A Study on the Correlation Between Tarceva (Erlotinib) - Induced Rash and Efficacy in EGFR Mutated Participants With Advanced Non-Small Cell Lung Cancer Receiving First-Line Therapy

PHASE2CompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

May 23, 2011

Primary Completion Date

December 20, 2016

Study Completion Date

December 20, 2016

Conditions
Non-Squamous Non-Small Cell Lung Cancer
Interventions
DRUG

erlotinib [Tarceva]

150 mg orally daily, with dose-reductions to 100 mg or 50 mg orally daily according to protocol

Trial Locations (16)

13100

Ziv Medical Center; Oncology Department, Sefad

15208

Poria Hospital; Oncology, Tiberias

18101

Haemek Hospital; Oncology, Afula

22100

Nahariya Hospital; Oncology, Nahariya

34362

Carmel Hospital; Oncology Unit, Haifa

58100

Wolfson Hospital; Oncology, Holon

78278

Barzilai; Oncology, Ashkelon

91031

Shaare Zedek Medical Center; Oncology Dept, Jerusalem

3525408

Rambam Medical Center; Oncology, Haifa

4428164

Meir Medical Center; Oncology, Kfar Saba

5262100

Chaim Sheba Medical Center; Oncology Dept, Ramat Gan

6093000

Assaf Harofeh; Oncology, Ẕerifin

7610001

Kaplan Medical Center; Oncology Inst., Rehovot

8410101

Soroka Medical Center; Oncology Dept, Beersheba

9112001

Hadassah Ein Karem Hospital; Oncology Dept, Jerusalem

64239-06

Sourasky / Ichilov Hospital; Oncology Department, Tel Aviv

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Clalit Health Services

OTHER

lead

Hoffmann-La Roche

INDUSTRY