CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 1,069 enrolled
Drug / intervention
PF-02341066drug
Likely dose
PF-02341066 250 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/NCT00932451
NCT00932451Phase 2Completed

Phase 2, Open-label Single Arm Study Of The Efficacy And Safety Of Pf-02341066 In Patients With Advanced Non-small Cell Lung Cancer (Nsclc) Harboring A Translocation Or Inversion Involving The Anaplastic Lymphoma Kinase (Alk) Gene Locus

Pfizer·interventional·Posted Jul 3, 2009·Updated Jan 13, 2017

In Brief

A Phase 2 clinical trial evaluating PF-02341066 for Carcinoma, Non-Small-Cell Lung. Completed, enrolled 1,069 participants across 280 sites in 22 countries.

Detailed Summary

This is a Phase 2 trial that will evaluate the safety and efficacy of PF-02341066 in patients with advanced non-small cell lung cancer with a specific gene profile involving the ALK gene. This trial will also allow patients from a Phase 3 trial who received standard of care chemotherapy (Study A8081007) to receive PF-02341066.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Brazil, Bulgaria, Canada, China, France, Germany, Greece, Hong Kong, Hungary, Ireland, Italy, Japan, Netherlands, Poland, Russia, South Korea, Spain, Sweden, Taiwan, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedJul 3, 2009
Enrollment StartJan 1, 2010
Primary CompletionMar 1, 2015
Study CompletionDec 1, 2015
TodayJul 2, 2026
Enrollment to primary: 5.2 yearsPosted 17.0 years ago

Interventions

PF-02341066drug

PF-02341066, 250 mg BID, will be administered orally on a continuous schedule