gram-negative severe sepsis. GR270773 will be administered as a three-day continuous intravenous infusion.

Study identification

NCT ID
NCT00089986
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,415 participants

Conditions and interventions

Conditions

Interventions

Drug · Other

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
Sep 1, 2004 (Type not available)
Primary completion
Apr 1, 2007 (Actual)
Completion
Apr 15, 2007 (Actual)
Last update posted
Aug 21, 2017

2004 – 2007

United States locations

U.S. sites
132
U.S. states
41
U.S. cities
113
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35294 —
GSK Investigational Site Phoenix Arizona 85006 —
GSK Investigational Site Tucson Arizona 85711 —
GSK Investigational Site Tucson Arizona 85724 —
GSK Investigational Site Bentonville Arkansas 71712 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Fresno California 93720 —
GSK Investigational Site Fullerton California 92835 —
GSK Investigational Site Loma Linda California 92534 —
GSK Investigational Site Los Angeles California 90089 —
GSK Investigational Site Orange California 92868 —
GSK Investigational Site Sacramento California 95816 —
GSK Investigational Site Sacramento California 95819 —
GSK Investigational Site San Jose California 95119 —
GSK Investigational Site Stanford California 94305 —
GSK Investigational Site Torrance California 90509 —
GSK Investigational Site Walnut Creek California 94598 —
GSK Investigational Site Colorado Springs Colorado 80919 —
GSK Investigational Site Denver Colorado 80204 —
GSK Investigational Site Denver Colorado 80210 —
GSK Investigational Site Denver Colorado 80218 —
GSK Investigational Site Fort Collins Colorado 80524 —
GSK Investigational Site Stamford Connecticut 06902 —
GSK Investigational Site Waterbury Connecticut 06708 —
GSK Investigational Site Newark Delaware 19718 —
GSK Investigational Site Washington D.C. District of Columbia 20010 —
GSK Investigational Site Atlantis Florida 33462 —
GSK Investigational Site Bay Pines Florida 33744 —
GSK Investigational Site Fort Lauderdale Florida 33316 —
GSK Investigational Site Melbourne Florida 32901 —
GSK Investigational Site New Port Richey Florida 34655 —
GSK Investigational Site Ocala Florida 34471 —
GSK Investigational Site Orlando Florida 32803 —
GSK Investigational Site Sarasota Florida 34239 —
GSK Investigational Site Tampa Florida 33601 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Augusta Georgia 30909 —
GSK Investigational Site Decatur Georgia 30033 —
GSK Investigational Site Rome Georgia 30165 —
GSK Investigational Site Honolulu Hawaii 96813 —
GSK Investigational Site Honolulu Hawaii 96816 —
GSK Investigational Site Honolulu Hawaii 96817 —
GSK Investigational Site Chicago Illinois 60611 —
GSK Investigational Site Chicago Illinois 60612-7230 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Maywood Illinois 60153 —
GSK Investigational Site Naperville Illinois 60540 —
GSK Investigational Site North Chicago Illinois 60064 —
GSK Investigational Site Oak Park Illinois 60302 —
GSK Investigational Site Peoria Illinois 62526 —
GSK Investigational Site Indianapolis Indiana 46280 —
GSK Investigational Site New Albany Indiana 47510 —
GSK Investigational Site Des Moines Iowa 50314 —
GSK Investigational Site Iowa City Iowa 52242 —
GSK Investigational Site Kansas City Kansas 66160 —
GSK Investigational Site Wichita Kansas 67214 —
GSK Investigational Site Lexington Kentucky 40536-0293 —
GSK Investigational Site Baton Rouge Louisiana 70806 —
GSK Investigational Site New Orleans Louisiana 70112 —
GSK Investigational Site Shreveport Louisiana 77103 —
GSK Investigational Site Slidell Louisiana 70458 —
GSK Investigational Site Baltimore Maryland 21201 —
GSK Investigational Site Baltimore Maryland 21237-3998 —
GSK Investigational Site Baltimore Maryland 21287-5554 —
