A Clinical Study of MIL93 in Solid Tumors.

PHASE1RecruitingINTERVENTIONAL
Enrollment

228

Participants

Timeline

Start Date

April 21, 2021

Primary Completion Date

August 31, 2025

Study Completion Date

August 31, 2025

Conditions
Advanced Malignancies
Interventions
DRUG

Recombinant Humanized Monoclonal Antibody MIL93

"PART I :The patients confirming to the eligibility criteria will be assigned to the 6 dose groups (0.3mg/kg, 1mg/kg, 3mg/kg, 10mg/kg, 20mg/kg, 30mg/kg,respectively) based on the sequence of inclusion. Each patient will receive an intravenous infusion of MIL93 every 3 or 2 week on Day 1.~PART II:One recommended dose will be conducted from 6 dose groups based on results of PART I."

Trial Locations (1)

Unknown

RECRUITING

Cancer Hospital,Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing

All Listed Sponsors
lead

Beijing Mabworks Biotech Co., Ltd.

INDUSTRY

NCT04671875 - A Clinical Study of MIL93 in Solid Tumors. | Biotech Hunter | Biotech Hunter