Safety and anti-tumor activity of lisavanbulin administered as 48-hour infusion in patients with ovarian cancer or recurrent glioblastoma: a phase 2a study

Conclusion.  This study demonstrated a favorable safety and tolerability profile of 48-hour continuous IV infusion of lisavanbulin in patients with solid extracranial tumors or glioblastoma.  Clinicaltrials.gov registration: NCT02895360.
Source: Investigational New Drugs - Category: Drugs & Pharmacology Source Type: research