Study identifier:D791AC00008
ClinicalTrials.gov identifier:NCT00683306
EudraCT identifier:N/A
CTIS identifier:N/A
Multicentre, open label, extension study of treatment with gefitinib(IRESSA™) for patients completing other gefitinib clinical studies who may benefit from gefitinib treatment
Non small cell lung cancer (NSCLC)
N/A
No
ZD1839 (Iressa)
All
94
Expanded Access
18 Years - 130 Years
Allocation: N/A
Endpoint Classification: -
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Aug 2018 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: 1 ZD 1839 (Iressa) | Drug: ZD1839 (Iressa) Gefitinib supplied for oral use at the dose and schedule that the patient received in the previous gefitinib clinical study. In the case of placebo patients, the gefitinib dose will be as described in the protocol of their previous gefitinib clinical study. Other Name: Iressa |