drugset / Trial / NCT06054477

Study of ALE.C04 in Patients With Head and Neck Cancer

NCT06054477 ↗

Phase 1/2 Terminated 21 enrolled Alentis Therapeutics AG
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety profile of ALE.C04 monotherapy and in combination with pembrolizumab, to characterize pharmacokinetics profile of ALE.C04, recommended Phase II dose (RP2D) for ALE.C04 in combination with pembrolizumab and to assess anti-tumor activity of ALE.C04 in combination with pembrolizumab in patients with Head and Neck Cancer.

Timeline

Start
2023-10-30
Primary completion
2025-02-12
Completion
2025-02-12

Outcome

Outcome not reported

Stopped: “Reprioritization of Trial”

Drugs

EvaluationDrugModalityDoseRoute
Subject ECLUTATUG Monoclonal antibody — —
Subject Pembrolizumab Monoclonal antibody 200 mg —