Study identifier:1839IL/0052
ClinicalTrials.gov identifier:NCT00684385
EudraCT identifier:N/A
CTIS identifier:N/A
An International Expanded Access Clinical Programme with ZD1839 (IRESSA) for Patients with Advanced Non-small Cell Lung Cancer(NSCLC) and patients with Recurrent or Metastatic or Both Recurrent and Metastatic Squamous Cell Carcinoma of the Head and Neck (H&NC)
Non Small Cell Lung Cancer
N/A
No
ZD1839
All
265
Expanded Access
18 Years - 130 Years
Allocation: N/A
Endpoint Classification: None
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Feb 2019 by AstraZeneca
AstraZeneca
-
The purpose of this study is to provide ZD1839 for those patients with locally advanced and/or metastatic non-operable non-small cell lung cancer (stage III or IV) or recurrent and/or metastatic squamous cell head and neck cancer who receive the therapy on an expanded access basis due to their inability to meet eligibility criteria for on-going recruiting trials, inability to participate in other clinical trials (e.g., poor performance status, lack of geographic proximity), or because other medical interventions are not considered appropriate or acceptable.
Location
Location
Trier, Germany, 54292
Location
Großhansdorf, Germany, 22927
Location
Mainz, Germany, 55131
Location
Kiel, Germany, 24105
Location
Göttingen, Germany, 37075
Location
Berlin, Germany, 10117
Location
Freiburg, Germany, 79106
Location
Essen, Germany, 45122
Arms | Assigned Interventions |
---|---|
Experimental: 1 | Drug: ZD1839 250mg administered daily for patients with NSCLC and500mg daily for patients with H&NC. Treatment dispensed to patients on Day 1 and every 12 weeks thereafter until the patient withdraws. Patients with NSCLC will take one tablet at each dose administration; patients with squamous cell H&NC will take two tablets at each dose administration. Other Name: Iressa |
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