drugset / Trial / NCT06835569

A Study to Learn About Study Medicine ALTA3263 in Adults With Advanced Solid Tumors With KRAS Mutations

NCT06835569

Phase 1 Recruiting 448 enrolled Alterome Therapeutics, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to characterize the safety and tolerability of ALTA3263 in adults with advanced solid tumors with KRAS mutations.

Timeline

Start
2025-03-05
Primary completion
2029-05
Completion
2029-08

Drugs

EvaluationDrugModalityDoseRoute
Subject ALTA3263 Unknown Oral
Subject Carboplatin Small molecule Intravenous
Subject Cetuximab Monoclonal antibody Intravenous
Subject Cisplatin Other / unclassified Intravenous
Subject Gemcitabine Small molecule
Subject Irinotecan Small molecule
Subject Leucovorin Small molecule
Subject Midazolam Small molecule Oral
Subject Oxaliplatin Small molecule
Subject Paclitaxel Small molecule
Subject Pembrolizumab Monoclonal antibody Intravenous
Subject Pemetrexed Small molecule Intravenous
Subject fluorouracil Small molecule