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.
Primary Objective:
- To characterize the safety, dose limiting toxicities (DLTs), maximum tolerated dose (MTD) or maximum administered dose (MAD) and recommended Phase 2 dose (RP2D) of APR 1051.
Secondary Objectives:
1. To characterize the pharmacokinetics of APR-1051 and major metabolites and active metabolites of APR-1051 in serum including but not limited to Cmax, Tmax, AUC, t1/2, and Cmin.
2. To assess preliminary efficacy of APR-1051 according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 (PCWG3 criteria for patients with mCRPC) as measured by:
- Objective response rate (ORR: CR and PR)
- Duration of response (DOR)
- Clinical benefit rate (CBR: CR, PR, and SD)
- Duration of clinical benefit (DOCB)
- Time to response (TTR)
- Progression-free survival (PFS)
- Overall survival (OS)
- Rutgers University
Inclusion Criteria: - Age ≥ 18 years - Diagnosis of advanced/metastatic solid tumor - Measurable or evaluable disease per RECIST version 1.1 (radiographic disease progression per PCWG3 criteria for patients with mCRPC) - Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1 or Karnofsky Performance Status (KPS) ≥ 70% - Patients must have recovered to Grade 1 or baseline levels from toxicity or adverse events related to prior treatment for their cancer, excluding Grade ≤ 2 neuropathy, alopecia, or skin pigmentation - Adequate bone marrow and organ function - Women of child-bearing potential (WOCBP) or men of child-fathering potential must agree to use adequate contraception prior to study entry Exclusion Criteria: - Patient has had prior systemic anti-cancer therapy (cytotoxic chemotherapy, immunotherapy, targeted therapy) within 3 weeks (6 weeks in cases of mitomycin C, nitrosourea, lomustine) or at least 5 half-lives (whichever is shorter, but no less than 2 weeks) prior to Day 1 - Prior radiation therapy at the target lesion unless there is evidence of disease progression. If patient has had prior radiation therapy for disease progression, see Exclusion Criterion 1 for allowed interval between radiotherapy and Day 1 and recovery of AEs - Treatment with any investigational agent administered within 30 days or 5 half-lives, whichever is shorter, before the first dose of APR-1051 - Major surgery within 21 days prior to Day 1 - Concomitant treatment with other anti-cancer therapy, including chemotherapy, immunotherapy, biological therapy, radiation therapy (except palliative local radiation therapy), or other novel anti-cancer agents. Note: endocrine therapy for breast and prostate cancer is allowed along with agents to treat or prevent skeletal related events (zoledronic acid, pamidronate, denosumab) - Subjects with active (uncontrolled, metastatic) second malignancies or requiring therapy
Please note that we have obtained the inclusion and exclusion criteria information from the National Institutes of Health’s clinical trials web site ClinicalTrials.gov. The listed criteria may not necessarily reflect recent amendments to the protocol and the current criteria.
For further information about clinical trials, please contact us at 732-235-7356.