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Completed Phase 1 Interventional Results available

Study Evaluating SKI-606 (Bosutinib) In Advanced Malignant Solid Tumors

ClinicalTrials.gov ID: NCT00195260

Public ClinicalTrials.gov record NCT00195260. 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 5, 2026, 11:09 PM EDT

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

Official title

Phase I Dose-Escalation Study Of Oral SKI-606 In Subjects With Advanced Malignant Solid Tumors

Brief summary

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

To evaluate the safety and tolerability of oral SKI-606 (bosutinib) administered on a daily schedule to subjects with advanced malignant solid tumors and to define a maximum tolerated dose (MTD) in this subject population.

Study identification

NCT ID
NCT00195260
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Pfizer
Industry
Enrollment
151 participants

Conditions and interventions

Conditions

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 30, 2004
Primary completion
Oct 31, 2007
Completion
Oct 31, 2007
Last update posted
Feb 10, 2013

2004 – 2007

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Pfizer Investigational Site Birmington Alabama 35233
Pfizer Investigational Site Scottsdale Arizona 85258
Pfizer Investigational Site Los Angeles California 90033
Pfizer Investigational Site Tampa Florida 33612
Pfizer Investigational Site Atlanta Georgia 30341
Pfizer Investigational Site Indianpolis Indiana 46202
Pfizer Investigational Site Baltimore Maryland 21287
Pfizer Investigational Site Detroit Michigan 48202
Pfizer Investigational Site Lansing Michigan 48910
Pfizer Investigational Site New York New York 10016
Pfizer Investigational Site New York New York 10032
Pfizer Investigational Site Charlotte North Carolina 28203
Pfizer Investigational Site Charlotte North Carolina 28211
Pfizer Investigational Site UNC Chapel Hill North Carolina 27514
Pfizer Investigational Site UNC Chapel Hill North Carolina 27759
Pfizer Investigational Site Cleveland Ohio 44106-1736
Pfizer Investigational Site San Antonio Texas 78258
Pfizer Investigational Site Tyler Texas 75702
Pfizer Investigational Site Seattle Washington 98104

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 NCT00195260, 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 10, 2013 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00195260 live on ClinicalTrials.gov.

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