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NCT00096837 · ClinicalTrials.gov registry record · Phase 2

A Study of Motexafin Gadolinium for the Treatment of Relapsed or Refractory Multiple Myeloma

A Phase 2 study of Multiple Myeloma, sponsored by Pharmacyclics.

Completed
Registry status
Phase 2
Development phase
25
Enrollment target
1
Study location

NCT00096837: Completed Phase 2 study of Multiple Myeloma, sponsored by Pharmacyclics.

NCT00096837 is a Phase 2 study of Multiple Myeloma that has completed, run by Pharmacyclics. The registered enrollment target is 25 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.

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The verdict

NCT00096837, a Phase 2 study of Multiple Myeloma, has completed, sponsored by Pharmacyclics.

COMPLETED
Registry status
Phase 2
Development phase
25 participants
Enrollment target
1
Study location

Study Summary

The purpose of the study is to determine if the drug motexafin gadolinium will be an effective treatment for patients who have relapsed or refractory multiple myeloma.

Conditions Studied

Interventions

  • DRUG Motexafin Gadolinium Injection

Study Locations (1)

Illinois

  • Robert H. Lurie Comprehensive Cancer Center - Chicago

Trial Details

FieldValue
Enrollment Target 25 participants
Phase Phase 2
Pharmacyclics

54 total trials

What the finished NCT00096837 record still lists

NCT00096837 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 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 Motexafin Gadolinium Injection is the first listed.

NCT00096837 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT00096837 about?

NCT00096837 is a clinical study titled "A Study of Motexafin Gadolinium for the Treatment of Relapsed or Refractory Multiple Myeloma". The purpose of the study is to determine if the drug motexafin gadolinium will be an effective treatment for patients who have relapsed or refractory multiple myeloma.

What is the current status of trial NCT00096837?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 25 participants.

What conditions does trial NCT00096837 study?

This clinical trial studies the following conditions: Multiple Myeloma.

What interventions are being tested in trial NCT00096837?

The interventions under investigation include: Motexafin Gadolinium Injection (DRUG).

Who is sponsoring clinical trial NCT00096837?

This trial is sponsored by Pharmacyclics, which has 54 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00096837 being conducted?

This trial has 1 study location across Illinois. 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 NCT00096837's enrollment target sits among peer trials

25 366th of 438 higher than 63 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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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT00096837, the US trial registry maintained by the National Library of Medicine. NCT00096837 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.