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Terminated Phase 3 Interventional

A Stratified Sickle Event Randomized Trial (ASSERT)

ClinicalTrials.gov ID: NCT00102791

Public ClinicalTrials.gov record NCT00102791. 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 21, 2026, 5:27 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 Phase III Multicenter, 52-Week, Randomized, Double-Blind, Placebo-Controlled Study of the Clinical Efficacy and Safety of ICA-17043 With or Without HU Therapy in Patients With Sickle Cell Disease Who Have Had =>2 Acute Sickle-Related Painful Crises Within the Preceding 12 Months

Brief summary

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

The purpose of this study is to compare the effects of ICA-17043 to placebo with or without hydroxyurea (an oral drug used for treatment of sickle cell disease) in patients with sickle cell disease who have had 2 or more acute sickle-related painful crises requiring a visit to a medical facility within the past 12 months.

Study identification

NCT ID
NCT00102791
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Icagen
Industry
Enrollment
297 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
16 Years to 65 Years
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
Feb 2005 (Type not available)
Primary completion
Not listed
Completion
Jun 2007 (Actual)
Last update posted
Mar 27, 2008

2005 – 2007

United States locations

U.S. sites
42
U.S. states
26
U.S. cities
42
Facility City State ZIP Site status
Not listed Mobile Alabama — —
Not listed Little Rock Arkansas — —
Not listed Davis California — —
Not listed Los Angeles California — —
Not listed Oakland California — —
Not listed Denver Colorado — —
Not listed Hartford Connecticut — —
Not listed Washington D.C. District of Columbia — —
Not listed Holly Hill Florida — —
Not listed Hollywood Florida — —
Not listed Jacksonville Florida — —
Not listed Augusta Georgia — —
Not listed Savannah Georgia — —
Not listed Chicago Illinois — —
Not listed Iowa City Iowa — —
Not listed New Orleans Louisiana — —
Not listed Shreveport Louisiana — —
Not listed Baltimore Maryland — —
Not listed Boston Massachusetts — —
Not listed Detroit Michigan — —
Not listed Jackson Mississippi — —
Not listed Kansas City Missouri — —
Not listed Las Vegas Nevada — —
Not listed Hackensack New Jersey — —
Not listed New Brunswick New Jersey — —
Not listed Newark New Jersey — —
Not listed Brooklyn New York — —
Not listed The Bronx New York — —
Not listed Chapel Hill North Carolina — —
Not listed Durham North Carolina — —
Not listed Greenville North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Cleveland Ohio — —
Not listed Philadelphia Pennsylvania — —
Not listed Pittsburgh Pennsylvania — —
Not listed Charleston South Carolina — —
Not listed Memphis Tennessee — —
Not listed Nashville Tennessee — —
Not listed Houston Texas — —
Not listed San Antonio Texas — —
Not listed Richmond Virginia — —

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00102791, 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 Mar 27, 2008 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00102791 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →