APL-501 Study for Select Advanced or Relapsed/Recurrent Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

March 27, 2017

Primary Completion Date

February 25, 2022

Study Completion Date

February 25, 2022

Conditions
Solid TumorMicrosatellite InstabilityMismatch Repair DeficiencyCancer of Unknown Primary Site
Interventions
DRUG

APL-501

"Subjects will be assigned to a dose level in the order of study entry. Treatment includes a minimum of four 28-day cycles at three planned dose levels (1, 3, and 10 mg/kg). In the Dose Escalation Segment, each treatment cycle is comprised of 2 doses of study drug administered on Days 1 and 15 of a 28-day cycle. In the Cohort Extension, the treatment cycle will consist of 2 doses of study drug administered on Days 1 and 15 of a 28-day cycle.~In Dose and Disease Expansion, the treatment cycle will consist of 2 doses of study drug (non-weight based dosing of 400 mg) administered on Days 1 and 15 of a 28-day cycle."

Trial Locations (5)

2050

Chris O'Brien Lifehouse, Camperdown

3000

Peter MaCallum Cancer Centre, Melbourne

3004

Nucleus Network, Melbourne

3144

Cabrini Health Limited, Malvern

6009

Linear Clinical Research, Nedlands

All Listed Sponsors
collaborator

Novotech (Australia) Pty Limited

INDUSTRY

collaborator

Apollomics Inc. (formerly CBT Pharmaceuticals, Inc.)

UNKNOWN

lead

Apollomics (Australia) Pty. Ltd.

INDUSTRY

NCT03053466 - APL-501 Study for Select Advanced or Relapsed/Recurrent Solid Tumors | Biotech Hunter | Biotech Hunter