A Study to Evaluate Safety and Efficacy of ACT001 and Anti-PD-1 in Patients With Surgically Accessible Recurrent Glioblastoma Multiforme

PHASE1/PHASE2UnknownINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

September 22, 2021

Primary Completion Date

November 30, 2022

Study Completion Date

November 30, 2023

Conditions
Recurrent Glioblastoma Multiforme(GBM)
Interventions
DRUG

ACT001

Phase1b - Starting approximately 2 weeks prior to the scheduled surgery, patient will receive an assigned dose of ACT001 by mouth in combination with a single dose of 200 mg pembrolizumab via an intravenous (IV-through a tube in vain) infusion in the clinic. Then patient will self administer ACT001 capsules twice daily by mouth, at the dose to which patient is assigned, until the evening prior to scheduled surgery. Patient will then undergo surgery to remove all or part of tumor. This a standard 3+3 dose escalation.

DRUG

ACT001 + Pembrolizumab

Phase 2a - Starting approximately 2 weeks prior to the scheduled surgery, patient will receive a single dose of 200 mg pembrolizumab via an intravenous (IV) infusion in the clinic (an IV infusion means the drug will be delivered through a tube in your vein). Patient will then self-administer ACT001 capsules twice daily by mouth, at the dose to which patient is assigned, until the evening prior to scheduled surgery. Patient then will undergo surgery to remove all or part of tumor.

Trial Locations (1)

77030

RECRUITING

UT MD Anderson Cancer Center, Dept of Neuro-Oncology, Houston

All Listed Sponsors
collaborator

C3 Research Associates

UNKNOWN

collaborator

Avance Clinical Pty Ltd.

INDUSTRY

lead

Accendatech USA Inc.

INDUSTRY