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NCT00550615 · ClinicalTrials.gov registry record · Phase 1

Dasatinib in Relapsed or Refractory Non-Hodgkin's Lymphoma

A Phase 1 study, sponsored by University of Nebraska.

Completed
Registry status
Phase 1
Development phase
38
Enrollment target

NCT00550615 is a Phase 1 study that has completed, run by University of Nebraska. The registered enrollment target is 38 participants.

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The verdict

NCT00550615, a Phase 1 study, has completed, sponsored by University of Nebraska.

COMPLETED
Registry status
Phase 1
Development phase
38 participants
Enrollment target

Study Summary

Primary Objective: * To determine the maximum tolerated dose (MTD) of Dasatinib in relapsed or refractory non-hodgkin's lymphoma (NHL) patients and to determine the safety of Dasatinib in NHL. Secondary Objectives: * To assess the complete and overall response rates for all Phase I and Phase II patients and to determine overall survival and event free survival for all Phase I and Phase II patients. * To assay the levels of kinase activity in NHL specimens and correlate this activity to patient outcomes.

Interventions

  • DRUG Dasatinib
  • DRUG Dasatinib Maximum Tolerated Dose

Trial Details

FieldValue
Enrollment Target 38 participants
Start Date 2007-09-17
Est. Completion 2017-12-01
Phase Phase 1

Sponsor

University of Nebraska

407 total trials

What the Registry Record Tells You About NCT00550615

The ClinicalTrials.gov registry entry for NCT00550615 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 38 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Nebraska, which has 407 total studies on file at ClinicalTrials.gov.

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

NCT00550615 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00550615 about?

NCT00550615 is a clinical study titled "Dasatinib in Relapsed or Refractory Non-Hodgkin's Lymphoma". Primary Objective: * To determine the maximum tolerated dose (MTD) of Dasatinib in relapsed or refractory non-hodgkin's lymphoma (NHL) patients and to determine the safety of Dasatinib in NHL. Secondary Objectives: * To assess the complete and overall response rates for all Phase I and Phase II p...

What is the current status of trial NCT00550615?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 38 participants. The study started on 2007-09-17. Estimated completion is 2017-12-01.

What interventions are being tested in trial NCT00550615?

The interventions under investigation include: Dasatinib (DRUG), Dasatinib Maximum Tolerated Dose (DRUG).

Who is sponsoring clinical trial NCT00550615?

This trial is sponsored by University of Nebraska, which has 407 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.