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NCT00383565 · ClinicalTrials.gov registry record · Phase 2

FR901228 in Treating Patients With Relapsed or Refractory Non-Hodgkin's Lymphoma

A Phase 2 study, sponsored by National Cancer Institute (NCI).

Terminated
Registry status
Phase 2
Development phase
9
Enrollment target

NCT00383565: Clinical Trial Phase 2 study, sponsored by National Cancer Institute (NCI).

NCT00383565 is a Phase 2 study that was terminated before completion, run by National Cancer Institute (NCI). The registered enrollment target is 9 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00383565, a Phase 2 study, was terminated before completion, sponsored by National Cancer Institute (NCI).

TERMINATED
Registry status
Phase 2
Development phase
9 participants
Enrollment target

Study Summary

FR901228 may stop the growth of cancer cells by blocking some of the enzymes needed for cell to grow and by blocking blood flow to the cancer. This phase II trial is studying how well FR901228 works in treating patients with relapsed or refractory non-Hodgkin's lymphoma.

Primary Outcome

International Working Group response for non- Hodgkin's lymphoma: Complete Response (CR) - disappearance all detectable clinical/radiographic evidence of disease and disappearance of all disease-related symptoms (present before therapy) and normalization of those biochemical abnormalities; Partial Response (PR) - ≥50% decrease in sum products of greatest diameters (SPD) of 6 largest dominant nodes or nodal masses, selected by clearly measurable in at least two perpendicular dimensions, from disp

Interventions

  • DRUG romidepsin

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2006-09
Est. Completion 2011-04
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

Why NCT00383565 stopped before completion

NCT00383565 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 9 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (93% lower).

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

NCT00383565 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00383565 about?

NCT00383565 is a clinical study titled "FR901228 in Treating Patients With Relapsed or Refractory Non-Hodgkin's Lymphoma". FR901228 may stop the growth of cancer cells by blocking some of the enzymes needed for cell to grow and by blocking blood flow to the cancer. This phase II trial is studying how well FR901228 works in treating patients with relapsed or refractory non-Hodgkin's lymphoma.

What is the current status of trial NCT00383565?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 9 participants. The study started on 2006-09. Estimated completion is 2011-04.

What interventions are being tested in trial NCT00383565?

The interventions under investigation include: romidepsin (DRUG).

Who is sponsoring clinical trial NCT00383565?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00383565's enrollment target sits among peer trials

9 1989th of 2000 higher than 11 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 NCT00383565, the US trial registry maintained by the National Library of Medicine. NCT00383565 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.