A Study of MIL62 in Treatment of CD20 Positive B-cell Lymphomas

PHASE1CompletedINTERVENTIONAL
Enrollment

27

Participants

Timeline

Start Date

February 10, 2017

Primary Completion Date

May 30, 2019

Study Completion Date

May 29, 2020

Conditions
CD20-positive B Cell Non-Hodgkin Lymphoma
Interventions
DRUG

Recombinant Humanized Monoclonal Antibody MIL62 Injection

The patients confirming to the eligibility criteria will be assigned to the 5 dose groups (200mg, 400mg, 800mg, 1000mg, and 1500mg, respectively) based on the sequence of inclusion. Each patient received an intravenous infusion of MIL62 on Days 1, 8, and 15 of Cycle 1 and on Day 1 of Cycles 2-8 for a maximum of 8 cycles and 10 infusions. Each cycle was 21 days.

Trial Locations (1)

100021

Chinese Academy of Medical Sciences (CAMS) & Peking Union Medical College (PUMC), Beijing

All Listed Sponsors
lead

Beijing Mabworks Biotech Co., Ltd.

INDUSTRY

NCT04103905 - A Study of MIL62 in Treatment of CD20 Positive B-cell Lymphomas | Biotech Hunter | Biotech Hunter