drugset / Trial / NCT07123103

A Study of XB371 Administered in Participants With Locally Advanced or Metastatic Solid Tumors

NCT07123103 ↗

Phase 1 Recruiting 150 enrolled Exelixis
Non-randomizedSequentialOpen-labelTreatment

Summary

The primary purpose of the study is to characterize the safety and tolerability of XB371. The dose-escalation cohorts and Part B of the expansion cohorts are non-randomized. Part A of the expansion cohorts is randomized.

Timeline

Start
2025-08-18
Primary completion
2027-11
Completion
2028-02

Drugs

EvaluationDrugModalityDoseRoute
Subject XB371 Unknown — Intravenous

Indications