drugset / Trial / NCT07040943

Clinical Trial of IL - 22BP Safety, Tolerability, and Antitumor Activity in Refractory Solid Tumors.

NCT07040943 ↗

Phase 1 Recruiting 6 enrolled West China Hospital
NaSingle-groupOpen-labelTreatment

Summary

This study aims to investigate the safety and efficacy of the IL-22BP in patients with refractory malignant solid tumors.

Timeline

Start
2025-06-29
Primary completion
2026-07-01
Completion
2026-07-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject IL-22BP Unknown 25 ug Other
Subject IL-22BP Unknown 50 ug Other