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NCT01015222 · ClinicalTrials.gov registry record · Phase 1

Dasatinib, Bevacizumab, Paclitaxel in Patients With Advanced Malignancies

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

Completed
Registry status
Phase 1
Development phase
122
Enrollment target

NCT01015222: Completed Phase 1 study, sponsored by M.D. Anderson Cancer Center.

NCT01015222 is a Phase 1 study that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 122 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (103% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT01015222, a Phase 1 study, has completed, sponsored by M.D. Anderson Cancer Center.

COMPLETED
Registry status
Phase 1
Development phase
122 participants
Enrollment target

Study Summary

The goal of this clinical research study is to find the highest tolerable dose of the combination of dasatinib, bevacizumab, and paclitaxel with or without Methylnaltrexone that can be given to patients with advanced cancer. The safety of this drug combination will also be studied.

Primary Outcome

MTD defined as the highest dose below any dose that has one third or more patients with dose limiting toxicities (DLT).

Interventions

  • DRUG Bevacizumab
  • DRUG Paclitaxel
  • DRUG Dasatinib

Trial Details

FieldValue
Enrollment Target 122 participants
Start Date 2009-11
Est. Completion 2021-05-27
Phase Phase 1
M.D. Anderson Cancer Center

2,692 total trials

What the finished NCT01015222 record still lists

NCT01015222 is an interventional study that assigns participants to a tested intervention. The registered 122 participants enrollment target is mid-sized for trials with a published cap, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (103% higher).

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

NCT01015222 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01015222 about?

NCT01015222 is a clinical study titled "Dasatinib, Bevacizumab, Paclitaxel in Patients With Advanced Malignancies". The goal of this clinical research study is to find the highest tolerable dose of the combination of dasatinib, bevacizumab, and paclitaxel with or without Methylnaltrexone that can be given to patients with advanced cancer. The safety of this drug combination will also be studied.

What is the current status of trial NCT01015222?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 122 participants. The study started on 2009-11. Estimated completion is 2021-05-27.

What interventions are being tested in trial NCT01015222?

The interventions under investigation include: Bevacizumab (DRUG), Paclitaxel (DRUG), Dasatinib (DRUG).

Who is sponsoring clinical trial NCT01015222?

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 NCT01015222's enrollment target sits among peer trials

122 475th of 2000 higher than 1,525 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 NCT01015222, the US trial registry maintained by the National Library of Medicine. NCT01015222 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.