A Phase 1/2 Study Evaluating AMG 337 in Asian Subjects

• Status: Completed
• Trial end date: 2018-12-07
• Target enrollment: 0
• Participant gender: All

Summary

This is a multicenter, Phase 1/2 study. The study will evaluate the tolerability, safety and activity of AMG 337 in Asian subjects who have advanced solid tumors (Phase 1) or subjects with MET amplified tumors with a focus on gastric/gastroesophageal junction/esophageal adenocarcinoma (Phase 2).

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Amgen

Criteria

Inclusion Criteria:

• Able to self administer daily AMG 337 as a whole capsule

• Male or female 20 years of age or over

• Phase 1: Subjects must have a pathologically confirmed, advanced solid tumor for which the subjects have received prior therapy for advanced disease, for which no standard therapy exists, or the subject refuses standard therapy.

• Phase 2: Subjects must have a pathologically confirmed, advanced G/GEJ/E adenocarcinoma (cohort 1) or other solid tumor (cohort 2) for which the subjects have received prior therapy for advanced disease, or for which no standard therapy exists, or the subject refuses standard therapy.

• Tumor MET amplified by protocol-specified centralized testing (phase 2 only).

• Phase 1: Measurable or non-measurable disease per RECIST v1.1

• Phase 2: Measurable disease per RECIST v1.1 guidelines. Cohort 2 may include subjects with advanced MET amplified G/GEJ/E adenocarcinoma with non-measurable tumor per RECIST v1.1.

• (ECOG) Performance Status of 0, 1, or 2

• Other protocol defined inclusion criteria may apply.

Exclusion Criteria:

• Known central nervous system metastases.

• Subject is a candidate for curative surgery or definitive chemoradiation.

• Peripheral edema > grade 1.

• Subjects who have persistent gastric outlet obstruction, complete dysphagia or are dependent upon jejunostomy for feeding. Significant gastrointestinal disorder(s) that in the opinion of the Investigator may influence drug absorption.

• Currently receiving any anti-tumor treatments, or less than 14 days prior to enrollment since ending anti-tumor treatment.

• Prior treatment with small molecule inhibitors of the MET pathway.

• Other protocol defined exclusion criteria may apply.