12
Participants
Start Date
January 31, 2016
Primary Completion Date
December 31, 2016
Study Completion Date
December 31, 2016
K-001
In case of severe adverse reactions associated with the test drug, or if half of the participants show adverse reactions at Ⅲ level and above, the test should be terminated. The maximum dosage not causing the above-described situation shall be considered as the maximum tolerated dose or the biologically effective dose. After the test, continuous medication shall be given upon request from patients.
Shanghai General Hospital, Shanghai
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
OTHER