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NCT01636622 · ClinicalTrials.gov registry record · Phase 1

Study of Vemurafenib, Carboplatin, and Paclitaxel

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

Completed
Registry status
Phase 1
Development phase
21
Enrollment target
1
Study location

NCT01636622 is a Phase 1 study of Advanced Cancers that has completed, run by M.D. Anderson Cancer Center. The registered enrollment target is 21 participants, below the 68-participant average among 10 other Advanced Cancers trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01636622, a Phase 1 study of Advanced Cancers, has completed, sponsored by M.D. Anderson Cancer Center.

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

Study Summary

The goal of this clinical research study is to find the highest tolerable dose of vemurafenib that can be given in combination with carboplatin and paclitaxel patients with advanced cancer. The safety of the study drug combination will also be studied. Vemurafenib is designed to block a protein (called mutated BRAF) that is only found in moles (spots) of the skin and certain types of cancer cells. This drug may slow the growth of or kill these cells. Carboplatin is designed to slow the growth of cancer cells by stopping them from making new DNA (the genetic material of cells). Paclitaxel is designed to slow the growth of cancer cells by stopping them from dividing into new cells.

Conditions Studied

Interventions

  • DRUG Carboplatin
  • DRUG Paclitaxel
  • DRUG Vemurafenib

Study Locations (1)

Texas

  • University of Texas MD Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2012-07-09
Est. Completion 2020-04-21
Phase Phase 1

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT01636622

The ClinicalTrials.gov registry entry for NCT01636622 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 68-participant average among 10 other Advanced Cancers trials with a reported enrollment target (69% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Advanced Cancers appearing as the primary indexed condition, and to 3 interventions - of which Carboplatin is the first listed.

NCT01636622 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT01636622 about?

NCT01636622 is a clinical study titled "Study of Vemurafenib, Carboplatin, and Paclitaxel". The goal of this clinical research study is to find the highest tolerable dose of vemurafenib that can be given in combination with carboplatin and paclitaxel patients with advanced cancer. The safety of the study drug combination will also be studied. Vemurafenib is designed to block a protein (ca...

What is the current status of trial NCT01636622?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 21 participants. The study started on 2012-07-09. Estimated completion is 2020-04-21.

What conditions does trial NCT01636622 study?

This clinical trial studies the following conditions: Advanced Cancers.

What interventions are being tested in trial NCT01636622?

The interventions under investigation include: Carboplatin (DRUG), Paclitaxel (DRUG), Vemurafenib (DRUG).

Who is sponsoring clinical trial NCT01636622?

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

Where is trial NCT01636622 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.