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NCT02264873 · ClinicalTrials.gov registry record · Phase 1

Phase I, Dose Escalation Study of Decitabine

A Phase 1 study, sponsored by University of Florida.

Completed
Registry status
Phase 1
Development phase
3
Enrollment target

NCT02264873: Completed Phase 1 study, sponsored by University of Florida.

NCT02264873 is a Phase 1 study that has completed, run by University of Florida. The registered enrollment target is 3 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02264873, a Phase 1 study, has completed, sponsored by University of Florida.

COMPLETED
Registry status
Phase 1
Development phase
3 participants
Enrollment target

Study Summary

Decitabine is a hypomethylating agent that has shown significant anti-leukemic effect in Myelodysplastic Syndrome (MDS) and Acute Myeloblastic Leukemia (AML). This study is based on the hypothesis that Decitabine delivered after allo-hematopoietic stem cell transplant (HSCT) in patients with leukemia will enhance disease control by the allogeneic immune system and lead to a longer disease free survival. The study is designed to provide safety data of low-dosing in the post-transplant setting.

Primary Outcome

This is a dose escalation study of decitabine maintenance therapy after allo-HSCT for the maximally tolerated dose in pediatric patients without adverse events.

Interventions

  • DRUG Decitabine

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2014-10
Est. Completion 2018-09-18
Phase Phase 1
University of Florida

1,106 total trials

What the finished NCT02264873 record still lists

NCT02264873 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (95% lower).

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

NCT02264873 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02264873 about?

NCT02264873 is a clinical study titled "Phase I, Dose Escalation Study of Decitabine". Decitabine is a hypomethylating agent that has shown significant anti-leukemic effect in Myelodysplastic Syndrome (MDS) and Acute Myeloblastic Leukemia (AML). This study is based on the hypothesis that Decitabine delivered after allo-hematopoietic stem cell transplant (HSCT) in patients with leukemi...

What is the current status of trial NCT02264873?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 3 participants. The study started on 2014-10. Estimated completion is 2018-09-18.

What interventions are being tested in trial NCT02264873?

The interventions under investigation include: Decitabine (DRUG).

Who is sponsoring clinical trial NCT02264873?

This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02264873's enrollment target sits among peer trials

3 1999th of 2000 higher than 1 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 NCT02264873, the US trial registry maintained by the National Library of Medicine. NCT02264873 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.