CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 36 enrolled
Drug / intervention
AG-013736 +5 moredrug
Likely dose
AG-013736 10 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01469052
NCT01469052Phase 1Completed

Phase I, Open-Label, Multicenter, Dose-Escalation Study Of The Tyrosine Kinase Inhibitor Of VEGFR-2, AG013736, In Patients With Advanced Solid Tumors

Pfizer·interventional·Posted Nov 10, 2011·Updated Mar 26, 2012

In Brief

A Phase 1 clinical trial evaluating AG-013736 for Advanced Solid Tumors. Completed, enrolled 36 participants across 3 sites.

Detailed Summary

The purpose of the study was to characterize the safety of investigational agent AG-013736, in patients with solid tumors in this First In Human trial.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 1CompletedFinished
2003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedNov 10, 2011
Enrollment StartNov 1, 2002
Primary CompletionJul 1, 2004
Study CompletionAug 1, 2004
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 14.6 years ago

Interventions

AG-013736drug

Axitinib continuous oral dosing (10 mg once a day, 10 mg twice a day, 20 mg twice a day or 30 mg twice day) in the fed state

AG-013736drug

Axitinib continuous oral dosing (20 mg twice a day) in the fed state

AG-013736drug

Axitinib continuous oral dosing (5 mg twice a day) in the fed state

AG-013736drug

Axitinib continuous oral dosing (15 mg once a day) in the fed state

AG-013736drug

Axitinib continuous oral dosing (5 mg twice a day) in the fasted state

AG-013736drug

Axitinib continuous oral dosing (2 mg twice a day on the first day of dosing, followed by 5 mg twice a day) in the fasted state