U.S., June 25 -- ClinicalTrials.gov registry received information related to the study (NCT07664150) titled 'CW-301 FIH Study of CAN016' on June 14.
Brief Summary: A Phase I/II, Open-Label, Non-Randomized, Multi-Centre First-in-Human Study of CAN016 in Patients with Advanced Solid Tumors
Study Start Date: June 18
Study Type: INTERVENTIONAL
Condition:
Patients With Advanced Solid Tumors
Intervention:
DRUG: CAN016
CAN016 will be administered intravenously into each patient on Day 1 of Cycle 1. Patients will continue to receive CAN016 Q3W until unacceptable toxicity, progressive disease, or withdrawal of consent, death, lost to F/U, or other discontinuation criteria is met.
DRUG: CAN016
an initial dose of CAN016 0.75 mg/kg will be ad...