A Phase 1b/2 Study of Sabizabulin, a Novel Oral Cytoskeleton Disruptor, in Men With Metastatic Castration-Resistant Prostate Cancer with Progression on an Androgen Receptor Targeting Agent.

Sabizabulin, an oral cytoskeleton disruptor was tested in a Phase 1b/2 clinical study in men with metastatic castration resistant prostate cancer (mCRPC).

The Phase 1b portion utilized a 3+3 design with escalating daily oral doses of 4. 5 mg - 81 mg and increasing schedule in 39 mCRPC patients treated with one or more androgen receptor targeting agents. Prior taxane chemotherapy was allowed. The Phase 2 portion tested a daily dose of 63 mg in 41 patients with no prior chemotherapy. Efficacy was assessed using PCWG3 and RECIST 1.1 criteria.

The MTD was not defined in the Phase 1b and the recommended Phase 2 dose was set at 63 mg/day. The most common adverse events (>10% frequency) at the 63 mg oral daily dosing (combined Phase 1b/2 data) were predominantly Grade 1-2 events. Grade ³3 events included diarrhea (7.4%), fatigue (5.6%) and ALT/AST elevations (5.6% and 3.7%, respectively). Neurotoxicity and neutropenia were not observed. Preliminary efficacy data in patients treated with {greater than or equal to}1 continuous cycle of 63 mg or higher included objective response rate in 6/29 (20.7%) patients with measurable disease (1 complete, 5 partial) and 14/48 (29.2%) patients had PSA declines. The Kaplan-Meier median radiographic progression-free survival was estimated to be 11.4 months (n=55). Durable responses lasting >2.75 years were observed.

This clinical trial demonstrated that chronic oral daily dosing of sabizabulin has a favorable safety profile with preliminary antitumor activity. These data support the ongoing Phase 3 VERACITY trial of sabizabulin in men with mCRPC.

Clinical cancer research : an official journal of the American Association for Cancer Research. 2022 Apr 13 [Epub ahead of print]

Mark C Markowski, Ronald Tutrone, Christopher Pieczonka, K Gary Barnette, Robert H Getzenberg, Domingo Rodriguez, MItchell S Steiner, Daniel R Saltzstein, Mario A Eisenberger, Emmanuel S Antonarakis

Johns Hopkins University School of Medicine, Baltimore, MD, United States., Chesapeake Urology Research Associates, Baltimore, Maryland, United States., Associated Medical Professionals of NY, Manlius, United States., Veru Inc, Miami, FL, United States., Urology San Antonio, San Antonio, TX, United States., Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD, United States., University of Minnesota, Minneapolis, United States.