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NCT00059618 · ClinicalTrials.gov registry record · Phase 1

PS-341 Plus Carboplatin in Platinum and Taxane Resistant Recurrent Ovarian Cancer, Primary Peritoneal Cancer, and Fallopian Tube Cancer

A Phase 1 study, sponsored by M.D. Anderson Cancer Center.

Completed
Registry status
Phase 1
Development phase
21
Enrollment target

NCT00059618: Completed Phase 1 study, sponsored by M.D. Anderson Cancer Center.

NCT00059618 is a Phase 1 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 21 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00059618, a Phase 1 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
21 participants
Enrollment target

Study Summary

The goal of this clinical research study is to find the highest safe dose of PS-341 that can be given with carboplatin chemotherapy as a treatment for patients with ovarian, abdominal, or fallopian tube cancer. Researchers also hope to find out if giving these drugs together will help shrink or slow the growth of tumors in patients who are considered resistant to platinum drugs. The safety of these drugs will also be studied.

Interventions

  • DRUG Carboplatin
  • DRUG PS-341 (Bortezomib)

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2003-04
Est. Completion 2007-04
Phase Phase 1
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT00059618 record still lists

NCT00059618 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (65% lower).

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

NCT00059618 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00059618 about?

NCT00059618 is a clinical study titled "PS-341 Plus Carboplatin in Platinum and Taxane Resistant Recurrent Ovarian Cancer, Primary Peritoneal Cancer, and Fallopian Tube Cancer". The goal of this clinical research study is to find the highest safe dose of PS-341 that can be given with carboplatin chemotherapy as a treatment for patients with ovarian, abdominal, or fallopian tube cancer. Researchers also hope to find out if giving these drugs together will help shrink or slow...

What is the current status of trial NCT00059618?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 21 participants. The study started on 2003-04. Estimated completion is 2007-04.

What interventions are being tested in trial NCT00059618?

The interventions under investigation include: Carboplatin (DRUG), PS-341 (Bortezomib) (DRUG).

Who is sponsoring clinical trial NCT00059618?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00059618's enrollment target sits among peer trials

21 1615th of 2000 higher than 372 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 NCT00059618, the US trial registry maintained by the National Library of Medicine. NCT00059618 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.