Venetoclax and Lintuzumab-Ac225 in AML Patients

PHASE1/PHASE2UnknownINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

January 15, 2020

Primary Completion Date

November 30, 2023

Study Completion Date

June 30, 2024

Conditions
Acute Myeloid LeukemiaRelapsed Adult AML
Interventions
BIOLOGICAL

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.

DRUG

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.

DRUG

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.

Trial Locations (5)

10021

RECRUITING

Weill Cornell Medicine, New York

40202

RECRUITING

University of Louisville, Louisville

70121

RECRUITING

Ochsner Clinic Foundation, New Orleans

90095

RECRUITING

University of California, Los Angeles

98109

RECRUITING

Fred Hutchinson Cancer Research Center, Seattle

Sponsors
All Listed Sponsors
lead

Actinium Pharmaceuticals

INDUSTRY