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NCT00693433 · ClinicalTrials.gov registry record · Phase 1

Temsirolimus and Dexamethasone in Treating Patients With Recurrent or Refractory Multiple Myeloma

A Phase 1 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 1
Development phase
15
Enrollment target

NCT00693433: Completed Phase 1 study, sponsored by National Cancer Institute (NCI).

NCT00693433 is a Phase 1 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 15 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (75% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00693433, a Phase 1 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 1
Development phase
15 participants
Enrollment target

Study Summary

This phase I trial is studying the side effects and best dose of temsirolimus when given together with dexamethasone in treating patients with recurrent or refractory multiple myeloma. Temsirolimus may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as dexamethasone, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving temsirolimus together with dexamethasone may kill more cancer cells.

Primary Outcome

The MTD is the dose level at which less than 2 out of 6 subjects experience DLT. Assessed according to the NCI Common Toxicity Criteria (CTC).

Interventions

  • OTHER laboratory biomarker analysis
  • DRUG dexamethasone
  • DRUG temsirolimus

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2008-12
Phase Phase 1
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00693433 record still lists

NCT00693433 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 15 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (75% lower).

The record links to 0 conditions, and to 3 interventions - of which laboratory biomarker analysis is the first listed.

NCT00693433 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00693433 about?

NCT00693433 is a clinical study titled "Temsirolimus and Dexamethasone in Treating Patients With Recurrent or Refractory Multiple Myeloma". This phase I trial is studying the side effects and best dose of temsirolimus when given together with dexamethasone in treating patients with recurrent or refractory multiple myeloma. Temsirolimus may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Drugs used...

What is the current status of trial NCT00693433?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 15 participants. The study started on 2008-12.

What interventions are being tested in trial NCT00693433?

The interventions under investigation include: laboratory biomarker analysis (OTHER), dexamethasone (DRUG), temsirolimus (DRUG).

Who is sponsoring clinical trial NCT00693433?

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 NCT00693433's enrollment target sits among peer trials

15 1798th of 2000 higher than 157 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00693433, the US trial registry maintained by the National Library of Medicine. NCT00693433 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.