Safety, Tolerability, Pharmacokinetics (PK), and Primary Clinical Efficacy of LY01616 in Patients With Advanced Solid Tumors

PHASE1/PHASE2Enrolling by invitationINTERVENTIONAL
Enrollment

78

Participants

Timeline

Start Date

April 22, 2021

Primary Completion Date

August 31, 2024

Study Completion Date

October 30, 2024

Conditions
Advanced Solid Tumors
Interventions
DRUG

LY010616

IV infusion was 90min (±5min), with an interval of 3 weeks between the first administration and the second administration, and once every 2 weeks thereafter

Trial Locations (1)

Unknown

Cancer Hospital, Chinese Academy of Medical Sciences, Beijing

All Listed Sponsors
lead

Luye Pharma Group Ltd.

INDUSTRY