An open-label phase I dose-escalation study of the safety and pharmacokinetics of DMUC4064A in patients with platinum-resistant ovarian cancer
Published date:
10/06/2021
Excerpt:
DMUC4064A was administered once every 3 weeks to patients in 1.0–5.6 mg/kg dose escalation cohorts, followed by cohort expansion at the recommended Phase II dose (RP2D)....Among the 54 patients with high MUC16 immunohistochemistry scores, the clinical benefit rate was 46% (25 patients).