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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 ↗

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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
Callisto Pharmaceuticals

4 total trials

What the finished NCT00086216 record still lists

NCT00086216 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (95% lower).

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 a single indexed study location in 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.

Where NCT00086216's enrollment target sits among peer trials

30 338th of 438 higher than 80 of 438 other Multiple Myeloma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Multiple Myeloma 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 NCT00086216, the US trial registry maintained by the National Library of Medicine. NCT00086216 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.