AZD4573 in Novel Combinations With Anti-cancer Agents in Patients With Advanced Blood Cancer

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

February 17, 2021

Primary Completion Date

September 8, 2023

Study Completion Date

February 27, 2025

Conditions
Advanced Haematological Malignancies
Interventions
DRUG

AZD4573

AZD4573 will be administered as an absolute (flat) dose, 2-hour (± 15 minutes) IV infusion once weekly (as monotherapy for Module 2 only) and in combination with orally administered acalabrutinib twice daily continuously. For both Part A and Part B of this study, Cycle 1 consists of 5 weeks, with a dose ramp-up. Subsequent cycles are 21 days (3 weeks) with once weekly dosing of AZD4573 in combination with acalabrutinib twice daily continuously (in Module 1 and Module 2, period 2).

DRUG

Acalabrutinib

Oral Acalabrutinib capsule will be administered twice daily continuously from Day 1 of Cycle 1 Week 1 in combination with AZD4573.

Trial Locations (17)

3168

Research Site, Clayton

6009

Research Site, Nedlands

59037

Research Site, Lille

77030

Research Site, Houston

84112

Research Site, Salt Lake City

91010

Research Site, Duarte

92093-0052

Research Site, La Jolla

G1R 2J6

Research Site, Québec

D08 NHY1

Research Site, Dublin

H91 YR71

Research Site, Galway

30-510

Research Site, Krakow

03080

Research Site, Seoul

05505

Research Site, Seoul

06351

Research Site, Seoul

08035

Research Site, Barcelona

07120

Research Site, Palma de Mallorca

PL6 8DH

Research Site, Plymouth

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Parexel

INDUSTRY

lead

AstraZeneca

INDUSTRY