A Study Evaluating AMG 193 in Combination With Other Therapies in Participants With Advanced Gastrointestinal, Biliary Tract, or Pancreatic Cancers With Homozygous Methylthioadenosine Phosphorylase (MTAP)-Deletion

Description

The study aims to determine maximum tolerated dose (MTD) or recommended combination dose of the MTA-cooperative PRMT5 inhibitor AMG 193 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 AMG 193 administered in combination with other therapies in adult participants with metastatic or locally advanced MTAP-deleted gastrointestinal, biliary tract, or pancreatic cancers.

Conditions

Advanced Gastrointestinal, Biliary Tract, and Pancreatic Cancers

Study Overview

Study Details

Study overview

The study aims to determine maximum tolerated dose (MTD) or recommended combination dose of the MTA-cooperative PRMT5 inhibitor AMG 193 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 AMG 193 administered in combination with other therapies in adult participants with metastatic or locally advanced MTAP-deleted gastrointestinal, biliary tract, or pancreatic cancers.

A Phase 1b Study Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of AMG 193 in Combination With Other Therapies in Subjects With Advanced Gastrointestinal, Biliary Tract, or Pancreatic Cancers With Homozygous MTAP-deletion

A Study Evaluating AMG 193 in Combination With Other Therapies in Participants With Advanced Gastrointestinal, Biliary Tract, or Pancreatic Cancers With Homozygous Methylthioadenosine Phosphorylase (MTAP)-Deletion

Condition
Advanced Gastrointestinal, Biliary Tract, and Pancreatic Cancers
Intervention / Treatment

-

Contacts and Locations

Bakersfield

Comprehensive Blood and Cancer Center, Bakersfield, California, United States, 93309

Duarte

City of Hope National Medical Center, Duarte, California, United States, 91010

Los Angeles

Translational Research in Oncology US Inc, Trio Central Pharmacy, Los Angeles, California, United States, 90095

Santa Monica

University of California Los Angeles, Santa Monica, California, United States, 90404

Aurora

Rocky Mountain Cancer Centers, Aurora, Colorado, United States, 80012

Hartford

Hartford Hospital, Hartford, Connecticut, United States, 06106

Norwalk

Norwalk Hospital, Norwalk, Connecticut, United States, 06856

Indianapolis

Indiana University, Indianapolis, Indiana, United States, 46202

Louisville

Norton Cancer Institute, Louisville, Kentucky, United States, 40202

Boston

Dana-Farber Cancer Institute, Boston, Massachusetts, United States, 02215

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    18 Years to 100 Years

    Sexes Eligible for Study

    ALL

    Accepts Healthy Volunteers

    No

    Collaborators and Investigators

    Amgen,

    MD, STUDY_DIRECTOR, Amgen

    Study Record Dates

    2028-04-30