38
Participants
Start Date
January 15, 2020
Primary Completion Date
November 30, 2023
Study Completion Date
June 30, 2024
Lintuzumab-Ac225
In the Phase I, patients will be enrolled into the following dose escalation cohorts: 0.50 μCi/kg, 1.0 μCi/kg, and 1.5 μCi/kg. If the 0.50 μCi/kg dose is determined to exceed the MTD, a 0.25 μCi/kg dose will be explored.
Venetoclax
400 mg daily will be taken orally on Days 1-21 of a 28-day cycle. There will be a ramp up of venetoclax dosing in the first cycle, with 100 mg administered on Day 1, 200 mg on Day 2, and 400 mg on Day 3 and Day 4 and later. Patients on antifungal azoles should receive one-half these doses, up to a maximum of 200 mg of venetoclax.
Spironolactone
25 mg by mouth daily, administered on Cycle 1 Day 15 and continued for 12 months after the subject's last treatment with lintuzumab-Ac225.
RECRUITING
Weill Cornell Medicine, New York
RECRUITING
University of Louisville, Louisville
RECRUITING
Ochsner Clinic Foundation, New Orleans
RECRUITING
University of California, Los Angeles
RECRUITING
Fred Hutchinson Cancer Research Center, Seattle
Lead Sponsor
Actinium Pharmaceuticals
INDUSTRY