30
Participants
Start Date
October 30, 2023
Primary Completion Date
October 30, 2024
Study Completion Date
December 31, 2025
PM1021, PM8001
Participants will be administered with PM1021 on Part A Day 1. Participants will be administered with PM1021 and PM8001 on Part B Day 1. PM1021 and PM8001 combination therapy administrated every 3 weeks from Part C Day 1 until disease progression, intolerable toxicity, until the patient withdraws/is withdrawn, or study completion.
Lead Sponsor
Biotheus Inc.
INDUSTRY