A Study of ATG-018 (ATR Inhibitor) Treatment in Patients With Advanced Solid Tumors and Hematological Malignancies

PHASE1TerminatedINTERVENTIONAL
Enrollment

22

Participants

Timeline

Start Date

July 8, 2022

Primary Completion Date

January 8, 2024

Study Completion Date

January 8, 2024

Conditions
Advanced Solid TumorsHematological Malignancies
Interventions
DRUG

ATG-018

"Dose Escalation Phase:~For both dose escalation groups, subjects will receive a single dose of ATG-018 monotherapy on Cycle 1 Day 1 (C1D1) for single dose PK samples' collection. From the morning dose on Cycle 1 Day 2, twice daily dosing (except Dose Level 1: 5 mg QD) will be initiated. Subject(s) will receive intermittent dosing in a 3 days on/4 days off schedule in 21-day cycles until disease progression or unacceptable toxicity.~Dose Expansion Phase :~Dose Expansion Phase will begin at the defined MTD/RP2D for solid tumors and hematological malignancies groups, to further evaluate the safety, tolerability, and PDx profile of ATG-018. Subjects with solid tumors and hematological malignancies will be enrolled."

Trial Locations (5)

Unknown

Icon Cancer Centre South Brisbane, Brisbane

Chris O'Brien Lifehouse, Camperdown

Austin Health, Heidelberg

Alfred Health, Melbourne

Liverpool Hospital, Sydney

Sponsors
All Listed Sponsors
lead

Antengene Discovery Limited

INDUSTRY

NCT05338346 - A Study of ATG-018 (ATR Inhibitor) Treatment in Patients With Advanced Solid Tumors and Hematological Malignancies | Biotech Hunter | Biotech Hunter