GSK Investigational Site Boston Massachusetts 02114 —
GSK Investigational Site Boston Massachusetts 02115 —
GSK Investigational Site Springfield Massachusetts 01199 —
GSK Investigational Site Ann Arbor Michigan 48109 —
GSK Investigational Site Detroit Michigan 48202 —
GSK Investigational Site East Lansing Michigan 48824 —
GSK Investigational Site Flint Michigan 48503 —
GSK Investigational Site Kalamazoo Michigan 49048 —
GSK Investigational Site Duluth Minnesota 55805 —
GSK Investigational Site Jackson Mississippi 39202 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site Butte Montana 59701 —
GSK Investigational Site Camden New Jersey 08103-1489 —
GSK Investigational Site Piscataway New Jersey 08854 —
GSK Investigational Site Somers Point New Jersey 08244 —
GSK Investigational Site Albany New York 12208 —
GSK Investigational Site Buffalo New York 14215 —
GSK Investigational Site New York New York 10021 —
GSK Investigational Site New York New York 10029 —
GSK Investigational Site New York New York 10065 —
GSK Investigational Site Syracuse New York 13210 —
GSK Investigational Site The Bronx New York 10461 —
GSK Investigational Site The Bronx New York 10467-2490 —
GSK Investigational Site Durham North Carolina 27705 —
GSK Investigational Site Greensboro North Carolina 27410 —
GSK Investigational Site Greenville North Carolina 27858 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Akron Ohio 44307 —
GSK Investigational Site Columbus Ohio 43210 —
GSK Investigational Site Columbus Ohio 43215 —
GSK Investigational Site Toledo Ohio 43614-5809 —
GSK Investigational Site Oklahoma City Oklahoma 73104 —
GSK Investigational Site Bend Oregon 97701 —
GSK Investigational Site Corvallis Oregon 97330 —
GSK Investigational Site Bethlehem Pennsylvania 18018 —
GSK Investigational Site Monroeville Pennsylvania 15146 —
GSK Investigational Site Philadelphia Pennsylvania 19140 —
GSK Investigational Site Philadelphia Pennsylvania 19141 —
GSK Investigational Site Pittsburgh Pennsylvania 15261 —
GSK Investigational Site Pawtucket Rhode Island 02860 —
GSK Investigational Site Providence Rhode Island 02903 —
GSK Investigational Site Charleston South Carolina 29425 —
GSK Investigational Site Columbia South Carolina 29203 —
GSK Investigational Site Greenville South Carolina 29605 —
GSK Investigational Site Chattanooga Tennessee 37403 —
GSK Investigational Site Knoxville Tennessee 37920 —
GSK Investigational Site Nashville Tennessee 37212 —
GSK Investigational Site Nashville Tennessee 37232 —
GSK Investigational Site Dallas Texas 75231 —
GSK Investigational Site Dallas Texas 75390-9113 —
GSK Investigational Site Fort Worth Texas 76104 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Lackland Air Force Base Texas 78236-5300 —
GSK Investigational Site Lubbock Texas 79430-8183 —
GSK Investigational Site Salt Lake City Utah 84132 —
GSK Investigational Site Burlington Vermont 05401 —
GSK Investigational Site Lynchburg Virginia 24501 —
GSK Investigational Site Norfolk Virginia 23507 —
GSK Investigational Site Richmond Virginia 23249 —
GSK Investigational Site Salem Virginia 24153 —
GSK Investigational Site Bellingham Washington 98226 —
GSK Investigational Site Everett Washington 98201 —
GSK Investigational Site Seattle Washington 98101 —
GSK Investigational Site Tacoma Washington 98405 —
GSK Investigational Site Huntington West Virginia 25701-1693 —
GSK Investigational Site Marshfield Wisconsin 54449 —
GSK Investigational Site Milwaukee Wisconsin 53215 —
GSK Investigational Site Milwaukee Wisconsin 53226 —

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 258 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00089986, 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 Aug 21, 2017 · Synced Nov 6, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00089986 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →