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NCT00337376 · ClinicalTrials.gov registry record · Phase 1

A Study of the mTOR Inhibitor Rapamycin (Rapamune, Sirolimus) in Combination With Abraxane in Advanced Solid Cancers

A Phase 1 study, sponsored by Yale University.

Terminated
Registry status
Phase 1
Development phase
23
Enrollment target

NCT00337376: Clinical Trial Phase 1 study, sponsored by Yale University.

NCT00337376 is a Phase 1 study that was terminated before completion, run by Yale University. The registered enrollment target is 23 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00337376, a Phase 1 study, was terminated before completion, sponsored by Yale University.

TERMINATED
Registry status
Phase 1
Development phase
23 participants
Enrollment target

Study Summary

Rapamycin is a drug that has been approved by the Food and Drug Administration (government) for use in patients receiving a kidney transplant to prevent the patient's body from rejecting the transplanted kidney. It has shown antitumor effects in the laboratory, but has not been approved at this time for the treatment of cancer. Abraxane is a new form of chemotherapy that has been approved by the Food and Drug Administration for the treatment of metastatic breast cancer, and is a promising drug that is being evaluated in clinical trials for treatment of other cancers. This is a phase I study designed to find out if different doses of Rapamycin, when combined with Abraxane, are safe and well tolerated.

Interventions

  • DRUG Abraxane
  • DRUG Rapamune

Trial Details

FieldValue
Enrollment Target 23 participants
Start Date 2006-02
Est. Completion 2010-07
Phase Phase 1
Yale University

1,492 total trials

Why NCT00337376 stopped before completion

NCT00337376 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% lower).

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

NCT00337376 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00337376 about?

NCT00337376 is a clinical study titled "A Study of the mTOR Inhibitor Rapamycin (Rapamune, Sirolimus) in Combination With Abraxane in Advanced Solid Cancers". Rapamycin is a drug that has been approved by the Food and Drug Administration (government) for use in patients receiving a kidney transplant to prevent the patient's body from rejecting the transplanted kidney. It has shown antitumor effects in the laboratory, but has not been approved at this time...

What is the current status of trial NCT00337376?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2006-02. Estimated completion is 2010-07.

What interventions are being tested in trial NCT00337376?

The interventions under investigation include: Abraxane (DRUG), Rapamune (DRUG).

Who is sponsoring clinical trial NCT00337376?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00337376's enrollment target sits among peer trials

23 1596th of 2000 higher than 400 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 NCT00337376, the US trial registry maintained by the National Library of Medicine. NCT00337376 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.