drugset / Trial / NCT06154291

FIH XON7 in Advanced/Metastatic Solid Tumors

NCT06154291 ↗

Phase 1/2 Recruiting 255 enrolled Xenothera SAS
NaSingle-groupOpen-labelTreatment

Summary

This is a two-stage trial consisting of a Part I, dose escalation and dose-finding component to establish the Maximal Tolerated Dose (MTD), if any, and Recommended Part 2 Dose (RP2D) of XON7, followed by a Part II component to investigate anti-tumors efficacy in selected solid tumor types and to further evaluate safety and tolerability of XON7 at RP2D.

Timeline

Start
2023-11-14
Primary completion
2026-12
Completion
2027-11

Drugs

EvaluationDrugModalityDoseRoute
Subject XON7 Unknown 1.5 mg/kg Intravenous
Subject XON7 Unknown 3 mg/kg Intravenous
Subject XON7 Unknown 6 mg/kg Intravenous
Subject XON7 Unknown 12 mg/kg Intravenous
Subject XON7 Unknown 16 mg/kg Intravenous
Subject XON7 Unknown 20 mg/kg Intravenous