Clinical Trial

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

Completed Phase 1
View on ClinicalTrials.gov →
Summary
This study aims to investigate the safety and efficacy of the IL-22BP in patients with refractory malignant solid tumors.
Protocol Amendment History 2 changes
critical Trial completed 2026-07-31
notable Primary completion moved earlier: 2026-07-01 -> 2026-01-20 2026-07-31
Trial Details
NCT Number NCT07040943
Lead Sponsor West China Hospital
Conditions Refractory Malignant Solid Tumors, mRNA Vaccine, Interleukin
Enrollment 6 participants
Start Date 2025-06-29
Primary Completion 2026-01-20 (estimated)
Study Completion 2026-07-20 (estimated)
Updated on ClinicalTrials.gov 2026-07-30