drugset / Trial / NCT06248411

A Clinical Study of KK2260 in Patients With Advanced or Metastatic Solid Tumors

NCT06248411 ↗

Phase 1 Recruiting 189 enrolled Kyowa Kirin, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This is the first in human study of KK2260. In Part 1a, the maximum tolerated dose (MTD) will be determined while evaluating the safety and tolerability of KK2260 in patients with advanced or metastatic solid tumors (any cancer type). In Part 1b and Part 2, at least two dosing regimens and two dosing regimens by cancer type, respectively, will be selected, and the safety, tolerability, and efficacy of each regimen will be evaluated.

Timeline

Start
2023-11-01
Primary completion
2029-10-31
Completion
2030-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject KK2260 Unknown — Intravenous

Indications

No indication recorded.