drugset / Trial / NCT04762225

RPTR-168 in Patients With Human Papillomavirus Strain 16 (HPV-16) E6/E7 Positive Tumors and Melanoma

NCT04762225 ↗

Phase 1 Terminated 7 enrolled Repertoire Immune Medicines
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety and tolerability of escalating doses of RPTR-168 as a monotherapy in patients with HPV-16 E6/E7 positive tumors (HNSCC, cervical) and melanoma.

Timeline

Start
2021-05-10
Primary completion
2022-09-14
Completion
2022-10-11

Outcome

Outcome not reported

Stopped: “Development program terminated”

Drugs

EvaluationDrugModalityDoseRoute
Subject RPTR-168 Unknown — Intravenous