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This is the phase II, single-arm, single-center study assessing the efficacy of weekly docetaxel plus carboplatin in second-line treatment of malignant melanoma (unresectable or metastatic) who has failed dacarbazine or temozolomide contained therapy. The primary end point is overall response rate according to RECIST 1.1 criteria assessed using CT or MRI and secondary end point includes disease control rate, progression free survival, overall survival and safety.
Age
20 - No limit years
Sex
ALL
Healthy Volunteers
No
Severance Hospital
Seoul, Seoul, South Korea
Start Date
July 1, 2011
Primary Completion Date
August 1, 2014
Completion Date
August 1, 2014
Last Updated
August 29, 2014
30
ACTUAL participants
docetaxel 35mg/m2
DRUG
Carboplatin AUC3
DRUG
Lead Sponsor
Yonsei University
NCT07371663
NCT01898039
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06209580