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NCT00294541 · ClinicalTrials.gov registry record · Phase 3

A Study Evaluating the Long-Term Safety of ICA-17043 in Sickle Cell Disease Patients With or Without Hydroxyurea Therapy

A Phase 3 study, sponsored by Icagen.

Terminated
Registry status
Phase 3
Development phase
51
Enrollment target

NCT00294541: Clinical Trial Phase 3 study, sponsored by Icagen.

NCT00294541 is a Phase 3 study that was terminated before completion, run by Icagen. The registered enrollment target is 51 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00294541, a Phase 3 study, was terminated before completion, sponsored by Icagen.

TERMINATED
Registry status
Phase 3
Development phase
51 participants
Enrollment target

Study Summary

This trial is a follow-up companion study to Protocol ICA-17043-10, a Phase III, multi-center, efficacy and safety study of ICA-17043. This is an open-label extension study collecting safety data on the use of ICA-17043 in subjects with sickle cell disease (SCD) (e.g., HbSS, HbSC, HbSb0-thalassemia, HbSb+-thalassemia subjects). All subjects who have successfully completed ICA-17043-10 will, if deemed appropriate by their study Investigator and appropriate consent by subject is given, enroll in the ICA-17043-12 study (Study 12). Only patients who participated in ICA-17043-10 are eligible for this open label study

Interventions

  • DRUG ICA-17043

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2006-02
Est. Completion 2007-06
Phase Phase 3
Icagen

4 total trials

Why NCT00294541 stopped before completion

NCT00294541 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (93% lower).

The record links to 0 conditions, and to 1 intervention - of which ICA-17043 is the first listed.

NCT00294541 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00294541 about?

NCT00294541 is a clinical study titled "A Study Evaluating the Long-Term Safety of ICA-17043 in Sickle Cell Disease Patients With or Without Hydroxyurea Therapy". This trial is a follow-up companion study to Protocol ICA-17043-10, a Phase III, multi-center, efficacy and safety study of ICA-17043. This is an open-label extension study collecting safety data on the use of ICA-17043 in subjects with sickle cell disease (SCD) (e.g., HbSS, HbSC, HbSb0-thalassemia,...

What is the current status of trial NCT00294541?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 51 participants. The study started on 2006-02. Estimated completion is 2007-06.

What interventions are being tested in trial NCT00294541?

The interventions under investigation include: ICA-17043 (DRUG).

Who is sponsoring clinical trial NCT00294541?

This trial is sponsored by Icagen, which has 4 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00294541's enrollment target sits among peer trials

51 1842nd of 2000 higher than 157 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00294541, the US trial registry maintained by the National Library of Medicine. NCT00294541 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.