Study of LM-102 in Subjects in Advanced Tumors

PHASE1TerminatedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

May 27, 2021

Primary Completion Date

May 19, 2022

Study Completion Date

May 19, 2022

Conditions
Advanced Solid Tumors
Interventions
DRUG

Drug:LM-102

Traditional '3+3' escalation design will be used. Dose escalation consists of five ascending dose levels of LM-102 (3 mg/kg, 10 mg/kg, 20 mg/kg, 30 mg/kg and 40 mg/kg). All subjects will be administered every 3 weeks (1 cycle=21 days) with a dose of LM-102 as a 2 h (120±10 min) intravenous (IV) infusion until the disease progression, intolerance, subject discontinuation/informed consent withdrawal, or at the discretion of the investigator in consultation with sponsor, at most till by one year.

Trial Locations (6)

44718

Gabrail Cancer and Research Center, Canton

46202

Indiana University Melvin and Bren Simon Cancer Center, Indianapolis

48202

Henry Ford Cancer Institute, Detroit

73104

Oklahoma University- Stephenson Cancer Center, Oklahoma City

77030

University of Texas MD Anderson Cancer Center, Houston

201203

Sarcoma Oncology Research Center, Cancer Center of Southern California, California City

Sponsors
All Listed Sponsors
lead

LaNova Medicines Limited

INDUSTRY