Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00086216 · ClinicalTrials.gov registry record · Phase 1

Safety and Efficacy of Atiprimod for Patients With Refractory Multiple Myeloma

A Phase 1 study of Multiple Myeloma, sponsored by Callisto Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
30
Enrollment target
1
Study location

NCT00086216: Completed Phase 1 study of Multiple Myeloma, sponsored by Callisto Pharmaceuticals.

NCT00086216 is a Phase 1 study of Multiple Myeloma that has completed, run by Callisto Pharmaceuticals. The registered enrollment target is 30 participants, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00086216, a Phase 1 study of Multiple Myeloma, has completed, sponsored by Callisto Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

This is a Phase I/IIa clinical trial to identify the maximum tolerated dose of atiprimod and to evaluate the safety of atiprimod in patients with refractory or relapsed multiple myeloma.

Conditions Studied

Interventions

  • DRUG Atiprimod

Study Locations (1)

Texas

  • MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2004-05
Est. Completion 2007-11
Phase Phase 1

Sponsor

Callisto Pharmaceuticals

4 total trials

What the Registry Record Tells You About NCT00086216

The ClinicalTrials.gov registry entry for NCT00086216 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (95% lower). The listed sponsor is Callisto Pharmaceuticals, which has 4 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Multiple Myeloma appearing as the primary indexed condition, and to 1 intervention - of which Atiprimod is the first listed.

NCT00086216 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT00086216 about?

NCT00086216 is a clinical study titled "Safety and Efficacy of Atiprimod for Patients With Refractory Multiple Myeloma". This is a Phase I/IIa clinical trial to identify the maximum tolerated dose of atiprimod and to evaluate the safety of atiprimod in patients with refractory or relapsed multiple myeloma.

What is the current status of trial NCT00086216?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 30 participants. The study started on 2004-05. Estimated completion is 2007-11.

What conditions does trial NCT00086216 study?

This clinical trial studies the following conditions: Multiple Myeloma.

What interventions are being tested in trial NCT00086216?

The interventions under investigation include: Atiprimod (DRUG).

Who is sponsoring clinical trial NCT00086216?

This trial is sponsored by Callisto Pharmaceuticals, which has 4 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00086216 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Multiple Myeloma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

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

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, the data changelog, or report a data error.