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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)

Protocol Number: 052606
Phase: Phase I
Applicable Disease Sites: Any Site
Drugs Involved: APR-1051
Principal Investigator: Sanjay Goel
Scope: National
Therapies Involved: Chemotherapy single agent systemic
Participating Institutions:
  • Rutgers University
Inclusion & Exclusion Criteria ►

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.

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