The purpose of this study is to determine the recommended Phase 2 dose(s) (RP2D\[s\]) and maximum tolerated dose (MTD) of JNJ-70218902 in Part 1, and to determine the safety of JNJ-70218902 RP2D(s) in Part 2.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Part 1 and Part 2: Number of Participants with Adverse Events (AEs) as a Measure of Safety and Tolerability
Timeframe: Up to 2.5 years
Part 1: Number of Participants with Dose-Limiting Toxicity (DLT)
Timeframe: Up to 21 days
Part 1 and Part 2: Number of Participants with AEs by Severity
Timeframe: Up to 2.5 years