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NCT00664677 · ClinicalTrials.gov registry record · Phase 1

Phase 1 Study of Terameprocol (EM-1421) in Patients With Leukemia

A Phase 1 study, sponsored by Erimos Pharmaceuticals.

Terminated
Registry status
Phase 1
Development phase
16
Enrollment target

NCT00664677: Clinical Trial Phase 1 study, sponsored by Erimos Pharmaceuticals.

NCT00664677 is a Phase 1 study that was terminated before completion, run by Erimos Pharmaceuticals. The registered enrollment target is 16 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00664677, a Phase 1 study, was terminated before completion, sponsored by Erimos Pharmaceuticals.

TERMINATED
Registry status
Phase 1
Development phase
16 participants
Enrollment target

Study Summary

This study is designed to determine the safety, maximum tolerated dose,dose limiting toxicity of Terameprocol(EM-1421)and determine the pharmacokinetics (clearance from the blood)of Terameprocol(EM-1421)given as intravenous infusion three times a week in patients with leukemia.

Interventions

  • DRUG Terameprocol (EM-1421)

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2007-08
Est. Completion 2009-06
Phase Phase 1
Erimos Pharmaceuticals

5 total trials

Why NCT00664677 stopped before completion

NCT00664677 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower).

The record links to 0 conditions, and to 1 intervention - of which Terameprocol (EM-1421) is the first listed.

NCT00664677 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00664677 about?

NCT00664677 is a clinical study titled "Phase 1 Study of Terameprocol (EM-1421) in Patients With Leukemia". This study is designed to determine the safety, maximum tolerated dose,dose limiting toxicity of Terameprocol(EM-1421)and determine the pharmacokinetics (clearance from the blood)of Terameprocol(EM-1421)given as intravenous infusion three times a week in patients with leukemia.

What is the current status of trial NCT00664677?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2007-08. Estimated completion is 2009-06.

What interventions are being tested in trial NCT00664677?

The interventions under investigation include: Terameprocol (EM-1421) (DRUG).

Who is sponsoring clinical trial NCT00664677?

This trial is sponsored by Erimos Pharmaceuticals, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00664677's enrollment target sits among peer trials

16 1786th of 2000 higher than 203 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00664677, the US trial registry maintained by the National Library of Medicine. NCT00664677 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.