Clinical Trials

Sponsor: Replimune, Inc.

Sponsor Study ID: RPL-001-16

Study Title: An Open Label, Multicenter, Phase 1/2 Study of RP1 as a Single Agent and in Combination with PD1 Blockade in Patients with Solid Tumors

NCT Number: NCT03767348

Phase: II

Protocol Type: Treatment

Age Group: Adults

Disease Sites: Other Skin, Lung, Melanoma, Skin

Study Objectives: 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.



Study Documents    
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