drugset / Trial / NCT06600321

A Study to Evaluate ALN-BCAT in Patients With Hepatocellular Carcinoma

NCT06600321 ↗

Phase 1 Recruiting 158 enrolled Alnylam Pharmaceuticals
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the dose escalation part of the study is to characterize the safety and tolerability of ALN-BCAT as monotherapy and in combination with pembrolizumab; and to determine the recommended dose(s) for expansion (RDFE) of ALN-BCAT as monotherapy and in combination with pembrolizumab. The purpose of the dose expansion part of the of the study is to evaluate the antitumor activity of ALN-BCAT as monotherapy and in combination with pembrolizumab; to characterize the safety and tolerability of ALN-BCAT as monotherapy and in combination with pembrolizumab.

Timeline

Start
2024-12-30
Primary completion
2027-09-30
Completion
2027-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject ALN-BCAT Unknown — Intravenous
Subject Pembrolizumab Monoclonal antibody — Intravenous