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Completed Phase 1Phase 2 Interventional

A Phase 1/2 Trial of Perifosine in the Treatment of Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT00399789

Public ClinicalTrials.gov record NCT00399789. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 30, 2026, 10:47 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a study of the drug perifosine that consists of 2 parts. The first part of this study was designed to determine the highest dose of perifosine that can be administered to people every week without severe or prolonged nausea, vomiting and diarrhea. This study started with patients taking 900 mg/week and went up to 1800 mg/week. Part I of this study is completed. The MTD had been determined and incorporated in Part II. The goals in Part II are to: 1. Compare the gastrointestinal toxicity of 3 different dose-schedules and 2. Obtain preliminary information on the response rate of perifosine in non-small cell lung cancer.

Study identification

NCT ID
NCT00399789
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
AEterna Zentaris
Industry
Enrollment
121 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2004 (Type not available)
Primary completion
Dec 2010 (Actual)
Completion
Dec 2011 (Actual)
Last update posted
Feb 22, 2018

2004 – 2011

United States locations

U.S. sites
21
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
AOI Pharmaceuticals Investigative Site Tucson Arizona 85704 —
AOI Pharmaceuticals Investigative Site Pomona California 91767 —
AOI Pharmaceuticals Investigative Site Aventura Florida 33180 —
AOI Pharmaceuticals Investigative Site Hollywood Florida 33021 —
AOI Pharmaceuticals Investigative Site Lakeland Florida 33805 —
AOI Pharmaceuticals Investigative Site Ormond Beach Florida 32174 —
AOI Pharmaceuticals Investigative Site Lawrenceville Georgia 30045 —
AOI Pharmaceuticals Investigative Site Galesburg Illinois 61401 —
AOI Pharmaceuticals Investigative Site New Albany Indiana 47150 —
AOI Pharmaceuticals Investigative Site Grand Rapids Michigan 49546 —
AOI Pharmaceuticals Investigative Site Kalamazoo Michigan 49048 —
AOI Pharmaceuticals Investigative Site Billings Montana 59101 —
AOI Pharmaceuticals Investigative Site Albuquerque New Mexico 87109 —
AOI Pharmaceuticals Investigative Site Albany New York 12208 —
AOI Pharmaceuticals Investigative Site Armonk New York 10504 —
AOI Pharmaceuticals Investigative Site Greenville South Carolina 29605 —
AOI Pharmaceuticals Investigative Site Chattanooga Tennessee 37404 —
AOI Pharmaceuticals Investigative Site Nashville Tennessee 37203 —
AOI Pharmaceuticals Investigative Site Dallas Texas 75237 —
AOI Pharmaceuticals Investigative Site Dallas Texas 75246 —
AOI Pharmaceuticals Investigative Site Tyler Texas 75702 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00399789, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 22, 2018 · Synced Sep 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00399789 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →