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Clinical Trial 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 as monotherapy and to assess anti-tumor activity of ALE.C04 monotherapy and in combination with pembrolizumab in patients with Head and Neck Cancer.


Clinical Trial Description

The study comprises a phase I and a phase II. The phase I dose escalation part for both ALE.C04 monotherapy and in combination with pembrolizumab and a recommended dose for expansion (RDE) part for both ALE.C04 monotherapy and in combination with pembrolizumab. The phase II comprises a 1:1 randomized 2 arms assessing 2 dose levels of ALE.C04 as monotherapy and a 1:1 randomized 2 arms assessing ALE.C04 and pembrolizumab given in combination versus pembrolizumab monotherapy ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06054477
Study type Interventional
Source Alentis Therapeutics AG
Contact Luigi Manenti, MD
Phone 41782304288
Email ale.c04.01@alentis.ch
Status Recruiting
Phase Phase 1/Phase 2
Start date October 30, 2023
Completion date February 2028

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