drugset / Trial / NCT04450901

Dose Escalation/Dose Expansion Study of YBL-006 in Patients With Advanced Solid Tumors

NCT04450901 ↗

Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase 1/2a, open-label, multicenter, dose-escalation/dose-expansion study of YBL-006, in participants with Advanced Solid Tumors. This multicenter study will be conducted in approximately 11-14 participants in the dose escalation phase, and approximately 39-76 participants in dose expansion phase.

Timeline

Start
2020-07-01
Primary completion
2023-03-31
Completion
2023-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject YBL-006 Unknown 0.5 mg/kg Intravenous
Subject YBL-006 Unknown 2 mg/kg Intravenous
Subject YBL-006 Unknown 5 mg/kg Intravenous
Subject YBL-006 Unknown 10 mg/kg Intravenous
Subject YBL-006 Unknown 200 mg Intravenous
Subject YBL-006 Unknown 300 mg Intravenous

Indications