A Study of FDA018-ADC in Patients with Advanced Solid Tumors

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

78

Participants

Timeline

Start Date

October 22, 2021

Primary Completion Date

December 31, 2029

Study Completion Date

December 31, 2029

Conditions
Advanced/ Metastatic Solid Tumors
Interventions
DRUG

FDA018-ADC

FDA018-ADC will be administered via IV infusion on Day 1, 15 and 22 of a 35-Day cycle (Cycle 1) and on Day 1, 15 and 22 of a 35-Day cycle (Cycle 1) and on Day 1 and 8 of a 21-day cycle (Cycle 2 \~ Cycle 5) in dose escalation phase, and on Day 1 and 8 of a 21-day cycle(Cycle 1 \~ Cycle 6) in dose expansion phase, and Day 1 and 8 of a 21-day cycle in follow-up period until disease progression, unacceptable toxicity or death.

Trial Locations (1)

200000

Fudan University Shanghai Cancer Center, Shanghai

All Listed Sponsors
lead

Shanghai Fudan-Zhangjiang Bio-Pharmaceutical Co., Ltd.

INDUSTRY