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NCT02282215 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy of Human Myeloid Progenitor Cells (CLT-008) During Chemotherapy for Acute Myeloid Leukemia

A Phase 2 study, sponsored by Cellerant Therapeutics.

Completed
Registry status
Phase 2
Development phase
163
Enrollment target

NCT02282215: Completed Phase 2 study, sponsored by Cellerant Therapeutics.

NCT02282215 is a Phase 2 study that has completed, run by Cellerant Therapeutics. The registered enrollment target is 163 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (23% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02282215, a Phase 2 study, has completed, sponsored by Cellerant Therapeutics.

COMPLETED
Registry status
Phase 2
Development phase
163 participants
Enrollment target

Study Summary

The purpose of the study is to explore the safety and efficacy of CLT-008 as an extra supportive care measure after induction chemotherapy for patients with acute myeloid leukemia (AML).

Interventions

  • BIOLOGICAL G-CSF
  • BIOLOGICAL CLT-008

Trial Details

FieldValue
Enrollment Target 163 participants
Start Date 2014-12
Est. Completion 2017-09-22
Phase Phase 2
Cellerant Therapeutics

3 total trials

What the finished NCT02282215 record still lists

NCT02282215 is an interventional study that assigns participants to a tested intervention. The registered 163 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (23% higher).

The record links to 0 conditions, and to 2 interventions - of which G-CSF is the first listed.

NCT02282215 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02282215 about?

NCT02282215 is a clinical study titled "Safety and Efficacy of Human Myeloid Progenitor Cells (CLT-008) During Chemotherapy for Acute Myeloid Leukemia". The purpose of the study is to explore the safety and efficacy of CLT-008 as an extra supportive care measure after induction chemotherapy for patients with acute myeloid leukemia (AML).

What is the current status of trial NCT02282215?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 163 participants. The study started on 2014-12. Estimated completion is 2017-09-22.

What interventions are being tested in trial NCT02282215?

The interventions under investigation include: G-CSF (BIOLOGICAL), CLT-008 (BIOLOGICAL).

Who is sponsoring clinical trial NCT02282215?

This trial is sponsored by Cellerant Therapeutics, which has 3 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02282215's enrollment target sits among peer trials

163 418th of 2000 higher than 1,583 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT02282215, the US trial registry maintained by the National Library of Medicine. NCT02282215 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.