drugset / Trial / NCT06360354

A Study Evaluating Anvumetostat in Combination With Other Therapies in Participants With Advanced Gastrointestinal, Biliary Tract, or Pancreatic Cancers With Homozygous Methylthioadenosine Phosphorylase (MTAP)-Deletion (MTAPESTRY 103)

NCT06360354

Phase 1 Active not recruiting 120 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 gastrointestinal, biliary tract, or pancreatic cancers. 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 gastrointestinal, biliary tract, or pancreatic cancers.

Timeline

Start
2024-05-29
Primary completion
2026-10-31
Completion
2026-11-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Anvumetostat Unknown Oral
Background Gemcitabine Small molecule Intravenous
Background Irinotecan Small molecule Intravenous
Background Oxaliplatin Small molecule Intravenous
Background Paclitaxel Small molecule Intravenous
Background daraxonrasib Small molecule Oral
Background fluorouracil Small molecule Intravenous
Background mFOLFIRINOX Unknown Intravenous