Overview

Part A of the study is a dose escalation by cohort study of NXP800 administered to patients with advanced cancers. The study will identify the maximum tolerated dose (MTD) and propose dose and dose schedules for future studies.

In Part B doses selected in Part A are administered to patients with platinum-resistant, ARID1a-mutated ovarian carcinoma.

Principal investigator

David Bender
Obstetrics/Gynecology

Participate in this trial

Are you interested in enrolling in this study? Learn more here.

I'm Interested In Participating