drugset / Trial / NCT06979674

Study of ESG406 in Adults With Solid Tumors

NCT06979674 ↗

Phase 1 Recruiting 556 enrolled Shanghai Escugen Biotechnology Co., Ltd
NaSingle-groupOpen-labelTreatment

Summary

This study is an open-label, dose-escalation and cohort expansion Phase I study, aiming to evaluate the safety, tolerability, PK characteristics and preliminary efficacy of ESG406, and determine the MTD, RP2D and administration regimens of ESG406. The study includes the dose escalation study in Phase Ia and the cohort expansion study in Phase Ib.

Timeline

Start
2025-06-04
Primary completion
2028-04
Completion
2028-06

Drugs

EvaluationDrugModalityDoseRoute
Subject ESG406 Unknown — Intravenous

Indications

No indication recorded.