drugset / Trial / NCT05564858

A Study of FDA022-BB05 in Subjects With Advanced Solid Malignant Tumors

NCT05564858 ↗

Non-randomizedSequentialOpen-labelTreatment

Summary

This is a Phase 1, open-label and two-part study to evaluate the safety, tolerability, pharmacokinetics and efficacy of FDA022-BB05 in participants with advanced/metastatic solid malignant tumors.

Timeline

Start
2023-01-16
Primary completion
2025-09
Completion
2025-11

Drugs

EvaluationDrugModalityDoseRoute
Subject FDA022-BB05 Monoclonal antibody — Intravenous

Indications