The purpose of this study is to determine whether the recombinant human EGF-rP64K/Montanide ISA 51 vaccine is safe, immunogenic and effective in the treatment of stage IIIb/IV non-small-cell lung cancer (NSCLC).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
230
Local Institution
Kubang Kerian, Kelantan, Malaysia
Local Institution
Kampung Baharu Nilai, Negeri Sembilan, Malaysia
Local Institution
Kuantan, Pahang, Malaysia
Local Institution
George Town, Pulau Pinang, Malaysia
Survival
Time frame: Two and a half years
Assessment of immunogenecity, safety as well as preliminary assessment of objective response, time of progression and quality of life
Time frame: Two and a half years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Local Institution
Kota Kinabalu, Sabah, Malaysia
Local Institution
Kota Kinabalu, Sabah, Malaysia
Local Institution
Klang, Selangor, Malaysia
Local Institution
Petaling Jaya, Selangor, Malaysia
Local Institution
Kuala Lumpur, Malaysia
Local Institution
Kuala Lumpur, Malaysia