Overview

Phase 1 Study of PTX-100 in Patients With Advanced Malignancies

Status:
Recruiting
Trial end date:
2023-04-30
Target enrollment:
Participant gender:
Summary
This is an open-label, non-randomized study to evaluate the PD, PK, and safety of 500 to 2000 mg/m2 PTX-100 in patients with advanced malignancies. PTX-100 will be administered by IV infusion over 60 minutes on days 1 to 5 of a 14-day cycle for 4 cycles unless toxicity is observed.
Phase:
Phase 1
Details
Lead Sponsor:
Prescient Therapeutics, Ltd.