A Phase 1, Open-Label, Multicenter, First-In-Human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of APR-1051 in Patients With Advanced Solid Tumors
Summary
The purpose of this study is to assess the safety and effectiveness of APR-1051 through the performance of a Phase 1, open-label, safety, PK, and preliminary efficacy study of oral APR-1051 in patients with advanced solid tumors.
Arms & interventions
- DrugAPR-1051
WEE1 Inhibitor
Outcome measures
Primary
Treatment-related adverse events
* Part 1 dose escalation: Incidence of adverse Events (AE), serious AEs (SAE), treatment-related AEs, AEs that would qualify as a dose-limiting toxicity (DLT), changes in clinical laboratory values, vital signs, ECG, ECHO * Part 1 dose escalation: Severity of adverse Events (AE), serious AEs (SAE), treatment-related AEs, and changes in clinical laboratory values, vital signs, ECG, ECHO according to National Cancer Institute Common Terminology Criteria for Adverse Events v5.0
Time frame: Day 1 to 28, each cycle is 28 days
Recommended dose of APR-1051
•Part 1 dose escalation: Recommended Phase 2 Dose (RP2D) of APR-1051 monotherapy \[Time frame: Day 1 through to start of dose expansion phase\]. The RP2D of will be determined based on review of safety, tolerability, pharmacokinetics/pharmacodynamics, and preliminary efficacy data
Time frame: Day 1 to 28, each cycle is 28 days
Secondary
Pharmacokinetics: Cmax/Cmin of APR-1051
Time frame: Day 1 to 112
Pharmacokinetics: Tmax of APR-1051
Time frame: Day 1 to 112
Pharmacokinetics: AUC of APR-1051
Time frame: Day 1 to 112
Pharmacokinetics: t1/2 of APR-1051
Time frame: Day 1 to 112
Eligibility criteria
Study locations (3)
MD Anderson Cancer Center (MDACC)
Houston, Texas, 77030
NEXT Oncology -Dallas
Irving, Texas, 75039
NEXT Oncology -San Antonio
San Antonio, Texas, 78229