drugset / Trial / NCT06333951

Anvumetostat Alone or in Combination With Other Therapies in Subjects With Advanced Thoracic Tumors With Homozygous MTAP-deletion (Master Protocol) (MTAPESTRY 104).

NCT06333951

Phase 1 Active not recruiting 49 enrolled Amgen
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The study aims to determine maximum tolerated dose (MTD) or recommended combination dose of the MTA-cooperative PRMT5 inhibitor Anvumetostat administered in combination with other therapies in adult participants with metastatic or locally advanced methylthioadenosine phosphorylase (MTAP)-deleted thoracic tumors. The study also aims to determine the safety profile of Anvumetostat administered in combination with other therapies in adult participants with metastatic or locally advanced MTAP-deleted thoracic tumors.

Timeline

Start
2024-09-17
Primary completion
2026-10-31
Completion
2026-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Anvumetostat Unknown Oral
Subject Carboplatin Small molecule Intravenous
Subject Paclitaxel Small molecule Intravenous
Subject Pembrolizumab Monoclonal antibody Intravenous
Subject Pemetrexed Small molecule Intravenous
Subject Sotorasib Small molecule Oral