drugset / Trial / NCT06208124

A Study of IMM-6-415 in RAS/RAF Mutant Solid Tumors

NCT06208124 ↗

Phase 1/2 Completed 30 enrolled Immuneering Corporation
NaSingle-groupOpen-labelTreatment

Summary

This is a FIH, ascending dose study to characterize the safety, tolerability, optimal dose and preliminary anti-tumor activity of IMM-6-415 in participants with advanced or metastatic solid tumors harboring RAS or RAF oncogenic mutations.

Timeline

Start
2024-02-27
Primary completion
2025-04-30
Completion
2025-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject IMM-6-415 Unknown — Oral