248
Participants
Start Date
April 21, 2022
Primary Completion Date
April 30, 2027
Study Completion Date
April 30, 2027
CM350 group1
CM350 will be administered intravenously (IV) once a week (QW) through step-up dosing until the participant discontinues study treatment, develops disease progression, initiates a new anti-tumor therapy, develops unacceptable toxicity, death, lost to follow-up, the investigator discontinue study treatment, or a female participant becomes pregnant (whichever occurs first).
CM350 group2
CM350 will be administered intravenously (IV) once a week (QW) through step-up dosing until the participant discontinues study treatment, develops disease progression, initiates a new anti-tumor therapy, develops unacceptable toxicity, death, lost to follow-up, the investigator discontinue study treatment, or a female participant becomes pregnant (whichever occurs first).
CM350 group3
CM350 will be administered intravenously (IV) once a week (QW). Individual subjects may continue study treatment until the participant discontinues study treatment, develops disease progression, initiates a new anti-tumor therapy, develops unacceptable toxicity, death, lost to follow-up, the investigator discontinue study treatment, or a female participant becomes pregnant (whichever occurs first).
RECRUITING
West China Hospital of Sichuan University, Chengdu
RECRUITING
Zhongshan Hospital Affiliated to Fudan University, Shanghai
Lead Sponsor
Keymed Biosciences Co.Ltd
INDUSTRY