9
Participants
Start Date
May 27, 2021
Primary Completion Date
May 19, 2022
Study Completion Date
May 19, 2022
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.
Gabrail Cancer and Research Center, Canton
Indiana University Melvin and Bren Simon Cancer Center, Indianapolis
Henry Ford Cancer Institute, Detroit
Oklahoma University- Stephenson Cancer Center, Oklahoma City
University of Texas MD Anderson Cancer Center, Houston
Sarcoma Oncology Research Center, Cancer Center of Southern California, California City
Lead Sponsor
LaNova Medicines Limited
INDUSTRY