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IMLT19000, Victor, RPL-001-16, Solid Tumor, RP1, Nivolumab

Research Question:
Is the drug RP1 alone and in combination with nivolumab safe and well tolerated in adult subjects with advanced and/or refractory solid tumors?

Basic Study Information

Purpose:
RPL-001-16 is a Phase 1/2, open label, dose escalation and expansion clinical study of RP1 alone and in combination with nivolumab in adult subjects with advanced and/or refractory solid tumors, to determine the maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D), as well as to evaluate preliminary efficacy.

Location: University of Rochester Medical Center
Study Reference #: IMLT19000

Lead Researcher (Principal Investigator)

Lead Researcher:  Adrienne Victor

Study Contact Information

Study Contact: Clinical Trials Office
Study Location: Wilmot Cancer Institute, University of Rochester Medical Center
Study Email: WCICTOResearch@urmc.rochester.edu

Additional Study Details

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