Department of Internal Medicine, National Taiwan University Hospital
Taipei, 100, Taiwan
NCT Number: NCT00172380
To assess the overall response rate to docetaxel plus CDDP as neoadjuvant chemotherapy prior to surgery, followed by adjuvant docetaxel plus CDDP in chemonaive patients NSCLC Stage IIIa and IIIb.
Looking for future studies?
Notify Me20 year and older
All sexes
Interventional
Phase 2
Taipei, 100, Taiwan
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
docetaxel 36mg/m2 and cisplatin 75mg/m2
Time frame: every cycle during 2nd-6th cycles
Time frame: resectability after treatment
Time frame: progression free survival after 1 year
Time frame: overall survival at 1 year
Looking for future studies?
Notify MeNational Taiwan University Hospital
Other
Phase II Study Evaluating Docetaxel and CDDP as Neoadjuvant Chemotherapy Prior to Surgery, Followed by Adjuvant Docetaxel Plus CDDP in Chemonaive Patients With NSCLC Stage III
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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