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Completed Phase 2 Interventional Results available

AZD9773 Dose Escalation Study

ClinicalTrials.gov ID: NCT00615017

Public ClinicalTrials.gov record NCT00615017. 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 Oct 17, 2026, 6:39 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 Placebo-controlled, Double-blind, Dose-escalation Study to Assess the Safety, Tolerability, and Pharmacokinetics and Pharmacodynamics of Single and Multiple Intravenous Infusions of CytoFab (AZD9773) in Patients With Severe Sepsis

Brief summary

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

This is a double-blind, placebo-controlled, multi-center, dose-escalation study to assess the safety, tolerability, Pharmacokinetics and Pharmacodynamics of single and multiple ascending intravenous infusions of CytoFab (AZD9773) in adult patients with severe sepsis.

Study identification

NCT ID
NCT00615017
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
70 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
Jan 2008 (Type not available)
Primary completion
Jul 2009 (Actual)
Completion
Jul 2009 (Actual)
Last update posted
Aug 22, 2013

2008 – 2009

United States locations

U.S. sites
26
U.S. states
16
U.S. cities
26
Facility City State ZIP Site status
Research Site Birmingham Alabama — —
Research Site Newark Delaware — —
Research Site Bay Pines Florida — —
Research Site Miami Florida — —
Research Site Chicago Illinois — —
Research Site Oak Park Illinois — —
Research Site Peoria Illinois — —
Research Site Indianapolis Indiana — —
Research Site Iowa City Iowa — —
Research Site Hazard Kentucky — —
Research Site Lexington Kentucky — —
Research Site Baltimore Maryland — —
Research Site Kansas City Missouri — —
Research Site Camden New Jersey — —
Research Site Newark New Jersey — —
Research Site Brooklyn New York — —
Research Site New York New York — —
Research Site Rochester New York — —
Research Site Durham North Carolina — —
Research Site Greensboro North Carolina — —
Research Site Winston-Salem North Carolina — —
Research Site Columbus Ohio — —
Research Site Oklahoma City Oklahoma — —
Research Site Nashville Tennessee — —
Research Site Galveston Texas — —
Research Site Houston Texas — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00615017, 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 22, 2013 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00615017 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →